Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1549 | 372 | 92 | 61 | 166 | 16 | 35 | 135 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0002 | 0/0 | 1549 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0003 | 0/0 | 1549 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0004 | 0/0 | 1549 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0005 | 0/0 | 1549 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4650 | 344 | 72 | 59 | 163 | 14 | 34 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0002 | 0/0 | 4650 | 19 | 19 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0003 | 0/0 | 4650 | 4 | 0 | 2 | 0 | 2 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0004 | 0/0 | 4650 | 3 | 0 | 0 | 0 | 2 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0005 | 0/0 | 4650 | 3 | 0 | 0 | 3 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0006 | 0/0 | 4650 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0007 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0008 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0009 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0010 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| c0011 | 0/0 | 4650 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8640 | 79 | 13 | 8 | 45 | 4 | 9 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0002 | 1/1 | 8640 | 65 | 5 | 21 | 20 | 7 | 10 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0003 | 0/0 | 8641 | 25 | 0 | 1 | 22 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0004 | 0/0 | 8641 | 23 | 0 | 0 | 22 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0005 | 0/0 | 8641 | 21 | 4 | 4 | 6 | 2 | 5 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0006 | 0/0 | 8639 | 18 | 0 | 3 | 11 | 3 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0007 | 0/0 | 8638 | 17 | 1 | 5 | 11 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0008 | 0/0 | 8639 | 16 | 16 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0009 | 0/0 | 8640 | 11 | 10 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0010 | 0/0 | 8643 | 9 | 1 | 1 | 5 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0011 | 0/0 | 8639 | 8 | 8 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0012 | 0/0 | 8640 | 6 | 0 | 6 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0013 | 0/0 | 8639 | 5 | 0 | 5 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0014 | 0/0 | 8643 | 5 | 0 | 0 | 5 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0015 | 0/0 | 8640 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0016 | 0/0 | 8643 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0017 | 0/0 | 8638 | 3 | 0 | 0 | 3 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0018 | 0/0 | 8641 | 3 | 0 | 1 | 0 | 1 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0019 | 0/0 | 8641 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0020 | 0/0 | 8637 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0021 | 0/0 | 8638 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0022 | 0/0 | 8640 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0023 | 0/0 | 8640 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0024 | 0/0 | 8640 | 2 | 0 | 2 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0025 | 0/0 | 8641 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0026 | 0/0 | 8638 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0027 | 0/0 | 8639 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0028 | 0/0 | 8640 | 2 | 0 | 1 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0029 | 0/0 | 8637 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0030 | 0/0 | 8641 | 2 | 0 | 0 | 0 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0031 | 0/0 | 8639 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0032 | 0/0 | 8642 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0033 | 0/0 | 8642 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0034 | 0/0 | 8640 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0035 | 0/0 | 8640 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0036 | 0/0 | 8640 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0037 | 0/0 | 8640 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0038 | 0/0 | 8638 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0039 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0040 | 0/0 | 8640 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0041 | 0/0 | 8640 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0042 | 0/0 | 8639 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0043 | 0/0 | 8640 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0044 | 0/0 | 8640 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0045 | 0/0 | 8641 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0046 | 0/0 | 8637 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0047 | 0/0 | 8641 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0048 | 0/0 | 8638 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0049 | 0/0 | 8639 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0050 | 0/0 | 8641 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0051 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0052 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0053 | 0/0 | 8640 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0054 | 0/0 | 8641 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0055 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0056 | 0/0 | 8642 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0057 | 0/0 | 8641 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0058 | 0/0 | 8641 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0059 | 0/0 | 8641 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0060 | 0/0 | 8627 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0061 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0062 | 0/0 | 8641 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0063 | 0/0 | 8641 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| t0064 | 0/0 | 8639 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4650 | 344 | 72 | 59 | 163 | 14 | 34 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0002 | 0/0 | 4650 | 19 | 19 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0003 | 0/0 | 4650 | 4 | 0 | 2 | 0 | 2 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0006 | 0/0 | 4650 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0007 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0008 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0011 | 0/0 | 4650 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0002c0004 | 0/0 | 4650 | 3 | 0 | 0 | 0 | 2 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0003c0005 | 0/0 | 4650 | 3 | 0 | 0 | 3 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0004c0010 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0005c0009 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | 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 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0002 | 1/1 | 13289 | 59 | 5 | 18 | 19 | 5 | 10 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0003 | 0/0 | 13290 | 25 | 0 | 1 | 22 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0004 | 0/0 | 13290 | 21 | 0 | 0 | 20 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0005 | 0/0 | 13290 | 20 | 4 | 4 | 6 | 2 | 4 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0006 | 0/0 | 13288 | 15 | 0 | 3 | 11 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0007 | 0/0 | 13287 | 17 | 1 | 5 | 11 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0009 | 0/0 | 13289 | 11 | 10 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0010 | 0/0 | 13292 | 9 | 1 | 1 | 5 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0011 | 0/0 | 13288 | 8 | 8 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0012 | 0/0 | 13289 | 6 | 0 | 6 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0013 | 0/0 | 13288 | 5 | 0 | 5 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0014 | 0/0 | 13292 | 5 | 0 | 0 | 5 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0015 | 0/0 | 13289 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0016 | 0/0 | 13292 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0017 | 0/0 | 13287 | 3 | 0 | 0 | 3 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0018 | 0/0 | 13290 | 3 | 0 | 1 | 0 | 1 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0019 | 0/0 | 13290 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0020 | 0/0 | 13286 | 3 | 3 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0021 | 0/0 | 13287 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0022 | 0/0 | 13289 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0023 | 0/0 | 13289 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0024 | 0/0 | 13289 | 2 | 0 | 2 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0025 | 0/0 | 13290 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0026 | 0/0 | 13287 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0028 | 0/0 | 13289 | 2 | 0 | 1 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0029 | 0/0 | 13286 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0030 | 0/0 | 13290 | 2 | 0 | 0 | 0 | 0 | 2 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0031 | 0/0 | 13288 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0032 | 0/0 | 13291 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0033 | 0/0 | 13291 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0034 | 0/0 | 13289 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0035 | 0/0 | 13289 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0036 | 0/0 | 13289 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0037 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0038 | 0/0 | 13287 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0039 | 0/0 | 13288 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0040 | 0/0 | 13289 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0041 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0042 | 0/0 | 13288 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0043 | 0/0 | 13289 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0044 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0045 | 0/0 | 13290 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0046 | 0/0 | 13286 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0047 | 0/0 | 13290 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0048 | 0/0 | 13287 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0049 | 0/0 | 13288 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0051 | 0/0 | 13288 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0053 | 0/0 | 13289 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0054 | 0/0 | 13290 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0055 | 0/0 | 13288 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0056 | 0/0 | 13291 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0057 | 0/0 | 13290 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0058 | 0/0 | 13290 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0059 | 0/0 | 13290 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0060 | 0/0 | 13276 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0061 | 0/0 | 13292 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0062 | 0/0 | 13290 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0063 | 0/0 | 13290 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0001t0064 | 0/0 | 13288 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0002t0008 | 0/0 | 13288 | 16 | 16 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0002t0027 | 0/0 | 13288 | 2 | 2 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0002t0050 | 0/0 | 13290 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0003t0002 | 0/0 | 13289 | 4 | 0 | 2 | 0 | 2 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0006t0004 | 0/0 | 13290 | 2 | 0 | 0 | 2 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0007t0052 | 0/0 | 13288 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0008t0001 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0001c0011t0005 | 0/0 | 13290 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0002c0004t0006 | 0/0 | 13288 | 3 | 0 | 0 | 0 | 2 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0003c0005t0001 | 0/0 | 13289 | 3 | 0 | 0 | 3 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0004c0010t0002 | 0/0 | 13289 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| a0005c0009t0002 | 0/0 | 13289 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | copy fasta | chr16 | 69560966 | 69709654 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0160 | 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 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0204 | 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 |
| a0001c0001t0003g0206 | 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 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0004g0254 | 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 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0006g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0010g0349 | 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 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0011g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0012g0123 | 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 |
| a0001c0001t0013g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0013g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0013g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0014g0348 | 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 |
| a0001c0001t0014g0353 | 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 |
| a0001c0001t0015g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0015g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0015g0319 | 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 |
| a0001c0001t0017g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0017g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0017g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0018g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0018g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0018g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0019g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0019g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0019g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0020g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0020g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0020g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0021g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0021g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0022g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0022g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0023g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0023g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0024g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0024g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0025g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0025g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0026g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0026g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0028g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0028g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0029g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0029g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0030g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0030g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0031g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0032g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0033g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0034g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0035g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0036g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0037g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0038g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0039g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0040g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0041g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0042g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0043g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0044g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0045g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0046g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0047g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0048g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0049g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0051g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0053g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0054g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0055g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0056g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0057g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0058g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0059g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0060g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0061g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0062g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0063g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0001t0064g0092 | 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 |
| a0001c0002t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0008g0181 | 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 |
| a0001c0002t0027g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0027g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0002t0050g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0006t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0006t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0007t0052g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0008t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0001c0011t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0002c0004t0006g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0002c0004t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0002c0004t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0003c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0003c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0003c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0004c0010t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| a0005c0009t0002g0288 | 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 | g0105 | EUR | GBR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | GBR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0279 | EUR | GBR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00140 | hp2 | a0001 | c0001 | t0035 | g0020 | EUR | GBR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0280 | EUR | FIN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0094 | EUR | FIN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0269 | 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 | g0183 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00423 | hp1 | a0001 | c0001 | t0044 | g0274 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00609 | hp2 | a0001 | c0001 | t0047 | g0086 | EAS | CHS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00733 | hp1 | a0001 | c0001 | t0012 | g0115 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0271 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0246 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0218 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0299 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0072 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01074 | hp1 | a0001 | c0001 | t0062 | g0237 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01074 | hp2 | a0004 | c0010 | t0002 | g0265 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01081 | hp2 | a0001 | c0001 | t0013 | g0034 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0117 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0266 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0252 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0074 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0253 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0301 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01255 | hp1 | a0001 | c0001 | t0043 | g0110 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01255 | hp2 | a0001 | c0001 | t0018 | g0375 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01256 | hp2 | a0001 | c0001 | t0013 | g0035 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01257 | hp1 | a0001 | c0001 | t0024 | g0230 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01258 | hp1 | a0001 | c0001 | t0024 | g0231 | 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 | g0108 | 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 | t0007 | g0069 | 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 | g0026 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0104 | 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 | t0028 | g0098 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01515 | hp1 | a0002 | c0004 | t0006 | g0103 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0256 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0272 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0270 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01517 | hp2 | a0002 | c0004 | t0006 | g0101 | EUR | IBS | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01884 | hp1 | a0001 | c0001 | t0019 | g0222 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01884 | hp2 | a0001 | c0002 | t0027 | g0173 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01891 | hp1 | a0001 | c0001 | t0021 | g0153 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01891 | hp2 | a0001 | c0002 | t0008 | g0166 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01928 | hp2 | a0001 | c0001 | t0013 | g0041 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01934 | hp1 | a0001 | c0001 | t0036 | g0046 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01943 | hp2 | a0001 | c0001 | t0012 | g0123 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0071 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02015 | hp1 | a0001 | c0001 | t0063 | g0350 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02015 | hp2 | a0005 | c0009 | t0002 | g0288 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02055 | hp1 | a0001 | c0002 | t0008 | g0168 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0340 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02129 | hp2 | a0001 | c0001 | t0045 | g0102 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02132 | hp2 | a0001 | c0001 | t0010 | g0349 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | CDX | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | CDX | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | CDX | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02257 | hp1 | a0001 | c0001 | t0059 | g0238 | 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 | g0319 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02273 | hp2 | a0001 | c0001 | t0007 | g0070 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02280 | hp2 | a0001 | c0002 | t0008 | g0162 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02300 | hp1 | a0001 | c0001 | t0012 | g0113 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0300 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02451 | hp2 | a0001 | c0001 | t0057 | g0245 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02572 | hp1 | a0001 | c0001 | t0020 | g0368 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02572 | hp2 | a0001 | c0001 | t0029 | g0373 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0243 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02615 | hp2 | a0001 | c0001 | t0020 | g0369 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0333 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0305 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0334 | 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 | g0241 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02683 | hp1 | a0002 | c0004 | t0006 | g0096 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02717 | hp1 | a0001 | c0001 | t0038 | g0136 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0258 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02723 | hp2 | a0001 | c0002 | t0008 | g0174 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0261 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0138 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0259 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0154 | 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 | t0026 | g0338 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02895 | hp2 | a0001 | c0002 | t0008 | g0171 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02896 | hp1 | a0001 | c0001 | t0046 | g0363 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0304 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0303 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02897 | hp2 | a0001 | c0002 | t0008 | g0167 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0224 | 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 | g0181 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0128 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02970 | hp2 | a0001 | c0002 | t0008 | g0163 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03017 | hp1 | a0001 | c0001 | t0028 | g0099 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03041 | hp1 | a0001 | c0001 | t0019 | g0234 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0367 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03098 | hp1 | a0001 | c0001 | t0026 | g0337 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03098 | hp2 | a0001 | c0001 | t0029 | g0372 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03130 | hp1 | a0001 | c0002 | t0050 | g0169 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0312 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0151 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03139 | hp2 | a0001 | c0001 | t0055 | g0240 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0326 | 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 | t0019 | g0235 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03209 | hp2 | a0001 | c0001 | t0056 | g0346 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03225 | hp2 | a0001 | c0001 | t0040 | g0158 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0024 | 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 | g0170 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0260 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0139 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03579 | hp2 | a0001 | c0001 | t0051 | g0257 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0251 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03688 | hp1 | a0001 | c0001 | t0030 | g0371 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0376 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03704 | hp2 | a0001 | c0001 | t0034 | g0056 | SAS | PJL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0324 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0254 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0197 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | BEB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04115 | hp1 | a0001 | c0001 | t0030 | g0090 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0044 | 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 | g0320 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04199 | hp2 | a0001 | c0011 | t0005 | g0226 | 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 | g0347 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | STU | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | CHB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | CHB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0247 | EAS | CHB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18906 | hp1 | a0001 | c0001 | t0021 | g0159 | AFR | YRI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18906 | hp2 | a0001 | c0002 | t0008 | g0164 | AFR | YRI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18939 | hp1 | a0001 | c0001 | t0007 | g0062 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0210 | 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 | g0255 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18957 | hp1 | a0001 | c0001 | t0007 | g0063 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18957 | hp2 | a0001 | c0001 | t0042 | g0285 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18963 | hp2 | a0001 | c0001 | t0060 | g0161 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18966 | hp2 | a0001 | c0001 | t0049 | g0047 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18972 | hp1 | a0003 | c0005 | t0001 | g0132 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18973 | hp2 | a0001 | c0001 | t0032 | g0028 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18977 | hp1 | a0001 | c0001 | t0014 | g0352 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0078 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18978 | hp1 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18980 | hp1 | a0001 | c0001 | t0033 | g0015 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18981 | hp1 | a0001 | c0001 | t0025 | g0277 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18982 | hp1 | a0003 | c0005 | t0001 | g0114 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18984 | hp2 | a0001 | c0001 | t0023 | g0116 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18985 | hp1 | a0001 | c0001 | t0037 | g0039 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18991 | hp1 | a0001 | c0001 | t0017 | g0075 | 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 | t0064 | g0092 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18992 | hp2 | a0003 | c0005 | t0001 | g0133 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18993 | hp2 | a0001 | c0001 | t0023 | g0118 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18994 | hp2 | a0001 | c0001 | t0017 | g0076 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19001 | hp1 | a0001 | c0001 | t0025 | g0308 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0354 | 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 | g0351 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0079 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19010 | hp2 | a0001 | c0001 | t0014 | g0348 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19012 | hp1 | a0001 | c0001 | t0017 | g0067 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19030 | hp1 | a0001 | c0001 | t0048 | g0341 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0318 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19043 | hp1 | a0001 | c0001 | t0061 | g0357 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19055 | hp2 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19058 | hp2 | a0001 | c0001 | t0058 | g0203 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19060 | hp1 | a0001 | c0001 | t0041 | g0119 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19066 | hp1 | a0001 | c0001 | t0014 | g0353 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19068 | hp1 | a0001 | c0008 | t0001 | g0033 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19078 | hp1 | a0001 | c0001 | t0022 | g0038 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19078 | hp2 | a0001 | c0006 | t0004 | g0182 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19080 | hp2 | a0001 | c0001 | t0010 | g0345 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19081 | hp1 | a0001 | c0001 | t0031 | g0120 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19084 | hp2 | a0001 | c0001 | t0022 | g0043 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19085 | hp2 | a0001 | c0001 | t0010 | g0355 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0014 | 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 | g0049 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19088 | hp2 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0084 | 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 | g0152 | AFR | ASW | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20752 | hp1 | a0001 | c0001 | t0018 | g0374 | EUR | TSI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0250 | EUR | TSI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0273 | EUR | TSI | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20905 | hp1 | a0001 | c0001 | t0054 | g0225 | SAS | GIH | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | GIH | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02109 | hp1 | a0001 | c0002 | t0027 | g0172 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02109 | hp2 | a0001 | c0001 | t0039 | g0050 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0313 | 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 | g0055 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0135 | AFR | ACB | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03471 | hp1 | a0001 | c0002 | t0008 | g0165 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0328 | AFR | MSL | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | USA | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| HG06807 | hp2 | a0001 | c0007 | t0052 | g0006 | AFR | USA | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0284 | 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 | t0007 | g0065 | AFR | USA | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| NA21309 | hp2 | a0001 | c0001 | t0053 | g0302 | AFR | LWK | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0298 | REF | REF | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0080 | REF | REF | NFAT5_chr16_69560966_69709654 | NFAT5 | chr16 | 69560966 | 69709654 |
| 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 |
| 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 |
| 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 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(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 | a0001c0001t0064 | 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 | 62 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(59): 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 | 19 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(16): 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 | a0001c0001t0054 | 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 | a0001c0001t0045 | 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 | a0001c0001t0063 | 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 | a0001c0001t0041 | 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 | 17 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(14): 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 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(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 | 7 | a0001c0001t0007a0001c0001t0013a0001c0001t0016others(4): 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 | a0001c0001t0024 | 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 | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(15): 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 | a0001c0001t0062 | 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 | 62 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(59): 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 | a0001c0001t0061 | 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 | a0001c0001t0053 | 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 | a0001c0001t0016a0001c0001t0046 | 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 | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(15): 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 | a0001c0001t0016a0001c0001t0018a0001c0001t0032others(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 | a0001c0001t0040 | 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 | a0001c0001t0020 | 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 | a0001c0001t0017a0001c0001t0057 | 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 | a0001c0001t0060 | 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 | a0001c0001t0010a0001c0001t0014a0001c0001t0033others(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 | a0001c0001t0046 | 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 | a0001c0001t0011a0001c0001t0021a0001c0001t0029others(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 | a0001c0001t0018a0001c0001t0029a0001c0007t0052 | 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 | a0001c0001t0041 | 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 | a0001c0001t0048 | 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 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(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 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(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 | a0001c0001t0051 | 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 | a0001c0001t0044 | 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 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(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 | a0001c0001t0011a0001c0001t0021a0001c0001t0039 | 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 | a0001c0002t0027 | 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 | 62 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(59): 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 | a0001c0001t0059a0001c0001t0062 | 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 | a0001c0001t0023a0001c0001t0031 | 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 | a0001c0001t0058 | 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 | a0001c0001t0034 | 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 | a0001c0001t0019 | 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 | a0001c0001t0037 | 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 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(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 | a0001c0001t0004a0001c0001t0058a0001c0006t0004 | 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 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(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 | a0001c0001t0058 | 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 | a0001c0001t0035 | 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 | 8 | a0001c0001t0006a0001c0001t0007a0001c0001t0017others(5): 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 | a0001c0001t0016a0001c0001t0046 | 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 | a0001c0001t0039 | 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 | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(6): 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 | 8 | a0001c0001t0006a0001c0001t0007a0001c0001t0017others(5): 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 | a0001c0001t0036 | 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 | a0001c0001t0048 | 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 | a0001c0001t0019 | 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 | a0001c0001t0022 | 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 | a0001c0001t0043 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8278C>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 15/15 | 9258 | chr16 | 69704629 |
| 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376 | 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 | a0001c0001t0030g0371 | 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 | a0001c0001t0020g0367a0001c0001t0020g0368a0001c0001t0020g0369 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0006g0004a0001c0001t0006g0005 | 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 | a0001c0001t0006g0004a0001c0001t0006g0005 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0010g0359a0001c0001t0010g0360 | 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 | a0001c0001t0010g0345a0001c0001t0010g0347a0001c0001t0010g0349others(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 | a0001c0001t0001g0008a0001c0001t0001g0009 | 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 | a0001c0001t0012g0343a0001c0001t0012g0344 | 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 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0004g0254others(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 | a0001c0001t0018g0376a0001c0001t0026g0338a0001c0001t0029g0372others(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 | a0001c0001t0001g0342 | 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 | a0001c0001t0011g0340 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0026g0337 | 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 | a0001c0001t0001g0317a0001c0001t0002g0263a0001c0001t0002g0264others(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 | a0001c0001t0002g0267a0001c0001t0002g0268a0001c0001t0002g0269others(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 | 21 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283others(18): Show | 21 | HG01069.hp1 HG02015.hp2 HG02080.hp1 others(18): 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 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0002g0310others(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 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0015g0319 | 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 | a0001c0001t0002g0320a0001c0001t0002g0321a0001c0001t0002g0322others(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 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0001t0002g0326 | 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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(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 | a0001c0001t0001g0332a0001c0001t0011g0333a0001c0001t0011g0334 | 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 | a0001c0001t0001g0335 | 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 | a0001c0001t0001g0336 | 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 | a0001c0001t0002g0339a0001c0001t0011g0340a0001c0001t0048g0341 | 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 | a0001c0001t0003g0228a0001c0001t0003g0229a0001c0001t0004g0227others(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 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177 | 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 | a0001c0001t0060g0161 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0033g0015 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0018a0001c0001t0001g0019 | 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 | a0001c0001t0035g0020 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023 | 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 | a0001c0001t0001g0024a0001c0001t0001g0025 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0027a0001c0001t0001g0342 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(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 | a0001c0001t0001g0036a0001c0001t0013g0002a0001c0001t0013g0034others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0013g0041others(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 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(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 | a0001c0001t0001g0051a0001c0001t0001g0052 | 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 | a0001c0001t0001g0003a0001c0001t0001g0053 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0034g0056 | 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 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 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 | a0001c0001t0001g0127a0001c0001t0006g0004a0001c0001t0006g0005others(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 | a0001c0001t0001g0131a0001c0001t0006g0100a0001c0001t0045g0102others(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 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(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 | a0001c0001t0002g0129a0001c0001t0015g0128 | 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 | a0001c0001t0002g0130a0001c0001t0002g0134a0001c0001t0015g0135 | 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 | a0001c0001t0001g0137a0001c0001t0011g0138a0001c0001t0038g0136 | 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 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(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 | a0001c0001t0001g0143a0001c0001t0001g0145 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147 | 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 | a0001c0001t0001g0148a0001c0001t0001g0149 | 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 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0011g0151others(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 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(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 | a0001c0001t0040g0158 | 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 | a0001c0001t0021g0159 | 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 | a0001c0001t0001g0160 | 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 | 114 | a0001c0001t0001g0317a0001c0001t0001g0327a0001c0001t0001g0329others(111): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): 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 | a0001c0001t0007g0062a0001c0001t0007g0063a0001c0001t0007g0064others(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 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0032g0028 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0002t0008g0181 | 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 | a0001c0001t0003g0223a0001c0001t0005g0224a0001c0001t0054g0225others(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 | a0001c0001t0002g0236a0001c0001t0007g0062a0001c0001t0007g0063others(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 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(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 | a0001c0001t0001g0008a0001c0001t0005g0239a0001c0001t0005g0243others(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 | a0001c0001t0018g0376a0001c0001t0029g0372a0001c0001t0029g0373others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0005g0241 | 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 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0042others(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 | a0001c0001t0020g0368 | 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 | a0001c0001t0001g0061a0001c0001t0001g0144 | 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 | a0001c0001t0010g0345 | 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 | a0001c0001t0002g0306a0001c0001t0003g0175a0001c0001t0003g0176others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0056g0346 | 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 | a0001c0001t0001g0013 | 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 | a0001c0006t0004g0182a0001c0006t0004g0183 | 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 | a0001c0001t0019g0222a0001c0001t0019g0234a0001c0001t0019g0235 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0040g0158 | 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 | a0001c0011t0005g0226 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0001g0141a0001c0001t0002g0325a0001c0001t0003g0221others(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 | a0001c0002t0008g0181 | 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 | a0001c0001t0060g0161 | 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 | a0001c0001t0044g0274 | 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 | a0001c0001t0001g0017 | 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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0006g0079a0001c0001t0006g0084a0001c0001t0006g0085others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0047g0086 | 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 | a0001c0001t0002g0134a0001c0001t0002g0282a0001c0001t0002g0283others(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 | a0001c0001t0002g0281a0001c0001t0004g0184a0001c0001t0009g0303others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0029g0372others(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 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(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 | a0001c0001t0001g0112a0001c0001t0001g0127a0001c0001t0001g0131others(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 | a0001c0001t0001g0007a0001c0001t0001g0124a0001c0001t0001g0317others(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 | a0001c0001t0011g0328a0001c0001t0011g0333 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0145a0001c0001t0003g0180a0001c0001t0003g0220others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0012g0123 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0007t0052g0006 | 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 | a0001c0007t0052g0006 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | 77 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): 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 | a0001c0001t0004g0227 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0019g0222a0001c0001t0019g0234a0001c0001t0019g0235 | 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 | 320 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0004g0254a0001c0001t0005g0246a0001c0001t0005g0252others(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 | a0001c0002t0008g0174 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0002g0267a0001c0001t0002g0268a0001c0001t0002g0269others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0004g0219 | 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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | 5 | a0001c0001t0002g0129a0001c0001t0002g0263a0001c0001t0002g0264others(2): Show | 5 | HG00280.hp1 HG01099.hp2 HG01192.hp2 others(2): 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0020g0369 | 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 | a0001c0001t0002g0306a0001c0001t0002g0316a0001c0001t0002g0324 | 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 | a0001c0001t0006g0084a0001c0001t0006g0085a0001c0001t0006g0100 | 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 | a0001c0001t0001g0156a0001c0001t0002g0273a0001c0001t0006g0084others(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 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(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 | a0001c0001t0001g0025a0001c0001t0001g0054a0001c0001t0005g0241others(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 | a0001c0001t0002g0311 | 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 | a0001c0001t0011g0138a0001c0001t0039g0050 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0040g0158 | 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 | a0001c0001t0061g0357 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0034g0056 | 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 | a0001c0001t0005g0251 | 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 | a0001c0001t0025g0308 | 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 | a0001c0001t0022g0038a0001c0001t0022g0043 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0017g0067a0001c0001t0017g0075a0001c0001t0017g0076 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0037g0039 | 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 | a0001c0001t0030g0371 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0002g0320 | 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 | a0001c0001t0009g0318a0001c0001t0053g0302 | 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 | 330 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0031a0001c0001t0001g0144a0001c0001t0001g0154others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0004g0254a0001c0001t0005g0010a0001c0001t0005g0224others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0003g0221 | 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 | a0001c0011t0005g0226 | 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 | a0001c0001t0040g0158 | 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 | a0001c0001t0009g0260 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0011t0005g0226 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376 | 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 | 77 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0011g0139a0001c0001t0038g0136 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0068 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0005g0224a0001c0001t0005g0239 | 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 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0048others(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 | a0001c0001t0053g0302 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0006g0088 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0003g0217 | 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 | a0001c0001t0001g0332 | 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 | 2 | a0001c0001t0002g0129a0001c0001t0002g0298 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.127+11377T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 2/14 | chr16 | 69579925 | ||||||
| chr16:69579949
|
G | T | 1 | a0001c0001t0048g0341 | 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 | a0001c0001t0004g0254a0001c0001t0005g0246a0001c0001t0005g0252others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0001g0331 | 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 | a0001c0001t0037g0039 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338a0001c0001t0051g0257 | 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 | a0001c0007t0052g0006 | 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 | a0001c0001t0003g0180 | 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 | a0001c0002t0008g0162a0001c0002t0008g0163a0001c0002t0008g0164 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0002g0311 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0006g0004 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0011t0005g0226 | 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 | a0001c0001t0001g0018a0001c0001t0018g0374a0001c0001t0018g0375others(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 | a0001c0001t0048g0341 | 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 | a0001c0007t0052g0006 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(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 | a0001c0001t0055g0240 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0006g0085 | 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 | 327 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0001c0001t0060g0161 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0055g0240 | 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 | a0001c0001t0003g0180 | 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 | a0001c0001t0003g0186a0001c0001t0003g0228 | 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 | a0001c0001t0004g0254a0001c0001t0005g0010a0001c0001t0005g0224others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376 | 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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0006g0079 | 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 | a0001c0001t0010g0345a0001c0001t0010g0349a0001c0001t0010g0355others(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 | a0001c0001t0006g0088 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0063g0350 | 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 | a0001c0001t0002g0321 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0127a0001c0001t0001g0317 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0002g0325a0001c0001t0011g0138a0001c0001t0011g0139others(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 | 330 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0066others(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 | a0001c0001t0010g0218a0001c0001t0010g0345a0001c0001t0010g0347others(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 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0048others(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 | a0001c0001t0007g0069 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0007g0070 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0032g0028 | 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 | a0001c0001t0061g0357 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338a0001c0001t0051g0257 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0003g0178 | 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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0002g0107a0001c0001t0003g0229a0001c0001t0005g0247others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0002g0294a0001c0001t0044g0274 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0061g0357 | 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 | 77 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): 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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0009g0259 | 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 | a0001c0001t0002g0339 | 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 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0002t0008g0168others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0026others(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 | a0001c0001t0002g0111a0001c0001t0002g0282a0001c0001t0002g0283others(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 | a0001c0001t0001g0018a0001c0001t0003g0187a0001c0001t0018g0376others(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 | a0001c0001t0003g0175a0001c0001t0003g0178a0001c0001t0003g0180others(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 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0179others(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 | a0001c0001t0003g0212a0001c0001t0003g0228a0001c0001t0010g0349others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(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 | a0001c0001t0005g0241a0001c0001t0011g0138a0001c0001t0011g0139others(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 | a0001c0001t0009g0259 | 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 | a0001c0001t0003g0220 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0003g0211 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0004g0210 | 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 | a0001c0001t0023g0116a0001c0001t0023g0118a0001c0001t0031g0120 | 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 | a0001c0001t0001g0331 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0005g0241 | 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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0011g0151 | 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 | a0001c0001t0001g0154 | 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 | a0001c0007t0052g0006 | 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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0007g0073 | 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 | a0001c0001t0006g0094 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0034g0056 | 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 | a0001c0011t0005g0226 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(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 | 7 | a0001c0001t0002g0129a0001c0001t0002g0298a0001c0001t0002g0325others(4): Show | 7 | HG00597.hp1 HG01099.hp2 HG01256.hp1 others(4): 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0032a0001c0001t0003g0180a0001c0001t0005g0224others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0007g0068 | 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 | a0001c0001t0019g0222a0001c0001t0019g0234a0001c0001t0019g0235 | 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 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0141others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | 77 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): 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 | a0001c0001t0003g0187a0001c0001t0003g0201a0001c0001t0003g0217others(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 | a0001c0001t0001g0141 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260others(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 | a0001c0001t0001g0137a0001c0001t0013g0041 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0005g0251 | 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 | a0001c0001t0019g0222 | 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 | a0001c0006t0004g0182a0001c0006t0004g0183 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0108 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0010g0349 | 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 | a0001c0001t0030g0090 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0006g0082a0001c0001t0006g0093 | 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 | a0001c0001t0006g0100 | 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 | a0003c0005t0001g0132a0003c0005t0001g0133 | 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 | a0001c0001t0012g0117 | 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 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0060others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0002g0134a0001c0001t0002g0307a0001c0001t0002g0322others(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 | a0001c0001t0003g0185a0001c0001t0003g0188a0001c0001t0003g0204others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0012g0113 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0048others(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 | a0001c0001t0005g0241 | 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 | a0001c0007t0052g0006 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | 10 | a0001c0001t0001g0060a0001c0001t0001g0145a0001c0001t0001g0327others(7): Show | 10 | HG00639.hp2 HG01175.hp2 HG02738.hp2 others(7): 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 | a0001c0001t0002g0323a0001c0001t0003g0217a0001c0001t0005g0249others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0004g0214 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0005g0244 | 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 | a0001c0001t0029g0373 | 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 | a0001c0001t0001g0160 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0040a0001c0001t0003g0220a0001c0001t0026g0337others(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 | a0001c0001t0003g0209 | 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 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0066others(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 | a0001c0001t0010g0349 | 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 | 327 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0001c0001t0002g0339 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0002g0297a0001c0001t0003g0186a0001c0001t0003g0201others(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 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0061others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0006g0082a0001c0001t0006g0093 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0024a0001c0001t0001g0060 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0007g0062 | 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 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0032others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | 330 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0242 | 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 | a0001c0001t0002g0232 | 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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0301 | 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 | 243 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0004g0254a0001c0001t0005g0010a0001c0001t0005g0224others(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 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0060others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0002g0307a0001c0001t0006g0089a0001c0001t0006g0095others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0005g0250a0001c0001t0016g0362a0001c0001t0016g0364others(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 | a0001c0001t0001g0036 | 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 | a0001c0001t0055g0240 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0005g0243 | 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 | a0001c0001t0019g0222a0001c0001t0019g0234a0001c0001t0019g0235 | 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 | a0001c0001t0029g0372a0001c0001t0029g0373 | 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 | a0001c0001t0004g0199 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0061g0357 | 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 | a0001c0001t0002g0134a0001c0001t0002g0307a0001c0001t0002g0322others(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 | a0001c0001t0048g0341a0001c0002t0008g0001a0001c0002t0008g0162others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0010g0347 | 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 | a0002c0004t0006g0096 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0035g0020 | 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 | a0001c0001t0009g0303a0001c0001t0009g0304 | 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 | a0001c0001t0002g0316 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | 330 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0001c0001t0055g0240 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | 330 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0001c0001t0010g0349 | 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 | a0001c0001t0004g0219 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0002t0027g0172a0001c0002t0027g0173 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0127a0001c0001t0001g0317 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0002c0004t0006g0096 | 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 | a0001c0001t0005g0247a0001c0001t0005g0248a0001c0001t0005g0255others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0007g0081 | 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 | a0001c0001t0045g0102 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0002g0282 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0003g0217 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0002g0273 | 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 | a0001c0001t0007g0077 | 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 | a0001c0001t0004g0184a0001c0001t0004g0213a0001c0001t0004g0214others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0007g0071 | 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 | a0001c0001t0020g0369 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0125 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0160a0001c0001t0002g0297a0001c0001t0006g0084others(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 | a0001c0001t0001g0045a0001c0001t0002g0311a0001c0001t0003g0175others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0010g0347 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0122a0001c0001t0001g0149 | 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 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0060others(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 | a0001c0001t0029g0373 | 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 | a0001c0001t0001g0330 | 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 | a0001c0001t0010g0345a0001c0001t0010g0349a0001c0001t0010g0355others(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 | a0001c0001t0001g0014 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0325 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | 327 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0004g0195a0001c0001t0004g0196a0001c0001t0004g0215 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0005g0241 | 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 | a0001c0001t0020g0368 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376 | 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 | a0001c0001t0005g0250 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0007g0065a0001c0001t0007g0071a0001c0001t0007g0078others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0003g0176 | 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 | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): 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 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0058others(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 | a0001c0008t0001g0033 | 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 | a0001c0001t0005g0261a0001c0001t0016g0362a0001c0001t0016g0364others(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 | a0001c0001t0001g0016a0001c0001t0002g0233a0001c0001t0002g0286others(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 | a0001c0001t0006g0079 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0049 | 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 | a0001c0002t0008g0168 | 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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0035g0020 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0020g0368 | 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 | a0001c0001t0010g0347 | 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 | a0001c0001t0010g0347 | 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 | a0001c0001t0055g0240 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0059a0001c0001t0003g0217a0001c0001t0006g0097others(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 | a0001c0001t0001g0003a0001c0001t0002g0309a0001c0001t0006g0089others(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 | a0001c0001t0001g0055 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0035g0020 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0010g0345a0001c0001t0010g0349a0001c0001t0010g0355others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0279others(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 | 77 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0003g0187a0001c0001t0003g0201a0001c0001t0003g0217others(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 | a0001c0001t0001g0018a0001c0001t0002g0104a0001c0001t0002g0109others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0002g0279 | 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 | a0001c0001t0020g0368 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0002g0309a0001c0001t0002g0321 | 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 | a0001c0008t0001g0033 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0020g0367a0001c0001t0020g0368a0001c0001t0020g0369 | 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 | a0001c0001t0020g0368 | 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 | a0001c0001t0003g0221 | 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 | a0001c0001t0001g0054 | 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 | a0004c0010t0002g0265 | 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 | 327 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0001c0001t0051g0257 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0003g0185a0001c0001t0003g0188a0001c0001t0003g0204others(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 | a0001c0001t0002g0339 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0011t0005g0226 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0037a0001c0001t0001g0042 | 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 | a0001c0001t0028g0098a0001c0001t0028g0099 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0291a0001c0001t0002g0311a0001c0001t0003g0175others(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 | a0001c0001t0001g0125 | 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 | a0001c0001t0011g0139a0001c0001t0011g0328a0001c0001t0011g0333others(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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0053a0001c0001t0001g0146a0001c0001t0001g0327 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0030g0090a0001c0001t0030g0371 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | 277 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(274): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0001t0001g0125a0001c0001t0003g0176a0001c0001t0003g0177others(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 | 330 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0003g0209 | 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 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0042others(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 | a0001c0001t0002g0287a0001c0001t0002g0289a0001c0001t0018g0374others(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 | a0001c0001t0002g0264 | 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 | 330 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0020g0367a0001c0001t0020g0368a0001c0001t0020g0369others(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 | a0001c0001t0002g0134a0001c0001t0002g0267a0001c0001t0002g0293others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0003g0178others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0001g0036 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0001g0061 | 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 | 77 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): 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 | a0001c0001t0011g0151a0001c0001t0011g0152a0001c0001t0011g0334others(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 | a0001c0001t0057g0245 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0001g0329 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0007g0065 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0140others(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 | a0001c0001t0002g0307a0001c0001t0011g0333a0001c0001t0043g0110others(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 | a0001c0001t0001g0013a0001c0001t0002g0233a0001c0001t0002g0323others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0013a0003c0005t0001g0133 | 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 | a0001c0001t0001g0327 | 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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0042others(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 | a0001c0001t0061g0357 | 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 | a0001c0001t0041g0119 | 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 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017 | 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 | a0001c0001t0002g0134a0001c0001t0002g0307a0001c0001t0002g0322others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0005g0241 | 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 | a0001c0001t0004g0202 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0002g0108 | 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 | a0001c0001t0002g0129 | 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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0007g0069 | 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 | a0001c0001t0007g0070a0001c0001t0007g0072a0001c0001t0007g0074 | 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 | a0001c0001t0007g0065 | 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 | a0001c0001t0006g0005a0001c0001t0006g0085a0001c0001t0006g0093 | 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 | a0001c0001t0006g0084a0001c0001t0006g0088a0001c0001t0007g0066others(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 | a0001c0001t0007g0062a0001c0001t0007g0073a0001c0001t0019g0235 | 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 | a0001c0001t0006g0100a0001c0001t0006g0299a0001c0001t0007g0063others(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 | a0001c0001t0007g0071a0001c0001t0017g0067a0001c0001t0017g0075others(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 | a0001c0001t0006g0095 | 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 | a0001c0001t0006g0087a0001c0001t0006g0089 | 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 | a0001c0001t0006g0097a0001c0001t0007g0091a0001c0001t0064g0092 | 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 | a0002c0004t0006g0101a0002c0004t0006g0103 | 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 | a0002c0004t0006g0096 | 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 | a0001c0001t0002g0284a0001c0001t0015g0135 | 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 | a0001c0001t0002g0134a0001c0001t0002g0281a0001c0001t0002g0326others(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 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(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 | 67 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(64): Show | 70 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(67): 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 | a0001c0001t0005g0224a0001c0001t0005g0250a0001c0001t0009g0258others(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 | a0001c0001t0001g0336a0001c0001t0004g0184a0001c0001t0005g0010others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0031others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0001t0001g0145a0001c0001t0016g0362a0001c0001t0016g0364others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0007g0066 | 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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0007g0068 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0002g0294a0001c0001t0044g0274 | 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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0017g0067a0001c0001t0017g0075a0001c0001t0017g0076 | 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 | a0001c0001t0010g0218 | 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 | a0001c0001t0004g0193a0001c0001t0004g0194 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0335 | 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 | 77 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.253+3088T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69629616 | ||||||
| chr16:69629768
|
A | AT | 165 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(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 | a0001c0001t0003g0208a0001c0001t0003g0229a0001c0001t0004g0189others(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 | a0001c0001t0002g0311a0001c0001t0002g0320a0001c0001t0005g0224others(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 | a0001c0001t0044g0274 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0005g0197a0001c0001t0005g0246a0001c0001t0005g0252others(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 | a0001c0001t0006g0088 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0311 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0001g0023 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0029g0373 | 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 | 329 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(326): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0011g0328a0001c0001t0011g0333 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0005g0248 | 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 | a0001c0001t0002g0268a0001c0001t0002g0269a0004c0010t0002g0265 | 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 | a0001c0001t0006g0094 | 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 | a0001c0001t0047g0086 | 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 | 74 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): 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 | a0001c0001t0051g0257 | 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 | 2 | a0001c0001t0002g0129a0001c0001t0002g0298 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253+6406A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | chr16 | 69632934 | ||||||
| chr16:69632982
|
A | G | 12 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0002g0322 | 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 | a0002c0004t0006g0096 | 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 | a0001c0001t0048g0341a0001c0002t0008g0001a0001c0002t0008g0162others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0002g0310 | 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 | a0001c0001t0006g0089a0001c0001t0006g0095a0001c0001t0006g0097others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0019g0235 | 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 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(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 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0112others(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 | a0001c0001t0029g0373a0001c0001t0048g0341a0001c0002t0008g0001others(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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0060g0161 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0001g0027a0001c0001t0001g0032 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0056g0346 | 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 | a0001c0001t0002g0104a0001c0001t0002g0134a0001c0001t0002g0232others(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 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0026others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0060a0001c0001t0005g0256a0001c0001t0011g0138others(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 | a0001c0001t0001g0023 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0006g0084a0001c0001t0006g0085a0001c0001t0006g0100 | 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 | a0001c0001t0051g0257 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0039g0050 | 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 | a0001c0001t0006g0094 | 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 | a0001c0001t0010g0345a0001c0001t0010g0349a0001c0001t0010g0355others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0026g0338 | 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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0005g0250 | 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 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338a0001c0001t0055g0240 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0147others(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 | a0001c0001t0002g0267a0001c0001t0002g0268a0001c0001t0002g0269others(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 | a0001c0001t0026g0337a0001c0001t0026g0338a0001c0001t0051g0257 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0001g0144 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0018g0375 | 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 | a0001c0001t0004g0196 | 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 | a0001c0001t0001g0051 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0046g0363 | 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 | a0001c0001t0048g0341a0001c0002t0008g0001a0001c0002t0008g0162others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0022a0001c0001t0002g0236a0001c0001t0002g0276others(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 | a0001c0001t0001g0030a0001c0001t0001g0122a0001c0001t0001g0126others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0005g0241 | 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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0140a0001c0001t0009g0300a0001c0001t0009g0301others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0009g0318 | 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 | a0001c0001t0004g0184a0001c0001t0004g0189a0001c0001t0004g0190others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0002g0263a0001c0001t0002g0273a0001c0001t0002g0275others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0025a0001c0001t0003g0206a0001c0001t0005g0010others(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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0012g0123 | 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 | a0001c0001t0002g0292a0001c0001t0002g0293a0001c0001t0002g0296 | 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 | a0001c0001t0039g0050a0001c0001t0048g0341a0001c0002t0008g0001others(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 | a0001c0001t0004g0190 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0020g0367a0001c0001t0020g0368a0001c0001t0020g0369others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0042others(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 | a0001c0001t0001g0052a0001c0001t0002g0281a0001c0001t0004g0214others(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 | a0001c0001t0033g0015 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0003g0229 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0142 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0002g0276a0001c0001t0002g0278a0001c0001t0025g0277 | 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 | a0001c0001t0006g0089a0001c0001t0006g0095a0001c0001t0006g0097others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0005g0241 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0030g0090 | 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 | a0001c0001t0057g0245 | 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 | a0001c0001t0060g0161 | 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 | a0001c0001t0001g0044a0001c0001t0003g0175a0001c0001t0003g0176others(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 | a0001c0001t0005g0010a0001c0001t0005g0197a0001c0001t0005g0243others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0006g0079 | 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 | a0001c0001t0006g0079 | 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 | a0001c0001t0002g0326 | 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 | a0001c0006t0004g0182a0001c0006t0004g0183 | 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 | a0001c0001t0045g0102 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0001g0143a0001c0001t0001g0332a0001c0001t0001g0336 | 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 | a0001c0001t0001g0027a0001c0001t0001g0112a0001c0001t0001g0160others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0002g0134a0001c0001t0002g0307a0001c0001t0002g0322others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0002g0264 | 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 | a0001c0001t0029g0372a0001c0001t0029g0373 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0011g0151a0001c0001t0011g0152a0001c0001t0011g0334others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0003g0220 | 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 | a0001c0001t0011g0328 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0002g0289a0001c0001t0002g0361 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0006g0079 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0003g0221others(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 | a0001c0001t0048g0341a0001c0002t0008g0001a0001c0002t0008g0162others(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 | a0001c0001t0035g0020 | 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 | a0001c0001t0006g0095 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0010g0354a0001c0001t0014g0348a0001c0001t0014g0351others(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 | ||||||
| chr16:69652454
|
A | G | 1 | a0001c0001t0002g0298 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.813-782A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4/14 | chr16 | 69652454 | ||||||
| chr16:69652745
|
GGTTT | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0048g0341a0001c0002t0008g0001a0001c0002t0008g0162others(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 | a0001c0001t0002g0129 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0236a0001c0001t0002g0295a0001c0001t0002g0297others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0289a0001c0001t0003g0188a0001c0001t0005g0010others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0022g0038a0001c0001t0022g0043 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0017g0067a0001c0001t0017g0075a0001c0001t0017g0076 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0130a0001c0001t0002g0306a0001c0001t0002g0316others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0002t0008g0162a0001c0002t0008g0163a0001c0002t0008g0164others(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 | a0001c0001t0001g0044a0001c0001t0003g0175a0001c0001t0003g0176others(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 | a0001c0001t0029g0373 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0015g0135 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260others(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 | a0001c0001t0044g0274 | 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 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0018others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0316a0001c0001t0004g0190a0001c0001t0007g0064others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0013g0002a0001c0001t0013g0035 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376 | 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 | a0001c0001t0010g0345a0001c0001t0010g0349a0001c0001t0010g0355others(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 | a0001c0001t0002g0289 | 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 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0060others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0003g0178 | 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 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0001g0125others(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 | a0001c0001t0029g0372 | 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 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0079others(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 | a0001c0001t0001g0143a0001c0001t0001g0332a0001c0001t0001g0336 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0001g0141 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0012g0117 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0125 | 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 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0066others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0053a0001c0001t0001g0146a0001c0001t0001g0327others(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 | a0001c0001t0003g0223 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0029g0372a0001c0001t0029g0373 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0046g0363 | 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 | a0001c0001t0006g0089a0001c0001t0006g0095a0001c0001t0006g0097others(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 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(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 | a0001c0001t0007g0062 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0134a0001c0001t0015g0128a0001c0001t0015g0135others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0030g0090 | 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 | a0001c0001t0006g0093a0001c0001t0018g0374a0001c0001t0018g0375others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0015g0135 | 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 | a0001c0001t0011g0328a0001c0001t0011g0333 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0005g0251 | 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 | a0001c0001t0060g0161 | 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 | a0001c0001t0005g0010a0001c0001t0005g0197a0001c0001t0005g0224others(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 | a0001c0001t0035g0020 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0005g0249 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0018others(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 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0286others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0002t0008g0168 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0002g0295a0001c0001t0004g0198a0001c0001t0026g0337others(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 | a0001c0001t0001g0156a0001c0001t0004g0195a0001c0001t0006g0004others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0020g0367 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0036a0001c0001t0001g0329a0001c0001t0001g0330others(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 | a0001c0001t0016g0364a0001c0001t0016g0365a0001c0001t0018g0374others(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 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0187others(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 | a0001c0001t0003g0175a0001c0001t0003g0179a0001c0001t0003g0186others(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 | a0001c0001t0003g0178a0001c0001t0003g0185a0001c0001t0003g0228others(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 | a0001c0001t0003g0180a0001c0001t0003g0220a0001c0001t0005g0010others(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 | a0001c0001t0002g0236a0001c0001t0005g0239a0001c0001t0005g0261others(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 | a0001c0001t0002g0278a0001c0001t0011g0139a0001c0001t0011g0333others(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 | a0001c0001t0002g0276a0001c0001t0011g0328 | 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(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 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0026others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0016a0001c0001t0001g0327 | 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 | a0001c0001t0001g0053a0001c0001t0001g0146 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0147a0001c0001t0002g0105a0001c0001t0007g0091others(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 | a0001c0001t0001g0331 | 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 | a0001c0001t0004g0189 | 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 | a0001c0007t0052g0006 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(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 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0286others(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 | a0001c0001t0012g0113a0001c0001t0012g0115a0001c0001t0012g0123others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0002g0134a0001c0001t0002g0284a0001c0001t0002g0295others(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 | a0001c0001t0002g0233a0001c0001t0002g0324a0001c0001t0007g0068others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0164others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0002t0008g0166 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0057g0245 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0005g0224 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0046g0363 | 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 | a0001c0001t0002g0263a0001c0001t0002g0280 | 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 | a0001c0001t0001g0048a0001c0001t0049g0047 | 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 | a0001c0001t0007g0078 | 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 | a0001c0001t0060g0161 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0037others(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 | a0001c0001t0001g0052a0001c0001t0001g0147a0001c0001t0002g0267others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0004g0184 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0001g0061a0001c0001t0006g0004a0001c0001t0006g0005others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0003g0205 | 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 | a0001c0001t0055g0240 | 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 | a0001c0001t0005g0010a0001c0001t0005g0197a0001c0001t0005g0224others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0002g0295 | 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 | 2 | a0001c0001t0002g0129a0001c0001t0002g0298 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1370-4508A>G | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 7/14 | chr16 | 69665469 | ||||||
| chr16:69665646
|
G | A | 130 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0003c0005t0001g0114 | 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 | a0001c0001t0029g0372 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0002g0287 | 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 | a0001c0001t0002g0232 | 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 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0079others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0051g0257 | 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 | a0001c0007t0052g0006 | 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 | a0001c0002t0008g0166 | 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 | a0001c0001t0005g0010a0001c0001t0005g0197a0001c0001t0005g0224others(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 | a0001c0001t0047g0086 | 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 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0079others(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 | a0001c0001t0001g0331 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0036 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0005g0249a0001c0002t0008g0001a0001c0002t0008g0162others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0328others(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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0079others(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 | a0001c0001t0001g0125a0001c0001t0001g0126 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0042others(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 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0024g0230others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0005g0241 | 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 | a0001c0001t0006g0082a0001c0001t0006g0093 | 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 | a0001c0001t0001g0127a0001c0001t0001g0317 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0011g0333 | 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 | a0001c0001t0003g0185a0001c0001t0003g0205a0001c0001t0003g0207others(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 | a0001c0001t0060g0161 | 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 | a0001c0001t0001g0143a0001c0001t0001g0332a0001c0001t0001g0336 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0057g0245 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0005g0244a0001c0001t0005g0247a0001c0001t0005g0248others(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 | a0001c0001t0002g0325 | 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 | a0001c0002t0008g0162a0001c0002t0008g0163a0001c0002t0008g0164 | 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 | a0001c0001t0002g0281a0001c0001t0002g0284a0001c0001t0002g0291others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0006g0097 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012 | 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 | a0001c0001t0005g0241 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0006g0084 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0019g0222a0001c0001t0019g0234a0001c0001t0019g0235 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0055g0240 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0289 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0029g0373 | 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 | a0001c0001t0009g0318a0001c0001t0053g0302 | 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 | a0001c0001t0057g0245 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0013g0002a0001c0001t0013g0035 | 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 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0002g0130a0001c0001t0005g0197a0001c0001t0005g0246others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0004g0195others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0051 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0011g0138 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0058g0203 | 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 | a0001c0001t0010g0345 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0335 | 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 | a0001c0001t0002g0320 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0003g0223 | 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 | a0001c0001t0003g0209 | 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 | a0001c0001t0020g0367a0001c0001t0020g0368a0001c0001t0020g0369others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0006g0088 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0079others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0330a0001c0001t0001g0335 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0026g0337a0001c0001t0026g0338a0001c0001t0051g0257 | 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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0328others(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 | a0001c0001t0029g0372 | 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 | a0001c0002t0008g0170 | 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 | a0001c0001t0030g0090 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338a0001c0001t0051g0257 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0004g0213 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0002g0280 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0026g0337a0001c0001t0026g0338a0001c0001t0051g0257 | 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 | a0001c0001t0004g0184 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0045g0102 | 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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0001t0011g0138a0001c0001t0039g0050 | 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 | a0001c0001t0001g0024a0001c0001t0001g0060 | 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 | a0001c0001t0020g0367a0001c0001t0020g0368a0001c0001t0020g0369others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0048g0341a0001c0002t0008g0001a0001c0002t0008g0162others(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 | a0001c0001t0003g0223a0001c0001t0003g0229a0001c0001t0011g0151others(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 | a0001c0001t0002g0276 | 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 | a0001c0001t0018g0375 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0010g0218 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0002g0134a0001c0001t0002g0263a0001c0001t0002g0273others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0016g0362a0001c0001t0016g0364a0001c0001t0016g0365others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0051g0257 | 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 | a0001c0007t0052g0006 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0001g0060 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0003g0187a0001c0001t0003g0201a0001c0001t0003g0217others(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 | a0001c0001t0009g0318a0001c0001t0053g0302 | 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 | a0001c0001t0004g0213 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0038g0136 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0307 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0011a0001c0001t0001g0329a0001c0001t0002g0134others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0040g0158 | 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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0005g0243 | 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 | a0001c0001t0040g0158 | 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 | a0001c0001t0010g0218a0001c0001t0010g0345a0001c0001t0010g0347others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0001g0160a0001c0001t0037g0039 | 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 | a0001c0001t0002g0311 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0005g0241a0001c0001t0018g0374a0001c0001t0018g0375others(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 | a0001c0001t0029g0372a0001c0001t0029g0373 | 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 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0286others(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 | a0001c0001t0001g0121a0001c0001t0001g0332a0001c0001t0001g0336others(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 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(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 | a0001c0001t0001g0025a0001c0001t0001g0058a0001c0001t0001g0150others(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 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0031others(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 | a0001c0001t0001g0003a0001c0001t0001g0122a0001c0001t0009g0318others(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 | a0001c0001t0001g0024a0001c0001t0001g0143a0001c0002t0008g0166 | 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 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0328others(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 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0127others(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 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0009g0303others(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 | a0001c0001t0002g0109a0001c0001t0007g0081a0001c0001t0007g0083others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0002g0233a0001c0001t0002g0295a0001c0001t0006g0004others(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 | a0001c0001t0002g0276a0001c0001t0002g0278a0001c0001t0003g0178others(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 | a0001c0001t0011g0151a0001c0001t0011g0152a0001c0001t0011g0334others(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 | a0001c0001t0002g0279a0001c0001t0002g0281a0001c0001t0002g0284others(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 | a0001c0001t0002g0130a0001c0001t0002g0242a0001c0001t0002g0268others(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 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0084others(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 | a0001c0001t0003g0185a0001c0001t0003g0187a0001c0001t0003g0188others(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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0001g0045a0001c0001t0001g0054 | 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 | a0001c0001t0001g0013a0001c0001t0001g0059a0001c0001t0001g0143others(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 | a0001c0001t0004g0195 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0284a0001c0001t0002g0297 | 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 | a0001c0001t0048g0341 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0006g0082a0001c0001t0006g0093a0001c0001t0009g0258others(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 | a0001c0001t0029g0372 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0006g0082a0001c0001t0006g0093 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0025a0001c0001t0001g0058a0001c0001t0001g0150others(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 | a0001c0001t0029g0372 | 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 | a0001c0001t0018g0374a0001c0001t0018g0375a0001c0001t0018g0376others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0105a0001c0001t0002g0233a0001c0001t0002g0322others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0048g0341 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0006g0079a0001c0001t0006g0084a0001c0001t0006g0085others(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 | a0002c0004t0006g0096 | 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 | a0001c0001t0026g0337a0001c0001t0026g0338a0001c0001t0051g0257 | 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 | a0001c0001t0051g0257 | 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 | a0001c0001t0002g0280 | 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 | a0001c0001t0002g0104a0001c0001t0002g0134a0001c0001t0002g0233others(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 | a0001c0001t0003g0185a0001c0001t0003g0187a0001c0001t0003g0188others(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 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(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 | a0001c0001t0004g0216a0001c0001t0009g0300a0001c0001t0009g0303 | 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 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0312others(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 | a0001c0001t0009g0301a0001c0001t0009g0318a0001c0001t0010g0359others(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 | a0001c0001t0005g0239a0001c0001t0010g0347a0001c0001t0010g0349others(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 | a0001c0001t0010g0345a0001c0001t0010g0354a0001c0001t0010g0355others(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 | a0001c0001t0005g0243a0001c0001t0005g0247a0001c0001t0005g0249others(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 | a0001c0001t0002g0236a0001c0001t0002g0276a0001c0001t0002g0278others(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 | a0001c0001t0059g0238 | 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 | a0001c0001t0005g0262a0001c0006t0004g0182 | 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 | a0001c0001t0055g0240 | 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 | a0001c0001t0019g0235 | 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 | a0001c0001t0005g0197a0001c0001t0019g0222a0001c0001t0019g0234 | 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 | a0001c0001t0003g0178a0001c0001t0005g0261a0001c0001t0005g0366 | 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 | a0001c0001t0003g0179a0001c0001t0003g0180 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0229others(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 | a0001c0001t0004g0189a0001c0001t0004g0192a0001c0001t0004g0194others(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 | a0001c0001t0003g0220a0001c0001t0004g0202a0001c0001t0004g0227 | 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 | a0001c0001t0004g0193a0001c0001t0010g0218 | 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 | a0001c0001t0061g0357 | 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 | a0001c0001t0004g0210a0001c0001t0005g0250a0001c0006t0004g0183 | 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 | a0001c0001t0004g0219 | 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 | a0001c0001t0002g0269 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(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 | a0001c0001t0049g0047a0001c0008t0001g0033 | 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 | a0001c0001t0001g0053a0001c0001t0001g0146a0001c0001t0011g0334others(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 | a0001c0001t0001g0018a0001c0001t0012g0113a0001c0001t0012g0115others(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 | a0001c0001t0004g0200 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0011g0152a0001c0001t0011g0334a0001c0001t0011g0340 | 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 | a0001c0001t0011g0138a0001c0001t0011g0139a0001c0001t0011g0151others(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 | a0001c0001t0021g0153a0001c0001t0021g0159 | 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 | a0001c0001t0005g0251 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0006g0004 | 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 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0060others(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 | a0001c0001t0005g0239 | 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 | a0001c0002t0008g0165a0001c0002t0008g0167a0001c0002t0008g0168others(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 | a0001c0001t0005g0244 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0026g0337a0001c0001t0026g0338 | 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 | a0001c0001t0003g0211 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0051g0257 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 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 | a0001c0001t0003g0223 | 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 | a0001c0001t0048g0341 | 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 | a0001c0001t0002g0290 | 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 | a0001c0001t0002g0264 | 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 | a0001c0001t0006g0087 | 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 | a0001c0001t0019g0222a0001c0001t0019g0234a0001c0001t0019g0235 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0060others(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 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(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 | 2 | a0001c0001t0002g0129a0001c0001t0002g0298 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1775-378G>A | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 11/14 | chr16 | 69690562 | ||||||
| chr16:69690568
|
G | A | 1 | a0001c0001t0028g0099 | 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 | a0001c0001t0006g0088 | 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 | a0001c0008t0001g0033 | 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 | a0001c0001t0011g0139a0001c0001t0038g0136 | 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 | a0001c0001t0051g0257 | 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 | a0001c0002t0008g0001a0001c0002t0008g0162a0001c0002t0008g0163others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0044 | 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 | a0001c0003t0002g0271 | 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 | a0001c0001t0001g0330a0001c0001t0001g0335 | 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 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0060others(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 | a0001c0001t0007g0081 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0005g0250 | 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 | a0001c0001t0002g0264 | 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 | a0001c0001t0003g0188 | 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 | a0001c0001t0001g0140a0001c0001t0001g0148 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0040others(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 | a0001c0001t0047g0086 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0016 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.*9-146T>C | NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 14/14 | chr16 | 69696214 |