Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10725 |
| ensemblid | ENSG00000102908.23 |
| hgncid | 7774 |
| symbol | NFAT5 |
| name | nuclear factor of activated T cells 5 |
| refseq_nuc | NM_138713.4 |
| refseq_prot | NP_619727.2 |
| ensembl_nuc | ENST00000349945.7 |
| ensembl_prot | ENSP00000338806.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 69565966 |
| end | 69704654 |
| strand | + |
| ver | v1.2 |
| region | chr16:69565966-69704654 |
| region5000 | chr16:69560966-69709654 |
| regionname0 | NFAT5_chr16_69565966_69704654 |
| regionname5000 | NFAT5_chr16_69560966_69709654 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1549 | 372 | 92 | 61 | 166 | 16 | 35 | 135 | NFAT5_chr16_69560966_69709654 | NFAT5 | MPSDF others(1544): Show |
chr16 | 69560966 | 69709654 |
| a0002 | 0/0 | 1549 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | MPSDF others(1544): Show |
chr16 | 69560966 | 69709654 |
| a0003 | 0/0 | 1549 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NFAT5_chr16_69560966_69709654 | NFAT5 | MPSDF others(1544): Show |
chr16 | 69560966 | 69709654 |
| a0004 | 0/0 | 1549 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | MPSDF others(1544): Show |
chr16 | 69560966 | 69709654 |
| a0005 | 0/0 | 1549 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | MPSDF others(1544): Show |
chr16 | 69560966 | 69709654 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4647 | 344 | 72 | 59 | 163 | 14 | 34 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0001c0002 | 0/0 | 4647 | 19 | 19 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0001c0003 | 0/0 | 4647 | 4 | 0 | 2 | 0 | 2 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0001c0006 | 0/0 | 4647 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0001c0007 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0001c0008 | 0/0 | 4647 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0001c0011 | 0/0 | 4647 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0002c0004 | 0/0 | 4647 | 3 | 0 | 0 | 0 | 2 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0003c0005 | 0/0 | 4647 | 3 | 0 | 0 | 3 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0004c0010 | 0/0 | 4647 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 | ||
| a0005c0009 | 0/0 | 4647 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | ATGCC others(4642): Show |
chr16 | 69560966 | 69709654 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 13289 | 75 | 13 | 8 | 41 | 4 | 9 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0002 | 1/1 | 13289 | 59 | 5 | 18 | 19 | 5 | 10 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0003 | 0/0 | 13290 | 26 | 0 | 1 | 23 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0004 | 0/0 | 13290 | 21 | 0 | 0 | 20 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0005 | 0/0 | 13290 | 21 | 5 | 4 | 6 | 2 | 4 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0006 | 0/0 | 13287 | 20 | 1 | 5 | 14 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13282): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0007 | 0/0 | 13288 | 15 | 0 | 3 | 11 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0009 | 0/0 | 13289 | 11 | 10 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0010 | 0/0 | 13292 | 9 | 1 | 1 | 5 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13287): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0011 | 0/0 | 13288 | 8 | 8 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0012 | 0/0 | 13289 | 6 | 0 | 6 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0013 | 0/0 | 13288 | 5 | 0 | 5 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0014 | 0/0 | 13292 | 5 | 0 | 0 | 5 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13287): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0015 | 0/0 | 13289 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0016 | 0/0 | 13292 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13287): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0017 | 0/0 | 13290 | 3 | 0 | 1 | 0 | 1 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0018 | 0/0 | 13290 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0019 | 0/0 | 13286 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13281): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0020 | 0/0 | 13287 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13282): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0021 | 0/0 | 13289 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0022 | 0/0 | 13289 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0023 | 0/0 | 13289 | 2 | 0 | 2 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0024 | 0/0 | 13290 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0025 | 0/0 | 13287 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13282): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0027 | 0/0 | 13289 | 2 | 0 | 1 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0028 | 0/0 | 13286 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13281): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0029 | 0/0 | 13290 | 2 | 0 | 0 | 0 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0030 | 0/0 | 13288 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0031 | 0/0 | 13291 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13286): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0032 | 0/0 | 13291 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13286): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0033 | 0/0 | 13289 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0034 | 0/0 | 13289 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0035 | 0/0 | 13289 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0036 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0037 | 0/0 | 13287 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13282): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0038 | 0/0 | 13288 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0039 | 0/0 | 13289 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0040 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0041 | 0/0 | 13288 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0042 | 0/0 | 13289 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0043 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0044 | 0/0 | 13290 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0045 | 0/0 | 13286 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13281): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0046 | 0/0 | 13290 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0047 | 0/0 | 13287 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13282): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0048 | 0/0 | 13288 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0050 | 0/0 | 13288 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0052 | 0/0 | 13289 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0053 | 0/0 | 13290 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0054 | 0/0 | 13288 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0055 | 0/0 | 13291 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13286): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0056 | 0/0 | 13290 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0057 | 0/0 | 13290 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0058 | 0/0 | 13292 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13287): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0059 | 0/0 | 13290 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0060 | 0/0 | 13290 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0001t0061 | 0/0 | 13288 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0002t0008 | 0/0 | 13288 | 16 | 16 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0002t0026 | 0/0 | 13288 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0002t0049 | 0/0 | 13290 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0003t0002 | 0/0 | 13289 | 4 | 0 | 2 | 0 | 2 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0006t0004 | 0/0 | 13290 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0001c0007t0051 | 0/0 | 13288 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0001c0008t0001 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0001c0011t0005 | 0/0 | 13290 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13285): Show |
chr16 | 69560966 | 69709654 |
| a0002c0004t0007 | 0/0 | 13288 | 3 | 0 | 0 | 0 | 2 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13283): Show |
chr16 | 69560966 | 69709654 |
| a0003c0005t0001 | 0/0 | 13289 | 3 | 0 | 0 | 3 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0004c0010t0002 | 0/0 | 13289 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| a0005c0009t0002 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | AGATT others(13284): Show |
chr16 | 69560966 | 69709654 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0338 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0013g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0013g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0013g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0013g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0014g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0014g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0014g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0014g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0014g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0015g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0015g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0015g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0016g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0016g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0016g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0017g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0017g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0017g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0018g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0018g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0019g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0019g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0019g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0020g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0020g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0021g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0021g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0022g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0022g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0023g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0023g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0024g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0024g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0025g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0025g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0027g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0027g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0028g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0028g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0029g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0029g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0030g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0031g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0032g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0033g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0034g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0035g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0036g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0037g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0038g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0039g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0040g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0041g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0042g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0043g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0044g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0045g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0046g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0047g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0048g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0050g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0052g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0053g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0054g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0055g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0056g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0057g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0058g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0059g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0060g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0061g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0026g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0026g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0049g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0006t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0006t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0007t0051g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0008t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0011t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0002c0004t0007g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0002c0004t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0002c0004t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0003c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0003c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0003c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0004c0010t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0005c0009t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0093 | EUR | GBR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | GBR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00140 | hp2 | a0001 | c0001 | t0034 | g0284 | EUR | GBR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0115 | EUR | FIN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0184 | EUR | FIN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0067 | EUR | FIN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00408 | hp2 | a0001 | c0006 | t0004 | g0027 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00423 | hp1 | a0001 | c0001 | t0043 | g0204 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0032 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00609 | hp2 | a0001 | c0001 | t0046 | g0033 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00733 | hp1 | a0001 | c0001 | t0012 | g0260 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0069 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0320 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0164 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0180 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0174 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01074 | hp1 | a0001 | c0001 | t0059 | g0034 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01074 | hp2 | a0004 | c0010 | t0002 | g0040 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01081 | hp2 | a0001 | c0001 | t0013 | g0242 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0264 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0064 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0331 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0189 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0333 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0198 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01255 | hp1 | a0001 | c0001 | t0042 | g0079 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01255 | hp2 | a0001 | c0001 | t0017 | g0375 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01256 | hp2 | a0001 | c0001 | t0013 | g0273 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01257 | hp1 | a0001 | c0001 | t0023 | g0321 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01258 | hp1 | a0001 | c0001 | t0023 | g0322 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01258 | hp2 | a0001 | c0001 | t0013 | g0002 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01261 | hp2 | a0001 | c0001 | t0013 | g0002 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0366 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01358 | hp2 | a0001 | c0001 | t0012 | g0343 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01496 | hp1 | a0001 | c0001 | t0012 | g0344 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01496 | hp2 | a0001 | c0001 | t0027 | g0052 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01515 | hp1 | a0002 | c0004 | t0007 | g0179 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0335 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0070 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0068 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01517 | hp2 | a0002 | c0004 | t0007 | g0171 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01884 | hp1 | a0001 | c0001 | t0018 | g0209 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01884 | hp2 | a0001 | c0002 | t0026 | g0023 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01891 | hp1 | a0001 | c0001 | t0020 | g0217 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01891 | hp2 | a0001 | c0002 | t0008 | g0016 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01928 | hp2 | a0001 | c0001 | t0013 | g0239 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01934 | hp1 | a0001 | c0001 | t0035 | g0281 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01943 | hp2 | a0001 | c0001 | t0012 | g0307 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0173 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02015 | hp1 | a0001 | c0001 | t0060 | g0349 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02015 | hp2 | a0005 | c0009 | t0002 | g0081 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02055 | hp1 | a0001 | c0002 | t0008 | g0018 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0341 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0050 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02129 | hp2 | a0001 | c0001 | t0044 | g0172 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02132 | hp2 | a0001 | c0001 | t0010 | g0348 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | CDX | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CDX | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CDX | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | CDX | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02257 | hp1 | a0001 | c0001 | t0057 | g0037 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02257 | hp2 | a0001 | c0001 | t0016 | g0362 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0045 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0169 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02280 | hp2 | a0001 | c0002 | t0008 | g0012 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02300 | hp1 | a0001 | c0001 | t0012 | g0246 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0197 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0319 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02572 | hp1 | a0001 | c0001 | t0019 | g0368 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02572 | hp2 | a0001 | c0001 | t0028 | g0373 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0161 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02615 | hp2 | a0001 | c0001 | t0019 | g0369 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0309 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0203 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0310 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02647 | hp1 | a0001 | c0002 | t0008 | g0370 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02683 | hp1 | a0002 | c0004 | t0007 | g0186 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02717 | hp1 | a0001 | c0001 | t0037 | g0215 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0117 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02723 | hp2 | a0001 | c0002 | t0008 | g0024 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0329 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0313 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0118 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02886 | hp2 | a0001 | c0002 | t0008 | g0001 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02895 | hp1 | a0001 | c0001 | t0025 | g0340 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02895 | hp2 | a0001 | c0002 | t0008 | g0021 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02896 | hp1 | a0001 | c0001 | t0045 | g0363 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0202 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0201 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02897 | hp2 | a0001 | c0002 | t0008 | g0017 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02922 | hp2 | a0001 | c0002 | t0008 | g0001 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02965 | hp1 | a0001 | c0002 | t0008 | g0028 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0087 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02970 | hp2 | a0001 | c0002 | t0008 | g0013 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03017 | hp1 | a0001 | c0001 | t0027 | g0175 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0336 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03041 | hp2 | a0001 | c0001 | t0019 | g0367 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03098 | hp1 | a0001 | c0001 | t0025 | g0339 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03098 | hp2 | a0001 | c0001 | t0028 | g0372 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03130 | hp1 | a0001 | c0002 | t0049 | g0019 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0211 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0311 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03139 | hp2 | a0001 | c0001 | t0054 | g0160 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03195 | hp2 | a0001 | c0002 | t0008 | g0001 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03209 | hp1 | a0001 | c0001 | t0018 | g0337 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03209 | hp2 | a0001 | c0001 | t0055 | g0345 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03225 | hp2 | a0001 | c0001 | t0039 | g0218 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03239 | hp2 | a0001 | c0001 | t0010 | g0360 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0365 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03453 | hp2 | a0001 | c0002 | t0008 | g0001 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0020 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0119 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03579 | hp2 | a0001 | c0001 | t0050 | g0194 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0330 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03688 | hp1 | a0001 | c0001 | t0029 | g0371 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03704 | hp1 | a0001 | c0001 | t0017 | g0376 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03704 | hp2 | a0001 | c0001 | t0033 | g0275 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0332 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0135 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04115 | hp1 | a0001 | c0001 | t0029 | g0056 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04199 | hp2 | a0001 | c0011 | t0005 | g0208 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0361 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04204 | hp2 | a0001 | c0001 | t0010 | g0346 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | CHB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | CHB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0325 | EAS | CHB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18906 | hp1 | a0001 | c0001 | t0020 | g0216 | AFR | YRI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18906 | hp2 | a0001 | c0002 | t0008 | g0014 | AFR | YRI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18939 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0193 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18943 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0356 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18957 | hp2 | a0001 | c0001 | t0041 | g0060 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18966 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18966 | hp2 | a0001 | c0001 | t0048 | g0300 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18972 | hp1 | a0003 | c0005 | t0001 | g0258 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0192 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18973 | hp2 | a0001 | c0001 | t0031 | g0244 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18977 | hp1 | a0001 | c0001 | t0014 | g0351 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18980 | hp1 | a0001 | c0001 | t0032 | g0230 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18981 | hp1 | a0001 | c0001 | t0024 | g0099 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18982 | hp1 | a0003 | c0005 | t0001 | g0248 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18982 | hp2 | a0001 | c0001 | t0007 | g0181 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18984 | hp2 | a0001 | c0001 | t0022 | g0263 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18985 | hp1 | a0001 | c0001 | t0036 | g0227 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18985 | hp2 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18991 | hp1 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18992 | hp1 | a0001 | c0001 | t0061 | g0178 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18992 | hp2 | a0003 | c0005 | t0001 | g0259 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18993 | hp2 | a0001 | c0001 | t0022 | g0265 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19001 | hp1 | a0001 | c0001 | t0024 | g0063 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0353 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19005 | hp2 | a0001 | c0001 | t0014 | g0350 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19010 | hp2 | a0001 | c0001 | t0014 | g0347 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19012 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19030 | hp1 | a0001 | c0001 | t0047 | g0342 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0200 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19043 | hp1 | a0001 | c0001 | t0058 | g0357 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19055 | hp2 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19058 | hp2 | a0001 | c0001 | t0056 | g0141 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19060 | hp1 | a0001 | c0001 | t0040 | g0266 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19065 | hp2 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19066 | hp1 | a0001 | c0001 | t0014 | g0352 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19068 | hp1 | a0001 | c0008 | t0001 | g0296 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19078 | hp1 | a0001 | c0001 | t0021 | g0226 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19078 | hp2 | a0001 | c0006 | t0004 | g0026 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19080 | hp2 | a0001 | c0001 | t0010 | g0355 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19081 | hp1 | a0001 | c0001 | t0030 | g0269 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19084 | hp2 | a0001 | c0001 | t0021 | g0235 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19085 | hp2 | a0001 | c0001 | t0010 | g0354 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19086 | hp2 | a0001 | c0001 | t0014 | g0358 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0359 | AFR | ASW | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0312 | AFR | ASW | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20752 | hp1 | a0001 | c0001 | t0017 | g0374 | EUR | TSI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0328 | EUR | TSI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | TSI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | TSI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20905 | hp1 | a0001 | c0001 | t0053 | g0162 | SAS | GIH | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | GIH | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02109 | hp1 | a0001 | c0002 | t0026 | g0022 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02109 | hp2 | a0001 | c0001 | t0038 | g0314 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0212 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0364 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0088 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03471 | hp1 | a0001 | c0002 | t0008 | g0015 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0213 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG06807 | hp2 | a0001 | c0007 | t0051 | g0006 | AFR | USA | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | USA | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | USA | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA21309 | hp2 | a0001 | c0001 | t0052 | g0199 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0338 | REF | REF | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0170 | REF | REF | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69684893 | C | G | 1 | a0003 | 3 | NA18972.hp1 NA18982.hp1 NA18992.hp2 |
missense_variant | MODERATE | c.1697C>G | p.Ala566Gly | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/15 | 2033/13289 | 1697/4650 | 566/1549 | chr16 | 69684893 | |||
| chr16:69691794 | T | G | 1 | a0002 | 3 | HG01515.hp1 HG01517.hp2 HG02683.hp1 |
missense_variant | MODERATE | c.1969T>G | p.Ser657Ala | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/15 | 2305/13289 | 1969/4650 | 657/1549 | chr16 | 69691794 | |||
| chr16:69692029 | A | T | 1 | a0004 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2204A>T | p.Gln735Leu | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/15 | 2540/13289 | 2204/4650 | 735/1549 | chr16 | 69692029 | |||
| chr16:69692166 | C | G | 1 | a0005 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2341C>G | p.Pro781Ala | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/15 | 2677/13289 | 2341/4650 | 781/1549 | chr16 | 69692166 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69647317 | G | A | 1 | a0001c0006 | 2 | HG00408.hp2 NA19078.hp2 |
synonymous_variant | LOW | c.543G>A | p.Gly181Gly | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/15 | 879/13289 | 543/4650 | 181/1549 | chr16 | 69647317 | |||
| chr16:69647467 | A | G | 1 | a0001c0011 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.693A>G | p.Lys231Lys | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/15 | 1029/13289 | 693/4650 | 231/1549 | chr16 | 69647467 | |||
| chr16:69659746 | T | C | 1 | a0001c0007 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1216T>C | p.Leu406Leu | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/15 | 1552/13289 | 1216/4650 | 406/1549 | chr16 | 69659746 | |||
| chr16:69691904 | G | A | 1 | a0001c0008 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.2079G>A | p.Leu693Leu | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/15 | 2415/13289 | 2079/4650 | 693/1549 | chr16 | 69691904 | |||
| chr16:69692351 | G | A | 1 | a0001c0003 | 4 | HG00733.hp2 HG01167.hp1 HG01516.hp2 others(1): Show |
synonymous_variant | LOW | c.2526G>A | p.Glu842Glu | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/15 | 2862/13289 | 2526/4650 | 842/1549 | chr16 | 69692351 | |||
| chr16:69693176 | T | C | 1 | a0001c0002 | 19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
synonymous_variant | LOW | c.3351T>C | p.Ile1117Ile | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/15 | 3687/13289 | 3351/4650 | 1117/1549 | chr16 | 69693176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69566046 | T | TC | 20 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(17): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-251dupC | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/15 | 250 | INFO_REALIGN_3_PRIME | chr16 | 69566046 | |||||
| chr16:69566155 | A | G | 1 | a0001c0001t0061 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-147A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/15 | 147 | chr16 | 69566155 | ||||||
| chr16:69696523 | A | G | 59 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(56): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*172A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 1152 | chr16 | 69696523 | ||||||
| chr16:69696652 | A | G | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(14): Show |
98 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*301A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 1281 | chr16 | 69696652 | ||||||
| chr16:69696885 | G | A | 1 | a0001c0001t0053 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 1514 | chr16 | 69696885 | ||||||
| chr16:69696916 | G | A | 1 | a0001c0001t0044 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*565G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 1545 | chr16 | 69696916 | ||||||
| chr16:69697205 | A | G | 1 | a0001c0001t0060 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*854A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 1834 | chr16 | 69697205 | ||||||
| chr16:69697907 | A | G | 1 | a0001c0001t0040 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1556A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 2536 | chr16 | 69697907 | ||||||
| chr16:69697939 | C | CT | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(12): Show |
97 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1605dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 2586 | INFO_REALIGN_3_PRIME | chr16 | 69697939 | |||||
| chr16:69697939 | CT | C | 28 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(25): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1605delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 2585 | INFO_REALIGN_3_PRIME | chr16 | 69697939 | |||||
| chr16:69697939 | CTT | C | 6 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0016 others(3): Show |
32 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1604_*1605delTT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 2584 | INFO_REALIGN_3_PRIME | chr16 | 69697939 | |||||
| chr16:69698411 | T | C | 1 | a0001c0001t0023 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2060T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 3040 | chr16 | 69698411 | ||||||
| chr16:69699106 | G | A | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(13): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2755G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 3735 | chr16 | 69699106 | ||||||
| chr16:69699144 | A | G | 1 | a0001c0001t0059 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2793A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 3773 | chr16 | 69699144 | ||||||
| chr16:69699557 | G | A | 59 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(56): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3206G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4186 | chr16 | 69699557 | ||||||
| chr16:69699667 | A | T | 1 | a0001c0001t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3316A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4296 | chr16 | 69699667 | ||||||
| chr16:69699686 | A | G | 1 | a0001c0001t0052 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3335A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4315 | chr16 | 69699686 | ||||||
| chr16:69699754 | T | C | 2 | a0001c0001t0016 a0001c0001t0045 |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3403T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4383 | chr16 | 69699754 | ||||||
| chr16:69699762 | T | G | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(13): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*3411T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4391 | chr16 | 69699762 | ||||||
| chr16:69699814 | T | TTC | 5 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0031 others(2): Show |
9 | HG01255.hp2 HG02129.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3485_*3486dupCT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4467 | INFO_REALIGN_3_PRIME | chr16 | 69699814 | |||||
| chr16:69699834 | C | T | 1 | a0001c0001t0039 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3483C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4463 | chr16 | 69699834 | ||||||
| chr16:69699834 | CTCTG | C | 1 | a0001c0001t0019 | 3 | HG02572.hp1 HG02615.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3485_*3488delCTGT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4465 | INFO_REALIGN_3_PRIME | chr16 | 69699834 | |||||
| chr16:69699838 | G | C | 2 | a0001c0001t0005 a0001c0001t0006 |
4 | HG02451.hp2 NA18991.hp1 NA18994.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3487G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4467 | chr16 | 69699838 | ||||||
| chr16:69699838 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0003 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3501_*3514delATGT others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4481 | INFO_REALIGN_3_PRIME | chr16 | 69699838 | |||||
| chr16:69699852 | A | ATG | 7 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0032 others(4): Show |
19 | HG00609.hp2 HG00738.hp2 HG02015.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3523_*3524dupGT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4505 | INFO_REALIGN_3_PRIME | chr16 | 69699852 | |||||
| chr16:69699852 | A | ATGTG | 1 | a0001c0001t0016 | 3 | HG02257.hp2 HG02486.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3521_*3524dupGTGT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4505 | INFO_REALIGN_3_PRIME | chr16 | 69699852 | |||||
| chr16:69699852 | A | G | 1 | a0001c0001t0045 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3501A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4481 | chr16 | 69699852 | ||||||
| chr16:69699852 | ATG | A | 5 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0028 others(2): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3523_*3524delGT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4503 | INFO_REALIGN_3_PRIME | chr16 | 69699852 | |||||
| chr16:69699856 | G | A | 1 | a0001c0001t0013 | 5 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3505G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4485 | chr16 | 69699856 | ||||||
| chr16:69699983 | A | G | 3 | a0001c0001t0017 a0001c0001t0028 a0001c0007t0051 |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3632A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4612 | chr16 | 69699983 | ||||||
| chr16:69700093 | C | T | 1 | a0001c0001t0040 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3742C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 4722 | chr16 | 69700093 | ||||||
| chr16:69700418 | G | A | 1 | a0001c0001t0047 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4067G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5047 | chr16 | 69700418 | ||||||
| chr16:69700600 | C | A | 21 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(18): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*4249C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5229 | chr16 | 69700600 | ||||||
| chr16:69700660 | C | T | 25 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(22): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4309C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5289 | chr16 | 69700660 | ||||||
| chr16:69700773 | T | C | 1 | a0001c0001t0050 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4422T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5402 | chr16 | 69700773 | ||||||
| chr16:69700870 | C | T | 1 | a0001c0001t0043 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4519C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5499 | chr16 | 69700870 | ||||||
| chr16:69700952 | C | CT | 19 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(16): Show |
108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*4614dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5595 | INFO_REALIGN_3_PRIME | chr16 | 69700952 | |||||
| chr16:69700952 | C | CTT | 3 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0038 |
11 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4613_*4614dupTT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5595 | INFO_REALIGN_3_PRIME | chr16 | 69700952 | |||||
| chr16:69700958 | T | A | 1 | a0001c0002t0026 | 2 | HG01884.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4607T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5587 | chr16 | 69700958 | ||||||
| chr16:69701368 | T | A | 59 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(56): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*5017T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 5997 | chr16 | 69701368 | ||||||
| chr16:69701456 | C | T | 2 | a0001c0001t0057 a0001c0001t0059 |
2 | HG01074.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5105C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 6085 | chr16 | 69701456 | ||||||
| chr16:69701494 | A | C | 2 | a0001c0001t0022 a0001c0001t0030 |
3 | NA18984.hp2 NA18993.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5143A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 6123 | chr16 | 69701494 | ||||||
| chr16:69701539 | G | T | 1 | a0001c0001t0056 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5188G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 6168 | chr16 | 69701539 | ||||||
| chr16:69701569 | T | G | 1 | a0001c0001t0015 | 3 | HG02258.hp1 HG02559.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5218T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 6198 | chr16 | 69701569 | ||||||
| chr16:69701657 | G | A | 1 | a0001c0001t0033 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5306G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 6286 | chr16 | 69701657 | ||||||
| chr16:69701989 | A | G | 1 | a0001c0001t0018 | 3 | HG01884.hp1 HG03041.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5638A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 6618 | chr16 | 69701989 | ||||||
| chr16:69702616 | A | C | 1 | a0001c0001t0036 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6265A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 7245 | chr16 | 69702616 | ||||||
| chr16:69702647 | GC | G | 32 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(29): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*6301delC | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 7281 | INFO_REALIGN_3_PRIME | chr16 | 69702647 | |||||
| chr16:69702827 | G | A | 3 | a0001c0001t0004 a0001c0001t0056 a0001c0006t0004 |
24 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6476G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 7456 | chr16 | 69702827 | ||||||
| chr16:69702948 | G | A | 29 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(26): Show |
143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*6597G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 7577 | chr16 | 69702948 | ||||||
| chr16:69703186 | G | C | 1 | a0001c0001t0056 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6835G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 7815 | chr16 | 69703186 | ||||||
| chr16:69703402 | T | G | 1 | a0001c0001t0034 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7051T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8031 | chr16 | 69703402 | ||||||
| chr16:69703565 | C | G | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0027 others(4): Show |
43 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*7214C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8194 | chr16 | 69703565 | ||||||
| chr16:69703587 | C | T | 1 | a0001c0001t0012 | 6 | HG00733.hp1 HG01099.hp1 HG01358.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7236C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8216 | chr16 | 69703587 | ||||||
| chr16:69703726 | C | G | 2 | a0001c0001t0016 a0001c0001t0045 |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7375C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8355 | chr16 | 69703726 | ||||||
| chr16:69703867 | A | G | 1 | a0001c0001t0038 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7516A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8496 | chr16 | 69703867 | ||||||
| chr16:69703943 | G | C | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(5): Show |
62 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*7592G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8572 | chr16 | 69703943 | ||||||
| chr16:69704005 | C | T | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0027 others(4): Show |
43 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*7654C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8634 | chr16 | 69704005 | ||||||
| chr16:69704011 | C | T | 1 | a0001c0001t0035 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7660C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8640 | chr16 | 69704011 | ||||||
| chr16:69704032 | G | A | 1 | a0001c0001t0047 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7681G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 8661 | chr16 | 69704032 | ||||||
| chr16:69704503 | T | C | 1 | a0001c0001t0018 | 3 | HG01884.hp1 HG03041.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8152T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 9132 | chr16 | 69704503 | ||||||
| chr16:69704507 | G | T | 1 | a0001c0001t0021 | 2 | NA19078.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8156G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 9136 | chr16 | 69704507 | ||||||
| chr16:69704629 | C | A | 1 | a0001c0001t0042 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8278C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 9258 | chr16 | 69704629 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69566409 | GGGGAGAC others(1): Show |
G | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.73+55_73+62delAGAC others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69566409 | ||||||
| chr16:69566432 | C | T | 3 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 |
3 | HG01255.hp2 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.73+58C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69566432 | |||||||
| chr16:69566455 | C | T | 1 | a0001c0001t0029g0371 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.73+81C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69566455 | |||||||
| chr16:69566504 | C | A | 1 | a0001c0001t0001g0003 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.73+130C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69566504 | |||||||
| chr16:69566511 | G | T | 1 | a0001c0002t0008g0370 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73+137G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69566511 | |||||||
| chr16:69566569 | C | G | 3 | a0001c0001t0019g0367 a0001c0001t0019g0368 a0001c0001t0019g0369 |
3 | HG02572.hp1 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.73+195C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69566569 | |||||||
| chr16:69566739 | C | T | 1 | a0001c0001t0005g0366 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.73+365C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69566739 | |||||||
| chr16:69567014 | ATTTTC | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.73+650_73+654delCT others(3): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69567014 | ||||||
| chr16:69567067 | T | A | 2 | a0001c0001t0007g0004 a0001c0001t0007g0005 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.73+693T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69567067 | |||||||
| chr16:69567068 | C | A | 2 | a0001c0001t0007g0004 a0001c0001t0007g0005 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.73+694C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69567068 | |||||||
| chr16:69567698 | A | G | 1 | a0001c0001t0002g0361 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.74-797A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69567698 | |||||||
| chr16:69567739 | G | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.74-756G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69567739 | |||||||
| chr16:69567881 | G | C | 1 | a0001c0001t0001g0007 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.74-614G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69567881 | |||||||
| chr16:69567939 | A | G | 2 | a0001c0001t0010g0359 a0001c0001t0010g0360 |
2 | HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.74-556A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69567939 | |||||||
| chr16:69568027 | A | T | 16 | a0001c0001t0010g0346 a0001c0001t0010g0348 a0001c0001t0010g0353 others(13): Show |
16 | HG02015.hp1 HG02132.hp2 HG03209.hp2 others(13): Show |
intron_variant | MODIFIER | c.74-468A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568027 | |||||||
| chr16:69568042 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG00408.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.74-453G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568042 | |||||||
| chr16:69568142 | G | A | 1 | a0001c0001t0005g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.74-353G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568142 | |||||||
| chr16:69568234 | C | T | 2 | a0001c0001t0012g0343 a0001c0001t0012g0344 |
2 | HG01358.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.74-261C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568234 | |||||||
| chr16:69568334 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0011 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.74-157_74-148dupAT others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568334 | ||||||
| chr16:69568334 | GTA | G | 22 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0004g0332 others(19): Show |
22 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.74-149_74-148delAT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568334 | ||||||
| chr16:69568334 | GTATA | G | 5 | a0001c0001t0017g0376 a0001c0001t0025g0340 a0001c0001t0028g0372 others(2): Show |
5 | HG02572.hp2 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-151_74-148delAT others(2): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568334 | ||||||
| chr16:69568336 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.74-159A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568336 | |||||||
| chr16:69568342 | A | ATGTGTGT others(15): Show |
1 | a0001c0001t0011g0341 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.74-152_74-151insGT others(20): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568342 | ||||||
| chr16:69568342 | A | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.74-153A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568342 | |||||||
| chr16:69568342 | ATATATG | A | 3 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0025g0339 |
3 | HG01255.hp2 HG03098.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.74-151_74-146delAT others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568342 | ||||||
| chr16:69568344 | A | ATG | 11 | a0001c0001t0001g0240 a0001c0001t0002g0114 a0001c0001t0002g0116 others(8): Show |
11 | HG01192.hp2 HG01243.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.74-150_74-149insGT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTG | 12 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(9): Show |
12 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.74-150_74-149insGT others(2): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTG | 20 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(17): Show |
20 | HG01069.hp1 HG02015.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.74-150_74-149insGT others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(1): Show |
6 | a0001c0001t0002g0072 a0001c0001t0002g0082 a0001c0001t0002g0098 others(3): Show |
6 | HG01069.hp2 HG01081.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-150_74-149insGT others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0015g0045 |
3 | HG01943.hp1 HG02258.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.74-150_74-149insGT others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(5): Show |
4 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0089 others(1): Show |
4 | HG01243.hp2 HG02280.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-150_74-149insGT others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(7): Show |
3 | a0001c0001t0002g0073 a0001c0001t0002g0111 a0001c0001t0002g0206 |
3 | HG01256.hp1 HG03195.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.74-150_74-149insGT others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0001g0221 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.74-150_74-149insGT others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(17): Show |
4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0268 others(1): Show |
4 | HG01175.hp1 HG02717.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-150_74-149insGT others(22): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(19): Show |
3 | a0001c0001t0001g0255 a0001c0001t0011g0309 a0001c0001t0011g0310 |
3 | HG01109.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.74-150_74-149insGT others(24): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(21): Show |
1 | a0001c0001t0001g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.74-150_74-149insGT others(26): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | ATGTGTGT others(35): Show |
1 | a0001c0001t0001g0278 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-150_74-149insGT others(40): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | A | G | 3 | a0001c0001t0002g0104 a0001c0001t0011g0341 a0001c0001t0047g0342 |
3 | HG02055.hp2 HG04228.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.74-151A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568344 | |||||||
| chr16:69568344 | ATATG | A | 4 | a0001c0001t0003g0123 a0001c0001t0003g0157 a0001c0001t0004g0059 others(1): Show |
4 | HG01168.hp1 HG01884.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-149_74-146delAT others(2): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | ATATGTG | A | 59 | a0001c0001t0003g0047 a0001c0001t0003g0121 a0001c0001t0003g0122 others(56): Show |
59 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.74-149_74-144delAT others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | ATATGTGT others(1): Show |
A | 3 | a0001c0001t0003g0126 a0001c0001t0003g0148 a0001c0001t0003g0149 |
3 | HG02155.hp1 NA18983.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.74-149_74-142delAT others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568344 | ATATGTGT others(5): Show |
A | 1 | a0001c0001t0003g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.74-149_74-138delAT others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568344 | ||||||
| chr16:69568346 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0222 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.74-148_74-147insAT others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0317 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.74-148_74-147insAT others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0238 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.74-148_74-147insAT others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATAT others(13): Show |
1 | a0001c0001t0032g0230 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.74-148_74-147insAT others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.74-148_74-147insAT others(20): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0315 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.74-148_74-147insAT others(24): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATGT others(3): Show |
2 | a0001c0001t0001g0234 a0001c0001t0001g0236 |
2 | HG02738.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.74-148_74-147insAT others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATGT others(9): Show |
1 | a0001c0001t0034g0284 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.74-148_74-147insAT others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATGT others(11): Show |
1 | a0001c0001t0001g0285 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.74-148_74-147insAT others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATGT others(13): Show |
2 | a0001c0001t0001g0225 a0001c0001t0001g0299 |
2 | HG03017.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.74-148_74-147insAT others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATGT others(15): Show |
2 | a0001c0001t0001g0210 a0001c0001t0001g0272 |
2 | HG00323.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.74-148_74-147insAT others(20): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATGT others(17): Show |
1 | a0001c0001t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.74-148_74-147insAT others(22): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATATGT others(21): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0288 |
2 | HG02132.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.74-148_74-147insAT others(26): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(5): Show |
4 | a0001c0001t0001g0237 a0001c0001t0001g0276 a0001c0001t0001g0287 others(1): Show |
4 | HG02071.hp1 NA18986.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-148_74-147insAT others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(7): Show |
4 | a0001c0001t0001g0290 a0001c0001t0013g0002 a0001c0001t0013g0242 others(1): Show |
5 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-148_74-147insAT others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(9): Show |
1 | a0001c0001t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.74-148_74-147insAT others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(11): Show |
5 | a0001c0001t0001g0233 a0001c0001t0001g0280 a0001c0001t0013g0239 others(2): Show |
5 | HG01928.hp2 HG02602.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.74-148_74-147insAT others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(13): Show |
8 | a0001c0001t0001g0267 a0001c0001t0001g0270 a0001c0001t0001g0301 others(5): Show |
8 | HG01934.hp1 HG02109.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.74-148_74-147insAT others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(15): Show |
2 | a0001c0001t0001g0295 a0001c0001t0001g0302 |
2 | HG03490.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.74-148_74-147insAT others(20): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(17): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0223 |
2 | HG01346.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.74-148_74-147insAT others(22): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(19): Show |
1 | a0001c0001t0001g0274 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.74-148_74-147insAT others(24): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(21): Show |
1 | a0001c0001t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.74-148_74-147insAT others(26): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(23): Show |
3 | a0001c0001t0001g0294 a0001c0001t0001g0298 a0001c0001t0033g0275 |
3 | HG03704.hp2 NA18981.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.74-148_74-147insAT others(28): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATATGTGT others(25): Show |
3 | a0001c0001t0001g0283 a0001c0001t0001g0297 a0001c0001t0001g0306 |
3 | HG00639.hp2 HG02965.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.74-148_74-147insAT others(30): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATG | 20 | a0001c0001t0001g0243 a0001c0001t0006g0177 a0001c0001t0007g0004 others(17): Show |
20 | HG00280.hp2 HG00609.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.74-119_74-118dupGT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTG | 7 | a0001c0001t0001g0245 a0001c0001t0007g0032 a0001c0001t0044g0172 others(4): Show |
7 | HG00597.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-121_74-118dupGT others(2): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTG | 5 | a0001c0001t0002g0074 a0001c0001t0002g0076 a0001c0001t0002g0078 others(2): Show |
5 | HG01255.hp1 HG01261.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.74-123_74-118dupGT others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0002g0113 a0001c0001t0015g0087 |
2 | HG01099.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.74-127_74-118dupGT others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(5): Show |
3 | a0001c0001t0002g0044 a0001c0001t0002g0086 a0001c0001t0015g0088 |
3 | HG02559.hp2 HG03516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.74-129_74-118dupGT others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(7): Show |
3 | a0001c0001t0001g0289 a0001c0001t0011g0313 a0001c0001t0037g0215 |
3 | HG02717.hp1 HG02809.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.74-131_74-118dupGT others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(9): Show |
5 | a0001c0001t0001g0224 a0001c0001t0001g0247 a0001c0001t0001g0249 others(2): Show |
5 | HG03540.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.74-133_74-118dupGT others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(11): Show |
2 | a0001c0001t0001g0282 a0001c0001t0001g0308 |
2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.74-135_74-118dupGT others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(13): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0252 |
2 | HG02523.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.74-137_74-118dupGT others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(15): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0291 |
2 | NA18944.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.74-139_74-118dupGT others(20): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(17): Show |
4 | a0001c0001t0001g0277 a0001c0001t0001g0293 a0001c0001t0011g0311 others(1): Show |
4 | HG02258.hp2 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-141_74-118dupGT others(22): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(19): Show |
4 | a0001c0001t0001g0250 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG01257.hp2 HG01515.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-143_74-118dupGT others(24): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(23): Show |
1 | a0001c0001t0039g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.74-147_74-118dupGT others(28): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(27): Show |
1 | a0001c0001t0020g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.74-118_74-117insGT others(32): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | ATGTGTGT others(31): Show |
1 | a0001c0001t0001g0231 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.74-118_74-117insGT others(36): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568346 | A | G | 113 | a0001c0001t0001g0221 a0001c0001t0001g0240 a0001c0001t0001g0253 others(110): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.74-149A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568346 | |||||||
| chr16:69568346 | ATG | A | 16 | a0001c0001t0006g0049 a0001c0001t0006g0053 a0001c0001t0006g0055 others(13): Show |
16 | HG01070.hp1 HG01168.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.74-119_74-118delGT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568346 | ||||||
| chr16:69568348 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0257 a0001c0001t0031g0244 |
3 | NA18951.hp2 NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.74-147G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568348 | |||||||
| chr16:69568370 | GTGTGTGT others(5): Show |
G | 15 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(12): Show |
18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.74-123_74-112delGT others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568370 | ||||||
| chr16:69568372 | GTGTGTAT others(3): Show |
G | 1 | a0001c0002t0008g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.74-121_74-112delGT others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568372 | ||||||
| chr16:69568374 | GTGTATA | G | 4 | a0001c0001t0003g0046 a0001c0001t0005g0159 a0001c0001t0053g0162 others(1): Show |
4 | HG02922.hp1 HG04199.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-119_74-114delGT others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568374 | ||||||
| chr16:69568376 | G | A | 4 | a0001c0001t0002g0096 a0001c0001t0006g0055 a0001c0001t0006g0167 others(1): Show |
4 | NA18939.hp1 NA18957.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-119G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568376 | |||||||
| chr16:69568376 | G | GTGTGTA | 7 | a0001c0001t0002g0075 a0001c0001t0002g0092 a0001c0001t0002g0093 others(4): Show |
7 | HG00099.hp1 HG01433.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-118_74-117insGT others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568376 | ||||||
| chr16:69568376 | GTATA | G | 8 | a0001c0001t0001g0008 a0001c0001t0005g0048 a0001c0001t0005g0161 others(5): Show |
8 | HG00408.hp1 HG01074.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.74-104_74-101delTA others(2): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568376 | ||||||
| chr16:69568376 | GTATATAT others(1): Show |
G | 4 | a0001c0001t0017g0376 a0001c0001t0028g0372 a0001c0001t0028g0373 others(1): Show |
4 | HG02572.hp2 HG03098.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-108_74-101delTA others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568376 | ||||||
| chr16:69568378 | A | G | 231 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(228): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.74-117A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568378 | |||||||
| chr16:69568380 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.74-115A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568380 | |||||||
| chr16:69568382 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.74-113A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568382 | |||||||
| chr16:69568384 | A | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.74-111A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568384 | |||||||
| chr16:69568386 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.74-109A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568386 | |||||||
| chr16:69568387 | TATATATA others(5): Show |
T | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.74-106_74-95delTAT others(9): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 69568387 | ||||||
| chr16:69568388 | A | G | 18 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0247 others(15): Show |
18 | HG00639.hp2 HG01433.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.74-107A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568388 | |||||||
| chr16:69568389 | T | C | 1 | a0001c0001t0019g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.74-106T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568389 | |||||||
| chr16:69568390 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0306 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.74-105A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568390 | |||||||
| chr16:69568391 | T | C | 1 | a0001c0001t0010g0355 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.74-104T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568391 | |||||||
| chr16:69568393 | T | C | 96 | a0001c0001t0002g0110 a0001c0001t0003g0046 a0001c0001t0003g0047 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.74-102T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568393 | |||||||
| chr16:69568395 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.74-100C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568395 | |||||||
| chr16:69568407 | T | C | 1 | a0001c0001t0055g0345 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.74-88T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568407 | |||||||
| chr16:69568494 | G | T | 1 | a0001c0001t0001g0317 | 1 | NA19057.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.74-1G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 1/14 | chr16 | 69568494 | |||||||
| chr16:69568571 | G | A | 2 | a0001c0006t0004g0026 a0001c0006t0004g0027 |
2 | HG00408.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.127+23G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69568571 | |||||||
| chr16:69568774 | A | G | 3 | a0001c0001t0018g0209 a0001c0001t0018g0336 a0001c0001t0018g0337 |
3 | HG01884.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.127+226A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69568774 | |||||||
| chr16:69569194 | T | C | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+646T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569194 | |||||||
| chr16:69569242 | T | A | 1 | a0001c0001t0039g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+694T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569242 | |||||||
| chr16:69569257 | A | G | 1 | a0001c0011t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.127+709A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569257 | |||||||
| chr16:69569319 | G | C | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+771G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569319 | |||||||
| chr16:69569324 | CA | C | 6 | a0001c0001t0001g0316 a0001c0001t0002g0206 a0001c0001t0003g0207 others(3): Show |
6 | HG01255.hp2 HG01256.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+790delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69569324 | ||||||
| chr16:69569353 | G | A | 1 | a0001c0002t0008g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127+805G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569353 | |||||||
| chr16:69569361 | A | G | 1 | a0001c0001t0003g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.127+813A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569361 | |||||||
| chr16:69569370 | G | T | 1 | a0001c0001t0043g0204 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.127+822G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569370 | |||||||
| chr16:69569477 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.127+929A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569477 | |||||||
| chr16:69569558 | A | G | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.127+1010A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569558 | |||||||
| chr16:69569668 | C | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+1120C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569668 | |||||||
| chr16:69569832 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+1284A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69569832 | |||||||
| chr16:69570106 | TACAG | T | 23 | a0001c0001t0001g0011 a0001c0001t0001g0219 a0001c0001t0001g0220 others(20): Show |
23 | HG00597.hp2 HG02132.hp1 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+1562_127+1565d others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69570106 | ||||||
| chr16:69570186 | T | G | 4 | a0001c0001t0007g0029 a0001c0001t0007g0030 a0001c0001t0007g0031 others(1): Show |
4 | HG00597.hp1 NA18948.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+1638T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69570186 | |||||||
| chr16:69570380 | A | G | 1 | a0001c0001t0005g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.127+1832A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69570380 | |||||||
| chr16:69570557 | AATT | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.127+2016_127+2018d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69570557 | ||||||
| chr16:69570718 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127+2170A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69570718 | |||||||
| chr16:69571101 | G | A | 1 | a0001c0001t0046g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.127+2553G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571101 | |||||||
| chr16:69571129 | T | TA | 39 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(36): Show |
39 | HG00735.hp2 HG01074.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.127+2609dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | T | TAA | 11 | a0001c0001t0002g0035 a0001c0001t0004g0036 a0001c0001t0009g0200 others(8): Show |
11 | HG02027.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+2608_127+2609d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | T | TAAA | 6 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0028g0372 others(3): Show |
6 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+2607_127+2609d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | T | TAAAAA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0210 a0001c0001t0001g0228 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.127+2605_127+2609d others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | T | TAAAAAA | 39 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(36): Show |
40 | HG00408.hp1 HG00733.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.127+2604_127+2609d others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | T | TAAAAAAA | 11 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0243 others(8): Show |
11 | HG00597.hp2 HG01081.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+2603_127+2609d others(9): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | T | TAAAAAAA others(1): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
7 | HG01928.hp2 HG02027.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+2602_127+2609d others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | T | TAAAAAAA others(4): Show |
2 | a0001c0001t0011g0213 a0001c0001t0011g0309 |
2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.127+2599_127+2609d others(13): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+2595_127+2609d others(17): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | TA | T | 7 | a0001c0001t0001g0308 a0001c0001t0003g0195 a0001c0001t0003g0196 others(4): Show |
7 | HG01516.hp1 HG01891.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+2609delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | TAAAAAAA others(2): Show |
T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+2601_127+2609d others(11): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571129 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0012g0307 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.127+2597_127+2609d others(15): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571129 | ||||||
| chr16:69571159 | C | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127+2611C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571159 | |||||||
| chr16:69571308 | A | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.127+2760A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571308 | |||||||
| chr16:69571314 | C | CAACA | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2785_127+2788d others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69571314 | ||||||
| chr16:69571338 | T | A | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127+2790T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571338 | |||||||
| chr16:69571341 | G | T | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127+2793G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571341 | |||||||
| chr16:69571365 | C | G | 24 | a0001c0001t0001g0011 a0001c0001t0001g0219 a0001c0001t0001g0220 others(21): Show |
24 | HG00597.hp2 HG02132.hp1 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.127+2817C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571365 | |||||||
| chr16:69571446 | T | C | 76 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+2898T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571446 | |||||||
| chr16:69571542 | C | T | 1 | a0001c0001t0004g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.127+2994C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571542 | |||||||
| chr16:69571595 | T | C | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.127+3047T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571595 | |||||||
| chr16:69571698 | A | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+3150A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571698 | |||||||
| chr16:69571708 | T | G | 3 | a0001c0001t0018g0209 a0001c0001t0018g0336 a0001c0001t0018g0337 |
3 | HG01884.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.127+3160T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571708 | |||||||
| chr16:69571709 | G | T | 319 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(316): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.127+3161G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571709 | |||||||
| chr16:69571710 | G | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(238): Show |
245 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.127+3162G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571710 | |||||||
| chr16:69571711 | G | T | 6 | a0001c0001t0004g0332 a0001c0001t0005g0320 a0001c0001t0005g0331 others(3): Show |
6 | HG00735.hp2 HG01167.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+3163G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571711 | |||||||
| chr16:69571737 | C | T | 1 | a0001c0002t0008g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.127+3189C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571737 | |||||||
| chr16:69571918 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+3370C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571918 | |||||||
| chr16:69571921 | G | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+3373G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571921 | |||||||
| chr16:69571984 | G | C | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(6): Show |
9 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+3436G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69571984 | |||||||
| chr16:69572031 | G | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+3483G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572031 | |||||||
| chr16:69572065 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+3517G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572065 | |||||||
| chr16:69572191 | A | G | 1 | a0001c0001t0004g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.127+3643A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572191 | |||||||
| chr16:69572199 | A | G | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.127+3651A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572199 | |||||||
| chr16:69572340 | A | G | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | HG00280.hp1 HG01099.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+3792A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572340 | |||||||
| chr16:69572444 | TA | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+3897delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572444 | |||||||
| chr16:69572499 | A | C | 1 | a0001c0001t0001g0306 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127+3951A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572499 | |||||||
| chr16:69572558 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+4010G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572558 | |||||||
| chr16:69572795 | G | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+4247G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69572795 | |||||||
| chr16:69573126 | G | A | 105 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(102): Show |
105 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.127+4578G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69573126 | |||||||
| chr16:69573195 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+4647G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69573195 | |||||||
| chr16:69573298 | A | G | 1 | a0001c0001t0019g0369 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+4750A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69573298 | |||||||
| chr16:69573308 | A | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0112 |
3 | HG03669.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.127+4760A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69573308 | |||||||
| chr16:69573537 | A | G | 3 | a0001c0001t0007g0029 a0001c0001t0007g0031 a0001c0001t0007g0032 |
3 | HG00597.hp1 NA18948.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.127+4989A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69573537 | |||||||
| chr16:69573869 | C | CT | 6 | a0001c0001t0001g0305 a0001c0001t0002g0071 a0001c0001t0006g0192 others(3): Show |
6 | HG01515.hp2 HG03688.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+5342dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69573869 | ||||||
| chr16:69573869 | CT | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0210 others(180): Show |
184 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.127+5342delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69573869 | ||||||
| chr16:69573869 | CTT | C | 7 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0005g0025 others(4): Show |
7 | HG00323.hp1 HG01256.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+5341_127+5342d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69573869 | ||||||
| chr16:69573910 | G | T | 1 | a0001c0001t0002g0109 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.127+5362G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69573910 | |||||||
| chr16:69573938 | A | G | 2 | a0001c0001t0011g0313 a0001c0001t0038g0314 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.127+5390A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69573938 | |||||||
| chr16:69573950 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+5402C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69573950 | |||||||
| chr16:69574150 | C | T | 1 | a0001c0001t0039g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+5602C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574150 | |||||||
| chr16:69574166 | C | T | 1 | a0001c0001t0058g0357 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127+5618C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574166 | |||||||
| chr16:69574263 | A | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+5715A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574263 | |||||||
| chr16:69574288 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127+5740A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574288 | |||||||
| chr16:69574385 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+5837C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574385 | |||||||
| chr16:69574386 | G | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+5838G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574386 | |||||||
| chr16:69574608 | A | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+6060A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574608 | |||||||
| chr16:69574697 | C | T | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+6149C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574697 | |||||||
| chr16:69574754 | T | C | 1 | a0001c0001t0033g0275 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.127+6206T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574754 | |||||||
| chr16:69574795 | A | G | 1 | a0001c0001t0005g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.127+6247A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574795 | |||||||
| chr16:69574831 | G | T | 1 | a0001c0001t0024g0063 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.127+6283G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574831 | |||||||
| chr16:69574904 | T | G | 2 | a0001c0001t0021g0226 a0001c0001t0021g0235 |
2 | NA19078.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.127+6356T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69574904 | |||||||
| chr16:69575080 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+6532G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69575080 | |||||||
| chr16:69575138 | A | G | 7 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(4): Show |
7 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+6590A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69575138 | |||||||
| chr16:69575374 | G | T | 3 | a0001c0001t0006g0058 a0001c0001t0006g0190 a0001c0001t0006g0191 |
3 | NA18991.hp1 NA18994.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.127+6826G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69575374 | |||||||
| chr16:69575456 | T | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+6908T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69575456 | |||||||
| chr16:69575557 | G | C | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+7009G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69575557 | |||||||
| chr16:69575564 | C | T | 1 | a0001c0001t0036g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.127+7016C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69575564 | |||||||
| chr16:69575669 | T | G | 1 | a0001c0001t0029g0371 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.127+7121T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69575669 | |||||||
| chr16:69575678 | TA | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.127+7138delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69575678 | ||||||
| chr16:69575949 | T | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+7401T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69575949 | |||||||
| chr16:69576007 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.127+7459G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576007 | |||||||
| chr16:69576078 | G | A | 2 | a0001c0001t0009g0200 a0001c0001t0052g0199 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.127+7530G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576078 | |||||||
| chr16:69576099 | A | G | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.127+7551A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576099 | |||||||
| chr16:69576130 | G | A | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.127+7582G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576130 | |||||||
| chr16:69576166 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+7618G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576166 | |||||||
| chr16:69576178 | C | T | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+7630C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576178 | |||||||
| chr16:69576291 | C | CA | 29 | a0001c0001t0001g0228 a0001c0001t0001g0247 a0001c0001t0001g0276 others(26): Show |
32 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.127+7763dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69576291 | ||||||
| chr16:69576343 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.127+7795C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576343 | |||||||
| chr16:69576368 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.127+7820A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576368 | |||||||
| chr16:69576409 | A | T | 25 | a0001c0001t0004g0332 a0001c0001t0005g0010 a0001c0001t0005g0025 others(22): Show |
25 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.127+7861A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576409 | |||||||
| chr16:69576554 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127+8006A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576554 | |||||||
| chr16:69576602 | G | T | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127+8054G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576602 | |||||||
| chr16:69576642 | G | A | 1 | a0001c0001t0003g0207 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.127+8094G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576642 | |||||||
| chr16:69576765 | T | C | 1 | a0001c0011t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.127+8217T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576765 | |||||||
| chr16:69576828 | G | A | 1 | a0001c0001t0039g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+8280G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576828 | |||||||
| chr16:69576973 | A | C | 1 | a0001c0001t0001g0007 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.127+8425A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69576973 | |||||||
| chr16:69577433 | A | G | 1 | a0001c0001t0009g0119 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127+8885A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69577433 | |||||||
| chr16:69577438 | A | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+8890A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69577438 | |||||||
| chr16:69577547 | G | C | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+8999G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69577547 | |||||||
| chr16:69577679 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.127+9131A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69577679 | |||||||
| chr16:69577710 | T | C | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+9162T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69577710 | |||||||
| chr16:69577726 | C | T | 1 | a0001c0011t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.127+9178C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69577726 | |||||||
| chr16:69577729 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+9181A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69577729 | |||||||
| chr16:69577950 | G | A | 3 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 |
3 | HG01255.hp2 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.127+9402G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69577950 | |||||||
| chr16:69577990 | CA | C | 76 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+9452delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69577990 | ||||||
| chr16:69578000 | A | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+9452A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578000 | |||||||
| chr16:69578164 | C | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+9616C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578164 | |||||||
| chr16:69578209 | T | C | 2 | a0001c0001t0011g0214 a0001c0001t0037g0215 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127+9661T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578209 | |||||||
| chr16:69578264 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+9716C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578264 | |||||||
| chr16:69578573 | G | A | 3 | a0001c0001t0006g0049 a0001c0001t0006g0166 a0001c0001t0006g0167 |
3 | NA18957.hp1 NA18978.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.127+10025G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578573 | |||||||
| chr16:69578613 | A | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127+10065A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578613 | |||||||
| chr16:69578707 | T | C | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+10159T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578707 | |||||||
| chr16:69578821 | T | C | 2 | a0001c0001t0005g0048 a0001c0001t0005g0159 |
2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.127+10273T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578821 | |||||||
| chr16:69578877 | G | GT | 10 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0298 others(7): Show |
10 | HG02300.hp1 NA18942.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+10344dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69578877 | ||||||
| chr16:69578935 | C | T | 1 | a0001c0001t0052g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.127+10387C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69578935 | |||||||
| chr16:69579129 | C | T | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+10581C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579129 | |||||||
| chr16:69579154 | G | A | 1 | a0001c0001t0007g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.127+10606G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579154 | |||||||
| chr16:69579199 | G | T | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+10651G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579199 | |||||||
| chr16:69579205 | C | A | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127+10657C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579205 | |||||||
| chr16:69579240 | A | G | 1 | a0001c0001t0003g0158 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.127+10692A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579240 | |||||||
| chr16:69579906 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.127+11358C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579906 | |||||||
| chr16:69579925 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.127+11377T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579925 | |||||||
| chr16:69579949 | G | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+11401G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579949 | |||||||
| chr16:69580225 | C | T | 7 | a0001c0001t0004g0332 a0001c0001t0005g0320 a0001c0001t0005g0329 others(4): Show |
7 | HG00735.hp2 HG01167.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+11677C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69580225 | |||||||
| chr16:69580292 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127+11744C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69580292 | |||||||
| chr16:69580391 | C | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+11843C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69580391 | |||||||
| chr16:69580524 | T | TA | 119 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.127+11991dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69580524 | ||||||
| chr16:69580766 | C | T | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.127+12218C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69580766 | |||||||
| chr16:69581105 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127+12557G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69581105 | |||||||
| chr16:69581270 | G | A | 1 | a0001c0001t0036g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.127+12722G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69581270 | |||||||
| chr16:69581291 | T | G | 3 | a0001c0001t0025g0339 a0001c0001t0025g0340 a0001c0001t0050g0194 |
3 | HG02895.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.127+12743T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69581291 | |||||||
| chr16:69581293 | G | T | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127+12745G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69581293 | |||||||
| chr16:69581398 | C | T | 1 | a0001c0001t0003g0196 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.127+12850C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69581398 | |||||||
| chr16:69581805 | ATATT | A | 3 | a0001c0002t0008g0012 a0001c0002t0008g0013 a0001c0002t0008g0014 |
3 | HG02280.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127+13261_127+1326 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69581805 | ||||||
| chr16:69581909 | A | G | 97 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(94): Show |
97 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.127+13361A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69581909 | |||||||
| chr16:69582071 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.127+13523G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69582071 | |||||||
| chr16:69582389 | C | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.127+13841C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69582389 | |||||||
| chr16:69582496 | C | T | 1 | a0001c0001t0007g0005 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+13948C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69582496 | |||||||
| chr16:69582573 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+14025A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69582573 | |||||||
| chr16:69582577 | G | A | 1 | a0001c0011t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.127+14029G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69582577 | |||||||
| chr16:69582678 | C | CT | 6 | a0001c0001t0001g0234 a0001c0001t0017g0374 a0001c0001t0017g0375 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+14143dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69582678 | ||||||
| chr16:69582705 | A | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+14157A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69582705 | |||||||
| chr16:69583071 | A | C | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127+14523A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583071 | |||||||
| chr16:69583075 | T | C | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.127+14527T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583075 | |||||||
| chr16:69583300 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.127+14752A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583300 | |||||||
| chr16:69583379 | TA | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0252 a0001c0001t0001g0253 others(40): Show |
44 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.127+14846delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69583379 | ||||||
| chr16:69583380 | A | T | 1 | a0001c0001t0054g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127+14832A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583380 | |||||||
| chr16:69583538 | A | T | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+14990A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583538 | |||||||
| chr16:69583543 | G | C | 1 | a0001c0001t0007g0031 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.127+14995G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583543 | |||||||
| chr16:69583610 | C | G | 326 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(323): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.127+15062C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583610 | |||||||
| chr16:69583682 | A | G | 1 | a0001c0001t0003g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.127+15134A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583682 | |||||||
| chr16:69583753 | T | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+15205T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583753 | |||||||
| chr16:69583815 | G | A | 1 | a0001c0001t0054g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127+15267G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583815 | |||||||
| chr16:69583994 | G | A | 1 | a0001c0001t0003g0196 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.127+15446G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69583994 | |||||||
| chr16:69584097 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.127+15549G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584097 | |||||||
| chr16:69584320 | C | CT | 45 | a0001c0001t0004g0332 a0001c0001t0005g0010 a0001c0001t0005g0025 others(42): Show |
45 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+15786dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69584320 | ||||||
| chr16:69584340 | A | G | 3 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 |
3 | HG01255.hp2 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.127+15792A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584340 | |||||||
| chr16:69584367 | T | A | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127+15819T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584367 | |||||||
| chr16:69584415 | G | A | 1 | a0001c0001t0007g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.127+15867G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584415 | |||||||
| chr16:69584422 | A | T | 4 | a0001c0001t0010g0348 a0001c0001t0010g0354 a0001c0001t0010g0355 others(1): Show |
4 | HG02132.hp2 NA18950.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+15874A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584422 | |||||||
| chr16:69584553 | T | C | 1 | a0001c0001t0007g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.127+16005T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584553 | |||||||
| chr16:69584633 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.127+16085A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584633 | |||||||
| chr16:69584788 | A | G | 1 | a0001c0001t0010g0360 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.127+16240A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584788 | |||||||
| chr16:69584916 | A | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+16368A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584916 | |||||||
| chr16:69584983 | A | G | 1 | a0001c0001t0060g0349 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.127+16435A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69584983 | |||||||
| chr16:69585030 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.127+16482G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69585030 | |||||||
| chr16:69585100 | C | T | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+16552C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69585100 | |||||||
| chr16:69585181 | T | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+16633T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69585181 | |||||||
| chr16:69585301 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0243 |
2 | HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.127+16753G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69585301 | |||||||
| chr16:69585305 | A | C | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+16757A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69585305 | |||||||
| chr16:69585311 | AT | A | 15 | a0001c0001t0002g0206 a0001c0001t0011g0213 a0001c0001t0011g0214 others(12): Show |
15 | HG01256.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.127+16776delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69585311 | ||||||
| chr16:69585485 | T | G | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.127+16937T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69585485 | |||||||
| chr16:69585535 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.127+16987A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69585535 | |||||||
| chr16:69585720 | C | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+17172C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69585720 | |||||||
| chr16:69586029 | A | C | 7 | a0001c0001t0006g0049 a0001c0001t0006g0057 a0001c0001t0006g0166 others(4): Show |
7 | HG02083.hp2 NA18957.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+17481A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586029 | |||||||
| chr16:69586047 | AAAAC | A | 17 | a0001c0001t0010g0164 a0001c0001t0010g0346 a0001c0001t0010g0348 others(14): Show |
17 | HG00738.hp2 HG02015.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.127+17502_127+1750 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69586047 | ||||||
| chr16:69586158 | AT | A | 8 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0298 others(5): Show |
8 | NA18942.hp1 NA18953.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+17611delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586158 | |||||||
| chr16:69586161 | T | C | 1 | a0001c0001t0006g0168 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.127+17613T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586161 | |||||||
| chr16:69586320 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+17772A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586320 | |||||||
| chr16:69586375 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+17827G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586375 | |||||||
| chr16:69586399 | T | C | 1 | a0001c0001t0006g0169 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.127+17851T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586399 | |||||||
| chr16:69586662 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+18114C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586662 | |||||||
| chr16:69586685 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0257 a0001c0001t0031g0244 |
3 | NA18951.hp2 NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.127+18137G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586685 | |||||||
| chr16:69586698 | C | T | 1 | a0001c0001t0058g0357 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127+18150C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69586698 | |||||||
| chr16:69587242 | AT | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+18706delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69587242 | ||||||
| chr16:69587290 | G | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127+18742G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587290 | |||||||
| chr16:69587362 | C | CTGTAAA | 88 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
88 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.127+18814_127+1881 others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587362 | |||||||
| chr16:69587362 | C | CTGTAAAA | 34 | a0001c0001t0001g0003 a0001c0001t0001g0252 a0001c0001t0001g0253 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+18814_127+1881 others(11): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587362 | |||||||
| chr16:69587364 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+18816C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587364 | |||||||
| chr16:69587365 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+18817C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587365 | |||||||
| chr16:69587427 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+18879C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587427 | |||||||
| chr16:69587579 | G | A | 3 | a0001c0001t0025g0339 a0001c0001t0025g0340 a0001c0001t0050g0194 |
3 | HG02895.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.127+19031G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587579 | |||||||
| chr16:69587716 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.127+19168A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587716 | |||||||
| chr16:69587864 | A | T | 1 | a0001c0001t0003g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.127+19316A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587864 | |||||||
| chr16:69587910 | A | G | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127+19362A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69587910 | |||||||
| chr16:69587944 | C | CT | 100 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
100 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.127+19422dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69587944 | ||||||
| chr16:69587944 | C | CTT | 24 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0220 others(21): Show |
25 | HG00140.hp2 HG00597.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.127+19421_127+1942 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69587944 | ||||||
| chr16:69587944 | CT | C | 11 | a0001c0001t0002g0074 a0001c0001t0003g0157 a0001c0001t0005g0325 others(8): Show |
11 | HG01168.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+19422delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69587944 | ||||||
| chr16:69587944 | CTT | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+19421_127+1942 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69587944 | ||||||
| chr16:69588056 | G | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+19508G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588056 | |||||||
| chr16:69588201 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+19653C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588201 | |||||||
| chr16:69588310 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.127+19762G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588310 | |||||||
| chr16:69588404 | A | G | 2 | a0001c0001t0002g0105 a0001c0001t0043g0204 |
2 | HG00423.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.127+19856A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588404 | |||||||
| chr16:69588513 | C | CACTTATT others(1): Show |
145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.127+19966_127+1997 others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588513 | ||||||
| chr16:69588613 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+20065A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588613 | |||||||
| chr16:69588795 | C | A | 1 | a0001c0001t0058g0357 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127+20247C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588795 | |||||||
| chr16:69588859 | G | A | 76 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+20311G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588859 | |||||||
| chr16:69588894 | C | T | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.127+20346C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588894 | |||||||
| chr16:69588962 | C | T | 1 | a0001c0001t0009g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127+20414C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588962 | |||||||
| chr16:69588963 | C | G | 1 | a0001c0001t0002g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.127+20415C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69588963 | |||||||
| chr16:69588976 | ACTT | A | 5 | a0001c0001t0004g0153 a0001c0001t0004g0154 a0001c0002t0008g0018 others(2): Show |
5 | HG02055.hp1 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+20432_127+2043 others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588976 | ||||||
| chr16:69588977 | CTTCT | C | 12 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(9): Show |
15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.127+20432_127+2043 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588977 | ||||||
| chr16:69588980 | C | CT | 56 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0251 others(53): Show |
56 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.127+20463dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69588980 | C | CTT | 17 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0061 others(14): Show |
17 | HG01192.hp1 HG01255.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.127+20462_127+2046 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69588980 | C | CTTT | 6 | a0001c0001t0001g0234 a0001c0001t0003g0124 a0001c0001t0017g0376 others(3): Show |
6 | HG02683.hp1 HG02738.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+20461_127+2046 others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69588980 | C | CTTTT | 27 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0125 others(24): Show |
27 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.127+20460_127+2046 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69588980 | C | CTTTTT | 22 | a0001c0001t0003g0121 a0001c0001t0003g0122 a0001c0001t0003g0142 others(19): Show |
22 | HG01168.hp1 HG02027.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.127+20459_127+2046 others(9): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69588980 | C | CTTTTTT | 6 | a0001c0001t0003g0123 a0001c0001t0003g0152 a0001c0001t0010g0348 others(3): Show |
6 | HG02132.hp2 HG03239.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+20458_127+2046 others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69588980 | CT | C | 26 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0257 others(23): Show |
26 | HG00140.hp2 HG01074.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.127+20463delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69588980 | CTTTTTTT others(3): Show |
C | 13 | a0001c0001t0005g0025 a0001c0001t0011g0213 a0001c0001t0011g0214 others(10): Show |
13 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.127+20454_127+2046 others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69588980 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0009g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127+20453_127+2046 others(15): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69588980 | ||||||
| chr16:69589074 | A | G | 1 | a0001c0001t0003g0195 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.127+20526A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589074 | |||||||
| chr16:69589096 | G | A | 105 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(102): Show |
105 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.127+20548G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589096 | |||||||
| chr16:69589119 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.127+20571C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589119 | |||||||
| chr16:69589155 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+20607C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589155 | |||||||
| chr16:69589248 | C | G | 1 | a0001c0001t0004g0150 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.127+20700C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589248 | |||||||
| chr16:69589471 | T | A | 3 | a0001c0001t0022g0263 a0001c0001t0022g0265 a0001c0001t0030g0269 |
3 | NA18984.hp2 NA18993.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.127+20923T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589471 | |||||||
| chr16:69589573 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127+21025G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589573 | |||||||
| chr16:69589610 | G | C | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.127+21062G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589610 | |||||||
| chr16:69589715 | T | A | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127+21167T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589715 | |||||||
| chr16:69589734 | AT | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(21): Show |
24 | HG00408.hp1 HG00733.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.127+21193delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69589734 | ||||||
| chr16:69589753 | G | A | 1 | a0001c0001t0011g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127+21205G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589753 | |||||||
| chr16:69589859 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127+21311A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589859 | |||||||
| chr16:69589982 | C | T | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127+21434C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69589982 | |||||||
| chr16:69590090 | C | T | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.127+21542C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69590090 | |||||||
| chr16:69590151 | G | A | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+21603G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69590151 | |||||||
| chr16:69590192 | T | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(141): Show |
148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.127+21644T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69590192 | |||||||
| chr16:69590192 | T | G | 1 | a0001c0001t0016g0364 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127+21644T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69590192 | |||||||
| chr16:69590472 | T | C | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+21924T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69590472 | |||||||
| chr16:69590774 | A | C | 1 | a0001c0001t0006g0188 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.127+22226A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69590774 | |||||||
| chr16:69590786 | G | A | 1 | a0001c0001t0007g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.127+22238G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69590786 | |||||||
| chr16:69591296 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+22748C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69591296 | |||||||
| chr16:69591635 | C | G | 1 | a0001c0001t0033g0275 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.127+23087C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69591635 | |||||||
| chr16:69591948 | A | T | 1 | a0001c0011t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.127+23400A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69591948 | |||||||
| chr16:69592047 | T | G | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+23499T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592047 | |||||||
| chr16:69592080 | C | CT | 116 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.127+23549dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69592080 | ||||||
| chr16:69592080 | C | CTT | 6 | a0001c0001t0002g0113 a0001c0001t0002g0206 a0001c0001t0006g0183 others(3): Show |
6 | HG00597.hp1 HG01099.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+23548_127+2354 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69592080 | ||||||
| chr16:69592080 | CT | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(236): Show |
243 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.127+23549delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69592080 | ||||||
| chr16:69592080 | CTT | C | 6 | a0001c0001t0001g0287 a0001c0001t0003g0196 a0001c0001t0005g0159 others(3): Show |
6 | HG01167.hp2 HG02922.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+23548_127+2354 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69592080 | ||||||
| chr16:69592091 | T | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127+23543T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592091 | |||||||
| chr16:69592184 | A | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.127+23636A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592184 | |||||||
| chr16:69592198 | A | T | 1 | a0001c0001t0006g0166 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.127+23650A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592198 | |||||||
| chr16:69592220 | C | T | 3 | a0001c0001t0018g0209 a0001c0001t0018g0336 a0001c0001t0018g0337 |
3 | HG01884.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.127+23672C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592220 | |||||||
| chr16:69592221 | G | A | 4 | a0001c0001t0001g0252 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
4 | HG02523.hp2 NA18995.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+23673G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592221 | |||||||
| chr16:69592229 | AC | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.127+23683delC | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69592229 | ||||||
| chr16:69592233 | C | A | 76 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+23685C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592233 | |||||||
| chr16:69592568 | C | T | 5 | a0001c0001t0003g0046 a0001c0001t0003g0124 a0001c0001t0003g0139 others(2): Show |
5 | NA18952.hp2 NA18980.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+24020C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592568 | |||||||
| chr16:69592864 | T | G | 1 | a0001c0001t0001g0316 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.127+24316T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69592864 | |||||||
| chr16:69593188 | A | C | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+24640A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593188 | |||||||
| chr16:69593344 | A | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.127+24796A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593344 | |||||||
| chr16:69593345 | T | A | 4 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 others(1): Show |
4 | HG02723.hp1 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+24797T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593345 | |||||||
| chr16:69593351 | T | A | 2 | a0001c0001t0001g0289 a0001c0001t0013g0239 |
2 | HG01928.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.127+24803T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593351 | |||||||
| chr16:69593411 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.127+24863A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593411 | |||||||
| chr16:69593477 | A | AT | 10 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(7): Show |
10 | HG02738.hp2 NA18943.hp2 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+24945dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69593477 | ||||||
| chr16:69593477 | AT | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.127+24945delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69593477 | ||||||
| chr16:69593479 | T | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+24931T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593479 | |||||||
| chr16:69593545 | G | C | 1 | a0001c0001t0005g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.127+24997G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593545 | |||||||
| chr16:69593637 | A | T | 1 | a0001c0001t0018g0209 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127+25089A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593637 | |||||||
| chr16:69593651 | G | A | 2 | a0001c0006t0004g0026 a0001c0006t0004g0027 |
2 | HG00408.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.127+25103G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593651 | |||||||
| chr16:69593851 | C | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127+25303C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593851 | |||||||
| chr16:69593890 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.127+25342G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593890 | |||||||
| chr16:69593935 | A | C | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+25387A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69593935 | |||||||
| chr16:69594192 | T | A | 1 | a0001c0001t0002g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.127+25644T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594192 | |||||||
| chr16:69594276 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.127+25728C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594276 | |||||||
| chr16:69594314 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.127+25766C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594314 | |||||||
| chr16:69594357 | G | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+25809G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594357 | |||||||
| chr16:69594466 | G | C | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+25918G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594466 | |||||||
| chr16:69594543 | C | T | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+25995C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594543 | |||||||
| chr16:69594725 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.127+26177A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594725 | |||||||
| chr16:69594776 | A | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+26228A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594776 | |||||||
| chr16:69594817 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.127+26269A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594817 | |||||||
| chr16:69594912 | C | T | 1 | a0001c0001t0010g0348 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127+26364C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69594912 | |||||||
| chr16:69595006 | GTTGTGCT others(9): Show |
G | 1 | a0001c0001t0029g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127+26461_127+2647 others(20): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69595006 | ||||||
| chr16:69595048 | G | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+26500G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595048 | |||||||
| chr16:69595250 | C | G | 27 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(24): Show |
30 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.127+26702C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595250 | |||||||
| chr16:69595328 | G | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+26780G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595328 | |||||||
| chr16:69595377 | G | T | 2 | a0001c0001t0007g0181 a0001c0001t0007g0182 |
2 | NA18966.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.127+26829G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595377 | |||||||
| chr16:69595550 | T | C | 1 | a0001c0001t0007g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.127+27002T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595550 | |||||||
| chr16:69595659 | G | A | 2 | a0003c0005t0001g0258 a0003c0005t0001g0259 |
2 | NA18972.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.127+27111G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595659 | |||||||
| chr16:69595666 | T | C | 1 | a0001c0001t0012g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.127+27118T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595666 | |||||||
| chr16:69595685 | A | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0283 a0001c0001t0001g0285 others(2): Show |
5 | HG00639.hp2 HG01123.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+27137A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595685 | |||||||
| chr16:69595829 | C | G | 1 | a0001c0001t0001g0262 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.127+27281C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595829 | |||||||
| chr16:69595830 | AAACACT | A | 8 | a0001c0001t0002g0044 a0001c0001t0002g0073 a0001c0001t0002g0089 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+27283_127+2728 others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595830 | |||||||
| chr16:69595864 | T | C | 10 | a0001c0001t0003g0121 a0001c0001t0003g0125 a0001c0001t0003g0142 others(7): Show |
10 | HG02083.hp1 NA18612.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+27316T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595864 | |||||||
| chr16:69595886 | A | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+27338A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69595886 | |||||||
| chr16:69596037 | G | T | 1 | a0001c0001t0012g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.127+27489G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596037 | |||||||
| chr16:69596138 | T | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+27590T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596138 | |||||||
| chr16:69596217 | G | C | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+27669G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596217 | |||||||
| chr16:69596524 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.127+27976G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596524 | |||||||
| chr16:69596589 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.127+28041G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596589 | |||||||
| chr16:69596622 | G | A | 8 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0298 others(5): Show |
8 | NA18942.hp1 NA18953.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+28074G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596622 | |||||||
| chr16:69596644 | G | A | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127+28096G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596644 | |||||||
| chr16:69596675 | G | A | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127+28127G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596675 | |||||||
| chr16:69596696 | C | T | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.127+28148C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596696 | |||||||
| chr16:69596717 | T | TA | 9 | a0001c0001t0001g0221 a0001c0001t0001g0283 a0001c0001t0001g0308 others(6): Show |
9 | HG00639.hp2 HG01175.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+28189dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69596717 | ||||||
| chr16:69596717 | TA | T | 14 | a0001c0001t0002g0091 a0001c0001t0003g0158 a0001c0001t0005g0319 others(11): Show |
14 | HG00423.hp1 HG01069.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.127+28189delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69596717 | ||||||
| chr16:69596929 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.127+28381A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596929 | |||||||
| chr16:69596950 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.127+28402C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69596950 | |||||||
| chr16:69597077 | G | T | 1 | a0001c0001t0004g0154 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.127+28529G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597077 | |||||||
| chr16:69597348 | T | A | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+28800T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597348 | |||||||
| chr16:69597439 | G | A | 34 | a0001c0001t0003g0047 a0001c0001t0003g0122 a0001c0001t0003g0123 others(31): Show |
34 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.127+28891G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597439 | |||||||
| chr16:69597446 | G | A | 1 | a0001c0001t0005g0318 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127+28898G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597446 | |||||||
| chr16:69597472 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.127+28924G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597472 | |||||||
| chr16:69597516 | C | T | 1 | a0001c0001t0028g0373 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.128-28887C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597516 | |||||||
| chr16:69597534 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.128-28869G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597534 | |||||||
| chr16:69597548 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-28855A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597548 | |||||||
| chr16:69597594 | C | CT | 6 | a0001c0001t0001g0233 a0001c0001t0003g0195 a0001c0001t0025g0339 others(3): Show |
6 | HG02602.hp2 HG02895.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-28794dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69597594 | ||||||
| chr16:69597622 | C | T | 1 | a0001c0001t0003g0147 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.128-28781C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597622 | |||||||
| chr16:69597653 | G | A | 6 | a0001c0001t0006g0049 a0001c0001t0006g0057 a0001c0001t0006g0166 others(3): Show |
6 | HG02083.hp2 NA18957.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-28750G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597653 | |||||||
| chr16:69597668 | C | T | 1 | a0001c0001t0010g0348 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.128-28735C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597668 | |||||||
| chr16:69597845 | A | G | 326 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(323): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.128-28558A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69597845 | |||||||
| chr16:69598148 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.128-28255C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69598148 | |||||||
| chr16:69598197 | AACATAAC others(3): Show |
A | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-28203_128-2819 others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69598197 | ||||||
| chr16:69598380 | T | TA | 11 | a0001c0001t0002g0108 a0001c0001t0003g0122 a0001c0001t0003g0139 others(8): Show |
11 | HG00280.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.128-28001dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69598380 | ||||||
| chr16:69598380 | TA | T | 18 | a0001c0001t0001g0274 a0001c0001t0001g0305 a0001c0001t0001g0306 others(15): Show |
18 | HG01070.hp2 HG01074.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.128-28001delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69598380 | ||||||
| chr16:69598380 | TAAAAAAA others(3): Show |
T | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-28010_128-2800 others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69598380 | ||||||
| chr16:69598433 | A | G | 2 | a0001c0001t0007g0181 a0001c0001t0007g0182 |
2 | NA18966.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.128-27970A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69598433 | |||||||
| chr16:69598524 | G | A | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-27879G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69598524 | |||||||
| chr16:69598885 | G | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-27518G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69598885 | |||||||
| chr16:69598949 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.128-27454G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69598949 | |||||||
| chr16:69598970 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0283 |
2 | HG00639.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.128-27433C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69598970 | |||||||
| chr16:69598971 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.128-27432G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69598971 | |||||||
| chr16:69599019 | T | G | 1 | a0001c0001t0006g0055 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.128-27384T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599019 | |||||||
| chr16:69599020 | C | CA | 25 | a0001c0001t0001g0009 a0001c0001t0001g0278 a0001c0001t0001g0287 others(22): Show |
25 | HG00408.hp2 HG00639.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.128-27363dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69599020 | ||||||
| chr16:69599058 | A | G | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.128-27345A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599058 | |||||||
| chr16:69599123 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-27280A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599123 | |||||||
| chr16:69599219 | A | AC | 32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
33 | HG00408.hp1 HG00733.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.128-27184_128-2718 others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599219 | |||||||
| chr16:69599222 | A | AC | 217 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0210 others(214): Show |
220 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.128-27180dupC | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69599222 | ||||||
| chr16:69599222 | A | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
34 | HG00408.hp1 HG00733.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.128-27181A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599222 | |||||||
| chr16:69599323 | T | G | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.128-27080T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599323 | |||||||
| chr16:69599342 | T | C | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.128-27061T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599342 | |||||||
| chr16:69599612 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.128-26791G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599612 | |||||||
| chr16:69599623 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.128-26780G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599623 | |||||||
| chr16:69599796 | A | G | 1 | a0001c0001t0002g0323 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.128-26607A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599796 | |||||||
| chr16:69599822 | G | A | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-26581G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599822 | |||||||
| chr16:69599980 | A | G | 1 | a0001c0001t0010g0360 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.128-26423A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69599980 | |||||||
| chr16:69600150 | G | GA | 13 | a0001c0001t0005g0319 a0001c0001t0009g0197 a0001c0001t0009g0198 others(10): Show |
13 | HG01243.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.128-26240dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69600150 | ||||||
| chr16:69600150 | GA | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.128-26240delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69600150 | ||||||
| chr16:69600168 | A | G | 1 | a0001c0001t0009g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128-26235A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69600168 | |||||||
| chr16:69600760 | G | GA | 242 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(239): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.128-25624dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69600760 | ||||||
| chr16:69600760 | G | GAA | 35 | a0001c0001t0004g0332 a0001c0001t0005g0010 a0001c0001t0005g0025 others(32): Show |
35 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.128-25625_128-2562 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69600760 | ||||||
| chr16:69600824 | C | G | 6 | a0001c0001t0001g0210 a0001c0001t0001g0283 a0001c0001t0001g0285 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-25579C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69600824 | |||||||
| chr16:69600854 | A | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.128-25549A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69600854 | |||||||
| chr16:69601156 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.128-25247A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69601156 | |||||||
| chr16:69601856 | G | A | 1 | a0001c0001t0005g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.128-24547G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69601856 | |||||||
| chr16:69602013 | A | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.128-24390A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69602013 | |||||||
| chr16:69602042 | T | G | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-24361T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69602042 | |||||||
| chr16:69602123 | CT | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.128-24271delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69602123 | ||||||
| chr16:69602248 | G | C | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-24155G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69602248 | |||||||
| chr16:69602270 | C | CT | 26 | a0001c0001t0002g0090 a0001c0001t0006g0177 a0001c0001t0007g0054 others(23): Show |
29 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.128-24117dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69602270 | ||||||
| chr16:69602376 | C | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-24027C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69602376 | |||||||
| chr16:69602424 | G | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.128-23979G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69602424 | |||||||
| chr16:69602598 | T | C | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-23805T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69602598 | |||||||
| chr16:69602779 | G | GT | 6 | a0001c0001t0005g0328 a0001c0001t0016g0362 a0001c0001t0016g0364 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-23613dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69602779 | ||||||
| chr16:69602780 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.128-23623T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69602780 | |||||||
| chr16:69603190 | G | A | 1 | a0001c0001t0054g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.128-23213G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69603190 | |||||||
| chr16:69603254 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.128-23149C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69603254 | |||||||
| chr16:69603446 | T | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-22957T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69603446 | |||||||
| chr16:69603481 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.128-22922G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69603481 | |||||||
| chr16:69603958 | A | G | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-22445A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69603958 | |||||||
| chr16:69604022 | A | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-22381A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69604022 | |||||||
| chr16:69604158 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.128-22245G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69604158 | |||||||
| chr16:69604324 | T | C | 3 | a0001c0001t0018g0209 a0001c0001t0018g0336 a0001c0001t0018g0337 |
3 | HG01884.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.128-22079T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69604324 | |||||||
| chr16:69604408 | A | G | 2 | a0001c0001t0028g0372 a0001c0001t0028g0373 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.128-21995A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69604408 | |||||||
| chr16:69604548 | C | T | 1 | a0001c0001t0004g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.128-21855C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69604548 | |||||||
| chr16:69604597 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.128-21806C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69604597 | |||||||
| chr16:69604636 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.128-21767C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69604636 | |||||||
| chr16:69605033 | A | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-21370A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605033 | |||||||
| chr16:69605135 | T | C | 1 | a0001c0001t0058g0357 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128-21268T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605135 | |||||||
| chr16:69605161 | C | T | 8 | a0001c0001t0002g0044 a0001c0001t0002g0073 a0001c0001t0002g0089 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-21242C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605161 | |||||||
| chr16:69605177 | C | T | 17 | a0001c0001t0047g0342 a0001c0002t0008g0001 a0001c0002t0008g0012 others(14): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.128-21226C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605177 | |||||||
| chr16:69605238 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.128-21165G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605238 | |||||||
| chr16:69605306 | G | C | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-21097G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605306 | |||||||
| chr16:69605312 | C | T | 7 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(4): Show |
7 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-21091C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605312 | |||||||
| chr16:69605330 | C | T | 1 | a0001c0001t0010g0346 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.128-21073C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605330 | |||||||
| chr16:69605371 | C | T | 1 | a0002c0004t0007g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.128-21032C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605371 | |||||||
| chr16:69605427 | G | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-20976G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605427 | |||||||
| chr16:69605428 | A | G | 1 | a0001c0001t0034g0284 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.128-20975A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605428 | |||||||
| chr16:69605437 | CAAAAAGA others(6): Show |
C | 2 | a0001c0001t0009g0201 a0001c0001t0009g0202 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.128-20961_128-2094 others(17): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69605437 | ||||||
| chr16:69605679 | T | G | 1 | a0001c0001t0002g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.128-20724T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605679 | |||||||
| chr16:69605729 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.128-20674C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605729 | |||||||
| chr16:69605761 | C | T | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-20642C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605761 | |||||||
| chr16:69605765 | C | G | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.128-20638C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605765 | |||||||
| chr16:69605868 | T | C | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.128-20535T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605868 | |||||||
| chr16:69605964 | C | T | 1 | a0001c0001t0054g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.128-20439C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69605964 | |||||||
| chr16:69606151 | A | G | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-20252A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606151 | |||||||
| chr16:69606156 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.128-20247G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606156 | |||||||
| chr16:69606314 | A | G | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.128-20089A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606314 | |||||||
| chr16:69606365 | G | A | 1 | a0001c0001t0010g0348 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.128-20038G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606365 | |||||||
| chr16:69606503 | C | T | 1 | a0001c0001t0004g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.128-19900C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606503 | |||||||
| chr16:69606504 | G | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-19899G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606504 | |||||||
| chr16:69606563 | G | A | 2 | a0001c0002t0026g0022 a0001c0002t0026g0023 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.128-19840G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606563 | |||||||
| chr16:69606687 | T | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.128-19716T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606687 | |||||||
| chr16:69606941 | C | T | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-19462C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606941 | |||||||
| chr16:69606964 | T | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.128-19439T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69606964 | |||||||
| chr16:69607105 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0243 |
2 | HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.128-19298A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69607105 | |||||||
| chr16:69607148 | G | C | 7 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0201 others(4): Show |
7 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-19255G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69607148 | |||||||
| chr16:69607235 | T | C | 1 | a0002c0004t0007g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.128-19168T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69607235 | |||||||
| chr16:69607430 | T | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0325 a0001c0001t0005g0326 others(1): Show |
4 | NA18612.hp1 NA18747.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-18973T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69607430 | |||||||
| chr16:69607573 | T | C | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-18830T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69607573 | |||||||
| chr16:69607890 | C | T | 1 | a0001c0001t0006g0176 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.128-18513C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69607890 | |||||||
| chr16:69608030 | G | A | 1 | a0001c0001t0044g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.128-18373G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608030 | |||||||
| chr16:69608193 | CA | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-18205delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69608193 | ||||||
| chr16:69608214 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.128-18189G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608214 | |||||||
| chr16:69608329 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-18074A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608329 | |||||||
| chr16:69608342 | A | G | 1 | a0001c0001t0005g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.128-18061A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608342 | |||||||
| chr16:69608405 | G | A | 1 | a0001c0001t0003g0158 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.128-17998G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608405 | |||||||
| chr16:69608521 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.128-17882C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608521 | |||||||
| chr16:69608539 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.128-17864G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608539 | |||||||
| chr16:69608572 | C | T | 1 | a0001c0001t0006g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.128-17831C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608572 | |||||||
| chr16:69608671 | A | G | 4 | a0001c0001t0004g0036 a0001c0001t0004g0153 a0001c0001t0004g0154 others(1): Show |
4 | HG02027.hp1 NA18948.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-17732A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608671 | |||||||
| chr16:69608701 | G | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-17702G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608701 | |||||||
| chr16:69608893 | G | A | 1 | a0001c0001t0006g0173 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.128-17510G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608893 | |||||||
| chr16:69608915 | A | G | 1 | a0001c0001t0002g0361 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-17488A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608915 | |||||||
| chr16:69608920 | G | A | 1 | a0001c0001t0019g0369 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.128-17483G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608920 | |||||||
| chr16:69608982 | G | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-17421G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69608982 | |||||||
| chr16:69609120 | C | CA | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-17270dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69609120 | ||||||
| chr16:69609122 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-17281A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69609122 | |||||||
| chr16:69609196 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.128-17207C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69609196 | |||||||
| chr16:69609450 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-16953A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69609450 | |||||||
| chr16:69609520 | T | G | 1 | a0001c0001t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.128-16883T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69609520 | |||||||
| chr16:69609819 | G | GA | 10 | a0001c0001t0001g0231 a0001c0001t0002g0108 a0001c0001t0006g0191 others(7): Show |
10 | HG02257.hp2 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-16562dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69609819 | ||||||
| chr16:69609819 | GA | G | 122 | a0001c0001t0001g0270 a0001c0001t0002g0109 a0001c0001t0003g0046 others(119): Show |
125 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.128-16562delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69609819 | ||||||
| chr16:69609836 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-16567A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69609836 | |||||||
| chr16:69610001 | AAGAG | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-16386_128-1638 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69610001 | ||||||
| chr16:69610021 | CAGAT | C | 66 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(63): Show |
66 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.128-16378_128-1637 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69610021 | ||||||
| chr16:69610146 | C | A | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.128-16257C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69610146 | |||||||
| chr16:69610331 | T | G | 1 | a0001c0001t0010g0346 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.128-16072T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69610331 | |||||||
| chr16:69610351 | T | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-16052T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69610351 | |||||||
| chr16:69610364 | T | G | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.128-16039T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69610364 | |||||||
| chr16:69610426 | A | C | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.128-15977A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69610426 | |||||||
| chr16:69610694 | G | A | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-15709G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69610694 | |||||||
| chr16:69610997 | T | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0291 |
2 | NA18747.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.128-15406T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69610997 | |||||||
| chr16:69611076 | T | C | 6 | a0001c0001t0001g0210 a0001c0001t0001g0283 a0001c0001t0001g0285 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-15327T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69611076 | |||||||
| chr16:69611184 | C | T | 1 | a0001c0001t0028g0373 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.128-15219C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69611184 | |||||||
| chr16:69611394 | T | G | 1 | a0001c0001t0001g0268 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.128-15009T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69611394 | |||||||
| chr16:69611553 | A | T | 4 | a0001c0001t0010g0348 a0001c0001t0010g0354 a0001c0001t0010g0355 others(1): Show |
4 | HG02132.hp2 NA18950.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-14850A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69611553 | |||||||
| chr16:69611570 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.128-14833G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69611570 | |||||||
| chr16:69611596 | A | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.128-14807A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69611596 | |||||||
| chr16:69611663 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-14740A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69611663 | |||||||
| chr16:69612088 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.128-14315G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69612088 | |||||||
| chr16:69612125 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0222 |
2 | NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.128-14278G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69612125 | |||||||
| chr16:69612219 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.128-14184C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69612219 | |||||||
| chr16:69612264 | C | A | 5 | a0001c0001t0002g0076 a0001c0001t0002g0078 a0001c0001t0002g0080 others(2): Show |
5 | HG01255.hp1 HG01261.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-14139C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69612264 | |||||||
| chr16:69612282 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.128-14121C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69612282 | |||||||
| chr16:69612424 | CTT | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.128-13977_128-1397 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69612424 | ||||||
| chr16:69612593 | C | T | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.128-13810C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69612593 | |||||||
| chr16:69612651 | G | C | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-13752G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69612651 | |||||||
| chr16:69612699 | G | GAC | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-13687_128-1368 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69612699 | ||||||
| chr16:69612875 | G | A | 326 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(323): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.128-13528G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69612875 | |||||||
| chr16:69612909 | AAAAAC | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-13489_128-1348 others(9): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69612909 | ||||||
| chr16:69613004 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-13399A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69613004 | |||||||
| chr16:69613005 | A | G | 3 | a0001c0001t0004g0133 a0001c0001t0004g0134 a0001c0001t0004g0155 |
3 | NA18942.hp2 NA18979.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.128-13398A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69613005 | |||||||
| chr16:69613207 | G | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-13196G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69613207 | |||||||
| chr16:69613298 | C | T | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.128-13105C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69613298 | |||||||
| chr16:69613634 | A | G | 1 | a0001c0001t0019g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.128-12769A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69613634 | |||||||
| chr16:69613763 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-12640A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69613763 | |||||||
| chr16:69613987 | T | C | 3 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 |
3 | HG01255.hp2 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.128-12416T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69613987 | |||||||
| chr16:69614086 | A | G | 1 | a0001c0001t0005g0328 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.128-12317A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614086 | |||||||
| chr16:69614158 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.128-12245T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614158 | |||||||
| chr16:69614251 | G | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-12152G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614251 | |||||||
| chr16:69614315 | C | T | 4 | a0001c0001t0006g0053 a0001c0001t0006g0173 a0001c0001t0006g0183 others(1): Show |
4 | HG01952.hp2 HG03098.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-12088C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614315 | |||||||
| chr16:69614592 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.128-11811T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614592 | |||||||
| chr16:69614724 | C | T | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.128-11679C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614724 | |||||||
| chr16:69614737 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.128-11666G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614737 | |||||||
| chr16:69614750 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.128-11653G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614750 | |||||||
| chr16:69614757 | C | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-11646C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614757 | |||||||
| chr16:69614862 | T | C | 1 | a0001c0001t0003g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.128-11541T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614862 | |||||||
| chr16:69614878 | C | CT | 285 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.128-11509dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69614878 | ||||||
| chr16:69614878 | C | CTT | 25 | a0001c0001t0001g0011 a0001c0001t0001g0253 a0001c0001t0001g0272 others(22): Show |
25 | HG00140.hp2 HG00323.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.128-11510_128-1150 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69614878 | ||||||
| chr16:69614940 | G | A | 1 | a0001c0008t0001g0296 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.128-11463G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69614940 | |||||||
| chr16:69615044 | A | AT | 7 | a0001c0001t0005g0329 a0001c0001t0016g0362 a0001c0001t0016g0364 others(4): Show |
7 | HG02257.hp2 HG02486.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-11342dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69615044 | ||||||
| chr16:69615044 | AT | A | 8 | a0001c0001t0001g0229 a0001c0001t0002g0061 a0001c0001t0002g0324 others(5): Show |
8 | HG01070.hp2 HG01257.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-11342delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69615044 | ||||||
| chr16:69615045 | T | A | 1 | a0001c0001t0007g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.128-11358T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615045 | |||||||
| chr16:69615195 | C | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.128-11208C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615195 | |||||||
| chr16:69615214 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.128-11189G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615214 | |||||||
| chr16:69615294 | G | A | 1 | a0001c0002t0008g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.128-11109G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615294 | |||||||
| chr16:69615505 | A | C | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-10898A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615505 | |||||||
| chr16:69615566 | A | G | 1 | a0001c0001t0034g0284 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.128-10837A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615566 | |||||||
| chr16:69615644 | C | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-10759C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615644 | |||||||
| chr16:69615787 | C | T | 1 | a0001c0001t0019g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.128-10616C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615787 | |||||||
| chr16:69615870 | C | G | 1 | a0001c0001t0010g0346 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.128-10533C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615870 | |||||||
| chr16:69615871 | T | A | 1 | a0001c0001t0010g0346 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.128-10532T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615871 | |||||||
| chr16:69615941 | A | G | 1 | a0001c0001t0054g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.128-10462A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615941 | |||||||
| chr16:69615975 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-10428A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69615975 | |||||||
| chr16:69616284 | A | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0253 a0001c0001t0001g0267 others(27): Show |
31 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.128-10119A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69616284 | |||||||
| chr16:69616361 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-10042A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69616361 | |||||||
| chr16:69616518 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.128-9885C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69616518 | |||||||
| chr16:69616619 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.128-9784C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69616619 | |||||||
| chr16:69616940 | C | CT | 24 | a0001c0001t0001g0297 a0001c0001t0003g0158 a0001c0001t0006g0192 others(21): Show |
24 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-9445dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69616940 | ||||||
| chr16:69616940 | CT | C | 6 | a0001c0001t0001g0003 a0001c0001t0002g0072 a0001c0001t0006g0177 others(3): Show |
6 | HG01109.hp1 HG01346.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-9445delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69616940 | ||||||
| chr16:69616946 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.128-9457T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69616946 | |||||||
| chr16:69617005 | G | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-9398G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617005 | |||||||
| chr16:69617104 | C | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-9299C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617104 | |||||||
| chr16:69617144 | G | A | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-9259G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617144 | |||||||
| chr16:69617164 | G | A | 1 | a0001c0001t0034g0284 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.128-9239G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617164 | |||||||
| chr16:69617273 | C | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.128-9130C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617273 | |||||||
| chr16:69617403 | G | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-9000G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617403 | |||||||
| chr16:69617611 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.128-8792C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617611 | |||||||
| chr16:69617741 | A | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-8662A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617741 | |||||||
| chr16:69617777 | C | G | 4 | a0001c0001t0010g0348 a0001c0001t0010g0354 a0001c0001t0010g0355 others(1): Show |
4 | HG02132.hp2 NA18950.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-8626C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617777 | |||||||
| chr16:69617798 | A | G | 98 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(95): Show |
98 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.128-8605A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617798 | |||||||
| chr16:69617954 | CG | C | 8 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(5): Show |
8 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-8448delG | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617954 | |||||||
| chr16:69617963 | C | T | 76 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.128-8440C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69617963 | |||||||
| chr16:69618014 | T | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.128-8389T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618014 | |||||||
| chr16:69618135 | G | A | 5 | a0001c0001t0003g0046 a0001c0001t0003g0124 a0001c0001t0003g0139 others(2): Show |
5 | NA18952.hp2 NA18980.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-8268G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618135 | |||||||
| chr16:69618158 | C | CA | 115 | a0001c0001t0001g0234 a0001c0001t0002g0078 a0001c0001t0002g0092 others(112): Show |
115 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.128-8228dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69618158 | ||||||
| chr16:69618191 | G | C | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.128-8212G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618191 | |||||||
| chr16:69618285 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.128-8118A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618285 | |||||||
| chr16:69618479 | T | C | 1 | a0001c0001t0019g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.128-7924T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618479 | |||||||
| chr16:69618508 | G | A | 1 | a0001c0001t0016g0364 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.128-7895G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618508 | |||||||
| chr16:69618542 | A | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-7861A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618542 | |||||||
| chr16:69618545 | C | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0072 |
2 | HG01109.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.128-7858C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618545 | |||||||
| chr16:69618623 | A | G | 1 | a0001c0008t0001g0296 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.128-7780A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618623 | |||||||
| chr16:69618705 | CTCTT | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-7695_128-7692d others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69618705 | ||||||
| chr16:69618943 | T | C | 3 | a0001c0001t0019g0367 a0001c0001t0019g0368 a0001c0001t0019g0369 |
3 | HG02572.hp1 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.128-7460T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69618943 | |||||||
| chr16:69619096 | G | A | 1 | a0001c0001t0019g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.128-7307G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69619096 | |||||||
| chr16:69619152 | C | T | 1 | a0001c0001t0003g0207 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.128-7251C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69619152 | |||||||
| chr16:69619317 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.128-7086C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69619317 | |||||||
| chr16:69619521 | A | G | 1 | a0004c0010t0002g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.128-6882A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69619521 | |||||||
| chr16:69619793 | C | G | 326 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(323): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.128-6610C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69619793 | |||||||
| chr16:69620026 | A | G | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-6377A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620026 | |||||||
| chr16:69620104 | G | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-6299G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620104 | |||||||
| chr16:69620342 | G | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.128-6061G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620342 | |||||||
| chr16:69620402 | G | A | 10 | a0001c0001t0003g0121 a0001c0001t0003g0125 a0001c0001t0003g0142 others(7): Show |
10 | HG02083.hp1 NA18612.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-6001G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620402 | |||||||
| chr16:69620560 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.128-5843C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620560 | |||||||
| chr16:69620563 | G | A | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-5840G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620563 | |||||||
| chr16:69620686 | C | A | 1 | a0001c0011t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.128-5717C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620686 | |||||||
| chr16:69620709 | A | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-5694A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620709 | |||||||
| chr16:69620754 | G | T | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.128-5649G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620754 | |||||||
| chr16:69620763 | A | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.128-5640A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620763 | |||||||
| chr16:69620887 | G | T | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.128-5516G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69620887 | |||||||
| chr16:69621052 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.128-5351G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621052 | |||||||
| chr16:69621135 | A | G | 2 | a0001c0001t0027g0052 a0001c0001t0027g0175 |
2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.128-5268A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621135 | |||||||
| chr16:69621156 | A | T | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-5247A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621156 | |||||||
| chr16:69621253 | TA | T | 51 | a0001c0001t0002g0097 a0001c0001t0002g0109 a0001c0001t0003g0047 others(48): Show |
51 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.128-5137delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69621253 | ||||||
| chr16:69621401 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.128-5002T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621401 | |||||||
| chr16:69621461 | T | C | 4 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-4942T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621461 | |||||||
| chr16:69621514 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.128-4889A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621514 | |||||||
| chr16:69621688 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0222 others(1): Show |
4 | HG00597.hp2 NA18971.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-4715G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621688 | |||||||
| chr16:69621804 | A | G | 1 | a0001c0001t0016g0362 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.128-4599A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621804 | |||||||
| chr16:69621815 | T | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0223 |
3 | NA18990.hp2 NA19054.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.128-4588T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621815 | |||||||
| chr16:69621914 | G | A | 1 | a0001c0001t0002g0361 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-4489G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69621914 | |||||||
| chr16:69621962 | CAAATA | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.128-4418_128-4414d others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69621962 | ||||||
| chr16:69622046 | A | T | 2 | a0001c0001t0029g0056 a0001c0001t0029g0371 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.128-4357A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69622046 | |||||||
| chr16:69622597 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.128-3806A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69622597 | |||||||
| chr16:69622629 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.128-3774G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69622629 | |||||||
| chr16:69622711 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.128-3692A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69622711 | |||||||
| chr16:69622798 | G | A | 4 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(1): Show |
4 | NA18979.hp1 NA18981.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-3605G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69622798 | |||||||
| chr16:69622832 | GA | G | 276 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(273): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.128-3557delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69622832 | ||||||
| chr16:69622832 | GAA | G | 95 | a0001c0001t0001g0261 a0001c0001t0003g0046 a0001c0001t0003g0121 others(92): Show |
95 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.128-3558_128-3557d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69622832 | ||||||
| chr16:69622986 | G | A | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.128-3417G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69622986 | |||||||
| chr16:69623110 | A | G | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-3293A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69623110 | |||||||
| chr16:69623328 | T | C | 1 | a0001c0001t0003g0147 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.128-3075T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69623328 | |||||||
| chr16:69623334 | C | CT | 23 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(20): Show |
23 | HG00099.hp1 HG01255.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.128-3054dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69623334 | ||||||
| chr16:69623334 | CT | C | 23 | a0001c0001t0002g0062 a0001c0001t0002g0084 a0001c0001t0017g0374 others(20): Show |
26 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.128-3054delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69623334 | ||||||
| chr16:69623734 | C | G | 1 | a0001c0001t0002g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.128-2669C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69623734 | |||||||
| chr16:69623753 | T | C | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.128-2650T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69623753 | |||||||
| chr16:69623770 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.128-2633G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69623770 | |||||||
| chr16:69623815 | T | C | 4 | a0001c0001t0005g0319 a0001c0001t0019g0367 a0001c0001t0019g0368 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-2588T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69623815 | |||||||
| chr16:69623853 | G | GA | 11 | a0001c0001t0002g0044 a0001c0001t0002g0065 a0001c0001t0002g0102 others(8): Show |
11 | HG00597.hp1 HG00639.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.128-2534dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69623853 | ||||||
| chr16:69623853 | GA | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0222 a0001c0001t0003g0047 others(11): Show |
14 | HG01255.hp2 HG02572.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.128-2534delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69623853 | ||||||
| chr16:69623853 | GAA | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(224): Show |
231 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.128-2535_128-2534d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69623853 | ||||||
| chr16:69623853 | GAAA | G | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-2536_128-2534d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69623853 | ||||||
| chr16:69623869 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.128-2534A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69623869 | |||||||
| chr16:69624041 | G | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-2362G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624041 | |||||||
| chr16:69624047 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-2356G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624047 | |||||||
| chr16:69624093 | T | G | 76 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.128-2310T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624093 | |||||||
| chr16:69624362 | C | T | 4 | a0001c0001t0011g0310 a0001c0001t0011g0311 a0001c0001t0011g0312 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-2041C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624362 | |||||||
| chr16:69624460 | G | C | 1 | a0001c0001t0005g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.128-1943G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624460 | |||||||
| chr16:69624496 | C | T | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.128-1907C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624496 | |||||||
| chr16:69624497 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.128-1906G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624497 | |||||||
| chr16:69624601 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-1802A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624601 | |||||||
| chr16:69624626 | A | G | 1 | a0001c0001t0006g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128-1777A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624626 | |||||||
| chr16:69624873 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.128-1530A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624873 | |||||||
| chr16:69624895 | C | CT | 96 | a0001c0001t0001g0224 a0001c0001t0001g0232 a0001c0001t0001g0247 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.128-1500dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69624895 | ||||||
| chr16:69624903 | T | A | 4 | a0001c0001t0002g0090 a0001c0001t0011g0309 a0001c0001t0042g0079 others(1): Show |
4 | HG01255.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1500T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624903 | |||||||
| chr16:69624903 | TA | T | 9 | a0001c0001t0001g0317 a0001c0001t0002g0091 a0001c0001t0002g0324 others(6): Show |
9 | HG01070.hp2 HG01516.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-1485delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69624903 | ||||||
| chr16:69624904 | A | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.128-1499A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624904 | |||||||
| chr16:69624905 | A | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.128-1498A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624905 | |||||||
| chr16:69624906 | A | T | 2 | a0001c0001t0001g0317 a0003c0005t0001g0259 |
2 | NA18992.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.128-1497A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624906 | |||||||
| chr16:69624960 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.128-1443C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624960 | |||||||
| chr16:69624990 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.128-1413C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69624990 | |||||||
| chr16:69625158 | T | C | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.128-1245T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69625158 | |||||||
| chr16:69625496 | A | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.128-907A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69625496 | |||||||
| chr16:69625532 | CT | C | 12 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(9): Show |
12 | HG01433.hp1 HG02559.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.128-859delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 69625532 | ||||||
| chr16:69625561 | A | C | 1 | a0001c0001t0058g0357 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128-842A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69625561 | |||||||
| chr16:69625728 | A | G | 1 | a0001c0001t0040g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.128-675A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69625728 | |||||||
| chr16:69625947 | T | C | 3 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0315 |
3 | NA18987.hp1 NA19007.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.128-456T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69625947 | |||||||
| chr16:69625961 | A | T | 32 | a0001c0001t0002g0044 a0001c0001t0002g0073 a0001c0001t0002g0089 others(29): Show |
35 | HG01069.hp1 HG01168.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.128-442A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69625961 | |||||||
| chr16:69625962 | T | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.128-441T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69625962 | |||||||
| chr16:69626101 | G | A | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.128-302G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69626101 | |||||||
| chr16:69626624 | T | A | 1 | a0001c0001t0004g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.253+96T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69626624 | |||||||
| chr16:69626634 | G | A | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.253+106G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69626634 | |||||||
| chr16:69626938 | A | G | 98 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(95): Show |
98 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.253+410A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69626938 | |||||||
| chr16:69626987 | A | T | 1 | a0001c0001t0002g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.253+459A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69626987 | |||||||
| chr16:69627156 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.253+628T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69627156 | |||||||
| chr16:69627224 | T | C | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.253+696T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69627224 | |||||||
| chr16:69627321 | AACATATA others(5): Show |
A | 1 | a0001c0001t0006g0168 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.253+795_253+806del others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627321 | ||||||
| chr16:69627321 | AACATATA others(7): Show |
A | 3 | a0001c0001t0006g0169 a0001c0001t0006g0174 a0001c0001t0006g0189 |
3 | HG01070.hp1 HG01168.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.253+795_253+808del others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627321 | ||||||
| chr16:69627323 | C | CATATATA others(11): Show |
1 | a0001c0001t0006g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.253+838_253+855dup others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CAT | C | 3 | a0001c0001t0007g0004 a0001c0001t0007g0031 a0001c0001t0007g0182 |
3 | HG01175.hp2 NA18948.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.253+854_253+855del others(2): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATAT | C | 6 | a0001c0001t0006g0057 a0001c0001t0006g0176 a0001c0001t0006g0183 others(3): Show |
6 | HG02083.hp2 HG03017.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.253+852_253+855del others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATAT | C | 3 | a0001c0001t0006g0055 a0001c0001t0006g0188 a0001c0001t0018g0337 |
3 | HG03209.hp1 NA18939.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.253+850_253+855del others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(1): Show |
C | 5 | a0001c0001t0006g0167 a0001c0001t0006g0191 a0001c0001t0006g0192 others(2): Show |
5 | HG00597.hp1 HG01069.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.253+848_253+855del others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(3): Show |
C | 4 | a0001c0001t0006g0058 a0001c0001t0006g0173 a0001c0001t0006g0190 others(1): Show |
4 | HG01884.hp1 HG01952.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+846_253+855del others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(5): Show |
C | 1 | a0001c0001t0007g0185 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.253+844_253+855del others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(7): Show |
C | 2 | a0001c0001t0007g0050 a0001c0001t0007g0054 |
2 | HG02080.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.253+842_253+855del others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(11): Show |
C | 3 | a0001c0001t0006g0177 a0001c0001t0007g0193 a0001c0001t0061g0178 |
3 | NA18940.hp1 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.253+838_253+855del others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(13): Show |
C | 2 | a0002c0004t0007g0171 a0002c0004t0007g0179 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.253+836_253+855del others(20): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(15): Show |
C | 1 | a0002c0004t0007g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.253+834_253+855del others(22): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(17): Show |
C | 2 | a0001c0001t0002g0043 a0001c0001t0015g0088 |
2 | HG02559.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.253+832_253+855del others(24): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(19): Show |
C | 9 | a0001c0001t0002g0035 a0001c0001t0002g0044 a0001c0001t0002g0073 others(6): Show |
9 | HG00280.hp2 HG02258.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.253+830_253+855del others(26): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(21): Show |
C | 13 | a0001c0001t0002g0062 a0001c0001t0002g0077 a0001c0001t0002g0084 others(10): Show |
13 | HG00099.hp1 HG00735.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.253+828_253+855del others(28): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(23): Show |
C | 66 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(63): Show |
69 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.253+826_253+855del others(30): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(25): Show |
C | 8 | a0001c0001t0005g0159 a0001c0001t0005g0328 a0001c0001t0009g0117 others(5): Show |
8 | HG00738.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+824_253+855del others(32): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(27): Show |
C | 31 | a0001c0001t0001g0278 a0001c0001t0004g0036 a0001c0001t0005g0010 others(28): Show |
31 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.253+822_253+855del others(34): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(29): Show |
C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0241 others(96): Show |
99 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.253+820_253+855del others(36): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(31): Show |
C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(94): Show |
98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.253+818_253+855del others(38): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627323 | CATATATA others(33): Show |
C | 6 | a0001c0001t0001g0308 a0001c0001t0016g0362 a0001c0001t0016g0364 others(3): Show |
6 | HG00609.hp2 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.253+816_253+855del others(40): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627323 | ||||||
| chr16:69627382 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.253+854A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69627382 | |||||||
| chr16:69627424 | A | G | 1 | a0001c0001t0006g0057 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.253+896A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69627424 | |||||||
| chr16:69627511 | A | G | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.253+983A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69627511 | |||||||
| chr16:69627582 | T | C | 1 | a0001c0001t0006g0166 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.253+1054T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69627582 | |||||||
| chr16:69627624 | TCAGGCTG others(7): Show |
T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.253+1099_253+1112d others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69627624 | ||||||
| chr16:69628103 | T | C | 98 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(95): Show |
98 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.253+1575T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69628103 | |||||||
| chr16:69628186 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.253+1658A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69628186 | |||||||
| chr16:69628373 | T | C | 2 | a0001c0001t0002g0105 a0001c0001t0043g0204 |
2 | HG00423.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.253+1845T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69628373 | |||||||
| chr16:69628798 | T | C | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.253+2270T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69628798 | |||||||
| chr16:69628842 | G | A | 3 | a0001c0001t0006g0058 a0001c0001t0006g0190 a0001c0001t0006g0191 |
3 | NA18991.hp1 NA18994.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.253+2314G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69628842 | |||||||
| chr16:69628901 | C | T | 1 | a0001c0001t0010g0164 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.253+2373C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69628901 | |||||||
| chr16:69628928 | G | A | 2 | a0001c0001t0004g0131 a0001c0001t0004g0132 |
2 | NA18971.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.253+2400G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69628928 | |||||||
| chr16:69629000 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.253+2472A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69629000 | |||||||
| chr16:69629006 | G | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.253+2478G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69629006 | |||||||
| chr16:69629468 | T | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(249): Show |
256 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.253+2940T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69629468 | |||||||
| chr16:69629469 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.253+2941G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69629469 | |||||||
| chr16:69629616 | T | C | 76 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.253+3088T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69629616 | |||||||
| chr16:69629768 | A | AT | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.253+3263dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69629768 | ||||||
| chr16:69629768 | A | ATT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0222 a0001c0001t0001g0234 others(8): Show |
11 | HG01952.hp1 HG02300.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+3262_253+3263d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69629768 | ||||||
| chr16:69629768 | AT | A | 13 | a0001c0001t0003g0146 a0001c0001t0003g0157 a0001c0001t0003g0205 others(10): Show |
13 | HG01074.hp1 HG01168.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.253+3263delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69629768 | ||||||
| chr16:69629940 | A | AT | 7 | a0001c0001t0002g0041 a0001c0001t0002g0109 a0001c0001t0005g0048 others(4): Show |
7 | HG01069.hp2 HG01192.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+3427dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69629940 | ||||||
| chr16:69629986 | G | C | 1 | a0001c0001t0043g0204 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.253+3458G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69629986 | |||||||
| chr16:69630117 | A | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.253+3589A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69630117 | |||||||
| chr16:69630144 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.253+3616C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69630144 | |||||||
| chr16:69630247 | C | G | 7 | a0001c0001t0005g0135 a0001c0001t0005g0320 a0001c0001t0005g0329 others(4): Show |
7 | HG00735.hp2 HG01167.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.253+3719C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69630247 | |||||||
| chr16:69630276 | C | T | 1 | a0001c0001t0007g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.253+3748C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69630276 | |||||||
| chr16:69630652 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.253+4124A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69630652 | |||||||
| chr16:69630746 | G | C | 1 | a0001c0001t0002g0109 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.253+4218G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69630746 | |||||||
| chr16:69630763 | CAT | C | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+4237_253+4238d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69630763 | ||||||
| chr16:69630899 | T | A | 1 | a0001c0001t0001g0299 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.253+4371T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69630899 | |||||||
| chr16:69630900 | C | G | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.253+4372C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69630900 | |||||||
| chr16:69631016 | T | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.253+4488T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631016 | |||||||
| chr16:69631162 | C | T | 1 | a0001c0001t0028g0373 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.253+4634C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631162 | |||||||
| chr16:69631305 | T | C | 328 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(325): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.253+4777T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631305 | |||||||
| chr16:69631470 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.253+4942A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631470 | |||||||
| chr16:69631493 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.253+4965G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631493 | |||||||
| chr16:69631565 | A | G | 1 | a0001c0001t0001g0316 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.253+5037A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631565 | |||||||
| chr16:69631588 | G | A | 2 | a0001c0001t0011g0213 a0001c0001t0011g0309 |
2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.253+5060G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631588 | |||||||
| chr16:69631621 | CTTTTGT | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0222 others(1): Show |
4 | HG00597.hp2 NA18971.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+5110_253+5115d others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69631621 | ||||||
| chr16:69631728 | C | T | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.253+5200C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631728 | |||||||
| chr16:69631957 | T | C | 1 | a0001c0001t0005g0326 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.253+5429T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631957 | |||||||
| chr16:69631968 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0004c0010t0002g0040 |
3 | HG00323.hp2 HG01074.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.253+5440G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69631968 | |||||||
| chr16:69632089 | C | T | 1 | a0001c0001t0007g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.253+5561C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69632089 | |||||||
| chr16:69632613 | G | A | 1 | a0001c0001t0046g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.253+6085G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69632613 | |||||||
| chr16:69632780 | G | A | 73 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(70): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.253+6252G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69632780 | |||||||
| chr16:69632812 | G | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.253+6284G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69632812 | |||||||
| chr16:69632934 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.253+6406A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69632934 | |||||||
| chr16:69632982 | A | G | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.253+6454A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69632982 | |||||||
| chr16:69633036 | C | T | 23 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(20): Show |
26 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.253+6508C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69633036 | |||||||
| chr16:69633067 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.253+6539C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69633067 | |||||||
| chr16:69633170 | T | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0253 a0001c0001t0001g0268 others(17): Show |
20 | HG00099.hp2 HG00323.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.253+6642T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69633170 | |||||||
| chr16:69633447 | A | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.253+6919A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69633447 | |||||||
| chr16:69633727 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.253+7199A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69633727 | |||||||
| chr16:69633737 | T | G | 1 | a0002c0004t0007g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.253+7209T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69633737 | |||||||
| chr16:69633783 | C | G | 17 | a0001c0001t0047g0342 a0001c0002t0008g0001 a0001c0002t0008g0012 others(14): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.253+7255C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69633783 | |||||||
| chr16:69633995 | G | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0222 others(15): Show |
18 | HG00597.hp2 HG02132.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.253+7467G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69633995 | |||||||
| chr16:69634015 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.253+7487T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634015 | |||||||
| chr16:69634028 | A | T | 5 | a0001c0001t0006g0177 a0001c0001t0007g0054 a0001c0001t0007g0185 others(2): Show |
5 | NA18940.hp1 NA18943.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.253+7500A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634028 | |||||||
| chr16:69634035 | T | C | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.253+7507T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634035 | |||||||
| chr16:69634035 | T | TG | 97 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(94): Show |
97 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.253+7513dupG | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69634035 | ||||||
| chr16:69634037 | G | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.253+7509G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634037 | |||||||
| chr16:69634227 | C | T | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+7699C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634227 | |||||||
| chr16:69634256 | C | T | 1 | a0001c0001t0018g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.253+7728C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634256 | |||||||
| chr16:69634277 | C | CA | 103 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(100): Show |
104 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.253+7771dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69634277 | ||||||
| chr16:69634277 | C | CAA | 26 | a0001c0001t0001g0222 a0001c0001t0001g0228 a0001c0001t0001g0229 others(23): Show |
26 | HG00140.hp2 HG01175.hp1 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.253+7770_253+7771d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69634277 | ||||||
| chr16:69634277 | C | CAAA | 6 | a0001c0001t0001g0220 a0001c0001t0001g0225 a0001c0001t0001g0231 others(3): Show |
6 | HG00597.hp2 HG02055.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.253+7769_253+7771d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69634277 | ||||||
| chr16:69634277 | CAA | C | 17 | a0001c0001t0028g0373 a0001c0001t0047g0342 a0001c0002t0008g0001 others(14): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.253+7770_253+7771d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69634277 | ||||||
| chr16:69634390 | C | G | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.253+7862C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634390 | |||||||
| chr16:69634568 | C | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0222 others(15): Show |
18 | HG00597.hp2 HG02132.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.253+8040C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634568 | |||||||
| chr16:69634593 | A | G | 1 | a0001c0001t0003g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.253+8065A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634593 | |||||||
| chr16:69634649 | C | T | 67 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(64): Show |
67 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.253+8121C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634649 | |||||||
| chr16:69634685 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | NA18995.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.253+8157G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634685 | |||||||
| chr16:69634719 | T | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.253+8191T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634719 | |||||||
| chr16:69634786 | G | A | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.253+8258G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634786 | |||||||
| chr16:69634837 | C | T | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.253+8309C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634837 | |||||||
| chr16:69634941 | C | T | 1 | a0001c0001t0055g0345 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.253+8413C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69634941 | |||||||
| chr16:69635023 | G | GT | 17 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0044 others(14): Show |
17 | HG00735.hp1 HG01109.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.253+8518dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69635023 | ||||||
| chr16:69635023 | GT | G | 95 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0001g0229 others(92): Show |
95 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.253+8518delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69635023 | ||||||
| chr16:69635023 | GTT | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(189): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.253+8517_253+8518d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69635023 | ||||||
| chr16:69635023 | GTTT | G | 8 | a0001c0001t0001g0283 a0001c0001t0005g0335 a0001c0001t0011g0313 others(5): Show |
8 | HG00639.hp2 HG01496.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+8516_253+8518d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69635023 | ||||||
| chr16:69635035 | T | G | 1 | a0001c0001t0001g0299 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.253+8507T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635035 | |||||||
| chr16:69635074 | G | T | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+8546G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635074 | |||||||
| chr16:69635080 | A | G | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.253+8552A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635080 | |||||||
| chr16:69635093 | C | G | 3 | a0001c0001t0007g0029 a0001c0001t0007g0031 a0001c0001t0007g0032 |
3 | HG00597.hp1 NA18948.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.253+8565C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635093 | |||||||
| chr16:69635113 | C | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.253+8585C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635113 | |||||||
| chr16:69635231 | G | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.253+8703G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635231 | |||||||
| chr16:69635253 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.253+8725C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635253 | |||||||
| chr16:69635254 | G | A | 3 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0315 |
3 | NA18987.hp1 NA19007.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.253+8726G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635254 | |||||||
| chr16:69635291 | G | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.253+8763G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635291 | |||||||
| chr16:69635524 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.253+8996G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635524 | |||||||
| chr16:69635527 | C | A | 1 | a0001c0001t0038g0314 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.253+8999C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635527 | |||||||
| chr16:69635752 | G | C | 1 | a0001c0001t0007g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.253+9224G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635752 | |||||||
| chr16:69635856 | T | C | 4 | a0001c0001t0010g0348 a0001c0001t0010g0354 a0001c0001t0010g0355 others(1): Show |
4 | HG02132.hp2 NA18950.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+9328T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69635856 | |||||||
| chr16:69636073 | C | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.253+9545C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636073 | |||||||
| chr16:69636223 | T | G | 1 | a0001c0001t0025g0340 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.253+9695T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636223 | |||||||
| chr16:69636260 | C | G | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.253+9732C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636260 | |||||||
| chr16:69636319 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.253+9791G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636319 | |||||||
| chr16:69636479 | T | C | 1 | a0001c0001t0005g0328 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.253+9951T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636479 | |||||||
| chr16:69636484 | G | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0163 a0001c0001t0003g0196 |
3 | NA18955.hp1 NA18984.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.253+9956G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636484 | |||||||
| chr16:69636537 | C | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+10009C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636537 | |||||||
| chr16:69636713 | C | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.253+10185C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636713 | |||||||
| chr16:69636715 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.253+10187C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636715 | |||||||
| chr16:69636847 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.254-10181C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69636847 | |||||||
| chr16:69637137 | G | A | 3 | a0001c0001t0025g0339 a0001c0001t0025g0340 a0001c0001t0054g0160 |
3 | HG02895.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.254-9891G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637137 | |||||||
| chr16:69637299 | C | G | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.254-9729C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637299 | |||||||
| chr16:69637378 | A | AT | 4 | a0001c0001t0001g0252 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
4 | HG02071.hp2 HG02523.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.254-9644dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69637378 | ||||||
| chr16:69637447 | G | GACAT | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(6): Show |
9 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.254-9578_254-9575d others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69637447 | ||||||
| chr16:69637488 | T | TA | 3 | a0001c0001t0025g0339 a0001c0001t0025g0340 a0001c0001t0050g0194 |
3 | HG02895.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.254-9539dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69637488 | ||||||
| chr16:69637491 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.254-9537A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637491 | |||||||
| chr16:69637550 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.254-9478A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637550 | |||||||
| chr16:69637552 | G | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.254-9476G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637552 | |||||||
| chr16:69637662 | C | T | 1 | a0001c0001t0016g0362 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.254-9366C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637662 | |||||||
| chr16:69637663 | G | A | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.254-9365G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637663 | |||||||
| chr16:69637685 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.254-9343C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637685 | |||||||
| chr16:69637827 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.254-9201G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637827 | |||||||
| chr16:69637969 | C | G | 1 | a0001c0001t0017g0375 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.254-9059C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637969 | |||||||
| chr16:69637974 | A | G | 1 | a0001c0001t0004g0134 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.254-9054A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637974 | |||||||
| chr16:69637995 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.254-9033C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69637995 | |||||||
| chr16:69638008 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.254-9020C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638008 | |||||||
| chr16:69638134 | G | A | 67 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(64): Show |
67 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.254-8894G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638134 | |||||||
| chr16:69638150 | C | T | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.254-8878C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638150 | |||||||
| chr16:69638231 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.254-8797A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638231 | |||||||
| chr16:69638352 | C | T | 3 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0045g0363 |
3 | HG02257.hp2 HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.254-8676C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638352 | |||||||
| chr16:69638469 | C | A | 17 | a0001c0001t0047g0342 a0001c0002t0008g0001 a0001c0002t0008g0012 others(14): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.254-8559C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638469 | |||||||
| chr16:69638507 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.254-8521G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638507 | |||||||
| chr16:69638608 | C | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.254-8420C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638608 | |||||||
| chr16:69638628 | C | T | 23 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(20): Show |
26 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.254-8400C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638628 | |||||||
| chr16:69638735 | C | CA | 105 | a0001c0001t0001g0225 a0001c0001t0002g0095 a0001c0001t0002g0096 others(102): Show |
105 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.254-8274dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69638735 | ||||||
| chr16:69638735 | CA | C | 26 | a0001c0001t0001g0237 a0001c0001t0001g0250 a0001c0001t0001g0262 others(23): Show |
26 | HG00323.hp2 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.254-8274delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69638735 | ||||||
| chr16:69638772 | G | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.254-8256G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638772 | |||||||
| chr16:69638773 | A | C | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-8255A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638773 | |||||||
| chr16:69638899 | CTG | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.254-8127_254-8126d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69638899 | ||||||
| chr16:69638947 | C | T | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.254-8081C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69638947 | |||||||
| chr16:69639066 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.254-7962C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69639066 | |||||||
| chr16:69639560 | A | T | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.254-7468A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69639560 | |||||||
| chr16:69639694 | T | C | 1 | a0001c0001t0001g0315 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.254-7334T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69639694 | |||||||
| chr16:69639724 | G | GT | 10 | a0001c0001t0001g0224 a0001c0001t0009g0197 a0001c0001t0009g0198 others(7): Show |
10 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-7297dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69639724 | ||||||
| chr16:69639816 | AAG | A | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-7206_254-7205d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69639816 | ||||||
| chr16:69639866 | T | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.254-7162T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69639866 | |||||||
| chr16:69639961 | A | T | 1 | a0001c0001t0016g0364 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.254-7067A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69639961 | |||||||
| chr16:69640079 | A | G | 1 | a0001c0001t0005g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.254-6949A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69640079 | |||||||
| chr16:69640495 | A | G | 1 | a0001c0001t0009g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.254-6533A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69640495 | |||||||
| chr16:69640537 | T | C | 24 | a0001c0001t0004g0036 a0001c0001t0004g0059 a0001c0001t0004g0127 others(21): Show |
24 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.254-6491T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69640537 | |||||||
| chr16:69640724 | G | A | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.254-6304G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69640724 | |||||||
| chr16:69640902 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.254-6126C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69640902 | |||||||
| chr16:69641016 | A | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.254-6012A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69641016 | |||||||
| chr16:69641277 | C | CA | 12 | a0001c0001t0002g0071 a0001c0001t0002g0075 a0001c0001t0002g0108 others(9): Show |
12 | HG01192.hp2 HG02486.hp2 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.254-5728dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69641277 | ||||||
| chr16:69641277 | CA | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
169 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.254-5728delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69641277 | ||||||
| chr16:69641277 | CAA | C | 44 | a0001c0001t0001g0272 a0001c0001t0003g0144 a0001c0001t0005g0010 others(41): Show |
47 | HG00323.hp1 HG00735.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.254-5729_254-5728d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69641277 | ||||||
| chr16:69641277 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.254-5739_254-5728d others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69641277 | ||||||
| chr16:69641277 | CAAAAAAA others(7): Show |
C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0222 others(15): Show |
18 | HG00597.hp2 HG02132.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.254-5741_254-5728d others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69641277 | ||||||
| chr16:69641392 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.254-5636A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69641392 | |||||||
| chr16:69641569 | A | G | 3 | a0001c0001t0003g0126 a0001c0001t0003g0148 a0001c0001t0003g0149 |
3 | HG02155.hp1 NA18983.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.254-5459A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69641569 | |||||||
| chr16:69642014 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.254-5014G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69642014 | |||||||
| chr16:69642158 | A | C | 1 | a0001c0001t0002g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.254-4870A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69642158 | |||||||
| chr16:69642183 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.254-4845T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69642183 | |||||||
| chr16:69642277 | G | A | 1 | a0001c0001t0012g0307 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.254-4751G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69642277 | |||||||
| chr16:69642742 | G | T | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0107 |
3 | NA18953.hp1 NA19066.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.254-4286G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69642742 | |||||||
| chr16:69642820 | AAAAAG | A | 18 | a0001c0001t0038g0314 a0001c0001t0047g0342 a0001c0002t0008g0001 others(15): Show |
21 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.254-4188_254-4184d others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69642820 | ||||||
| chr16:69642820 | AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0004g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.254-4193_254-4184d others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69642820 | ||||||
| chr16:69642826 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.254-4202A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69642826 | |||||||
| chr16:69642973 | G | A | 5 | a0001c0001t0005g0319 a0001c0001t0019g0367 a0001c0001t0019g0368 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.254-4055G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69642973 | |||||||
| chr16:69643034 | A | G | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.254-3994A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69643034 | |||||||
| chr16:69643217 | C | CA | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.254-3793dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69643217 | ||||||
| chr16:69643217 | C | CAA | 12 | a0001c0001t0001g0247 a0001c0001t0001g0250 a0001c0001t0001g0251 others(9): Show |
12 | HG01433.hp1 HG02559.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.254-3794_254-3793d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69643217 | ||||||
| chr16:69643217 | CA | C | 11 | a0001c0001t0001g0302 a0001c0001t0002g0035 a0001c0001t0004g0154 others(8): Show |
11 | HG02451.hp2 HG02572.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.254-3793delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69643217 | ||||||
| chr16:69643376 | A | G | 1 | a0001c0001t0032g0230 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.254-3652A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69643376 | |||||||
| chr16:69643448 | AT | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.254-3573delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 69643448 | ||||||
| chr16:69643564 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.254-3464C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69643564 | |||||||
| chr16:69643576 | T | G | 1 | a0001c0001t0003g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.254-3452T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69643576 | |||||||
| chr16:69643806 | A | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.254-3222A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69643806 | |||||||
| chr16:69643813 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.254-3215A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69643813 | |||||||
| chr16:69644123 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.254-2905A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69644123 | |||||||
| chr16:69644215 | A | G | 3 | a0001c0001t0002g0095 a0001c0001t0002g0100 a0001c0001t0024g0099 |
3 | NA18981.hp1 NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.254-2813A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69644215 | |||||||
| chr16:69644221 | G | C | 5 | a0001c0001t0006g0177 a0001c0001t0007g0054 a0001c0001t0007g0185 others(2): Show |
5 | NA18940.hp1 NA18943.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.254-2807G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69644221 | |||||||
| chr16:69644313 | A | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.254-2715A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69644313 | |||||||
| chr16:69644711 | C | T | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.254-2317C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69644711 | |||||||
| chr16:69644932 | G | A | 105 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(102): Show |
105 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.254-2096G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69644932 | |||||||
| chr16:69644947 | G | C | 1 | a0001c0001t0029g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.254-2081G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69644947 | |||||||
| chr16:69645855 | C | T | 1 | a0001c0001t0005g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.254-1173C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69645855 | |||||||
| chr16:69646297 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.254-731C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646297 | |||||||
| chr16:69646318 | A | G | 68 | a0001c0001t0001g0267 a0001c0001t0003g0046 a0001c0001t0003g0047 others(65): Show |
68 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.254-710A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646318 | |||||||
| chr16:69646455 | A | G | 20 | a0001c0001t0005g0010 a0001c0001t0005g0120 a0001c0001t0005g0135 others(17): Show |
20 | HG00735.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.254-573A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646455 | |||||||
| chr16:69646468 | A | G | 7 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0201 others(4): Show |
7 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.254-560A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646468 | |||||||
| chr16:69646701 | T | A | 1 | a0001c0001t0007g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.254-327T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646701 | |||||||
| chr16:69646702 | A | T | 1 | a0001c0001t0007g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.254-326A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646702 | |||||||
| chr16:69646781 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.254-247G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646781 | |||||||
| chr16:69646827 | A | G | 2 | a0001c0006t0004g0026 a0001c0006t0004g0027 |
2 | HG00408.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.254-201A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646827 | |||||||
| chr16:69646972 | A | G | 1 | a0001c0001t0044g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.254-56A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69646972 | |||||||
| chr16:69647720 | C | T | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.812+134C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69647720 | |||||||
| chr16:69647747 | A | C | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.812+161A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69647747 | |||||||
| chr16:69647839 | T | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.812+253T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69647839 | |||||||
| chr16:69647900 | G | A | 7 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0201 others(4): Show |
7 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.812+314G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69647900 | |||||||
| chr16:69647948 | G | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0278 a0001c0001t0001g0282 |
3 | HG01109.hp2 HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.812+362G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69647948 | |||||||
| chr16:69648176 | C | CA | 17 | a0001c0001t0001g0220 a0001c0001t0001g0231 a0001c0001t0001g0288 others(14): Show |
17 | HG00597.hp2 HG01243.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.812+603dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69648176 | ||||||
| chr16:69648193 | C | CA | 34 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(31): Show |
34 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.812+617dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69648193 | ||||||
| chr16:69648313 | T | C | 8 | a0001c0001t0002g0044 a0001c0001t0002g0073 a0001c0001t0002g0089 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.812+727T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69648313 | |||||||
| chr16:69648320 | C | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.812+734C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69648320 | |||||||
| chr16:69648552 | G | C | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.812+966G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69648552 | |||||||
| chr16:69648556 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.812+970G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69648556 | |||||||
| chr16:69648610 | A | G | 2 | a0001c0001t0028g0372 a0001c0001t0028g0373 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.812+1024A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69648610 | |||||||
| chr16:69648877 | T | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.812+1291T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69648877 | |||||||
| chr16:69648937 | A | C | 4 | a0001c0001t0011g0310 a0001c0001t0011g0311 a0001c0001t0011g0312 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.812+1351A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69648937 | |||||||
| chr16:69648952 | C | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.812+1366C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69648952 | |||||||
| chr16:69649745 | A | G | 1 | a0001c0001t0003g0195 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.812+2159A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69649745 | |||||||
| chr16:69649953 | G | A | 1 | a0001c0001t0011g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.812+2367G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69649953 | |||||||
| chr16:69649967 | TA | T | 7 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.812+2391delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69649967 | ||||||
| chr16:69650137 | T | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(27): Show |
30 | HG00408.hp1 HG00733.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.812+2551T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69650137 | |||||||
| chr16:69650170 | G | A | 3 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0315 |
3 | NA18987.hp1 NA19007.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.812+2584G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69650170 | |||||||
| chr16:69650174 | C | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.812+2588C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69650174 | |||||||
| chr16:69650217 | G | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.812+2631G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69650217 | |||||||
| chr16:69650220 | A | G | 2 | a0001c0001t0002g0084 a0001c0001t0002g0361 |
2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.812+2634A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69650220 | |||||||
| chr16:69650222 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.812+2636G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69650222 | |||||||
| chr16:69651009 | T | C | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.813-2227T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651009 | |||||||
| chr16:69651080 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.813-2156A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651080 | |||||||
| chr16:69651089 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.813-2147G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651089 | |||||||
| chr16:69651111 | A | G | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.813-2125A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651111 | |||||||
| chr16:69651131 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.813-2105A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651131 | |||||||
| chr16:69651222 | A | G | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.813-2014A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651222 | |||||||
| chr16:69651393 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.813-1843C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651393 | |||||||
| chr16:69651560 | A | G | 1 | a0001c0001t0007g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.813-1676A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651560 | |||||||
| chr16:69651671 | A | AT | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
240 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.813-1549dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69651671 | ||||||
| chr16:69651671 | A | ATT | 19 | a0001c0001t0001g0231 a0001c0001t0001g0277 a0001c0001t0003g0207 others(16): Show |
19 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.813-1550_813-1549d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69651671 | ||||||
| chr16:69651696 | GT | G | 17 | a0001c0001t0047g0342 a0001c0002t0008g0001 a0001c0002t0008g0012 others(14): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.813-1536delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69651696 | ||||||
| chr16:69651751 | A | T | 1 | a0001c0001t0034g0284 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.813-1485A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69651751 | |||||||
| chr16:69652031 | G | C | 1 | a0001c0001t0007g0185 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.813-1205G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69652031 | |||||||
| chr16:69652107 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.813-1129A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69652107 | |||||||
| chr16:69652325 | G | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.813-911G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69652325 | |||||||
| chr16:69652406 | T | C | 7 | a0001c0001t0010g0353 a0001c0001t0014g0347 a0001c0001t0014g0350 others(4): Show |
7 | HG02015.hp1 NA18977.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.813-830T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69652406 | |||||||
| chr16:69652745 | GGTTT | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.813-486_813-483del others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69652745 | ||||||
| chr16:69652773 | C | CTTTTT | 301 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(298): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.813-461_813-460ins others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69652773 | ||||||
| chr16:69652845 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(141): Show |
148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.813-391G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69652845 | |||||||
| chr16:69652964 | CT | C | 17 | a0001c0001t0047g0342 a0001c0002t0008g0001 a0001c0002t0008g0012 others(14): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.813-270delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 69652964 | ||||||
| chr16:69652985 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.813-251C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69652985 | |||||||
| chr16:69653009 | A | G | 309 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(306): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.813-227A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69653009 | |||||||
| chr16:69653196 | C | G | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.813-40C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69653196 | |||||||
| chr16:69653204 | T | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.813-32T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69653204 | |||||||
| chr16:69653554 | T | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1005+126T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69653554 | |||||||
| chr16:69653575 | A | AT | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0096 others(13): Show |
16 | HG01109.hp1 HG01255.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1005+165dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 69653575 | ||||||
| chr16:69653575 | AT | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
114 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1005+165delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 69653575 | ||||||
| chr16:69654022 | GA | G | 31 | a0001c0001t0002g0084 a0001c0001t0003g0125 a0001c0001t0005g0010 others(28): Show |
31 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1005+603delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 69654022 | ||||||
| chr16:69654049 | G | A | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005+621G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69654049 | |||||||
| chr16:69654290 | GTATTT | G | 18 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0222 others(15): Show |
18 | HG00597.hp2 HG02132.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.1005+865_1005+869d others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 69654290 | ||||||
| chr16:69654303 | G | A | 2 | a0001c0001t0021g0226 a0001c0001t0021g0235 |
2 | NA19078.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1005+875G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69654303 | |||||||
| chr16:69654372 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1005+944G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69654372 | |||||||
| chr16:69654377 | G | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1005+949G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69654377 | |||||||
| chr16:69654480 | C | G | 3 | a0001c0001t0006g0058 a0001c0001t0006g0190 a0001c0001t0006g0191 |
3 | NA18991.hp1 NA18994.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1005+1052C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69654480 | |||||||
| chr16:69654510 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1005+1082A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69654510 | |||||||
| chr16:69654517 | G | A | 5 | a0001c0001t0002g0041 a0001c0001t0002g0086 a0001c0001t0002g0110 others(2): Show |
5 | HG03669.hp1 HG03834.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1005+1089G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69654517 | |||||||
| chr16:69654912 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1006-697A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69654912 | |||||||
| chr16:69655048 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1006-561C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69655048 | |||||||
| chr16:69655217 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(141): Show |
148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1006-392G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69655217 | |||||||
| chr16:69655424 | GACTT | G | 4 | a0001c0002t0008g0012 a0001c0002t0008g0013 a0001c0002t0008g0014 others(1): Show |
4 | HG02280.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-180_1006-177d others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 69655424 | ||||||
| chr16:69655447 | A | G | 99 | a0001c0001t0001g0267 a0001c0001t0003g0046 a0001c0001t0003g0047 others(96): Show |
99 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1006-162A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69655447 | |||||||
| chr16:69655569 | A | G | 1 | a0001c0001t0028g0373 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1006-40A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 5/14 | chr16 | 69655569 | |||||||
| chr16:69655864 | T | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1196+65T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69655864 | |||||||
| chr16:69655874 | T | C | 1 | a0001c0001t0016g0364 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1196+75T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69655874 | |||||||
| chr16:69656070 | C | T | 1 | a0001c0001t0015g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1196+271C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69656070 | |||||||
| chr16:69656113 | T | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1196+314T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69656113 | |||||||
| chr16:69656142 | G | A | 6 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 others(3): Show |
6 | HG01255.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1196+343G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69656142 | |||||||
| chr16:69656258 | G | T | 1 | a0001c0001t0043g0204 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1196+459G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69656258 | |||||||
| chr16:69656282 | C | CA | 33 | a0001c0001t0001g0011 a0001c0001t0001g0224 a0001c0001t0001g0233 others(30): Show |
33 | HG00140.hp1 HG01261.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.1196+503dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69656282 | ||||||
| chr16:69656282 | CA | C | 26 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(23): Show |
29 | HG01243.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1196+503delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69656282 | ||||||
| chr16:69656452 | A | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1196+653A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69656452 | |||||||
| chr16:69656454 | C | CT | 6 | a0001c0001t0002g0112 a0001c0001t0004g0129 a0001c0001t0006g0049 others(3): Show |
6 | HG00609.hp1 HG00738.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1196+670dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69656454 | ||||||
| chr16:69656545 | A | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1196+746A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69656545 | |||||||
| chr16:69656641 | G | A | 2 | a0001c0001t0013g0002 a0001c0001t0013g0273 |
3 | HG01256.hp2 HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1196+842G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69656641 | |||||||
| chr16:69656774 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1196+975A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69656774 | |||||||
| chr16:69657008 | T | C | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1196+1209T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657008 | |||||||
| chr16:69657135 | AT | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1196+1348delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69657135 | ||||||
| chr16:69657140 | T | C | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1196+1341T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657140 | |||||||
| chr16:69657199 | C | T | 3 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 |
3 | HG01255.hp2 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1196+1400C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657199 | |||||||
| chr16:69657218 | C | T | 1 | a0001c0001t0005g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1196+1419C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657218 | |||||||
| chr16:69657219 | C | T | 4 | a0001c0001t0010g0348 a0001c0001t0010g0354 a0001c0001t0010g0355 others(1): Show |
4 | HG02132.hp2 NA18950.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196+1420C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657219 | |||||||
| chr16:69657221 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1196+1422C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657221 | |||||||
| chr16:69657454 | CTT | C | 6 | a0001c0001t0001g0210 a0001c0001t0001g0283 a0001c0001t0001g0285 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1196+1658_1196+165 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69657454 | ||||||
| chr16:69657468 | T | TA | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1196+1675dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69657468 | ||||||
| chr16:69657486 | C | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1196+1687C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657486 | |||||||
| chr16:69657632 | C | T | 34 | a0001c0001t0003g0047 a0001c0001t0003g0122 a0001c0001t0003g0123 others(31): Show |
34 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1196+1833C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657632 | |||||||
| chr16:69657705 | G | T | 1 | a0001c0001t0003g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1196+1906G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657705 | |||||||
| chr16:69657758 | CA | C | 21 | a0001c0001t0001g0255 a0001c0001t0001g0261 a0001c0001t0001g0278 others(18): Show |
21 | HG01109.hp2 HG01255.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1197-1950delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69657758 | ||||||
| chr16:69657873 | C | G | 1 | a0001c0001t0028g0372 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1197-1854C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657873 | |||||||
| chr16:69657956 | G | A | 45 | a0001c0001t0006g0049 a0001c0001t0006g0053 a0001c0001t0006g0055 others(42): Show |
45 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1197-1771G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657956 | |||||||
| chr16:69657965 | G | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0278 a0001c0001t0001g0282 |
3 | HG01109.hp2 HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1197-1762G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657965 | |||||||
| chr16:69657977 | C | T | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1197-1750C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657977 | |||||||
| chr16:69657986 | GAGGCAGG others(1): Show |
G | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1197-1740_1197-173 others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69657986 | |||||||
| chr16:69658028 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1197-1699G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658028 | |||||||
| chr16:69658036 | A | C | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1197-1691A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658036 | |||||||
| chr16:69658068 | G | T | 1 | a0001c0001t0012g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1197-1659G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658068 | |||||||
| chr16:69658092 | A | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1197-1635A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658092 | |||||||
| chr16:69658136 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1197-1591G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658136 | |||||||
| chr16:69658318 | A | C | 7 | a0001c0001t0006g0049 a0001c0001t0006g0057 a0001c0001t0006g0166 others(4): Show |
7 | HG02083.hp2 NA18957.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197-1409A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658318 | |||||||
| chr16:69658382 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1197-1345T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658382 | |||||||
| chr16:69658483 | CA | C | 8 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0223 others(5): Show |
8 | HG01168.hp2 HG02895.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1197-1228delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69658483 | ||||||
| chr16:69658530 | A | G | 1 | a0001c0001t0003g0046 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1197-1197A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658530 | |||||||
| chr16:69658565 | A | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1197-1162A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658565 | |||||||
| chr16:69658674 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197-1053A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658674 | |||||||
| chr16:69658697 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1197-1030C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658697 | |||||||
| chr16:69658735 | G | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197-992G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658735 | |||||||
| chr16:69658804 | G | A | 2 | a0001c0001t0028g0372 a0001c0001t0028g0373 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1197-923G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69658804 | |||||||
| chr16:69658851 | TA | T | 3 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0045g0363 |
3 | HG02257.hp2 HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1197-870delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69658851 | ||||||
| chr16:69659124 | T | A | 25 | a0001c0001t0005g0319 a0001c0001t0006g0177 a0001c0001t0007g0054 others(22): Show |
28 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1197-603T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659124 | |||||||
| chr16:69659128 | AT | A | 26 | a0001c0001t0001g0210 a0001c0001t0001g0225 a0001c0001t0001g0238 others(23): Show |
29 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1197-583delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69659128 | ||||||
| chr16:69659131 | T | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1197-596T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659131 | |||||||
| chr16:69659132 | T | A | 157 | a0001c0001t0001g0210 a0001c0001t0001g0225 a0001c0001t0001g0238 others(154): Show |
157 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1197-595T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659132 | |||||||
| chr16:69659133 | T | A | 1 | a0001c0001t0006g0055 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1197-594T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659133 | |||||||
| chr16:69659134 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1197-593T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659134 | |||||||
| chr16:69659135 | T | A | 13 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(10): Show |
13 | HG00733.hp2 HG01167.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1197-592T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659135 | |||||||
| chr16:69659136 | T | A | 5 | a0001c0001t0002g0044 a0001c0001t0015g0045 a0001c0001t0015g0087 others(2): Show |
5 | HG02258.hp1 HG02559.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197-591T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659136 | |||||||
| chr16:69659145 | A | T | 97 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(94): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1197-582A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659145 | |||||||
| chr16:69659165 | G | A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197-562G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659165 | |||||||
| chr16:69659355 | T | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197-372T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659355 | |||||||
| chr16:69659385 | G | A | 1 | a0001c0001t0029g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1197-342G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659385 | |||||||
| chr16:69659440 | C | CA | 7 | a0001c0001t0007g0182 a0001c0001t0017g0374 a0001c0001t0017g0375 others(4): Show |
7 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197-278dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 69659440 | ||||||
| chr16:69659618 | T | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1197-109T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659618 | |||||||
| chr16:69659685 | A | G | 1 | a0001c0001t0015g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1197-42A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 6/14 | chr16 | 69659685 | |||||||
| chr16:69660102 | A | G | 2 | a0001c0001t0011g0213 a0001c0001t0011g0309 |
2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1369+203A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660102 | |||||||
| chr16:69660129 | T | C | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1369+230T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660129 | |||||||
| chr16:69660271 | T | A | 1 | a0001c0001t0005g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1369+372T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660271 | |||||||
| chr16:69660338 | A | T | 1 | a0001c0001t0003g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1369+439A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660338 | |||||||
| chr16:69660384 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1369+485C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660384 | |||||||
| chr16:69660411 | CA | C | 24 | a0001c0001t0005g0010 a0001c0001t0005g0025 a0001c0001t0005g0048 others(21): Show |
24 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1369+513delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660411 | |||||||
| chr16:69660510 | T | G | 1 | a0001c0001t0034g0284 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1369+611T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660510 | |||||||
| chr16:69660594 | C | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1369+695C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660594 | |||||||
| chr16:69660798 | GTC | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(238): Show |
245 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1369+911_1369+912d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69660798 | ||||||
| chr16:69660840 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1369+941C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660840 | |||||||
| chr16:69660967 | A | T | 1 | a0001c0001t0005g0327 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1369+1068A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69660967 | |||||||
| chr16:69661082 | C | CT | 89 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(86): Show |
89 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.1369+1200dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661082 | ||||||
| chr16:69661082 | C | CTT | 47 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0224 others(44): Show |
48 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1369+1199_1369+120 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661082 | ||||||
| chr16:69661082 | CT | C | 6 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0061 others(3): Show |
6 | NA18957.hp2 NA18963.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.1369+1200delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661082 | ||||||
| chr16:69661082 | CTT | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1369+1199_1369+120 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661082 | ||||||
| chr16:69661097 | T | G | 1 | a0001c0002t0008g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1369+1198T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661097 | |||||||
| chr16:69661319 | C | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1369+1420C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661319 | |||||||
| chr16:69661380 | T | TA | 16 | a0001c0001t0002g0106 a0001c0001t0004g0136 a0001c0001t0025g0339 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1369+1497dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661380 | ||||||
| chr16:69661380 | TA | T | 8 | a0001c0001t0001g0305 a0001c0001t0004g0133 a0001c0001t0005g0319 others(5): Show |
8 | HG00738.hp1 HG01256.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1369+1497delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661380 | ||||||
| chr16:69661407 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1369+1508G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661407 | |||||||
| chr16:69661485 | A | G | 1 | a0001c0001t0019g0367 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1369+1586A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661485 | |||||||
| chr16:69661508 | C | CACTCCAG others(7): Show |
1 | a0001c0001t0001g0306 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1369+1611_1369+162 others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661508 | ||||||
| chr16:69661539 | T | TA | 37 | a0001c0001t0001g0253 a0001c0001t0001g0268 a0001c0001t0001g0290 others(34): Show |
37 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1369+1668dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAA | 7 | a0001c0001t0005g0319 a0001c0001t0016g0364 a0001c0001t0016g0365 others(4): Show |
7 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1369+1665_1369+166 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAA | 27 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0143 others(24): Show |
27 | HG00408.hp2 HG00423.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1369+1664_1369+166 others(9): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAA | 33 | a0001c0001t0003g0046 a0001c0001t0003g0122 a0001c0001t0003g0126 others(30): Show |
33 | HG00609.hp1 HG01168.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.1369+1663_1369+166 others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA | 16 | a0001c0001t0003g0047 a0001c0001t0003g0121 a0001c0001t0003g0123 others(13): Show |
16 | HG01167.hp2 HG01516.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.1369+1662_1369+166 others(11): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(1): Show |
13 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0005g0010 others(10): Show |
13 | HG00735.hp2 HG01192.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1369+1661_1369+166 others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(2): Show |
8 | a0001c0001t0002g0096 a0001c0001t0005g0048 a0001c0001t0005g0329 others(5): Show |
8 | HG01074.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1369+1660_1369+166 others(13): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(3): Show |
7 | a0001c0001t0002g0100 a0001c0001t0011g0214 a0001c0001t0011g0309 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1369+1659_1369+166 others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(4): Show |
2 | a0001c0001t0002g0095 a0001c0001t0011g0213 |
2 | HG03471.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1369+1658_1369+166 others(15): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(5): Show |
16 | a0001c0001t0001g0210 a0001c0001t0001g0222 a0001c0001t0001g0240 others(13): Show |
16 | HG00639.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1369+1657_1369+166 others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(6): Show |
30 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0220 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.1369+1656_1369+166 others(17): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(7): Show |
13 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0224 others(10): Show |
13 | HG01433.hp1 HG02132.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1369+1655_1369+166 others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0241 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1369+1654_1369+166 others(19): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(11): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0229 |
2 | NA18987.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1369+1651_1369+166 others(22): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0223 |
2 | NA18990.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1369+1650_1369+166 others(23): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | T | TAAAAAAA others(21): Show |
1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1369+1641_1369+166 others(32): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | TA | T | 7 | a0001c0001t0001g0252 a0001c0001t0002g0093 a0001c0001t0006g0177 others(4): Show |
7 | HG00099.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1369+1668delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0254 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1369+1659_1369+166 others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0004g0128 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1369+1658_1369+166 others(15): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661539 | TAAAAAAA others(5): Show |
T | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1369+1657_1369+166 others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69661539 | ||||||
| chr16:69661568 | G | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1369+1669G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661568 | |||||||
| chr16:69661686 | T | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0210 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1369+1787T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661686 | |||||||
| chr16:69661740 | G | A | 49 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0061 others(46): Show |
49 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1369+1841G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661740 | |||||||
| chr16:69661891 | A | G | 5 | a0001c0001t0012g0246 a0001c0001t0012g0260 a0001c0001t0012g0307 others(2): Show |
5 | HG00733.hp1 HG01358.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+1992A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661891 | |||||||
| chr16:69661983 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1369+2084G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69661983 | |||||||
| chr16:69662159 | G | A | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1369+2260G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662159 | |||||||
| chr16:69662249 | G | T | 1 | a0001c0001t0016g0364 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1369+2350G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662249 | |||||||
| chr16:69662442 | A | G | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1369+2543A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662442 | |||||||
| chr16:69662450 | C | CT | 29 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0044 others(26): Show |
29 | HG01496.hp2 HG01516.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1369+2575dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69662450 | ||||||
| chr16:69662450 | CT | C | 20 | a0001c0001t0002g0111 a0001c0001t0002g0324 a0001c0001t0006g0166 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1369+2575delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69662450 | ||||||
| chr16:69662450 | CTTT | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0231 others(25): Show |
28 | HG00408.hp1 HG00733.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1369+2573_1369+257 others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69662450 | ||||||
| chr16:69662450 | CTTTT | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(87): Show |
91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1369+2572_1369+257 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69662450 | ||||||
| chr16:69662451 | T | TTTC | 11 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0014 others(8): Show |
14 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1369+2554_1369+255 others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69662451 | ||||||
| chr16:69662457 | T | C | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1369+2558T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662457 | |||||||
| chr16:69662458 | T | C | 1 | a0001c0002t0008g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1369+2559T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662458 | |||||||
| chr16:69662495 | T | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1369+2596T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662495 | |||||||
| chr16:69662506 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1369+2607A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662506 | |||||||
| chr16:69662752 | G | A | 1 | a0001c0001t0005g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1369+2853G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662752 | |||||||
| chr16:69662902 | T | TC | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1369+3004dupC | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69662902 | ||||||
| chr16:69662903 | C | G | 1 | a0001c0001t0005g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1369+3004C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69662903 | |||||||
| chr16:69663035 | A | T | 3 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0045g0363 |
3 | HG02257.hp2 HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1369+3136A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69663035 | |||||||
| chr16:69663298 | G | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1369+3399G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69663298 | |||||||
| chr16:69663348 | C | A | 2 | a0001c0001t0001g0301 a0001c0001t0048g0300 |
2 | NA18953.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1369+3449C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69663348 | |||||||
| chr16:69663404 | T | C | 1 | a0001c0001t0006g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1369+3505T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69663404 | |||||||
| chr16:69663465 | T | C | 1 | a0001c0001t0003g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1369+3566T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69663465 | |||||||
| chr16:69663471 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1369+3572G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69663471 | |||||||
| chr16:69663564 | T | TA | 93 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0231 others(90): Show |
93 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.1369+3688dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69663564 | ||||||
| chr16:69663564 | TA | T | 16 | a0001c0001t0001g0252 a0001c0001t0001g0302 a0001c0001t0002g0065 others(13): Show |
16 | HG00639.hp1 HG01069.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1369+3688delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69663564 | ||||||
| chr16:69663564 | TAA | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1369+3687_1369+368 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69663564 | ||||||
| chr16:69663564 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0004g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1369+3677_1369+368 others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69663564 | ||||||
| chr16:69663690 | C | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1369+3791C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69663690 | |||||||
| chr16:69663712 | A | C | 47 | a0001c0001t0001g0306 a0001c0001t0006g0049 a0001c0001t0006g0053 others(44): Show |
47 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1369+3813A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69663712 | |||||||
| chr16:69664019 | T | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1369+4120T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69664019 | |||||||
| chr16:69664309 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1369+4410C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69664309 | |||||||
| chr16:69664431 | C | G | 1 | a0001c0001t0003g0143 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1369+4532C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69664431 | |||||||
| chr16:69664528 | G | A | 1 | a0001c0001t0054g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1369+4629G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69664528 | |||||||
| chr16:69664547 | G | T | 24 | a0001c0001t0005g0010 a0001c0001t0005g0025 a0001c0001t0005g0048 others(21): Show |
24 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1369+4648G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69664547 | |||||||
| chr16:69664763 | C | T | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1369+4864C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69664763 | |||||||
| chr16:69664900 | A | G | 250 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.1369+5001A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69664900 | |||||||
| chr16:69665086 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1370-4891C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665086 | |||||||
| chr16:69665102 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1370-4875T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665102 | |||||||
| chr16:69665267 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1370-4710G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665267 | |||||||
| chr16:69665270 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1370-4707G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665270 | |||||||
| chr16:69665469 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1370-4508A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665469 | |||||||
| chr16:69665646 | G | A | 130 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(127): Show |
133 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.1370-4331G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665646 | |||||||
| chr16:69665742 | G | C | 1 | a0003c0005t0001g0248 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1370-4235G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665742 | |||||||
| chr16:69665796 | C | T | 1 | a0001c0001t0028g0372 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1370-4181C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665796 | |||||||
| chr16:69665851 | T | C | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1370-4126T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665851 | |||||||
| chr16:69665856 | C | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1370-4121C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665856 | |||||||
| chr16:69666011 | T | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(248): Show |
255 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.1370-3966T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666011 | |||||||
| chr16:69666017 | A | G | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-3960A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666017 | |||||||
| chr16:69666032 | T | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1370-3945T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666032 | |||||||
| chr16:69666083 | T | G | 1 | a0001c0001t0002g0062 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1370-3894T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666083 | |||||||
| chr16:69666251 | T | C | 1 | a0001c0001t0002g0323 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1370-3726T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666251 | |||||||
| chr16:69666298 | A | G | 43 | a0001c0001t0006g0049 a0001c0001t0006g0053 a0001c0001t0006g0055 others(40): Show |
43 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1370-3679A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666298 | |||||||
| chr16:69666310 | A | G | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1370-3667A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666310 | |||||||
| chr16:69666326 | T | C | 3 | a0001c0001t0003g0126 a0001c0001t0003g0148 a0001c0001t0003g0149 |
3 | HG02155.hp1 NA18983.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1370-3651T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666326 | |||||||
| chr16:69666336 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1370-3641G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666336 | |||||||
| chr16:69666411 | A | C | 98 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(95): Show |
98 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1370-3566A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666411 | |||||||
| chr16:69666631 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1370-3346C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666631 | |||||||
| chr16:69666765 | G | A | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1370-3212G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666765 | |||||||
| chr16:69666817 | A | C | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1370-3160A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666817 | |||||||
| chr16:69666924 | G | A | 1 | a0001c0002t0008g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1370-3053G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69666924 | |||||||
| chr16:69666993 | TA | T | 24 | a0001c0001t0005g0010 a0001c0001t0005g0025 a0001c0001t0005g0048 others(21): Show |
24 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1370-2978delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69666993 | ||||||
| chr16:69667065 | C | G | 1 | a0001c0001t0046g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1370-2912C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667065 | |||||||
| chr16:69667128 | C | T | 48 | a0001c0001t0006g0049 a0001c0001t0006g0053 a0001c0001t0006g0055 others(45): Show |
48 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1370-2849C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667128 | |||||||
| chr16:69667145 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1370-2832G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667145 | |||||||
| chr16:69667228 | C | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-2749C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667228 | |||||||
| chr16:69667336 | A | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1370-2641A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667336 | |||||||
| chr16:69667337 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1370-2640A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667337 | |||||||
| chr16:69667399 | C | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1370-2578C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667399 | |||||||
| chr16:69667404 | G | C | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1370-2573G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667404 | |||||||
| chr16:69667494 | T | TA | 14 | a0001c0001t0005g0327 a0001c0002t0008g0001 a0001c0002t0008g0012 others(11): Show |
17 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1370-2467dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69667494 | ||||||
| chr16:69667494 | TA | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1370-2467delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69667494 | ||||||
| chr16:69667497 | A | G | 8 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1370-2480A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667497 | |||||||
| chr16:69667520 | C | T | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1370-2457C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667520 | |||||||
| chr16:69667584 | G | C | 45 | a0001c0001t0006g0049 a0001c0001t0006g0053 a0001c0001t0006g0055 others(42): Show |
45 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1370-2393G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667584 | |||||||
| chr16:69667585 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA18969.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1370-2392C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667585 | |||||||
| chr16:69667637 | G | A | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1370-2340G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667637 | |||||||
| chr16:69667742 | TTAATG | T | 12 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(9): Show |
12 | HG01433.hp1 HG02559.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1370-2230_1370-222 others(9): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 69667742 | ||||||
| chr16:69667766 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1370-2211C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667766 | |||||||
| chr16:69667788 | T | A | 4 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0023g0321 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-2189T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667788 | |||||||
| chr16:69667842 | A | G | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1370-2135A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69667842 | |||||||
| chr16:69668028 | G | A | 105 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(102): Show |
105 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.1370-1949G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668028 | |||||||
| chr16:69668092 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1370-1885G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668092 | |||||||
| chr16:69668168 | A | G | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1370-1809A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668168 | |||||||
| chr16:69668267 | C | T | 2 | a0001c0001t0007g0181 a0001c0001t0007g0182 |
2 | NA18966.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1370-1710C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668267 | |||||||
| chr16:69668283 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1370-1694C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668283 | |||||||
| chr16:69668284 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0243 |
2 | HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1370-1693G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668284 | |||||||
| chr16:69668516 | C | T | 96 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1370-1461C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668516 | |||||||
| chr16:69668541 | A | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1370-1436A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668541 | |||||||
| chr16:69668677 | T | A | 1 | a0001c0001t0011g0309 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1370-1300T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668677 | |||||||
| chr16:69668687 | A | T | 6 | a0001c0001t0003g0121 a0001c0001t0003g0143 a0001c0001t0003g0145 others(3): Show |
6 | HG02895.hp1 HG03098.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370-1290A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668687 | |||||||
| chr16:69668808 | A | G | 1 | a0001c0001t0003g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1370-1169A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668808 | |||||||
| chr16:69668935 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0278 a0001c0001t0001g0282 |
3 | HG01109.hp2 HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1370-1042C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668935 | |||||||
| chr16:69668936 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1370-1041G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668936 | |||||||
| chr16:69668940 | G | A | 1 | a0001c0001t0005g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1370-1037G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668940 | |||||||
| chr16:69668951 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1370-1026C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69668951 | |||||||
| chr16:69669027 | G | A | 6 | a0001c0001t0005g0120 a0001c0001t0005g0318 a0001c0001t0005g0325 others(3): Show |
6 | NA18612.hp1 NA18747.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370-950G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69669027 | |||||||
| chr16:69669054 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1370-923C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69669054 | |||||||
| chr16:69669522 | G | A | 3 | a0001c0002t0008g0012 a0001c0002t0008g0013 a0001c0002t0008g0014 |
3 | HG02280.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1370-455G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69669522 | |||||||
| chr16:69669674 | A | G | 5 | a0001c0001t0002g0035 a0001c0001t0002g0043 a0001c0001t0002g0097 others(2): Show |
5 | HG02015.hp2 HG02523.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1370-303A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69669674 | |||||||
| chr16:69669960 | C | A | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1370-17C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69669960 | |||||||
| chr16:69670187 | T | TA | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505-41dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 69670187 | ||||||
| chr16:69670219 | C | CTG | 313 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(310): Show |
317 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.1505-16_1505-15ins others(2): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 69670219 | ||||||
| chr16:69670301 | CT | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
260 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1557+20delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 69670301 | ||||||
| chr16:69670439 | T | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
260 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1557+151T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69670439 | |||||||
| chr16:69670624 | A | T | 3 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 |
3 | HG01255.hp2 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1557+336A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69670624 | |||||||
| chr16:69670835 | G | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+547G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69670835 | |||||||
| chr16:69671014 | T | C | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+726T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671014 | |||||||
| chr16:69671015 | A | T | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+727A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671015 | |||||||
| chr16:69671016 | G | A | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+728G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671016 | |||||||
| chr16:69671017 | A | T | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+729A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671017 | |||||||
| chr16:69671019 | G | C | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+731G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671019 | |||||||
| chr16:69671022 | G | A | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+734G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671022 | |||||||
| chr16:69671023 | C | G | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+735C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671023 | |||||||
| chr16:69671024 | A | T | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+736A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671024 | |||||||
| chr16:69671025 | A | G | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+737A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671025 | |||||||
| chr16:69671027 | A | T | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+739A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671027 | |||||||
| chr16:69671028 | A | G | 1 | a0001c0001t0007g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1557+740A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671028 | |||||||
| chr16:69671218 | A | G | 102 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(99): Show |
102 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1557+930A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671218 | |||||||
| chr16:69671586 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1557+1298G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671586 | |||||||
| chr16:69671744 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0222 |
2 | NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1557+1456G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69671744 | |||||||
| chr16:69672051 | C | G | 1 | a0001c0001t0005g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1557+1763C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672051 | |||||||
| chr16:69672211 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1557+1923G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672211 | |||||||
| chr16:69672243 | C | A | 1 | a0001c0001t0007g0029 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1557+1955C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672243 | |||||||
| chr16:69672407 | A | T | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+2119A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672407 | |||||||
| chr16:69672430 | T | A | 3 | a0001c0001t0018g0209 a0001c0001t0018g0336 a0001c0001t0018g0337 |
3 | HG01884.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1557+2142T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672430 | |||||||
| chr16:69672483 | G | T | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+2195G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672483 | |||||||
| chr16:69672530 | T | C | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1557+2242T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672530 | |||||||
| chr16:69672584 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+2296A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672584 | |||||||
| chr16:69672590 | A | C | 1 | a0001c0001t0054g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1557+2302A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672590 | |||||||
| chr16:69672723 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1557+2435T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672723 | |||||||
| chr16:69672949 | A | G | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1557+2661A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672949 | |||||||
| chr16:69672989 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG00408.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1557+2701A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69672989 | |||||||
| chr16:69673020 | TTC | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1557+2746_1557+274 others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 69673020 | ||||||
| chr16:69673103 | A | T | 1 | a0001c0001t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1557+2815A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69673103 | |||||||
| chr16:69673426 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1557+3138A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69673426 | |||||||
| chr16:69673679 | C | T | 98 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(95): Show |
98 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1557+3391C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69673679 | |||||||
| chr16:69673742 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1557+3454C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69673742 | |||||||
| chr16:69673853 | T | A | 1 | a0001c0001t0028g0373 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1558-3350T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69673853 | |||||||
| chr16:69673901 | C | A | 2 | a0001c0001t0009g0200 a0001c0001t0052g0199 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1558-3302C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69673901 | |||||||
| chr16:69674043 | G | A | 1 | a0001c0001t0005g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1558-3160G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674043 | |||||||
| chr16:69674046 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1558-3157C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674046 | |||||||
| chr16:69674116 | G | A | 33 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(30): Show |
33 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1558-3087G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674116 | |||||||
| chr16:69674174 | C | T | 2 | a0001c0001t0013g0002 a0001c0001t0013g0273 |
3 | HG01256.hp2 HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1558-3029C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674174 | |||||||
| chr16:69674203 | A | G | 10 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0231 others(7): Show |
10 | HG02132.hp1 NA18952.hp1 NA18985.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558-3000A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674203 | |||||||
| chr16:69674241 | C | CA | 13 | a0001c0001t0002g0086 a0001c0001t0005g0135 a0001c0001t0005g0319 others(10): Show |
14 | HG00735.hp2 HG01081.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558-2941dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 69674241 | ||||||
| chr16:69674241 | C | CAAA | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558-2943_1558-294 others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 69674241 | ||||||
| chr16:69674241 | CA | C | 61 | a0001c0001t0001g0225 a0001c0001t0001g0291 a0001c0001t0004g0133 others(58): Show |
61 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1558-2941delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 69674241 | ||||||
| chr16:69674518 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1558-2685G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674518 | |||||||
| chr16:69674795 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1558-2408C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674795 | |||||||
| chr16:69674922 | GCTCCCAA others(3): Show |
G | 1 | a0001c0001t0001g0295 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1558-2273_1558-226 others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 69674922 | ||||||
| chr16:69674927 | C | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-2276C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674927 | |||||||
| chr16:69674975 | T | A | 1 | a0001c0001t0011g0313 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1558-2228T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69674975 | |||||||
| chr16:69675124 | G | A | 100 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(97): Show |
100 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1558-2079G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69675124 | |||||||
| chr16:69675259 | A | G | 1 | a0001c0001t0056g0141 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1558-1944A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69675259 | |||||||
| chr16:69675410 | A | G | 1 | a0001c0001t0010g0355 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1558-1793A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69675410 | |||||||
| chr16:69675468 | G | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0222 others(15): Show |
18 | HG00597.hp2 HG02132.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.1558-1735G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69675468 | |||||||
| chr16:69675521 | A | C | 1 | a0001c0001t0001g0289 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1558-1682A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69675521 | |||||||
| chr16:69675750 | C | A | 65 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(62): Show |
65 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1558-1453C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69675750 | |||||||
| chr16:69675866 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-1337C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69675866 | |||||||
| chr16:69675902 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1558-1301A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69675902 | |||||||
| chr16:69676052 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1558-1151T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69676052 | |||||||
| chr16:69676396 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1558-807A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69676396 | |||||||
| chr16:69676519 | C | G | 1 | a0001c0001t0001g0301 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1558-684C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69676519 | |||||||
| chr16:69676569 | A | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(76): Show |
80 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1558-634A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69676569 | |||||||
| chr16:69676831 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1558-372G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69676831 | |||||||
| chr16:69676955 | G | C | 1 | a0001c0001t0003g0046 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1558-248G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69676955 | |||||||
| chr16:69676961 | A | G | 1 | a0001c0001t0003g0147 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1558-242A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 9/14 | chr16 | 69676961 | |||||||
| chr16:69677385 | T | C | 4 | a0001c0001t0005g0319 a0001c0001t0019g0367 a0001c0001t0019g0368 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+50T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69677385 | |||||||
| chr16:69677408 | A | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1690+73A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69677408 | |||||||
| chr16:69677579 | G | C | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1690+244G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69677579 | |||||||
| chr16:69677630 | T | C | 7 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0201 others(4): Show |
7 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+295T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69677630 | |||||||
| chr16:69677692 | G | T | 1 | a0001c0001t0007g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1690+357G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69677692 | |||||||
| chr16:69677980 | T | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
260 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1690+645T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69677980 | |||||||
| chr16:69677985 | T | G | 43 | a0001c0001t0006g0049 a0001c0001t0006g0053 a0001c0001t0006g0055 others(40): Show |
43 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1690+650T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69677985 | |||||||
| chr16:69678208 | AT | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(249): Show |
256 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1690+885delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69678208 | ||||||
| chr16:69678243 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0292 |
2 | HG00099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1690+908C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678243 | |||||||
| chr16:69678275 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+940C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678275 | |||||||
| chr16:69678277 | C | T | 35 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(32): Show |
35 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1690+942C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678277 | |||||||
| chr16:69678301 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+966A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678301 | |||||||
| chr16:69678339 | C | T | 3 | a0001c0001t0025g0339 a0001c0001t0025g0340 a0001c0001t0050g0194 |
3 | HG02895.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1690+1004C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678339 | |||||||
| chr16:69678504 | C | G | 8 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690+1169C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678504 | |||||||
| chr16:69678513 | C | G | 1 | a0001c0001t0028g0372 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1690+1178C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678513 | |||||||
| chr16:69678617 | C | T | 1 | a0001c0002t0008g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1690+1282C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678617 | |||||||
| chr16:69678751 | T | C | 1 | a0001c0001t0029g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1690+1416T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69678751 | |||||||
| chr16:69679037 | G | A | 3 | a0001c0001t0025g0339 a0001c0001t0025g0340 a0001c0001t0050g0194 |
3 | HG02895.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1690+1702G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69679037 | |||||||
| chr16:69679050 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1690+1715C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69679050 | |||||||
| chr16:69679216 | C | T | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0200 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690+1881C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69679216 | |||||||
| chr16:69679314 | C | G | 1 | a0001c0001t0004g0153 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1690+1979C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69679314 | |||||||
| chr16:69679428 | C | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2093C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69679428 | |||||||
| chr16:69679436 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1690+2101T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69679436 | |||||||
| chr16:69679737 | A | C | 1 | a0001c0001t0001g0316 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1690+2402A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69679737 | |||||||
| chr16:69679954 | A | G | 1 | a0001c0001t0001g0316 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1690+2619A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69679954 | |||||||
| chr16:69680011 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1690+2676A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69680011 | |||||||
| chr16:69680054 | C | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1690+2719C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69680054 | |||||||
| chr16:69680097 | G | A | 3 | a0001c0001t0025g0339 a0001c0001t0025g0340 a0001c0001t0050g0194 |
3 | HG02895.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1690+2762G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69680097 | |||||||
| chr16:69680659 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1690+3324G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69680659 | |||||||
| chr16:69680738 | ATTTTTTT others(1): Show |
A | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+3417_1690+342 others(12): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69680738 | ||||||
| chr16:69680865 | T | C | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1690+3530T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69680865 | |||||||
| chr16:69681002 | C | T | 1 | a0001c0001t0044g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1690+3667C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681002 | |||||||
| chr16:69681006 | C | T | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+3671C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681006 | |||||||
| chr16:69681170 | A | T | 2 | a0001c0001t0011g0313 a0001c0001t0038g0314 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1691-3717A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681170 | |||||||
| chr16:69681380 | T | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0283 |
2 | HG00639.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1691-3507T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681380 | |||||||
| chr16:69681640 | G | A | 4 | a0001c0001t0005g0319 a0001c0001t0019g0367 a0001c0001t0019g0368 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1691-3247G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681640 | |||||||
| chr16:69681640 | G | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1691-3247G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681640 | |||||||
| chr16:69681720 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1691-3167A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681720 | |||||||
| chr16:69681728 | TA | T | 17 | a0001c0001t0047g0342 a0001c0002t0008g0001 a0001c0002t0008g0012 others(14): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1691-3157delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69681728 | ||||||
| chr16:69681917 | GA | G | 24 | a0001c0001t0003g0046 a0001c0001t0003g0157 a0001c0001t0011g0310 others(21): Show |
27 | HG01168.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1691-2953delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69681917 | ||||||
| chr16:69681918 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1691-2969A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681918 | |||||||
| chr16:69681965 | G | A | 1 | a0001c0001t0017g0375 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1691-2922G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69681965 | |||||||
| chr16:69682186 | A | AT | 31 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(28): Show |
31 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1691-2685dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69682186 | ||||||
| chr16:69682186 | AT | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1691-2685delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69682186 | ||||||
| chr16:69682198 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1691-2689T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682198 | |||||||
| chr16:69682294 | A | AT | 130 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1691-2579dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69682294 | ||||||
| chr16:69682294 | AT | A | 113 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(110): Show |
113 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1691-2579delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69682294 | ||||||
| chr16:69682340 | G | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1691-2547G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682340 | |||||||
| chr16:69682377 | G | A | 1 | a0001c0001t0010g0164 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1691-2510G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682377 | |||||||
| chr16:69682377 | G | C | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1691-2510G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682377 | |||||||
| chr16:69682432 | A | AC | 16 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0044 others(13): Show |
16 | HG00597.hp1 HG01109.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1691-2444dupC | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69682432 | ||||||
| chr16:69682432 | AC | A | 107 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(104): Show |
107 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1691-2444delC | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69682432 | ||||||
| chr16:69682435 | C | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1691-2452C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682435 | |||||||
| chr16:69682441 | C | G | 4 | a0001c0001t0016g0362 a0001c0001t0016g0364 a0001c0001t0016g0365 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1691-2446C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682441 | |||||||
| chr16:69682443 | C | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1691-2444C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682443 | |||||||
| chr16:69682455 | A | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1691-2432A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682455 | |||||||
| chr16:69682481 | T | G | 132 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(129): Show |
135 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1691-2406T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682481 | |||||||
| chr16:69682504 | C | G | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1691-2383C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682504 | |||||||
| chr16:69682566 | C | T | 1 | a0001c0007t0051g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1691-2321C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682566 | |||||||
| chr16:69682624 | A | C | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1691-2263A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682624 | |||||||
| chr16:69682629 | T | G | 132 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(129): Show |
135 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1691-2258T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682629 | |||||||
| chr16:69682953 | T | C | 24 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(21): Show |
24 | HG00735.hp2 HG01167.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.1691-1934T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69682953 | |||||||
| chr16:69683014 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1691-1873C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683014 | |||||||
| chr16:69683050 | A | G | 102 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(99): Show |
102 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1691-1837A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683050 | |||||||
| chr16:69683061 | A | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1691-1826A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683061 | |||||||
| chr16:69683121 | G | C | 102 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(99): Show |
102 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1691-1766G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683121 | |||||||
| chr16:69683213 | AAAGAAAA others(4): Show |
A | 5 | a0001c0001t0003g0046 a0001c0001t0003g0124 a0001c0001t0003g0139 others(2): Show |
5 | NA18952.hp2 NA18980.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1691-1664_1691-165 others(15): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69683213 | ||||||
| chr16:69683288 | T | C | 2 | a0001c0001t0009g0200 a0001c0001t0052g0199 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1691-1599T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683288 | |||||||
| chr16:69683375 | T | C | 1 | a0001c0001t0004g0153 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1691-1512T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683375 | |||||||
| chr16:69683669 | T | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1691-1218T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683669 | |||||||
| chr16:69683778 | G | A | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1691-1109G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683778 | |||||||
| chr16:69683972 | G | A | 1 | a0001c0001t0037g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1691-915G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69683972 | |||||||
| chr16:69684064 | A | T | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1691-823A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684064 | |||||||
| chr16:69684095 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1691-792G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684095 | |||||||
| chr16:69684209 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1691-678G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684209 | |||||||
| chr16:69684255 | CA | C | 76 | a0001c0001t0001g0011 a0001c0001t0001g0253 a0001c0001t0002g0044 others(73): Show |
79 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1691-611delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69684255 | ||||||
| chr16:69684255 | CAA | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1691-612_1691-611d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69684255 | ||||||
| chr16:69684255 | CAAA | C | 36 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0315 others(33): Show |
36 | HG00735.hp2 HG01074.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1691-613_1691-611d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 69684255 | ||||||
| chr16:69684276 | A | T | 1 | a0001c0001t0039g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1691-611A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684276 | |||||||
| chr16:69684331 | C | T | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1691-556C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684331 | |||||||
| chr16:69684335 | T | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1691-552T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684335 | |||||||
| chr16:69684516 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1691-371C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684516 | |||||||
| chr16:69684570 | A | G | 1 | a0001c0001t0039g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1691-317A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684570 | |||||||
| chr16:69684790 | G | A | 17 | a0001c0001t0010g0164 a0001c0001t0010g0346 a0001c0001t0010g0348 others(14): Show |
17 | HG00738.hp2 HG02015.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.1691-97G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 10/14 | chr16 | 69684790 | |||||||
| chr16:69685069 | C | T | 98 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(95): Show |
98 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1774+99C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685069 | |||||||
| chr16:69685073 | G | T | 2 | a0001c0001t0001g0231 a0001c0001t0036g0227 |
2 | NA18985.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1774+103G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685073 | |||||||
| chr16:69685094 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1774+124A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685094 | |||||||
| chr16:69685106 | G | A | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1774+136G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685106 | |||||||
| chr16:69685166 | GTT | G | 5 | a0001c0001t0005g0025 a0001c0001t0017g0374 a0001c0001t0017g0375 others(2): Show |
5 | HG01255.hp2 HG02647.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1774+200_1774+201d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685166 | ||||||
| chr16:69685170 | T | A | 2 | a0001c0001t0028g0372 a0001c0001t0028g0373 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1774+200T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685170 | |||||||
| chr16:69685170 | T | TTA | 7 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0061 others(4): Show |
7 | HG03209.hp2 NA18957.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.1774+220_1774+221d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685170 | ||||||
| chr16:69685170 | TTA | T | 26 | a0001c0001t0001g0255 a0001c0001t0001g0271 a0001c0001t0001g0278 others(23): Show |
29 | HG01109.hp2 HG02055.hp1 HG02155.hp1 others(26): Show |
intron_variant | MODIFIER | c.1774+220_1774+221d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685170 | ||||||
| chr16:69685170 | TTATA | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(53): Show |
56 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1774+218_1774+221d others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685170 | ||||||
| chr16:69685170 | TTATATA | T | 5 | a0001c0001t0001g0253 a0001c0001t0001g0272 a0001c0001t0001g0293 others(2): Show |
5 | HG00323.hp1 HG01515.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1774+216_1774+221d others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685170 | ||||||
| chr16:69685185 | TATATA | T | 25 | a0001c0001t0001g0252 a0001c0001t0001g0267 a0001c0001t0001g0270 others(22): Show |
26 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1774+216_1774+220d others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685185 | |||||||
| chr16:69685186 | ATATAT | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0286 a0001c0001t0009g0200 others(4): Show |
7 | HG01346.hp2 HG02257.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1774+218_1774+222d others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685186 | ||||||
| chr16:69685187 | TATA | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0282 a0001c0002t0008g0016 |
3 | HG01891.hp2 HG03239.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1774+218_1774+220d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685187 | |||||||
| chr16:69685188 | A | T | 5 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0315 others(2): Show |
5 | HG02280.hp1 HG03225.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1774+218A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685188 | |||||||
| chr16:69685188 | ATAT | A | 8 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1774+220_1774+222d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685188 | ||||||
| chr16:69685188 | ATATT | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0240 a0001c0001t0001g0243 others(6): Show |
9 | HG00408.hp1 HG01099.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.1774+220_1774+223d others(6): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685188 | ||||||
| chr16:69685188 | ATATTT | A | 9 | a0001c0001t0009g0197 a0001c0001t0009g0198 a0001c0001t0009g0201 others(6): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1774+220_1774+224d others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685188 | ||||||
| chr16:69685189 | TA | T | 8 | a0001c0001t0002g0078 a0001c0001t0006g0176 a0001c0001t0006g0187 others(5): Show |
8 | HG01496.hp2 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+220delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685189 | |||||||
| chr16:69685190 | A | T | 61 | a0001c0001t0001g0011 a0001c0001t0001g0219 a0001c0001t0001g0220 others(58): Show |
64 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1774+220A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685190 | |||||||
| chr16:69685190 | AT | A | 41 | a0001c0001t0002g0106 a0001c0001t0002g0324 a0001c0001t0006g0053 others(38): Show |
41 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1774+231delT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685190 | ||||||
| chr16:69685190 | ATT | A | 83 | a0001c0001t0002g0095 a0001c0001t0002g0100 a0001c0001t0003g0046 others(80): Show |
83 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1774+230_1774+231d others(4): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685190 | ||||||
| chr16:69685190 | ATTT | A | 7 | a0001c0001t0011g0310 a0001c0001t0011g0311 a0001c0001t0011g0312 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1774+229_1774+231d others(5): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685190 | ||||||
| chr16:69685191 | T | TA | 8 | a0001c0001t0002g0035 a0001c0001t0002g0043 a0001c0001t0002g0083 others(5): Show |
8 | HG00140.hp1 HG02015.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+221_1774+222i others(3): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685191 | |||||||
| chr16:69685192 | T | A | 20 | a0001c0001t0002g0066 a0001c0001t0002g0077 a0001c0001t0002g0085 others(17): Show |
20 | HG00423.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1774+222T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685192 | |||||||
| chr16:69685193 | T | A | 8 | a0001c0001t0007g0004 a0001c0001t0007g0005 a0001c0001t0007g0029 others(5): Show |
8 | HG00280.hp2 HG00597.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1774+223T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685193 | |||||||
| chr16:69685194 | T | A | 25 | a0001c0001t0003g0121 a0001c0001t0003g0124 a0001c0001t0003g0125 others(22): Show |
25 | HG00738.hp2 HG02027.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.1774+224T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685194 | |||||||
| chr16:69685248 | A | G | 6 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1774+278A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685248 | |||||||
| chr16:69685316 | T | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0274 |
2 | NA18942.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1774+346T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685316 | |||||||
| chr16:69685546 | TA | T | 12 | a0001c0001t0001g0282 a0001c0001t0001g0297 a0001c0001t0001g0317 others(9): Show |
12 | HG01433.hp2 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1774+591delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69685546 | ||||||
| chr16:69685656 | G | T | 1 | a0001c0001t0004g0133 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1774+686G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685656 | |||||||
| chr16:69685742 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1774+772T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685742 | |||||||
| chr16:69685821 | A | G | 254 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(251): Show |
258 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1774+851A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685821 | |||||||
| chr16:69685986 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0108 |
2 | NA18955.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1774+1016G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69685986 | |||||||
| chr16:69686077 | G | T | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1774+1107G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69686077 | |||||||
| chr16:69686184 | A | C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1774+1214A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69686184 | |||||||
| chr16:69686352 | C | CA | 9 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0009g0117 others(6): Show |
9 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1774+1394dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69686352 | ||||||
| chr16:69686638 | T | G | 1 | a0001c0001t0028g0372 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1774+1668T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69686638 | |||||||
| chr16:69686900 | G | GTAAA | 302 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.1774+1932_1774+193 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69686900 | ||||||
| chr16:69687027 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1774+2057C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687027 | |||||||
| chr16:69687034 | A | G | 2 | a0001c0001t0007g0181 a0001c0001t0007g0182 |
2 | NA18966.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1774+2064A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687034 | |||||||
| chr16:69687061 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1774+2091G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687061 | |||||||
| chr16:69687266 | C | G | 5 | a0001c0001t0001g0253 a0001c0001t0001g0272 a0001c0001t0001g0293 others(2): Show |
5 | HG00323.hp1 HG01515.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1774+2296C>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687266 | |||||||
| chr16:69687383 | G | A | 1 | a0001c0001t0028g0372 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1774+2413G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687383 | |||||||
| chr16:69687403 | T | C | 5 | a0001c0001t0017g0374 a0001c0001t0017g0375 a0001c0001t0017g0376 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1774+2433T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687403 | |||||||
| chr16:69687415 | T | C | 100 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(97): Show |
100 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1774+2445T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687415 | |||||||
| chr16:69687436 | G | GA | 214 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(211): Show |
215 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1774+2485dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69687436 | ||||||
| chr16:69687436 | GA | G | 7 | a0001c0001t0002g0089 a0001c0001t0002g0093 a0001c0001t0002g0324 others(4): Show |
7 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1774+2485delA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69687436 | ||||||
| chr16:69687471 | T | C | 100 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(97): Show |
100 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1774+2501T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687471 | |||||||
| chr16:69687512 | G | A | 132 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(129): Show |
135 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1774+2542G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687512 | |||||||
| chr16:69687767 | TTATAA | T | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1774+2804_1774+280 others(9): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69687767 | ||||||
| chr16:69687917 | G | A | 109 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(106): Show |
109 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.1774+2947G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687917 | |||||||
| chr16:69687957 | G | A | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1775-2983G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69687957 | |||||||
| chr16:69688022 | G | T | 1 | a0001c0001t0001g0302 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1775-2918G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688022 | |||||||
| chr16:69688053 | G | A | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1775-2887G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688053 | |||||||
| chr16:69688149 | T | C | 4 | a0001c0001t0007g0029 a0001c0001t0007g0030 a0001c0001t0007g0031 others(1): Show |
4 | HG00597.hp1 NA18948.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1775-2791T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688149 | |||||||
| chr16:69688168 | A | G | 1 | a0002c0004t0007g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1775-2772A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688168 | |||||||
| chr16:69688174 | G | A | 3 | a0001c0001t0025g0339 a0001c0001t0025g0340 a0001c0001t0050g0194 |
3 | HG02895.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1775-2766G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688174 | |||||||
| chr16:69688189 | C | T | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1775-2751C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688189 | |||||||
| chr16:69688190 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1775-2750G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688190 | |||||||
| chr16:69688202 | C | CA | 23 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(20): Show |
23 | HG01070.hp2 HG01109.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1775-2714dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAA | 43 | a0001c0001t0003g0046 a0001c0001t0003g0121 a0001c0001t0003g0124 others(40): Show |
43 | HG00280.hp2 HG00609.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.1775-2716_1775-271 others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAA | 20 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0145 others(17): Show |
20 | HG00423.hp2 HG00597.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1775-2717_1775-271 others(8): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0004g0156 a0001c0001t0009g0197 a0001c0001t0009g0201 |
3 | HG02451.hp1 HG02897.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1775-2723_1775-271 others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0009g0202 a0001c0001t0009g0203 a0001c0001t0009g0211 others(2): Show |
5 | HG02486.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-2724_1775-271 others(15): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0009g0198 a0001c0001t0009g0200 a0001c0001t0010g0359 others(1): Show |
4 | HG01243.hp1 HG03239.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1775-2725_1775-271 others(16): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0005g0048 a0001c0001t0010g0346 a0001c0001t0010g0348 others(2): Show |
5 | HG02015.hp1 HG02132.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-2726_1775-271 others(17): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(7): Show |
9 | a0001c0001t0010g0353 a0001c0001t0010g0354 a0001c0001t0010g0355 others(6): Show |
9 | HG03209.hp2 NA18950.hp2 NA19004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1775-2727_1775-271 others(18): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0005g0161 a0001c0001t0005g0325 a0001c0001t0005g0327 others(1): Show |
4 | HG02602.hp1 NA18747.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1775-2728_1775-271 others(19): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(9): Show |
10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0100 others(7): Show |
10 | HG01074.hp1 HG02647.hp2 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.1775-2729_1775-271 others(20): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0057g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1775-2730_1775-271 others(21): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0005g0120 a0001c0006t0004g0026 |
2 | NA18612.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1775-2731_1775-271 others(22): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0054g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1775-2734_1775-271 others(25): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0018g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1775-2735_1775-271 others(26): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(16): Show |
3 | a0001c0001t0005g0135 a0001c0001t0018g0209 a0001c0001t0018g0336 |
3 | HG01884.hp1 HG03041.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1775-2736_1775-271 others(27): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(17): Show |
3 | a0001c0001t0003g0047 a0001c0001t0005g0329 a0001c0001t0005g0366 |
3 | HG01358.hp1 HG02738.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1775-2737_1775-271 others(28): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(18): Show |
2 | a0001c0001t0003g0163 a0001c0001t0003g0196 |
2 | NA18984.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1775-2714_1775-271 others(29): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0005g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1775-2714_1775-271 others(30): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0003g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1775-2714_1775-271 others(32): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(22): Show |
5 | a0001c0001t0003g0148 a0001c0001t0003g0149 a0001c0001t0003g0157 others(2): Show |
5 | HG01167.hp2 HG01168.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1775-2714_1775-271 others(33): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(24): Show |
11 | a0001c0001t0004g0127 a0001c0001t0004g0128 a0001c0001t0004g0132 others(8): Show |
11 | HG00735.hp2 HG01192.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1775-2714_1775-271 others(35): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(25): Show |
3 | a0001c0001t0003g0195 a0001c0001t0004g0059 a0001c0001t0004g0140 |
3 | HG02071.hp2 NA18965.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1775-2714_1775-271 others(36): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(26): Show |
2 | a0001c0001t0004g0131 a0001c0001t0010g0164 |
2 | HG00738.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1775-2714_1775-271 others(37): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0058g0357 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1775-2714_1775-271 others(39): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0016g0365 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1775-2714_1775-271 others(40): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(30): Show |
3 | a0001c0001t0004g0150 a0001c0001t0005g0328 a0001c0006t0004g0027 |
3 | HG00408.hp2 NA18950.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1775-2714_1775-271 others(41): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | CAAAAAAA others(31): Show |
1 | a0001c0001t0004g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1775-2714_1775-271 others(42): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688202 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1775-2738C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688202 | |||||||
| chr16:69688202 | CAAAAAAA others(2): Show |
C | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1775-2722_1775-271 others(13): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688202 | ||||||
| chr16:69688204 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1775-2727_1775-272 others(14): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688204 | ||||||
| chr16:69688212 | A | AACAAAC | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1775-2727_1775-272 others(10): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688212 | ||||||
| chr16:69688212 | A | C | 2 | a0001c0001t0048g0300 a0001c0008t0001g0296 |
2 | NA18966.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1775-2728A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688212 | |||||||
| chr16:69688213 | A | ACAAAC | 4 | a0001c0001t0001g0219 a0001c0001t0001g0223 a0001c0001t0011g0310 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1775-2727_1775-272 others(9): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688213 | |||||||
| chr16:69688216 | A | C | 8 | a0001c0001t0001g0234 a0001c0001t0012g0246 a0001c0001t0012g0260 others(5): Show |
8 | HG00733.hp1 HG01099.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1775-2724A>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688216 | |||||||
| chr16:69688225 | A | AAAAAAAA others(24): Show |
1 | a0001c0001t0004g0138 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1775-2714_1775-271 others(35): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688225 | ||||||
| chr16:69688227 | C | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1775-2713C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688227 | |||||||
| chr16:69688227 | C | CAAA | 9 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1775-2713_1775-271 others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688227 | |||||||
| chr16:69688227 | C | CAAACAAA | 3 | a0001c0001t0011g0310 a0001c0001t0011g0312 a0001c0001t0011g0341 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1775-2713_1775-271 others(11): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688227 | |||||||
| chr16:69688293 | G | A | 12 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0309 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1775-2647G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688293 | |||||||
| chr16:69688307 | G | A | 2 | a0001c0001t0020g0216 a0001c0001t0020g0217 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1775-2633G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688307 | |||||||
| chr16:69688362 | A | G | 1 | a0001c0001t0005g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1775-2578A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688362 | |||||||
| chr16:69688420 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1775-2520G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688420 | |||||||
| chr16:69688445 | G | A | 1 | a0001c0001t0007g0005 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1775-2495G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688445 | |||||||
| chr16:69688536 | C | CT | 5 | a0001c0001t0001g0210 a0001c0001t0001g0283 a0001c0001t0001g0285 others(2): Show |
5 | HG00639.hp2 HG01123.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-2397dupT | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688536 | ||||||
| chr16:69688575 | T | C | 1 | a0001c0001t0005g0048 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1775-2365T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688575 | |||||||
| chr16:69688656 | T | A | 4 | a0001c0002t0008g0015 a0001c0002t0008g0017 a0001c0002t0008g0018 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1775-2284T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688656 | |||||||
| chr16:69688659 | G | A | 1 | a0001c0001t0005g0318 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1775-2281G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688659 | |||||||
| chr16:69688852 | ATAG | A | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1775-2083_1775-208 others(7): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 69688852 | ||||||
| chr16:69688853 | T | G | 2 | a0001c0001t0025g0339 a0001c0001t0025g0340 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1775-2087T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688853 | |||||||
| chr16:69688890 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1775-2050C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688890 | |||||||
| chr16:69688894 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1775-2046T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688894 | |||||||
| chr16:69688998 | G | A | 12 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(9): Show |
15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1775-1942G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69688998 | |||||||
| chr16:69689207 | G | C | 1 | a0001c0001t0010g0360 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1775-1733G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689207 | |||||||
| chr16:69689211 | A | G | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1775-1729A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689211 | |||||||
| chr16:69689219 | G | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1775-1721G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689219 | |||||||
| chr16:69689389 | A | G | 3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1775-1551A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689389 | |||||||
| chr16:69689491 | G | T | 1 | a0001c0001t0003g0046 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1775-1449G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689491 | |||||||
| chr16:69689505 | A | G | 1 | a0001c0001t0047g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1775-1435A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689505 | |||||||
| chr16:69689527 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1775-1413T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689527 | |||||||
| chr16:69689624 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1775-1316A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689624 | |||||||
| chr16:69689729 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1775-1211G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689729 | |||||||
| chr16:69689862 | C | T | 3 | a0001c0001t0018g0209 a0001c0001t0018g0336 a0001c0001t0018g0337 |
3 | HG01884.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1775-1078C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69689862 | |||||||
| chr16:69690062 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1775-878A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690062 | |||||||
| chr16:69690206 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1775-734A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690206 | |||||||
| chr16:69690317 | G | A | 6 | a0001c0001t0001g0210 a0001c0001t0001g0283 a0001c0001t0001g0285 others(3): Show |
6 | HG00140.hp2 HG00639.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1775-623G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690317 | |||||||
| chr16:69690320 | A | G | 67 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0121 others(64): Show |
67 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1775-620A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690320 | |||||||
| chr16:69690562 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1775-378G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690562 | |||||||
| chr16:69690568 | G | A | 1 | a0001c0001t0027g0175 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1775-372G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690568 | |||||||
| chr16:69690764 | C | T | 1 | a0001c0001t0007g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1775-176C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690764 | |||||||
| chr16:69690827 | T | G | 1 | a0001c0008t0001g0296 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1775-113T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690827 | |||||||
| chr16:69690856 | C | T | 2 | a0001c0001t0011g0214 a0001c0001t0037g0215 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1775-84C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690856 | |||||||
| chr16:69690920 | T | C | 1 | a0001c0001t0050g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1775-20T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690920 | |||||||
| chr16:69691217 | A | G | 16 | a0001c0002t0008g0001 a0001c0002t0008g0012 a0001c0002t0008g0013 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1923+129A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 12/14 | chr16 | 69691217 | |||||||
| chr16:69691495 | A | T | 1 | a0001c0001t0010g0360 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1924-254A>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 12/14 | chr16 | 69691495 | |||||||
| chr16:69691627 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1924-122A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 12/14 | chr16 | 69691627 | |||||||
| chr16:69691689 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1924-60A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 12/14 | chr16 | 69691689 | |||||||
| chr16:69694479 | T | A | 1 | a0001c0003t0002g0069 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4414+240T>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/14 | chr16 | 69694479 | |||||||
| chr16:69694507 | G | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0292 |
2 | HG00099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.4414+268G>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/14 | chr16 | 69694507 | |||||||
| chr16:69694751 | A | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0283 a0001c0001t0001g0285 others(2): Show |
5 | HG00639.hp2 HG01123.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.4415-385A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/14 | chr16 | 69694751 | |||||||
| chr16:69694835 | C | T | 1 | a0001c0001t0006g0176 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4415-301C>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/14 | chr16 | 69694835 | |||||||
| chr16:69694895 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4415-241G>T | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/14 | chr16 | 69694895 | |||||||
| chr16:69694963 | G | A | 1 | a0001c0001t0005g0328 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4415-173G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/14 | chr16 | 69694963 | |||||||
| chr16:69695087 | C | A | 1 | a0001c0001t0002g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4415-49C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 13/14 | chr16 | 69695087 | |||||||
| chr16:69695485 | T | C | 1 | a0001c0001t0003g0125 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.*8+106T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | chr16 | 69695485 | |||||||
| chr16:69695566 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0232 |
2 | NA18944.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.*8+187G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | chr16 | 69695566 | |||||||
| chr16:69695621 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*8+242A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | chr16 | 69695621 | |||||||
| chr16:69695688 | C | CA | 107 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.*8+324dupA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 69695688 | ||||||
| chr16:69695688 | C | CAA | 7 | a0001c0001t0001g0210 a0001c0001t0001g0233 a0001c0001t0001g0253 others(4): Show |
7 | HG00639.hp2 HG01123.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.*8+323_*8+324dupAA | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 69695688 | ||||||
| chr16:69695818 | T | C | 1 | a0001c0001t0046g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.*8+439T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | chr16 | 69695818 | |||||||
| chr16:69695891 | T | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.*9-469T>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | chr16 | 69695891 | |||||||
| chr16:69696214 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.*9-146T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | chr16 | 69696214 |