Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4775 |
| ensemblid | ENSG00000072736.19 |
| hgncid | 7777 |
| symbol | NFATC3 |
| name | nuclear factor of activated T cells 3 |
| refseq_nuc | NM_173165.3 |
| refseq_prot | NP_775188.1 |
| ensembl_nuc | ENST00000346183.8 |
| ensembl_prot | ENSP00000300659.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 68085370 |
| end | 68229259 |
| strand | + |
| ver | v1.2 |
| region | chr16:68085370-68229259 |
| region5000 | chr16:68080370-68234259 |
| regionname0 | NFATC3_chr16_68085370_68229259 |
| regionname5000 | NFATC3_chr16_68080370_68234259 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1075 | 175 | 73 | 33 | 41 | 4 | 22 | 31 | NFATC3_chr16_68080370_68234259 | NFATC3 | MTTAN others(1070): Show |
chr16 | 68080370 | 68234259 |
| a0002 | 0/0 | 1075 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | MTTAN others(1070): Show |
chr16 | 68080370 | 68234259 |
| a0003 | 0/0 | 1075 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | MTTAN others(1070): Show |
chr16 | 68080370 | 68234259 |
| a0004 | 0/0 | 1075 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | MTTAN others(1070): Show |
chr16 | 68080370 | 68234259 |
| a0005 | 0/0 | 1075 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | MTTAN others(1070): Show |
chr16 | 68080370 | 68234259 |
| a0006 | 0/0 | 1075 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | MTTAN others(1070): Show |
chr16 | 68080370 | 68234259 |
| a0007 | 0/0 | 1075 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | MTTAN others(1070): Show |
chr16 | 68080370 | 68234259 |
| a0008 | 0/0 | 1075 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | MTTAN others(1070): Show |
chr16 | 68080370 | 68234259 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3225 | 171 | 72 | 30 | 41 | 4 | 22 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0001c0004 | 0/0 | 3225 | 3 | 1 | 2 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0001c0008 | 0/0 | 3225 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0002c0002 | 0/0 | 3225 | 4 | 4 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0003c0003 | 0/0 | 3225 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0004c0005 | 0/0 | 3225 | 2 | 0 | 0 | 2 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0005c0009 | 0/0 | 3225 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0006c0007 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0007c0010 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 | ||
| a0008c0006 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | ATGAC others(3220): Show |
chr16 | 68080370 | 68234259 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6328 | 44 | 20 | 6 | 11 | 0 | 6 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0002 | 0/0 | 6324 | 26 | 1 | 6 | 12 | 1 | 6 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6319): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0003 | 0/0 | 6329 | 14 | 8 | 1 | 4 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6324): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0004 | 0/0 | 6325 | 11 | 2 | 4 | 3 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6320): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0005 | 0/0 | 6329 | 10 | 8 | 0 | 0 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6324): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0006 | 0/0 | 6318 | 9 | 1 | 4 | 3 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6313): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0007 | 0/1 | 6327 | 8 | 2 | 3 | 0 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6322): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0008 | 0/0 | 6328 | 7 | 7 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0009 | 0/0 | 6321 | 7 | 1 | 4 | 1 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6316): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0010 | 0/0 | 6327 | 4 | 3 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6322): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0012 | 0/0 | 6330 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6325): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0013 | 0/0 | 6327 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6322): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0015 | 0/0 | 6329 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6324): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0016 | 0/0 | 6333 | 2 | 2 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6328): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0017 | 0/0 | 6328 | 2 | 2 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0018 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0019 | 0/0 | 6325 | 2 | 1 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6320): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0020 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6325): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0021 | 0/0 | 6328 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0023 | 0/0 | 6325 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6320): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0024 | 0/0 | 6288 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6283): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0025 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6319): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0026 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6305): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0027 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0028 | 0/0 | 6328 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0029 | 0/0 | 6328 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0030 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0031 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0032 | 0/0 | 6321 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6316): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0033 | 0/0 | 6318 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6313): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0035 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0001t0036 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6325): Show |
chr16 | 68080370 | 68234259 |
| a0001c0004t0001 | 0/0 | 6328 | 3 | 1 | 2 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0001c0008t0001 | 0/0 | 6328 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0002c0002t0014 | 0/0 | 6328 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0002c0002t0034 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6322): Show |
chr16 | 68080370 | 68234259 |
| a0003c0003t0011 | 0/0 | 6332 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6327): Show |
chr16 | 68080370 | 68234259 |
| a0004c0005t0004 | 0/0 | 6325 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6320): Show |
chr16 | 68080370 | 68234259 |
| a0004c0005t0022 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0005c0009t0020 | 0/0 | 6330 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6325): Show |
chr16 | 68080370 | 68234259 |
| a0006c0007t0001 | 0/0 | 6328 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0007c0010t0001 | 0/0 | 6328 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| a0008c0006t0018 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | AGGGC others(6323): Show |
chr16 | 68080370 | 68234259 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0009g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0009g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0010g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0012g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0013g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0013g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0016g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0017g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0018g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0019g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0019g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0020g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0021g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0023g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0024g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0025g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0026g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0027g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0028g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0029g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0030g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0031g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0032g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0033g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0035g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0036g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0008t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0002c0002t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0002c0002t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0002c0002t0014g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0002c0002t0034g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0003c0003t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0003c0003t0011g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0003c0003t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0004c0005t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0004c0005t0022g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0005c0009t0020g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0006c0007t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0007c0010t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0008c0006t0018g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00438 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | CHS | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | CHS | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0077 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0128 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01070 | hp1 | a0001 | c0001 | t0009 | g0126 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01070 | hp2 | a0001 | c0008 | t0001 | g0114 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0125 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01109 | hp2 | a0005 | c0009 | t0020 | g0028 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01169 | hp2 | a0001 | c0001 | t0021 | g0158 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0116 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0059 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0122 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0112 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0057 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01346 | hp1 | a0001 | c0001 | t0009 | g0123 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0010 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0088 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0001 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0089 | AMR | PEL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0108 | AMR | PEL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02055 | hp1 | a0001 | c0001 | t0019 | g0170 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02071 | hp2 | a0001 | c0001 | t0024 | g0169 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02080 | hp1 | a0001 | c0001 | t0035 | g0106 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02080 | hp2 | a0001 | c0001 | t0031 | g0052 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0076 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02132 | hp2 | a0001 | c0001 | t0023 | g0137 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0034 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0188 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0186 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02451 | hp1 | a0006 | c0007 | t0001 | g0093 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02572 | hp2 | a0002 | c0002 | t0014 | g0178 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02647 | hp1 | a0001 | c0001 | t0020 | g0029 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02717 | hp2 | a0002 | c0002 | t0014 | g0177 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0185 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02809 | hp1 | a0001 | c0001 | t0015 | g0031 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0184 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0032 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02886 | hp2 | a0002 | c0002 | t0014 | g0180 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0124 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0003 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02897 | hp2 | a0001 | c0001 | t0029 | g0002 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0006 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02976 | hp1 | a0002 | c0002 | t0034 | g0179 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03041 | hp2 | a0003 | c0003 | t0011 | g0182 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0011 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0004 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03225 | hp1 | a0003 | c0003 | t0011 | g0183 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03225 | hp2 | a0001 | c0001 | t0032 | g0007 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03491 | hp1 | a0001 | c0001 | t0033 | g0047 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03516 | hp1 | a0001 | c0001 | t0036 | g0030 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03540 | hp1 | a0001 | c0001 | t0017 | g0005 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0061 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | STU | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03927 | hp2 | a0001 | c0001 | t0019 | g0172 | SAS | BEB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0175 | SAS | STU | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0155 | SAS | STU | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0095 | SAS | STU | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG04204 | hp1 | a0001 | c0001 | t0030 | g0109 | SAS | STU | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0021 | SAS | STU | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18522 | hp1 | a0001 | c0001 | t0015 | g0026 | AFR | YRI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | YRI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | YRI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18940 | hp1 | a0004 | c0005 | t0022 | g0146 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18952 | hp1 | a0001 | c0001 | t0018 | g0097 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18975 | hp1 | a0001 | c0001 | t0026 | g0159 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18995 | hp2 | a0008 | c0006 | t0018 | g0096 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19010 | hp2 | a0004 | c0005 | t0004 | g0147 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | LWK | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | LWK | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | LWK | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19060 | hp2 | a0001 | c0001 | t0025 | g0130 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19240 | hp2 | a0003 | c0003 | t0011 | g0181 | AFR | YRI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0113 | EUR | TSI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA20752 | hp2 | a0001 | c0001 | t0009 | g0127 | EUR | TSI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA20805 | hp1 | a0001 | c0001 | t0027 | g0068 | EUR | TSI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0149 | EUR | TSI | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02486 | hp1 | a0007 | c0010 | t0001 | g0121 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02486 | hp2 | a0001 | c0001 | t0028 | g0040 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | USA | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | USA | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0086 | REF | REF | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0102 | REF | REF | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:68122088 | T | C | 1 | a0008 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.205T>C | p.Ser69Pro | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/10 | 517/6328 | 205/3228 | 69/1075 | chr16 | 68122088 | |||
| chr16:68122127 | A | G | 1 | a0004 | 2 | NA18940.hp1 NA19010.hp2 |
missense_variant | MODERATE | c.244A>G | p.Ser82Gly | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/10 | 556/6328 | 244/3228 | 82/1075 | chr16 | 68122127 | |||
| chr16:68122182 | T | C | 1 | a0006 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.299T>C | p.Leu100Ser | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/10 | 611/6328 | 299/3228 | 100/1075 | chr16 | 68122182 | |||
| chr16:68122196 | C | A | 1 | a0003 | 3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.313C>A | p.Pro105Thr | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/10 | 625/6328 | 313/3228 | 105/1075 | chr16 | 68122196 | |||
| chr16:68122295 | C | T | 2 | a0006 a0007 |
2 | HG02451.hp1 HG02486.hp1 |
missense_variant | MODERATE | c.412C>T | p.Arg138Trp | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/10 | 724/6328 | 412/3228 | 138/1075 | chr16 | 68122295 | |||
| chr16:68123027 | C | T | 1 | a0002 | 4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.1144C>T | p.Pro382Ser | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/10 | 1456/6328 | 1144/3228 | 382/1075 | chr16 | 68123027 | |||
| chr16:68191532 | C | G | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2863C>G | p.Pro955Ala | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/10 | 3175/6328 | 2863/3228 | 955/1075 | chr16 | 68191532 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:68122513 | T | C | 1 | a0001c0008 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.630T>C | p.Thr210Thr | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/10 | 942/6328 | 630/3228 | 210/1075 | chr16 | 68122513 | |||
| chr16:68191498 | A | G | 2 | a0006c0007 a0007c0010 |
2 | HG02451.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.2829A>G | p.Pro943Pro | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/10 | 3141/6328 | 2829/3228 | 943/1075 | chr16 | 68191498 | |||
| chr16:68191612 | G | A | 1 | a0001c0004 | 3 | HG01433.hp2 HG01934.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.2943G>A | p.Thr981Thr | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/10 | 3255/6328 | 2943/3228 | 981/1075 | chr16 | 68191612 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:68085411 | T | TG | 6 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0019 others(3): Show |
18 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-264dupG | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/10 | 263 | INFO_REALIGN_3_PRIME | chr16 | 68085411 | |||||
| chr16:68085522 | A | G | 1 | a0001c0001t0035 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-160A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/10 | 160 | chr16 | 68085522 | ||||||
| chr16:68085652 | G | A | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0019 others(7): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
5_prime_UTR_variant | MODIFIER | c.-30G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/10 | 30 | chr16 | 68085652 | ||||||
| chr16:68226499 | C | T | 2 | a0002c0002t0014 a0002c0002t0034 |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*28C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 28 | chr16 | 68226499 | ||||||
| chr16:68226644 | C | T | 1 | a0001c0001t0033 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 173 | chr16 | 68226644 | ||||||
| chr16:68226897 | C | CA | 4 | a0001c0001t0003 a0001c0001t0020 a0001c0001t0036 others(1): Show |
17 | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*452dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 453 | INFO_REALIGN_3_PRIME | chr16 | 68226897 | |||||
| chr16:68226897 | C | CAAA | 2 | a0001c0001t0016 a0003c0003t0011 |
5 | HG02280.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*452dupAAA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 453 | INFO_REALIGN_3_PRIME | chr16 | 68226897 | |||||
| chr16:68226897 | CA | C | 4 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0013 others(1): Show |
15 | HG00639.hp1 HG01192.hp1 HG01258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*452delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 452 | INFO_REALIGN_3_PRIME | chr16 | 68226897 | |||||
| chr16:68226897 | CAAA | C | 2 | a0001c0001t0004 a0004c0005t0004 |
12 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*452delAAA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 450 | INFO_REALIGN_3_PRIME | chr16 | 68226897 | |||||
| chr16:68226897 | CAAAA | C | 5 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0023 others(2): Show |
31 | HG00639.hp2 HG01099.hp2 HG01255.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*449_*452delAAAA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 449 | INFO_REALIGN_3_PRIME | chr16 | 68226897 | |||||
| chr16:68226897 | CAAAAAAA | C | 2 | a0001c0001t0009 a0001c0001t0032 |
8 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*446_*452delAAAAAA others(1): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 446 | INFO_REALIGN_3_PRIME | chr16 | 68226897 | |||||
| chr16:68226897 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0026 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435_*452delAAAAAA others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 435 | INFO_REALIGN_3_PRIME | chr16 | 68226897 | |||||
| chr16:68226914 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0006 a0001c0001t0033 |
10 | HG00438.hp1 HG01175.hp1 HG01255.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*458_*467delAAAAAG others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 458 | INFO_REALIGN_3_PRIME | chr16 | 68226914 | |||||
| chr16:68226916 | A | G | 1 | a0001c0001t0001 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 445 | chr16 | 68226916 | ||||||
| chr16:68226918 | A | G | 1 | a0001c0001t0001 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 447 | chr16 | 68226918 | ||||||
| chr16:68226929 | A | G | 1 | a0001c0001t0031 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 458 | chr16 | 68226929 | ||||||
| chr16:68227189 | T | C | 1 | a0001c0001t0027 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 718 | chr16 | 68227189 | ||||||
| chr16:68227444 | C | CT | 3 | a0001c0001t0012 a0001c0001t0016 a0003c0003t0011 |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*974dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 975 | INFO_REALIGN_3_PRIME | chr16 | 68227444 | |||||
| chr16:68227446 | A | C | 3 | a0001c0001t0012 a0001c0001t0016 a0003c0003t0011 |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*975A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 975 | chr16 | 68227446 | ||||||
| chr16:68227447 | G | T | 3 | a0001c0001t0012 a0001c0001t0016 a0003c0003t0011 |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*976G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 976 | chr16 | 68227447 | ||||||
| chr16:68227531 | G | A | 3 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0032 |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1060G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 1060 | chr16 | 68227531 | ||||||
| chr16:68227798 | T | TA | 3 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0023 |
6 | HG01884.hp1 HG02132.hp2 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1341dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 1342 | INFO_REALIGN_3_PRIME | chr16 | 68227798 | |||||
| chr16:68227847 | T | C | 1 | a0001c0001t0028 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1376T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 1376 | chr16 | 68227847 | ||||||
| chr16:68227848 | T | A | 2 | a0001c0001t0013 a0001c0001t0029 |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1377T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 1377 | chr16 | 68227848 | ||||||
| chr16:68228146 | A | T | 2 | a0001c0001t0018 a0008c0006t0018 |
2 | NA18952.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1675A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 1675 | chr16 | 68228146 | ||||||
| chr16:68228310 | C | T | 1 | a0001c0001t0025 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1839C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 1839 | chr16 | 68228310 | ||||||
| chr16:68228431 | A | G | 1 | a0001c0001t0030 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1960A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 1960 | chr16 | 68228431 | ||||||
| chr16:68228545 | GAAATGCT others(29): Show |
G | 1 | a0001c0001t0024 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2079_*2114delGCTT others(32): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 2079 | INFO_REALIGN_3_PRIME | chr16 | 68228545 | |||||
| chr16:68228768 | C | G | 1 | a0004c0005t0022 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2297C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 2297 | chr16 | 68228768 | ||||||
| chr16:68228769 | G | C | 1 | a0004c0005t0022 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2298G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 2298 | chr16 | 68228769 | ||||||
| chr16:68228974 | T | C | 2 | a0001c0001t0015 a0001c0001t0036 |
4 | HG02809.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2503T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 2503 | chr16 | 68228974 | ||||||
| chr16:68229055 | G | A | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(17): Show |
75 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2584G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 2584 | chr16 | 68229055 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:68085998 | C | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+214C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68085998 | |||||||
| chr16:68086126 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+342A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086126 | |||||||
| chr16:68086255 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+471A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086255 | |||||||
| chr16:68086485 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.103+701A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086485 | |||||||
| chr16:68086513 | A | G | 1 | a0001c0001t0005g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.103+729A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086513 | |||||||
| chr16:68086703 | A | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+919A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086703 | |||||||
| chr16:68086708 | T | G | 1 | a0001c0001t0032g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.103+924T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086708 | |||||||
| chr16:68086855 | G | A | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.103+1071G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086855 | |||||||
| chr16:68086859 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.103+1075A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086859 | |||||||
| chr16:68086976 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+1192A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68086976 | |||||||
| chr16:68087392 | C | T | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.103+1608C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68087392 | |||||||
| chr16:68087529 | G | A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.103+1745G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68087529 | |||||||
| chr16:68087533 | AT | A | 5 | a0001c0001t0001g0008 a0002c0002t0014g0177 a0002c0002t0014g0178 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+1757delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68087533 | ||||||
| chr16:68087568 | T | TATGAAAA | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+1785_103+1786i others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68087568 | ||||||
| chr16:68087760 | T | C | 1 | a0001c0001t0005g0009 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.103+1976T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68087760 | |||||||
| chr16:68088156 | A | G | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+2372A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68088156 | |||||||
| chr16:68088366 | T | C | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+2582T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68088366 | |||||||
| chr16:68088482 | G | GTATATAA others(18): Show |
1 | a0001c0001t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.103+2711_103+2712i others(27): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68088482 | ||||||
| chr16:68088482 | G | GTATATAA others(19): Show |
45 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.103+2711_103+2712i others(28): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68088482 | ||||||
| chr16:68088482 | G | GTATATAA others(11): Show |
28 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(25): Show |
28 | HG01433.hp1 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.103+2704_103+2721d others(20): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68088482 | ||||||
| chr16:68088482 | G | GTATATAA others(38): Show |
1 | a0001c0001t0010g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103+2721_103+2722i others(47): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68088482 | ||||||
| chr16:68088701 | G | C | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.103+2917G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68088701 | |||||||
| chr16:68088723 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+2939A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68088723 | |||||||
| chr16:68088801 | T | C | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+3017T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68088801 | |||||||
| chr16:68088823 | T | C | 68 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(65): Show |
68 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.103+3039T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68088823 | |||||||
| chr16:68088969 | T | G | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.103+3185T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68088969 | |||||||
| chr16:68089011 | A | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+3227A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68089011 | |||||||
| chr16:68089046 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.103+3262C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68089046 | |||||||
| chr16:68089183 | G | T | 1 | a0001c0001t0006g0122 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.103+3399G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68089183 | |||||||
| chr16:68089372 | C | T | 1 | a0001c0001t0015g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.103+3588C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68089372 | |||||||
| chr16:68089550 | G | GT | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+3773dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68089550 | ||||||
| chr16:68089606 | CT | C | 9 | a0001c0001t0001g0033 a0001c0001t0012g0185 a0001c0001t0012g0187 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.103+3830delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68089606 | ||||||
| chr16:68089837 | T | G | 1 | a0001c0004t0001g0034 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.103+4053T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68089837 | |||||||
| chr16:68089881 | G | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+4097G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68089881 | |||||||
| chr16:68090013 | A | T | 58 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(55): Show |
58 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.103+4229A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68090013 | |||||||
| chr16:68090293 | C | G | 1 | a0007c0010t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.103+4509C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68090293 | |||||||
| chr16:68090295 | AC | A | 137 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0043 others(134): Show |
137 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.103+4523delC | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68090295 | ||||||
| chr16:68090295 | ACC | A | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(10): Show |
13 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.103+4522_103+4523d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68090295 | ||||||
| chr16:68090322 | A | AAC | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.103+4555_103+4556d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68090322 | ||||||
| chr16:68090322 | AAC | A | 3 | a0001c0001t0001g0098 a0001c0001t0003g0100 a0001c0001t0005g0099 |
3 | HG01884.hp2 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.103+4555_103+4556d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68090322 | ||||||
| chr16:68090328 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.103+4544C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68090328 | |||||||
| chr16:68090339 | A | ACACACAC others(5): Show |
3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.103+4556_103+4557i others(14): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68090339 | ||||||
| chr16:68090339 | A | ACACACG | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+4556_103+4557i others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68090339 | ||||||
| chr16:68090339 | A | ACACG | 2 | a0001c0001t0017g0005 a0001c0001t0025g0130 |
2 | HG03540.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.103+4556_103+4557i others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68090339 | ||||||
| chr16:68090341 | G | A | 10 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.103+4557G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68090341 | |||||||
| chr16:68090341 | G | GCA | 73 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(70): Show |
73 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.103+4567_103+4568d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68090341 | ||||||
| chr16:68090395 | T | A | 1 | a0001c0001t0003g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.103+4611T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68090395 | |||||||
| chr16:68091057 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+5273A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091057 | |||||||
| chr16:68091223 | G | A | 2 | a0001c0001t0005g0021 a0001c0001t0005g0175 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.103+5439G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091223 | |||||||
| chr16:68091317 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+5533C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091317 | |||||||
| chr16:68091413 | A | G | 184 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0035 others(181): Show |
184 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(181): Show |
intron_variant | MODIFIER | c.103+5629A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091413 | |||||||
| chr16:68091720 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5936T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091720 | |||||||
| chr16:68091721 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5937A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091721 | |||||||
| chr16:68091722 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5938G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091722 | |||||||
| chr16:68091725 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5941A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091725 | |||||||
| chr16:68091726 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5942G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091726 | |||||||
| chr16:68091727 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5943C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091727 | |||||||
| chr16:68091731 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5947A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091731 | |||||||
| chr16:68091732 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5948G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091732 | |||||||
| chr16:68091734 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5950T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091734 | |||||||
| chr16:68091736 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+5952G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68091736 | |||||||
| chr16:68092014 | G | T | 12 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.103+6230G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092014 | |||||||
| chr16:68092069 | G | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+6285G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092069 | |||||||
| chr16:68092299 | T | C | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.103+6515T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092299 | |||||||
| chr16:68092318 | G | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+6534G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092318 | |||||||
| chr16:68092325 | C | T | 1 | a0001c0001t0010g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103+6541C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092325 | |||||||
| chr16:68092370 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0003g0100 a0001c0001t0005g0099 |
3 | HG01884.hp2 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.103+6586T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092370 | |||||||
| chr16:68092440 | A | G | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.103+6656A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092440 | |||||||
| chr16:68092452 | C | CA | 7 | a0001c0001t0001g0045 a0001c0001t0003g0044 a0001c0001t0003g0046 others(4): Show |
7 | HG01255.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+6682dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092452 | ||||||
| chr16:68092452 | CA | C | 5 | a0001c0001t0002g0161 a0001c0001t0013g0001 a0001c0001t0013g0003 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+6682delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092452 | ||||||
| chr16:68092459 | A | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+6675A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092459 | |||||||
| chr16:68092463 | A | T | 12 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 others(9): Show |
12 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.103+6679A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092463 | |||||||
| chr16:68092467 | T | A | 1 | a0001c0001t0001g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.103+6683T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092467 | |||||||
| chr16:68092609 | A | ATTAGCCG others(3134): Show |
4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+6829_103+6830i others(3143): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092609 | A | ATTAGCCG others(3139): Show |
3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.103+6829_103+6830i others(3148): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092609 | A | ATTAGCCG others(3139): Show |
4 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0016g0184 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+6829_103+6830i others(3148): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092609 | A | ATTAGCCG others(3140): Show |
1 | a0001c0001t0012g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.103+6829_103+6830i others(3149): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092609 | A | ATTAGCCG others(3139): Show |
42 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(39): Show |
42 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.103+6829_103+6830i others(3148): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092609 | A | ATTAGCCG others(3139): Show |
1 | a0001c0001t0021g0158 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.103+6829_103+6830i others(3148): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092609 | A | ATTAGCCG others(3139): Show |
1 | a0001c0001t0026g0159 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.103+6829_103+6830i others(3148): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092609 | A | ATTAGCCG others(3140): Show |
1 | a0001c0001t0002g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.103+6829_103+6830i others(3149): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092609 | A | ATTAGCCG others(3139): Show |
1 | a0001c0001t0002g0160 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.103+6829_103+6830i others(3148): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68092609 | ||||||
| chr16:68092703 | T | C | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.103+6919T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092703 | |||||||
| chr16:68092732 | C | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+6948C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092732 | |||||||
| chr16:68092833 | T | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+7049T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68092833 | |||||||
| chr16:68093061 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+7277C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68093061 | |||||||
| chr16:68093081 | TCCA | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+7301_103+7303d others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68093081 | ||||||
| chr16:68093135 | T | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+7351T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68093135 | |||||||
| chr16:68093319 | TAG | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+7538_103+7539d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68093319 | ||||||
| chr16:68093375 | A | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+7591A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68093375 | |||||||
| chr16:68093665 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.103+7881T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68093665 | |||||||
| chr16:68093943 | AT | A | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+8160delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68093943 | |||||||
| chr16:68094201 | A | G | 97 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(94): Show |
97 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.103+8417A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68094201 | |||||||
| chr16:68094366 | G | A | 1 | a0001c0001t0016g0184 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.103+8582G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68094366 | |||||||
| chr16:68094422 | CA | C | 11 | a0001c0001t0001g0103 a0001c0001t0003g0100 a0001c0001t0008g0018 others(8): Show |
11 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.103+8651delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68094422 | ||||||
| chr16:68094436 | T | A | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+8652T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68094436 | |||||||
| chr16:68094571 | G | C | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+8787G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68094571 | |||||||
| chr16:68094806 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+9022C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68094806 | |||||||
| chr16:68095100 | A | G | 1 | a0001c0001t0007g0095 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.103+9316A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68095100 | |||||||
| chr16:68095150 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.103+9366T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68095150 | |||||||
| chr16:68095164 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103+9380T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68095164 | |||||||
| chr16:68095198 | A | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+9414A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68095198 | |||||||
| chr16:68095214 | T | TGA | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+9437_103+9438d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68095214 | ||||||
| chr16:68095347 | A | AT | 72 | a0001c0001t0001g0048 a0001c0001t0001g0090 a0001c0001t0001g0091 others(69): Show |
72 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.103+9586dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68095347 | ||||||
| chr16:68095347 | A | ATT | 25 | a0001c0001t0002g0129 a0001c0001t0002g0153 a0001c0001t0002g0154 others(22): Show |
25 | HG00741.hp2 HG01109.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.103+9585_103+9586d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68095347 | ||||||
| chr16:68095347 | A | ATTT | 7 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0016 others(4): Show |
7 | HG02886.hp2 HG02896.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+9584_103+9586d others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68095347 | ||||||
| chr16:68095528 | ATTC | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+9747_103+9749d others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68095528 | ||||||
| chr16:68095530 | T | G | 1 | a0001c0001t0002g0151 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.103+9746T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68095530 | |||||||
| chr16:68095735 | A | G | 3 | a0001c0004t0001g0034 a0001c0004t0001g0088 a0001c0004t0001g0089 |
3 | HG01433.hp2 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.103+9951A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68095735 | |||||||
| chr16:68095897 | A | T | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103+10113A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68095897 | |||||||
| chr16:68096015 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.103+10231T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68096015 | |||||||
| chr16:68096039 | G | A | 1 | a0001c0001t0033g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.103+10255G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68096039 | |||||||
| chr16:68096090 | A | G | 1 | a0001c0001t0012g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.103+10306A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68096090 | |||||||
| chr16:68096212 | C | T | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+10428C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68096212 | |||||||
| chr16:68096330 | T | C | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+10546T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68096330 | |||||||
| chr16:68096354 | T | C | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+10570T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68096354 | |||||||
| chr16:68097239 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103+11455T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68097239 | |||||||
| chr16:68097386 | G | T | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.103+11602G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68097386 | |||||||
| chr16:68097504 | A | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+11720A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68097504 | |||||||
| chr16:68097829 | G | A | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.103+12045G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68097829 | |||||||
| chr16:68097891 | C | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+12107C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68097891 | |||||||
| chr16:68098206 | T | C | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.103+12422T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098206 | |||||||
| chr16:68098271 | C | CTAT | 2 | a0001c0001t0003g0041 a0001c0001t0032g0007 |
2 | HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.103+12516_103+1251 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098271 | ||||||
| chr16:68098294 | A | AT | 8 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0005g0021 others(5): Show |
8 | HG02280.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+12512dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098294 | ||||||
| chr16:68098294 | A | T | 3 | a0001c0001t0009g0125 a0001c0001t0009g0126 a0001c0001t0009g0127 |
3 | HG01070.hp1 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.103+12510A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098294 | |||||||
| chr16:68098294 | ATTATTAT others(3): Show |
A | 1 | a0001c0001t0004g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.103+12513_103+1252 others(14): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098294 | ||||||
| chr16:68098296 | TA | T | 3 | a0001c0001t0006g0115 a0001c0001t0033g0047 a0006c0007t0001g0093 |
3 | HG02071.hp1 HG02451.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.103+12513delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098296 | |||||||
| chr16:68098297 | A | AT | 7 | a0001c0001t0001g0070 a0001c0001t0001g0092 a0001c0001t0005g0022 others(4): Show |
7 | HG01109.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+12515dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098297 | ||||||
| chr16:68098297 | A | ATTTT | 3 | a0001c0001t0008g0012 a0001c0001t0008g0016 a0001c0001t0008g0018 |
3 | HG02622.hp2 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.103+12515_103+1251 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098297 | ||||||
| chr16:68098297 | A | T | 34 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0037 others(31): Show |
34 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.103+12513A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098297 | |||||||
| chr16:68098299 | TA | T | 3 | a0001c0001t0006g0113 a0001c0001t0006g0120 a0001c0008t0001g0114 |
3 | HG01070.hp2 NA19081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.103+12516delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098299 | |||||||
| chr16:68098300 | A | ATTTT | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0017 others(2): Show |
5 | HG01433.hp1 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+12532_103+1253 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098300 | ||||||
| chr16:68098300 | A | T | 98 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0035 others(95): Show |
98 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.103+12516A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098300 | |||||||
| chr16:68098300 | ATTTT | A | 35 | a0001c0001t0002g0129 a0001c0001t0002g0136 a0001c0001t0002g0138 others(32): Show |
35 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.103+12532_103+1253 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098300 | ||||||
| chr16:68098300 | ATTTTTTT others(3): Show |
A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+12526_103+1253 others(14): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098300 | ||||||
| chr16:68098301 | T | TTATTA | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+12518_103+1251 others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68098301 | ||||||
| chr16:68098302 | T | TATTATTA | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.103+12518_103+1251 others(11): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098302 | |||||||
| chr16:68098303 | T | A | 2 | a0001c0001t0001g0050 a0001c0001t0003g0042 |
2 | HG01099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.103+12519T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098303 | |||||||
| chr16:68098304 | T | A | 10 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(7): Show |
10 | HG01099.hp2 HG01255.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.103+12520T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098304 | |||||||
| chr16:68098305 | T | A | 7 | a0001c0001t0001g0051 a0001c0001t0013g0001 a0001c0001t0013g0003 others(4): Show |
7 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+12521T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098305 | |||||||
| chr16:68098306 | T | A | 1 | a0001c0001t0006g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.103+12522T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098306 | |||||||
| chr16:68098307 | T | A | 36 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(33): Show |
36 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.103+12523T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098307 | |||||||
| chr16:68098308 | T | A | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103+12524T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098308 | |||||||
| chr16:68098310 | T | A | 30 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(27): Show |
30 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.103+12526T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098310 | |||||||
| chr16:68098313 | T | A | 4 | a0001c0001t0002g0129 a0001c0001t0002g0136 a0001c0001t0002g0161 others(1): Show |
4 | NA18953.hp2 NA18961.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+12529T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098313 | |||||||
| chr16:68098339 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.103+12555C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68098339 | |||||||
| chr16:68099206 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.103+13422G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68099206 | |||||||
| chr16:68099360 | A | G | 102 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(99): Show |
102 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(99): Show |
intron_variant | MODIFIER | c.103+13576A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68099360 | |||||||
| chr16:68099434 | C | CA | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+13663dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68099434 | ||||||
| chr16:68099446 | A | T | 1 | a0001c0001t0006g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.103+13662A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68099446 | |||||||
| chr16:68099449 | A | T | 1 | a0001c0001t0006g0112 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.103+13665A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68099449 | |||||||
| chr16:68099607 | AAAT | A | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+13847_103+1384 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68099607 | ||||||
| chr16:68099634 | A | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+13850A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68099634 | |||||||
| chr16:68099876 | A | G | 1 | a0001c0001t0006g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.103+14092A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68099876 | |||||||
| chr16:68099916 | C | G | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.103+14132C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68099916 | |||||||
| chr16:68100087 | A | G | 1 | a0001c0001t0007g0095 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.103+14303A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100087 | |||||||
| chr16:68100242 | A | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0031 a0001c0001t0015g0032 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+14458A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100242 | |||||||
| chr16:68100299 | G | A | 1 | a0001c0001t0009g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.103+14515G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100299 | |||||||
| chr16:68100348 | A | G | 8 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0081 others(5): Show |
8 | HG00738.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.103+14564A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100348 | |||||||
| chr16:68100375 | C | T | 43 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(40): Show |
43 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.103+14591C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100375 | |||||||
| chr16:68100393 | T | C | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.103+14609T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100393 | |||||||
| chr16:68100489 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.103+14705G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100489 | |||||||
| chr16:68100489 | G | T | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.103+14705G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100489 | |||||||
| chr16:68100786 | T | C | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.103+15002T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100786 | |||||||
| chr16:68100887 | C | CTG | 4 | a0001c0001t0004g0145 a0001c0001t0005g0024 a0004c0005t0004g0147 others(1): Show |
4 | HG00438.hp2 NA18906.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+15120_103+1512 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68100887 | ||||||
| chr16:68100887 | C | CTGTG | 41 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(38): Show |
41 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.103+15118_103+1512 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68100887 | ||||||
| chr16:68100887 | C | CTGTGTG | 2 | a0001c0001t0002g0135 a0001c0001t0002g0153 |
2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.103+15116_103+1512 others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68100887 | ||||||
| chr16:68100887 | CTGTGTGT others(14): Show |
C | 1 | a0001c0001t0005g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.103+15122_103+1514 others(25): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68100887 | ||||||
| chr16:68100907 | G | GGT | 24 | a0001c0001t0005g0027 a0001c0001t0008g0012 a0001c0001t0008g0013 others(21): Show |
24 | HG01433.hp1 HG01884.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.103+15147_103+1514 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68100907 | ||||||
| chr16:68100907 | G | GGTGT | 4 | a0001c0001t0007g0078 a0001c0001t0007g0079 a0003c0003t0011g0182 others(1): Show |
4 | HG02622.hp1 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+15145_103+1514 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68100907 | ||||||
| chr16:68100907 | GGT | G | 7 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
7 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+15147_103+1514 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68100907 | ||||||
| chr16:68100909 | T | G | 2 | a0001c0001t0001g0101 a0001c0001t0031g0052 |
2 | HG02080.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.103+15125T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100909 | |||||||
| chr16:68100994 | A | C | 1 | a0001c0001t0024g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.103+15210A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68100994 | |||||||
| chr16:68101007 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+15223G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68101007 | |||||||
| chr16:68101057 | T | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+15273T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68101057 | |||||||
| chr16:68101135 | G | A | 1 | a0001c0001t0035g0106 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.103+15351G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68101135 | |||||||
| chr16:68101370 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103+15586T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68101370 | |||||||
| chr16:68101478 | G | GT | 8 | a0001c0001t0004g0145 a0001c0001t0032g0007 a0002c0002t0014g0178 others(5): Show |
8 | HG00438.hp2 HG02572.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+15705dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68101478 | ||||||
| chr16:68101478 | G | GTT | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+15704_103+1570 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68101478 | ||||||
| chr16:68101576 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+15792C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68101576 | |||||||
| chr16:68101577 | G | A | 4 | a0001c0001t0015g0026 a0001c0001t0015g0031 a0001c0001t0015g0032 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+15793G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68101577 | |||||||
| chr16:68101726 | G | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+15942G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68101726 | |||||||
| chr16:68101730 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.103+15946G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68101730 | |||||||
| chr16:68102013 | G | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0085 others(3): Show |
6 | HG00738.hp1 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.103+16229G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68102013 | |||||||
| chr16:68102090 | C | T | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+16306C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68102090 | |||||||
| chr16:68102098 | G | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+16314G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68102098 | |||||||
| chr16:68102301 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+16517G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68102301 | |||||||
| chr16:68102320 | C | T | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+16536C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68102320 | |||||||
| chr16:68102374 | G | GA | 55 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(52): Show |
55 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.103+16617dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68102374 | ||||||
| chr16:68102374 | GA | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0012g0185 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.103+16617delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68102374 | ||||||
| chr16:68102375 | A | G | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103+16591A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68102375 | |||||||
| chr16:68102665 | G | A | 1 | a0001c0001t0030g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.103+16881G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68102665 | |||||||
| chr16:68102719 | T | G | 77 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(74): Show |
77 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.103+16935T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68102719 | |||||||
| chr16:68103029 | G | T | 1 | a0001c0001t0006g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.103+17245G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103029 | |||||||
| chr16:68103190 | T | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+17406T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103190 | |||||||
| chr16:68103480 | G | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+17696G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103480 | |||||||
| chr16:68103517 | C | G | 32 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(29): Show |
32 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.103+17733C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103517 | |||||||
| chr16:68103570 | A | C | 7 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+17786A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103570 | |||||||
| chr16:68103583 | G | T | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.103+17799G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103583 | |||||||
| chr16:68103720 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103+17936A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103720 | |||||||
| chr16:68103844 | A | G | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.103+18060A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103844 | |||||||
| chr16:68103894 | T | G | 1 | a0001c0001t0001g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.104-18093T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103894 | |||||||
| chr16:68103897 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.104-18090T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103897 | |||||||
| chr16:68103957 | G | A | 1 | a0001c0001t0012g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.104-18030G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68103957 | |||||||
| chr16:68104188 | G | T | 1 | a0001c0001t0007g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.104-17799G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104188 | |||||||
| chr16:68104328 | T | C | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-17659T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104328 | |||||||
| chr16:68104446 | A | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-17541A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104446 | |||||||
| chr16:68104653 | G | GTT | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-17319_104-1731 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTT | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0016g0184 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-17321_104-1731 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTT | 36 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(33): Show |
36 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.104-17322_104-1731 others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTT | 13 | a0001c0001t0002g0143 a0001c0001t0002g0168 a0001c0001t0004g0152 others(10): Show |
13 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.104-17323_104-1731 others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(6): Show |
2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.104-17330_104-1731 others(17): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0008g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-17331_104-1731 others(18): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(8): Show |
1 | a0001c0001t0010g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.104-17332_104-1731 others(19): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(11): Show |
1 | a0003c0003t0011g0182 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.104-17318_104-1731 others(22): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(12): Show |
1 | a0003c0003t0011g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.104-17318_104-1731 others(23): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(13): Show |
3 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | HG03195.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.104-17318_104-1731 others(24): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(14): Show |
4 | a0001c0001t0008g0012 a0001c0001t0008g0016 a0001c0001t0008g0017 others(1): Show |
4 | HG02622.hp2 HG02896.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-17318_104-1731 others(25): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(15): Show |
1 | a0001c0001t0009g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.104-17318_104-1731 others(26): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0009g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.104-17318_104-1731 others(28): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104653 | G | GTTTTTTT others(18): Show |
2 | a0001c0001t0009g0123 a0001c0001t0009g0127 |
2 | HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.104-17318_104-1731 others(29): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68104653 | ||||||
| chr16:68104706 | C | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-17281C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104706 | |||||||
| chr16:68104713 | G | A | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-17274G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104713 | |||||||
| chr16:68104769 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-17218C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104769 | |||||||
| chr16:68104812 | G | A | 3 | a0001c0004t0001g0034 a0001c0004t0001g0088 a0001c0004t0001g0089 |
3 | HG01433.hp2 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.104-17175G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104812 | |||||||
| chr16:68104828 | G | C | 1 | a0001c0001t0008g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.104-17159G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104828 | |||||||
| chr16:68104890 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.104-17097A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104890 | |||||||
| chr16:68104996 | C | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-16991C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68104996 | |||||||
| chr16:68105091 | G | GT | 16 | a0001c0001t0001g0092 a0001c0001t0002g0142 a0001c0001t0010g0011 others(13): Show |
16 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.104-16879dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68105091 | ||||||
| chr16:68105180 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-16807T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68105180 | |||||||
| chr16:68105288 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.104-16699A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68105288 | |||||||
| chr16:68105326 | A | G | 3 | a0001c0001t0005g0009 a0001c0001t0005g0025 a0001c0001t0020g0029 |
3 | HG02451.hp2 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.104-16661A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68105326 | |||||||
| chr16:68105354 | G | A | 1 | a0001c0001t0016g0184 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.104-16633G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68105354 | |||||||
| chr16:68105520 | C | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-16467C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68105520 | |||||||
| chr16:68105828 | G | T | 3 | a0001c0001t0005g0009 a0001c0001t0005g0025 a0001c0001t0020g0029 |
3 | HG02451.hp2 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.104-16159G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68105828 | |||||||
| chr16:68105887 | C | CT | 5 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0025 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-16091dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68105887 | ||||||
| chr16:68105965 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.104-16022G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68105965 | |||||||
| chr16:68106121 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.104-15866C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106121 | |||||||
| chr16:68106156 | C | T | 3 | a0001c0001t0015g0026 a0001c0001t0015g0032 a0001c0001t0036g0030 |
3 | HG02818.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.104-15831C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106156 | |||||||
| chr16:68106256 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.104-15731C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106256 | |||||||
| chr16:68106334 | C | G | 1 | a0001c0001t0004g0157 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.104-15653C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106334 | |||||||
| chr16:68106416 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.104-15571C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106416 | |||||||
| chr16:68106537 | G | A | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-15450G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106537 | |||||||
| chr16:68106600 | A | G | 1 | a0001c0001t0010g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.104-15387A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106600 | |||||||
| chr16:68106736 | T | G | 20 | a0001c0001t0001g0043 a0001c0001t0001g0104 a0001c0001t0001g0107 others(17): Show |
20 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.104-15251T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106736 | |||||||
| chr16:68106742 | G | GT | 13 | a0001c0001t0001g0048 a0001c0001t0008g0012 a0001c0001t0008g0013 others(10): Show |
13 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.104-15235dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68106742 | ||||||
| chr16:68106742 | GT | G | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-15235delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68106742 | ||||||
| chr16:68106745 | T | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-15242T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106745 | |||||||
| chr16:68106746 | T | G | 1 | a0001c0001t0012g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.104-15241T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106746 | |||||||
| chr16:68106855 | T | A | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.104-15132T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106855 | |||||||
| chr16:68106877 | T | C | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-15110T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106877 | |||||||
| chr16:68106927 | C | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0009g0076 |
3 | HG01975.hp1 HG02132.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.104-15060C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68106927 | |||||||
| chr16:68107210 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.104-14777C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68107210 | |||||||
| chr16:68107367 | A | G | 10 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0025 others(7): Show |
10 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-14620A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68107367 | |||||||
| chr16:68107730 | T | TATA | 6 | a0001c0001t0002g0142 a0001c0001t0002g0168 a0001c0001t0004g0145 others(3): Show |
6 | HG00438.hp2 HG03704.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-14236_104-1423 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68107730 | ||||||
| chr16:68108238 | C | T | 1 | a0001c0001t0005g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-13749C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68108238 | |||||||
| chr16:68108648 | A | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0005c0009t0020g0028 |
3 | HG01109.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.104-13339A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68108648 | |||||||
| chr16:68108743 | G | C | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-13244G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68108743 | |||||||
| chr16:68109282 | A | C | 1 | a0001c0001t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104-12705A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109282 | |||||||
| chr16:68109478 | G | C | 1 | a0001c0001t0008g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.104-12509G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109478 | |||||||
| chr16:68109496 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0176 |
2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.104-12491T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109496 | |||||||
| chr16:68109548 | A | G | 6 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(3): Show |
6 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-12439A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109548 | |||||||
| chr16:68109580 | T | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-12407T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109580 | |||||||
| chr16:68109695 | T | G | 84 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(81): Show |
84 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.104-12292T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109695 | |||||||
| chr16:68109749 | A | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-12238A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109749 | |||||||
| chr16:68109774 | T | G | 1 | a0001c0001t0009g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.104-12213T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109774 | |||||||
| chr16:68109842 | G | A | 97 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(94): Show |
97 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.104-12145G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68109842 | |||||||
| chr16:68110236 | C | A | 1 | a0006c0007t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.104-11751C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68110236 | |||||||
| chr16:68110287 | G | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-11700G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68110287 | |||||||
| chr16:68110295 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.104-11692G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68110295 | |||||||
| chr16:68110308 | A | AT | 40 | a0001c0001t0001g0051 a0001c0001t0002g0129 a0001c0001t0002g0132 others(37): Show |
40 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.104-11662dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68110308 | ||||||
| chr16:68110308 | A | ATT | 9 | a0001c0001t0002g0135 a0001c0001t0002g0140 a0001c0001t0002g0153 others(6): Show |
9 | HG00741.hp1 HG01192.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-11663_104-1166 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68110308 | ||||||
| chr16:68110308 | AT | A | 13 | a0001c0001t0001g0090 a0001c0001t0001g0104 a0001c0001t0012g0185 others(10): Show |
13 | HG01071.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.104-11662delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68110308 | ||||||
| chr16:68110334 | A | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-11653A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68110334 | |||||||
| chr16:68110378 | G | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-11609G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68110378 | |||||||
| chr16:68110401 | C | T | 1 | a0001c0001t0004g0141 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.104-11586C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68110401 | |||||||
| chr16:68110616 | A | AT | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-11360dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68110616 | ||||||
| chr16:68110616 | AT | A | 64 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(61): Show |
64 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.104-11360delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68110616 | ||||||
| chr16:68110652 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0072 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-11335C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68110652 | |||||||
| chr16:68110754 | G | A | 2 | a0001c0001t0015g0026 a0001c0001t0036g0030 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.104-11233G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68110754 | |||||||
| chr16:68111002 | C | T | 3 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 |
3 | HG00738.hp2 HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.104-10985C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68111002 | |||||||
| chr16:68111078 | T | A | 1 | a0005c0009t0020g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.104-10909T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68111078 | |||||||
| chr16:68111137 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-10850A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68111137 | |||||||
| chr16:68111159 | C | T | 77 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(74): Show |
77 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.104-10828C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68111159 | |||||||
| chr16:68111540 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-10447G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68111540 | |||||||
| chr16:68111597 | T | C | 1 | a0001c0001t0004g0155 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.104-10390T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68111597 | |||||||
| chr16:68111757 | A | G | 27 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(24): Show |
27 | HG01109.hp2 HG01433.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.104-10230A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68111757 | |||||||
| chr16:68111895 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-10092C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68111895 | |||||||
| chr16:68112164 | CT | C | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-9821delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112164 | ||||||
| chr16:68112172 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-9815G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112172 | |||||||
| chr16:68112214 | C | T | 9 | a0001c0001t0010g0020 a0001c0001t0012g0185 a0001c0001t0012g0187 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-9773C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112214 | |||||||
| chr16:68112234 | C | T | 1 | a0001c0001t0008g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-9753C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112234 | |||||||
| chr16:68112268 | C | CT | 26 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0070 others(23): Show |
26 | HG00438.hp1 HG01070.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.104-9692dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112268 | C | CTT | 30 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0136 others(27): Show |
30 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.104-9693_104-9692d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112268 | C | CTTT | 12 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(9): Show |
12 | HG00639.hp2 HG01099.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-9694_104-9692d others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112268 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0012g0185 a0001c0001t0012g0188 a0001c0001t0016g0186 |
3 | HG02257.hp2 HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.104-9701_104-9692d others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112268 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0016g0184 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.104-9702_104-9692d others(13): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112268 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0012g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.104-9703_104-9692d others(14): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112268 | CT | C | 10 | a0001c0001t0007g0077 a0001c0001t0010g0011 a0001c0001t0010g0019 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-9692delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112268 | CTTTTTTT others(3): Show |
C | 3 | a0002c0002t0014g0178 a0002c0002t0014g0180 a0002c0002t0034g0179 |
3 | HG02572.hp2 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.104-9701_104-9692d others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112268 | CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0014g0177 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.104-9702_104-9692d others(13): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112268 | ||||||
| chr16:68112338 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0005c0009t0020g0028 |
3 | HG01109.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.104-9649C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112338 | |||||||
| chr16:68112399 | G | T | 7 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(4): Show |
7 | HG01109.hp2 HG01891.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-9588G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112399 | |||||||
| chr16:68112511 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-9476C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112511 | |||||||
| chr16:68112632 | A | ATTT | 97 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(94): Show |
97 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.104-9351_104-9349d others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112632 | ||||||
| chr16:68112645 | C | CT | 4 | a0001c0001t0002g0167 a0001c0001t0004g0156 a0001c0001t0024g0169 others(1): Show |
4 | HG02071.hp2 NA18952.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-9342_104-9341i others(3): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112645 | |||||||
| chr16:68112645 | CG | C | 13 | a0001c0001t0002g0173 a0001c0001t0010g0010 a0001c0001t0010g0011 others(10): Show |
13 | HG01109.hp2 HG01433.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.104-9341delG | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112645 | |||||||
| chr16:68112645 | CGT | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-9341_104-9340d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112645 | |||||||
| chr16:68112646 | G | GT | 16 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0092 others(13): Show |
16 | HG00438.hp1 HG00741.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.104-9318dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68112646 | ||||||
| chr16:68112646 | G | T | 60 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(57): Show |
60 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.104-9341G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112646 | |||||||
| chr16:68112690 | C | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-9297C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112690 | |||||||
| chr16:68112706 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0003g0083 |
2 | HG00738.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.104-9281C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112706 | |||||||
| chr16:68112781 | C | T | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-9206C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112781 | |||||||
| chr16:68112782 | CCGACA | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-9204_104-9200d others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112782 | |||||||
| chr16:68112786 | C | T | 1 | a0001c0001t0033g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.104-9201C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112786 | |||||||
| chr16:68112788 | T | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-9199T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112788 | |||||||
| chr16:68112956 | G | C | 77 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(74): Show |
77 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.104-9031G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68112956 | |||||||
| chr16:68113049 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-8938C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68113049 | |||||||
| chr16:68113087 | G | A | 2 | a0001c0001t0007g0078 a0001c0001t0007g0079 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.104-8900G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68113087 | |||||||
| chr16:68113115 | A | G | 1 | a0001c0001t0005g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.104-8872A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68113115 | |||||||
| chr16:68113223 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-8764T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68113223 | |||||||
| chr16:68113402 | C | G | 2 | a0001c0001t0001g0081 a0001c0001t0003g0082 |
2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.104-8585C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68113402 | |||||||
| chr16:68113626 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-8361C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68113626 | |||||||
| chr16:68113986 | T | G | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-8001T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68113986 | |||||||
| chr16:68114005 | T | C | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-7982T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114005 | |||||||
| chr16:68114026 | A | G | 1 | a0001c0001t0009g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.104-7961A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114026 | |||||||
| chr16:68114354 | C | T | 2 | a0001c0001t0002g0148 a0001c0001t0004g0152 |
2 | HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.104-7633C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114354 | |||||||
| chr16:68114573 | G | A | 1 | a0001c0001t0006g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.104-7414G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114573 | |||||||
| chr16:68114576 | C | CT | 64 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(61): Show |
64 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.104-7394dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68114576 | ||||||
| chr16:68114577 | TTTTTTTT others(20): Show |
T | 1 | a0001c0001t0003g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.104-7407_104-7381d others(29): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68114577 | ||||||
| chr16:68114599 | G | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0055 others(21): Show |
24 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.104-7388G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114599 | |||||||
| chr16:68114733 | C | T | 19 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(16): Show |
19 | HG01109.hp2 HG01433.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.104-7254C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114733 | |||||||
| chr16:68114834 | A | G | 2 | a0001c0001t0002g0139 a0001c0001t0004g0141 |
2 | NA18973.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.104-7153A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114834 | |||||||
| chr16:68114894 | A | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0003g0044 |
3 | HG02630.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.104-7093A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114894 | |||||||
| chr16:68114896 | C | T | 1 | a0001c0001t0004g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.104-7091C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114896 | |||||||
| chr16:68114910 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-7077T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114910 | |||||||
| chr16:68115413 | T | C | 81 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(78): Show |
81 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.104-6574T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115413 | |||||||
| chr16:68115413 | T | G | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.104-6574T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115413 | |||||||
| chr16:68115631 | G | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-6356G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115631 | |||||||
| chr16:68115672 | C | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-6315C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115672 | |||||||
| chr16:68115672 | C | G | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-6315C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115672 | |||||||
| chr16:68115725 | G | C | 1 | a0001c0001t0007g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.104-6262G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115725 | |||||||
| chr16:68115739 | G | T | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104-6248G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115739 | |||||||
| chr16:68115775 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0003g0044 |
3 | HG02630.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.104-6212T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115775 | |||||||
| chr16:68115869 | C | A | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-6118C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115869 | |||||||
| chr16:68115987 | C | T | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.104-6000C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68115987 | |||||||
| chr16:68116191 | A | T | 1 | a0001c0001t0003g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.104-5796A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68116191 | |||||||
| chr16:68116425 | A | G | 1 | a0001c0001t0010g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.104-5562A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68116425 | |||||||
| chr16:68116530 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-5457T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68116530 | |||||||
| chr16:68116571 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-5416A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68116571 | |||||||
| chr16:68116624 | A | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-5363A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68116624 | |||||||
| chr16:68116805 | CT | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-5170delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68116805 | ||||||
| chr16:68116840 | A | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-5147A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68116840 | |||||||
| chr16:68117090 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.104-4897T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68117090 | |||||||
| chr16:68117621 | C | A | 1 | a0001c0001t0006g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.104-4366C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68117621 | |||||||
| chr16:68117769 | C | T | 2 | a0001c0001t0010g0020 a0001c0001t0028g0040 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.104-4218C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68117769 | |||||||
| chr16:68118132 | A | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-3855A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68118132 | |||||||
| chr16:68118153 | C | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.104-3834C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68118153 | |||||||
| chr16:68118153 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.104-3834C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68118153 | |||||||
| chr16:68118254 | A | G | 84 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(81): Show |
84 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.104-3733A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68118254 | |||||||
| chr16:68118435 | ATAGT | A | 2 | a0001c0001t0001g0101 a0001c0001t0031g0052 |
2 | HG02080.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.104-3550_104-3547d others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68118435 | ||||||
| chr16:68118539 | ATTC | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-3442_104-3440d others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68118539 | ||||||
| chr16:68118931 | G | C | 2 | a0001c0001t0010g0020 a0001c0001t0028g0040 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.104-3056G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68118931 | |||||||
| chr16:68119159 | G | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-2828G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68119159 | |||||||
| chr16:68119297 | G | A | 75 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(72): Show |
75 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.104-2690G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68119297 | |||||||
| chr16:68119337 | T | G | 2 | a0001c0001t0010g0010 a0001c0001t0010g0011 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.104-2650T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68119337 | |||||||
| chr16:68119479 | G | C | 83 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.104-2508G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68119479 | |||||||
| chr16:68119483 | C | G | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-2504C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68119483 | |||||||
| chr16:68119589 | A | G | 1 | a0001c0001t0006g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.104-2398A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68119589 | |||||||
| chr16:68119650 | G | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-2337G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68119650 | |||||||
| chr16:68119780 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.104-2207A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68119780 | |||||||
| chr16:68120037 | G | A | 2 | a0001c0001t0013g0003 a0001c0001t0029g0002 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.104-1950G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120037 | |||||||
| chr16:68120077 | A | C | 1 | a0001c0001t0006g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.104-1910A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120077 | |||||||
| chr16:68120078 | G | A | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104-1909G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120078 | |||||||
| chr16:68120114 | C | CA | 21 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0070 others(18): Show |
21 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.104-1855dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68120114 | ||||||
| chr16:68120114 | CA | C | 7 | a0001c0001t0006g0119 a0001c0001t0012g0185 a0001c0001t0012g0187 others(4): Show |
7 | HG00438.hp1 HG01884.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-1855delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68120114 | ||||||
| chr16:68120152 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-1835G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120152 | |||||||
| chr16:68120248 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-1739C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120248 | |||||||
| chr16:68120279 | C | CA | 48 | a0001c0001t0001g0070 a0001c0001t0002g0129 a0001c0001t0002g0132 others(45): Show |
48 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.104-1692dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68120279 | ||||||
| chr16:68120327 | T | C | 75 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(72): Show |
75 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.104-1660T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120327 | |||||||
| chr16:68120477 | G | A | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-1510G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120477 | |||||||
| chr16:68120572 | G | GA | 25 | a0001c0001t0001g0043 a0001c0001t0007g0078 a0001c0001t0008g0012 others(22): Show |
25 | HG00741.hp2 HG01071.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.104-1394dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68120572 | ||||||
| chr16:68120641 | A | G | 83 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.104-1346A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120641 | |||||||
| chr16:68120726 | C | G | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.104-1261C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120726 | |||||||
| chr16:68120731 | T | TCAAA | 29 | a0001c0001t0002g0142 a0001c0001t0002g0160 a0001c0001t0008g0012 others(26): Show |
29 | HG01433.hp1 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.104-1235_104-1232d others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68120731 | ||||||
| chr16:68120731 | T | TCAAACAA others(1): Show |
44 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(41): Show |
44 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.104-1239_104-1232d others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68120731 | ||||||
| chr16:68120959 | G | A | 97 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(94): Show |
97 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.104-1028G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68120959 | |||||||
| chr16:68121091 | CA | C | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.104-884delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121091 | ||||||
| chr16:68121218 | G | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-769G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68121218 | |||||||
| chr16:68121242 | C | CT | 49 | a0001c0001t0001g0043 a0001c0001t0002g0129 a0001c0001t0002g0132 others(46): Show |
49 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.104-723dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121242 | ||||||
| chr16:68121242 | CT | C | 6 | a0001c0001t0007g0077 a0001c0001t0013g0001 a0001c0001t0013g0004 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-723delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121242 | ||||||
| chr16:68121242 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.104-732_104-723del others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121242 | ||||||
| chr16:68121247 | T | C | 11 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0006g0105 others(8): Show |
11 | HG00438.hp1 HG01071.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.104-740T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68121247 | |||||||
| chr16:68121248 | T | C | 7 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
7 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-739T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68121248 | |||||||
| chr16:68121365 | G | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-622G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68121365 | |||||||
| chr16:68121672 | C | CA | 10 | a0001c0001t0004g0156 a0001c0001t0005g0099 a0001c0001t0006g0105 others(7): Show |
10 | HG01175.hp1 HG01258.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-297dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121672 | ||||||
| chr16:68121672 | CA | C | 16 | a0001c0001t0002g0134 a0001c0001t0009g0123 a0001c0001t0009g0124 others(13): Show |
16 | HG00741.hp2 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.104-297delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121672 | ||||||
| chr16:68121957 | G | GT | 7 | a0001c0001t0003g0044 a0001c0001t0003g0069 a0001c0001t0003g0094 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-17dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121957 | ||||||
| chr16:68121957 | GT | G | 22 | a0001c0001t0002g0129 a0001c0001t0002g0136 a0001c0001t0002g0138 others(19): Show |
22 | HG02055.hp1 HG02132.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.104-17delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121957 | ||||||
| chr16:68121957 | GTT | G | 31 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(28): Show |
31 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-18_104-17delTT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 68121957 | ||||||
| chr16:68123324 | T | G | 3 | a0001c0001t0015g0026 a0001c0001t0015g0032 a0001c0001t0036g0030 |
3 | HG02818.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1238+203T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68123324 | |||||||
| chr16:68123325 | T | A | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238+204T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68123325 | |||||||
| chr16:68123497 | C | CA | 5 | a0001c0001t0001g0051 a0001c0001t0001g0070 a0001c0001t0001g0092 others(2): Show |
5 | HG02809.hp1 HG03688.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238+395dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 68123497 | ||||||
| chr16:68123497 | CA | C | 77 | a0001c0001t0001g0035 a0001c0001t0002g0129 a0001c0001t0002g0132 others(74): Show |
77 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.1238+395delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 68123497 | ||||||
| chr16:68123659 | A | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1238+538A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68123659 | |||||||
| chr16:68123709 | C | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1238+588C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68123709 | |||||||
| chr16:68123773 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238+652C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68123773 | |||||||
| chr16:68123808 | AACCGTGT others(15): Show |
A | 3 | a0001c0004t0001g0034 a0001c0004t0001g0088 a0001c0004t0001g0089 |
3 | HG01433.hp2 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1238+689_1238+710d others(24): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 68123808 | ||||||
| chr16:68123867 | C | T | 1 | a0001c0001t0027g0068 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1238+746C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68123867 | |||||||
| chr16:68124187 | G | A | 1 | a0007c0010t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1238+1066G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68124187 | |||||||
| chr16:68124277 | A | T | 4 | a0001c0001t0005g0024 a0003c0003t0011g0181 a0003c0003t0011g0182 others(1): Show |
4 | HG03041.hp2 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238+1156A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68124277 | |||||||
| chr16:68124286 | G | T | 2 | a0001c0001t0010g0020 a0001c0001t0028g0040 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1238+1165G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68124286 | |||||||
| chr16:68124300 | A | T | 2 | a0003c0003t0011g0182 a0003c0003t0011g0183 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1238+1179A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68124300 | |||||||
| chr16:68124334 | C | G | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238+1213C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68124334 | |||||||
| chr16:68124407 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1238+1286C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68124407 | |||||||
| chr16:68124431 | CT | C | 183 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0035 others(180): Show |
183 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(180): Show |
intron_variant | MODIFIER | c.1238+1327delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 68124431 | ||||||
| chr16:68124518 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1238+1397C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68124518 | |||||||
| chr16:68124722 | C | T | 2 | a0001c0001t0010g0020 a0001c0001t0028g0040 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1238+1601C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68124722 | |||||||
| chr16:68125063 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1239-1385C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68125063 | |||||||
| chr16:68125375 | A | G | 11 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(8): Show |
11 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1239-1073A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68125375 | |||||||
| chr16:68125904 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1239-544A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68125904 | |||||||
| chr16:68126125 | C | A | 1 | a0001c0001t0015g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1239-323C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68126125 | |||||||
| chr16:68126386 | T | G | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1239-62T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 2/9 | chr16 | 68126386 | |||||||
| chr16:68126861 | G | A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1401+251G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68126861 | |||||||
| chr16:68126875 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1401+265C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68126875 | |||||||
| chr16:68127030 | C | G | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1401+420C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68127030 | |||||||
| chr16:68127065 | G | T | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1401+455G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68127065 | |||||||
| chr16:68127084 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+474G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68127084 | |||||||
| chr16:68127419 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+809G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68127419 | |||||||
| chr16:68127500 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1401+890A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68127500 | |||||||
| chr16:68127604 | A | T | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1401+994A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68127604 | |||||||
| chr16:68127687 | C | CA | 54 | a0001c0001t0001g0090 a0001c0001t0002g0129 a0001c0001t0002g0132 others(51): Show |
54 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1401+1092dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68127687 | ||||||
| chr16:68127763 | G | T | 1 | a0001c0001t0009g0127 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1401+1153G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68127763 | |||||||
| chr16:68127770 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1401+1160T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68127770 | |||||||
| chr16:68128113 | G | A | 57 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(54): Show |
57 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1401+1503G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68128113 | |||||||
| chr16:68128292 | G | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+1682G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68128292 | |||||||
| chr16:68128520 | T | C | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1401+1910T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68128520 | |||||||
| chr16:68129138 | G | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+2528G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68129138 | |||||||
| chr16:68129457 | C | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0031 a0001c0001t0015g0032 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+2847C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68129457 | |||||||
| chr16:68129668 | C | T | 1 | a0006c0007t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1401+3058C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68129668 | |||||||
| chr16:68129669 | G | A | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+3059G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68129669 | |||||||
| chr16:68129671 | C | CT | 21 | a0001c0001t0001g0067 a0001c0001t0001g0104 a0001c0001t0003g0069 others(18): Show |
21 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1401+3083dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68129671 | ||||||
| chr16:68129671 | CT | C | 5 | a0001c0001t0001g0107 a0001c0001t0002g0142 a0001c0001t0002g0168 others(2): Show |
5 | HG01070.hp1 HG03669.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+3083delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68129671 | ||||||
| chr16:68129699 | C | A | 80 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(77): Show |
80 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1401+3089C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68129699 | |||||||
| chr16:68129759 | T | C | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1401+3149T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68129759 | |||||||
| chr16:68130362 | A | G | 2 | a0001c0001t0005g0021 a0001c0001t0005g0175 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1401+3752A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68130362 | |||||||
| chr16:68130442 | G | A | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1401+3832G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68130442 | |||||||
| chr16:68130503 | GT | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+3900delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68130503 | ||||||
| chr16:68130599 | G | A | 17 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(14): Show |
17 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1401+3989G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68130599 | |||||||
| chr16:68130859 | G | A | 2 | a0001c0001t0010g0020 a0001c0001t0028g0040 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1401+4249G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68130859 | |||||||
| chr16:68131046 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1401+4436G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131046 | |||||||
| chr16:68131152 | A | G | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+4542A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131152 | |||||||
| chr16:68131300 | CAG | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1401+4693_1401+469 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68131300 | ||||||
| chr16:68131336 | G | A | 5 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+4726G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131336 | |||||||
| chr16:68131340 | T | C | 57 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(54): Show |
57 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1401+4730T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131340 | |||||||
| chr16:68131362 | C | A | 4 | a0001c0001t0015g0026 a0001c0001t0015g0031 a0001c0001t0015g0032 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+4752C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131362 | |||||||
| chr16:68131528 | T | A | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+4918T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131528 | |||||||
| chr16:68131558 | G | A | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1401+4948G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131558 | |||||||
| chr16:68131650 | C | CTT | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+5055_1401+505 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68131650 | ||||||
| chr16:68131684 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1401+5074C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131684 | |||||||
| chr16:68131971 | G | T | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1401+5361G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131971 | |||||||
| chr16:68131991 | C | T | 2 | a0001c0001t0010g0020 a0001c0001t0028g0040 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1401+5381C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68131991 | |||||||
| chr16:68132058 | G | C | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1401+5448G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68132058 | |||||||
| chr16:68132510 | A | G | 5 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(2): Show |
5 | HG01099.hp2 HG01255.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1401+5900A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68132510 | |||||||
| chr16:68132566 | G | A | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1401+5956G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68132566 | |||||||
| chr16:68132962 | A | G | 1 | a0001c0001t0005g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1401+6352A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68132962 | |||||||
| chr16:68133068 | A | C | 57 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(54): Show |
57 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1401+6458A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133068 | |||||||
| chr16:68133078 | C | T | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1401+6468C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133078 | |||||||
| chr16:68133111 | C | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+6501C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133111 | |||||||
| chr16:68133504 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1401+6894C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133504 | |||||||
| chr16:68133618 | C | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1401+7008C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133618 | |||||||
| chr16:68133876 | CT | C | 5 | a0001c0001t0002g0154 a0001c0001t0004g0152 a0001c0001t0009g0124 others(2): Show |
5 | HG01070.hp1 HG02602.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1401+7274delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68133876 | ||||||
| chr16:68133877 | T | C | 1 | a0005c0009t0020g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1401+7267T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133877 | |||||||
| chr16:68133883 | T | A | 16 | a0001c0001t0009g0123 a0001c0001t0009g0125 a0001c0001t0009g0127 others(13): Show |
16 | HG00741.hp2 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.1401+7273T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133883 | |||||||
| chr16:68133884 | T | A | 79 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(76): Show |
79 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.1401+7274T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133884 | |||||||
| chr16:68133884 | TA | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0055 others(5): Show |
8 | HG02602.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1401+7288delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68133884 | ||||||
| chr16:68133973 | C | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+7363C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133973 | |||||||
| chr16:68134297 | C | G | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1401+7687C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68134297 | |||||||
| chr16:68134429 | T | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+7819T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68134429 | |||||||
| chr16:68134691 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1401+8081G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68134691 | |||||||
| chr16:68134983 | CT | C | 32 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(29): Show |
32 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1401+8383delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68134983 | ||||||
| chr16:68135117 | G | T | 1 | a0003c0003t0011g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1401+8507G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68135117 | |||||||
| chr16:68135185 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1401+8575G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68135185 | |||||||
| chr16:68135224 | C | T | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1401+8614C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68135224 | |||||||
| chr16:68135376 | TGA | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+8767_1401+876 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68135376 | |||||||
| chr16:68135429 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0055 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1401+8819A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68135429 | |||||||
| chr16:68135457 | C | CA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0056 a0001c0001t0001g0070 others(7): Show |
10 | HG01070.hp2 HG01192.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1401+8873dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68135457 | ||||||
| chr16:68135457 | CA | C | 16 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0023 others(13): Show |
16 | HG01934.hp1 HG01934.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1401+8873delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68135457 | ||||||
| chr16:68135457 | CAA | C | 6 | a0001c0001t0002g0160 a0001c0001t0005g0022 a0001c0001t0012g0185 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+8872_1401+887 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68135457 | ||||||
| chr16:68135457 | CAAA | C | 12 | a0001c0001t0002g0135 a0001c0001t0009g0123 a0001c0001t0009g0124 others(9): Show |
12 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1401+8871_1401+887 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68135457 | ||||||
| chr16:68135457 | CAAAA | C | 63 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(60): Show |
63 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.1401+8870_1401+887 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68135457 | ||||||
| chr16:68135457 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0001g0107 a0001c0001t0006g0105 a0001c0001t0006g0112 others(6): Show |
9 | HG01255.hp2 HG01256.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1401+8865_1401+887 others(13): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68135457 | ||||||
| chr16:68135791 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1401+9181G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68135791 | |||||||
| chr16:68136232 | T | C | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1401+9622T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136232 | |||||||
| chr16:68136387 | A | G | 1 | a0001c0001t0005g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1401+9777A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136387 | |||||||
| chr16:68136395 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+9785C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136395 | |||||||
| chr16:68136557 | C | A | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1401+9947C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136557 | |||||||
| chr16:68136604 | A | C | 2 | a0001c0001t0005g0021 a0001c0001t0005g0175 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1401+9994A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136604 | |||||||
| chr16:68136657 | C | T | 1 | a0001c0001t0005g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1401+10047C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136657 | |||||||
| chr16:68136844 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1401+10234A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136844 | |||||||
| chr16:68136894 | T | C | 1 | a0001c0001t0005g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1401+10284T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136894 | |||||||
| chr16:68137141 | T | A | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1401+10531T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137141 | |||||||
| chr16:68137618 | C | CT | 9 | a0001c0001t0001g0090 a0001c0001t0003g0100 a0001c0001t0005g0023 others(6): Show |
9 | HG01071.hp1 HG01192.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1401+11023dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68137618 | ||||||
| chr16:68137638 | C | CAG | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1401+11029_1401+11 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68137638 | ||||||
| chr16:68137676 | C | T | 17 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(14): Show |
17 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1401+11066C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137676 | |||||||
| chr16:68137722 | T | C | 1 | a0001c0001t0035g0106 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1401+11112T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137722 | |||||||
| chr16:68137731 | A | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+11121A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137731 | |||||||
| chr16:68137961 | A | T | 1 | a0004c0005t0022g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1401+11351A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137961 | |||||||
| chr16:68137972 | T | C | 1 | a0004c0005t0022g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1401+11362T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137972 | |||||||
| chr16:68137974 | A | T | 1 | a0004c0005t0022g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1401+11364A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137974 | |||||||
| chr16:68137976 | C | G | 1 | a0004c0005t0022g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1401+11366C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137976 | |||||||
| chr16:68137978 | C | G | 1 | a0004c0005t0022g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1401+11368C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137978 | |||||||
| chr16:68137979 | T | A | 1 | a0004c0005t0022g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1401+11369T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137979 | |||||||
| chr16:68137981 | T | G | 1 | a0004c0005t0022g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1401+11371T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137981 | |||||||
| chr16:68137983 | A | T | 1 | a0004c0005t0022g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1401+11373A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68137983 | |||||||
| chr16:68138031 | A | T | 1 | a0001c0001t0025g0130 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1401+11421A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138031 | |||||||
| chr16:68138065 | C | T | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1401+11455C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138065 | |||||||
| chr16:68138255 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1401+11645G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138255 | |||||||
| chr16:68138275 | A | G | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+11665A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138275 | |||||||
| chr16:68138513 | A | T | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1401+11903A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138513 | |||||||
| chr16:68138540 | C | A | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1401+11930C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138540 | |||||||
| chr16:68138587 | A | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+11977A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138587 | |||||||
| chr16:68138665 | C | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+12055C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138665 | |||||||
| chr16:68138684 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0104 others(1): Show |
4 | NA18940.hp2 NA18961.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+12074A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138684 | |||||||
| chr16:68138819 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1401+12209C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138819 | |||||||
| chr16:68138996 | G | A | 1 | a0001c0001t0030g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1401+12386G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68138996 | |||||||
| chr16:68139051 | A | T | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1401+12441A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68139051 | |||||||
| chr16:68139056 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+12446G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68139056 | |||||||
| chr16:68139080 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1401+12470C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68139080 | |||||||
| chr16:68139147 | A | C | 2 | a0001c0001t0001g0063 a0001c0001t0003g0064 |
2 | HG02027.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1401+12537A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68139147 | |||||||
| chr16:68139253 | T | C | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+12643T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68139253 | |||||||
| chr16:68139916 | G | C | 3 | a0001c0001t0004g0131 a0001c0001t0004g0150 a0001c0001t0019g0170 |
3 | HG02055.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1401+13306G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68139916 | |||||||
| chr16:68140117 | C | T | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1401+13507C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68140117 | |||||||
| chr16:68140536 | A | G | 2 | a0001c0001t0002g0135 a0001c0001t0002g0153 |
2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1401+13926A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68140536 | |||||||
| chr16:68140552 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+13942A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68140552 | |||||||
| chr16:68140648 | A | AT | 10 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(7): Show |
10 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1401+14049dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68140648 | ||||||
| chr16:68140845 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+14235A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68140845 | |||||||
| chr16:68141265 | T | C | 3 | a0001c0001t0015g0026 a0001c0001t0015g0032 a0001c0001t0036g0030 |
3 | HG02818.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1401+14655T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68141265 | |||||||
| chr16:68141386 | G | A | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+14776G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68141386 | |||||||
| chr16:68141521 | G | A | 17 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(14): Show |
17 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1401+14911G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68141521 | |||||||
| chr16:68141573 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+14963G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68141573 | |||||||
| chr16:68141958 | A | G | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+15348A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68141958 | |||||||
| chr16:68142267 | GTTC | G | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-15596_1402-15 others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68142267 | ||||||
| chr16:68142484 | A | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-15385A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68142484 | |||||||
| chr16:68142512 | C | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1402-15357C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68142512 | |||||||
| chr16:68142619 | G | A | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-15250G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68142619 | |||||||
| chr16:68142652 | G | C | 1 | a0001c0001t0003g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1402-15217G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68142652 | |||||||
| chr16:68142689 | C | T | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1402-15180C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68142689 | |||||||
| chr16:68143133 | G | C | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1402-14736G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68143133 | |||||||
| chr16:68143209 | T | TA | 23 | a0001c0001t0001g0050 a0001c0001t0001g0117 a0001c0001t0002g0129 others(20): Show |
23 | HG01109.hp1 HG01109.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1402-14639dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68143209 | ||||||
| chr16:68143209 | T | TAA | 6 | a0001c0001t0008g0018 a0001c0001t0013g0001 a0001c0001t0013g0003 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-14640_1402-14 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68143209 | ||||||
| chr16:68143209 | TAA | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-14640_1402-14 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68143209 | ||||||
| chr16:68143804 | A | G | 1 | a0001c0001t0030g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1402-14065A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68143804 | |||||||
| chr16:68144435 | GA | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-13423delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68144435 | ||||||
| chr16:68144443 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-13426A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68144443 | |||||||
| chr16:68144451 | T | C | 1 | a0001c0001t0024g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1402-13418T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68144451 | |||||||
| chr16:68144573 | G | C | 2 | a0001c0001t0010g0020 a0001c0001t0028g0040 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1402-13296G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68144573 | |||||||
| chr16:68144670 | A | T | 1 | a0001c0001t0021g0158 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1402-13199A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68144670 | |||||||
| chr16:68144743 | C | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1402-13126C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68144743 | |||||||
| chr16:68144877 | G | A | 2 | a0001c0001t0010g0020 a0001c0001t0028g0040 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1402-12992G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68144877 | |||||||
| chr16:68144948 | G | C | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-12921G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68144948 | |||||||
| chr16:68144988 | G | T | 1 | a0001c0001t0008g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1402-12881G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68144988 | |||||||
| chr16:68145001 | T | G | 1 | a0001c0001t0010g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1402-12868T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68145001 | |||||||
| chr16:68145133 | C | CT | 5 | a0001c0001t0001g0104 a0001c0001t0004g0145 a0001c0001t0021g0158 others(2): Show |
5 | HG00438.hp2 HG01169.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.1402-12719dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68145133 | ||||||
| chr16:68145248 | G | A | 3 | a0001c0004t0001g0034 a0001c0004t0001g0088 a0001c0004t0001g0089 |
3 | HG01433.hp2 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1402-12621G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68145248 | |||||||
| chr16:68145292 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1402-12577C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68145292 | |||||||
| chr16:68145317 | G | GT | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-12546dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68145317 | ||||||
| chr16:68145576 | C | T | 1 | a0001c0001t0009g0127 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1402-12293C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68145576 | |||||||
| chr16:68145617 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1402-12252T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68145617 | |||||||
| chr16:68145667 | G | C | 1 | a0001c0001t0018g0097 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1402-12202G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68145667 | |||||||
| chr16:68146339 | A | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1402-11530A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68146339 | |||||||
| chr16:68146410 | G | GA | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-11448dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68146410 | ||||||
| chr16:68146432 | T | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-11437T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68146432 | |||||||
| chr16:68146931 | T | G | 3 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 |
3 | HG00738.hp2 HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1402-10938T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68146931 | |||||||
| chr16:68147174 | C | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-10695C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147174 | |||||||
| chr16:68147216 | A | G | 1 | a0001c0001t0025g0130 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1402-10653A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147216 | |||||||
| chr16:68147226 | T | G | 2 | a0001c0001t0009g0125 a0001c0001t0009g0126 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1402-10643T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147226 | |||||||
| chr16:68147274 | C | A | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1402-10595C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147274 | |||||||
| chr16:68147327 | A | G | 2 | a0001c0001t0009g0125 a0001c0001t0009g0126 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1402-10542A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147327 | |||||||
| chr16:68147353 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1402-10516G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147353 | |||||||
| chr16:68147400 | G | A | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-10469G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147400 | |||||||
| chr16:68147509 | C | T | 1 | a0001c0001t0004g0157 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1402-10360C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147509 | |||||||
| chr16:68147755 | G | GA | 6 | a0001c0001t0001g0033 a0001c0001t0012g0185 a0001c0001t0012g0187 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-10095dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68147755 | ||||||
| chr16:68147755 | GA | G | 16 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(13): Show |
16 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1402-10095delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68147755 | ||||||
| chr16:68147755 | GAA | G | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-10096_1402-10 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68147755 | ||||||
| chr16:68147756 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1402-10113A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147756 | |||||||
| chr16:68147832 | A | AT | 7 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1402-10028dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68147832 | ||||||
| chr16:68147837 | T | C | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-10032T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147837 | |||||||
| chr16:68147994 | T | A | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1402-9875T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68147994 | |||||||
| chr16:68148107 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1402-9762C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68148107 | |||||||
| chr16:68148170 | C | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402-9699C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68148170 | |||||||
| chr16:68148217 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1402-9652T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68148217 | |||||||
| chr16:68149161 | T | A | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1402-8708T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68149161 | |||||||
| chr16:68149347 | A | G | 2 | a0001c0001t0009g0125 a0001c0001t0009g0126 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1402-8522A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68149347 | |||||||
| chr16:68150264 | T | C | 1 | a0001c0001t0027g0068 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1402-7605T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68150264 | |||||||
| chr16:68150318 | C | T | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1402-7551C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68150318 | |||||||
| chr16:68150347 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-7522C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68150347 | |||||||
| chr16:68150412 | T | TA | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(5): Show |
8 | HG00438.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-7434dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68150412 | ||||||
| chr16:68150412 | T | TAA | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-7435_1402-743 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68150412 | ||||||
| chr16:68150412 | TA | T | 15 | a0001c0001t0001g0070 a0001c0001t0003g0069 a0001c0001t0005g0065 others(12): Show |
15 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1402-7434delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68150412 | ||||||
| chr16:68150412 | TAAAAA | T | 11 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(8): Show |
11 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402-7438_1402-743 others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68150412 | ||||||
| chr16:68150467 | A | G | 2 | a0001c0001t0013g0003 a0001c0001t0029g0002 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1402-7402A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68150467 | |||||||
| chr16:68150804 | T | C | 1 | a0001c0001t0009g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1402-7065T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68150804 | |||||||
| chr16:68150954 | G | GC | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-6908dupC | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68150954 | ||||||
| chr16:68150966 | A | G | 3 | a0001c0001t0005g0009 a0001c0001t0005g0025 a0001c0001t0020g0029 |
3 | HG02451.hp2 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1402-6903A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68150966 | |||||||
| chr16:68151018 | C | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-6851C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151018 | |||||||
| chr16:68151133 | C | T | 1 | a0001c0001t0009g0127 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1402-6736C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151133 | |||||||
| chr16:68151205 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1402-6664A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151205 | |||||||
| chr16:68151251 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1402-6618T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151251 | |||||||
| chr16:68151257 | G | A | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1402-6612G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151257 | |||||||
| chr16:68151279 | CTA | C | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1402-6587_1402-658 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68151279 | ||||||
| chr16:68151487 | G | A | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1402-6382G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151487 | |||||||
| chr16:68151555 | G | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-6314G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151555 | |||||||
| chr16:68151668 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1402-6201A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151668 | |||||||
| chr16:68151789 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-6080T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151789 | |||||||
| chr16:68151807 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1402-6062G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151807 | |||||||
| chr16:68151930 | G | A | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-5939G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151930 | |||||||
| chr16:68151961 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-5908T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68151961 | |||||||
| chr16:68152064 | C | CA | 5 | a0001c0001t0001g0043 a0001c0001t0001g0110 a0001c0001t0001g0117 others(2): Show |
5 | HG01175.hp1 HG03704.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-5789dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152064 | ||||||
| chr16:68152064 | CA | C | 34 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0151 others(31): Show |
34 | HG00438.hp2 HG00741.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1402-5789delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152064 | ||||||
| chr16:68152064 | CAA | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-5790_1402-578 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152064 | ||||||
| chr16:68152064 | CAAA | C | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-5791_1402-578 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152064 | ||||||
| chr16:68152179 | A | G | 57 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(54): Show |
57 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1402-5690A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68152179 | |||||||
| chr16:68152205 | A | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-5664A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68152205 | |||||||
| chr16:68152209 | C | CA | 8 | a0001c0001t0001g0037 a0001c0001t0003g0064 a0002c0002t0014g0177 others(5): Show |
8 | HG02717.hp2 HG02886.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402-5640dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152209 | ||||||
| chr16:68152209 | CA | C | 43 | a0001c0001t0001g0050 a0001c0001t0002g0129 a0001c0001t0002g0132 others(40): Show |
43 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1402-5640delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152209 | ||||||
| chr16:68152283 | A | G | 75 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(72): Show |
75 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.1402-5586A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68152283 | |||||||
| chr16:68152378 | CA | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0045 others(93): Show |
96 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.1402-5468delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152378 | ||||||
| chr16:68152378 | CAA | C | 22 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(19): Show |
22 | HG01433.hp1 HG01891.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1402-5469_1402-546 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152378 | ||||||
| chr16:68152378 | CAAA | C | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1402-5470_1402-546 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68152378 | ||||||
| chr16:68152398 | A | G | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1402-5471A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68152398 | |||||||
| chr16:68152673 | G | A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1402-5196G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68152673 | |||||||
| chr16:68152780 | T | G | 1 | a0001c0001t0003g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1402-5089T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68152780 | |||||||
| chr16:68152909 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-4960A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68152909 | |||||||
| chr16:68153060 | C | CA | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-4808dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68153060 | ||||||
| chr16:68153247 | C | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-4622C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68153247 | |||||||
| chr16:68153469 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-4400C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68153469 | |||||||
| chr16:68153569 | C | T | 1 | a0001c0001t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1402-4300C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68153569 | |||||||
| chr16:68153667 | A | C | 1 | a0006c0007t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1402-4202A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68153667 | |||||||
| chr16:68153691 | G | A | 1 | a0001c0001t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1402-4178G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68153691 | |||||||
| chr16:68153774 | C | T | 5 | a0001c0001t0002g0149 a0001c0001t0013g0001 a0001c0001t0013g0003 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-4095C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68153774 | |||||||
| chr16:68153815 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1402-4054G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68153815 | |||||||
| chr16:68153879 | CT | C | 143 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(140): Show |
143 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1402-3988delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68153879 | ||||||
| chr16:68153884 | G | A | 1 | a0001c0001t0032g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1402-3985G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68153884 | |||||||
| chr16:68154167 | G | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-3702G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68154167 | |||||||
| chr16:68154294 | A | G | 4 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0004g0141 others(1): Show |
4 | HG02132.hp2 NA18973.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1402-3575A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68154294 | |||||||
| chr16:68154473 | C | T | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1402-3396C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68154473 | |||||||
| chr16:68154510 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-3359A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68154510 | |||||||
| chr16:68154561 | G | A | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402-3308G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68154561 | |||||||
| chr16:68154879 | C | A | 1 | a0001c0001t0032g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1402-2990C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68154879 | |||||||
| chr16:68155151 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1402-2718C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68155151 | |||||||
| chr16:68155361 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1402-2508T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68155361 | |||||||
| chr16:68155437 | G | A | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1402-2432G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68155437 | |||||||
| chr16:68155688 | T | TCAGTTAA others(4): Show |
82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1402-2178_1402-217 others(15): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68155688 | ||||||
| chr16:68155733 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1402-2136C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68155733 | |||||||
| chr16:68155815 | TAC | T | 2 | a0001c0001t0001g0091 a0001c0001t0005g0065 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1402-2042_1402-204 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68155815 | ||||||
| chr16:68155862 | C | G | 1 | a0002c0002t0034g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1402-2007C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68155862 | |||||||
| chr16:68156302 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1402-1567C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68156302 | |||||||
| chr16:68156318 | A | AAAC | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1402-1536_1402-153 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 68156318 | ||||||
| chr16:68156336 | A | C | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1402-1533A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68156336 | |||||||
| chr16:68156706 | G | A | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1402-1163G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68156706 | |||||||
| chr16:68156745 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0072 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1402-1124C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68156745 | |||||||
| chr16:68156747 | T | C | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1402-1122T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68156747 | |||||||
| chr16:68156854 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-1015G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68156854 | |||||||
| chr16:68156935 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-934T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68156935 | |||||||
| chr16:68157491 | G | A | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-378G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68157491 | |||||||
| chr16:68157501 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402-368A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68157501 | |||||||
| chr16:68157705 | A | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1402-164A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68157705 | |||||||
| chr16:68158194 | T | G | 5 | a0001c0001t0009g0123 a0001c0001t0009g0125 a0001c0001t0009g0126 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1601+126T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68158194 | |||||||
| chr16:68158465 | T | A | 1 | a0001c0001t0015g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1601+397T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68158465 | |||||||
| chr16:68158621 | C | A | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1601+553C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68158621 | |||||||
| chr16:68158769 | G | GA | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1601+701_1601+702i others(3): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68158769 | |||||||
| chr16:68159048 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1601+980A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159048 | |||||||
| chr16:68159404 | C | CT | 10 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0002g0160 others(7): Show |
10 | HG00741.hp2 HG01071.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1601+1352dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68159404 | ||||||
| chr16:68159404 | CT | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0110 others(3): Show |
6 | HG00639.hp1 HG00738.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601+1352delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68159404 | ||||||
| chr16:68159408 | T | C | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+1340T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159408 | |||||||
| chr16:68159409 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1601+1341T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159409 | |||||||
| chr16:68159415 | T | C | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+1347T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159415 | |||||||
| chr16:68159450 | G | GTC | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1601+1385_1601+138 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68159450 | ||||||
| chr16:68159493 | G | T | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601+1425G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159493 | |||||||
| chr16:68159579 | C | T | 1 | a0001c0001t0005g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1601+1511C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159579 | |||||||
| chr16:68159583 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1601+1515C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159583 | |||||||
| chr16:68159659 | G | A | 1 | a0001c0001t0002g0154 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1601+1591G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159659 | |||||||
| chr16:68159682 | T | C | 86 | a0001c0001t0001g0067 a0001c0001t0002g0129 a0001c0001t0002g0132 others(83): Show |
86 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.1601+1614T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159682 | |||||||
| chr16:68159852 | C | T | 1 | a0001c0001t0019g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1601+1784C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159852 | |||||||
| chr16:68159946 | C | T | 3 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 |
3 | HG00738.hp2 HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1601+1878C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68159946 | |||||||
| chr16:68160098 | C | T | 1 | a0001c0001t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1601+2030C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68160098 | |||||||
| chr16:68160381 | C | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0031 a0001c0001t0015g0032 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601+2313C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68160381 | |||||||
| chr16:68160693 | A | AT | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1601+2637dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68160693 | ||||||
| chr16:68160693 | AT | A | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1601+2637delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68160693 | ||||||
| chr16:68160708 | A | G | 1 | a0001c0001t0003g0042 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1601+2640A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68160708 | |||||||
| chr16:68160744 | T | G | 129 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(126): Show |
129 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.1601+2676T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68160744 | |||||||
| chr16:68160960 | CATCT | C | 100 | a0001c0001t0001g0067 a0001c0001t0002g0129 a0001c0001t0002g0132 others(97): Show |
100 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(97): Show |
intron_variant | MODIFIER | c.1601+2894_1601+289 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68160960 | ||||||
| chr16:68160986 | C | T | 5 | a0001c0001t0009g0123 a0001c0001t0009g0125 a0001c0001t0009g0126 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1601+2918C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68160986 | |||||||
| chr16:68161016 | A | G | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1601+2948A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68161016 | |||||||
| chr16:68161098 | A | G | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1601+3030A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68161098 | |||||||
| chr16:68161131 | C | T | 2 | a0001c0001t0002g0140 a0001c0001t0002g0173 |
2 | NA18978.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1601+3063C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68161131 | |||||||
| chr16:68161508 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1601+3440G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68161508 | |||||||
| chr16:68161692 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1601+3624A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68161692 | |||||||
| chr16:68161917 | A | G | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1601+3849A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68161917 | |||||||
| chr16:68161935 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1601+3867C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68161935 | |||||||
| chr16:68162226 | G | A | 1 | a0001c0001t0013g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1601+4158G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68162226 | |||||||
| chr16:68162293 | G | A | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1601+4225G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68162293 | |||||||
| chr16:68162438 | A | G | 2 | a0001c0001t0004g0163 a0001c0001t0004g0164 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1601+4370A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68162438 | |||||||
| chr16:68162589 | C | CT | 93 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(90): Show |
93 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.1602-4238dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68162589 | ||||||
| chr16:68162589 | C | CTT | 12 | a0001c0001t0001g0067 a0001c0001t0002g0140 a0001c0001t0009g0123 others(9): Show |
12 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1602-4239_1602-423 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68162589 | ||||||
| chr16:68162749 | A | T | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1602-4094A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68162749 | |||||||
| chr16:68162948 | TAAC | T | 86 | a0001c0001t0001g0067 a0001c0001t0002g0129 a0001c0001t0002g0132 others(83): Show |
86 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.1602-3891_1602-388 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68162948 | ||||||
| chr16:68162960 | C | T | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1602-3883C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68162960 | |||||||
| chr16:68163057 | G | A | 2 | a0003c0003t0011g0182 a0003c0003t0011g0183 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1602-3786G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163057 | |||||||
| chr16:68163204 | C | T | 1 | a0001c0001t0019g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1602-3639C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163204 | |||||||
| chr16:68163267 | G | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1602-3576G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163267 | |||||||
| chr16:68163273 | G | A | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1602-3570G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163273 | |||||||
| chr16:68163280 | G | A | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1602-3563G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163280 | |||||||
| chr16:68163342 | G | A | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1602-3501G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163342 | |||||||
| chr16:68163344 | G | A | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1602-3499G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163344 | |||||||
| chr16:68163438 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0091 a0001c0001t0005g0065 |
3 | HG02809.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1602-3405C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163438 | |||||||
| chr16:68163445 | G | GC | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1602-3397dupC | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 68163445 | ||||||
| chr16:68163471 | G | A | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1602-3372G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163471 | |||||||
| chr16:68163476 | T | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1602-3367T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163476 | |||||||
| chr16:68163516 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-3327G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163516 | |||||||
| chr16:68163578 | G | A | 9 | a0001c0001t0001g0067 a0001c0001t0009g0123 a0001c0001t0009g0124 others(6): Show |
9 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-3265G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163578 | |||||||
| chr16:68163610 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1602-3233C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163610 | |||||||
| chr16:68163621 | C | T | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1602-3222C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163621 | |||||||
| chr16:68163799 | C | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-3044C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163799 | |||||||
| chr16:68163820 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1602-3023C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163820 | |||||||
| chr16:68163821 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1602-3022G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163821 | |||||||
| chr16:68163962 | C | T | 50 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0002g0129 others(47): Show |
50 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1602-2881C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68163962 | |||||||
| chr16:68164006 | C | T | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1602-2837C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164006 | |||||||
| chr16:68164105 | A | G | 7 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602-2738A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164105 | |||||||
| chr16:68164154 | C | G | 1 | a0001c0001t0002g0160 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1602-2689C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164154 | |||||||
| chr16:68164158 | G | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0009g0076 |
3 | HG01975.hp1 HG02132.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1602-2685G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164158 | |||||||
| chr16:68164166 | G | A | 1 | a0001c0001t0013g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1602-2677G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164166 | |||||||
| chr16:68164185 | T | C | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1602-2658T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164185 | |||||||
| chr16:68164274 | C | T | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1602-2569C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164274 | |||||||
| chr16:68164311 | G | A | 1 | a0001c0001t0010g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1602-2532G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164311 | |||||||
| chr16:68164363 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1602-2480T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164363 | |||||||
| chr16:68164689 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1602-2154C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164689 | |||||||
| chr16:68164692 | G | A | 86 | a0001c0001t0001g0067 a0001c0001t0002g0129 a0001c0001t0002g0132 others(83): Show |
86 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.1602-2151G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164692 | |||||||
| chr16:68164750 | C | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-2093C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164750 | |||||||
| chr16:68164907 | A | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1602-1936A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68164907 | |||||||
| chr16:68165096 | A | C | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602-1747A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68165096 | |||||||
| chr16:68165154 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-1689A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68165154 | |||||||
| chr16:68165422 | A | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-1421A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68165422 | |||||||
| chr16:68165491 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-1352G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68165491 | |||||||
| chr16:68165615 | C | G | 3 | a0001c0001t0005g0009 a0001c0001t0005g0025 a0001c0001t0020g0029 |
3 | HG02451.hp2 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1602-1228C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68165615 | |||||||
| chr16:68165713 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1602-1130C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68165713 | |||||||
| chr16:68165898 | T | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-945T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68165898 | |||||||
| chr16:68166144 | T | C | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1602-699T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68166144 | |||||||
| chr16:68166213 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1602-630T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68166213 | |||||||
| chr16:68166226 | A | G | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1602-617A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68166226 | |||||||
| chr16:68166395 | C | A | 2 | a0001c0001t0015g0026 a0001c0001t0036g0030 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1602-448C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68166395 | |||||||
| chr16:68166595 | C | A | 1 | a0001c0001t0007g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1602-248C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68166595 | |||||||
| chr16:68166599 | T | A | 1 | a0001c0001t0007g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1602-244T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68166599 | |||||||
| chr16:68166645 | T | G | 1 | a0001c0001t0027g0068 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1602-198T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68166645 | |||||||
| chr16:68166718 | A | G | 5 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(2): Show |
5 | HG01099.hp2 HG01255.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602-125A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 4/9 | chr16 | 68166718 | |||||||
| chr16:68167095 | G | A | 1 | a0001c0001t0006g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1774+80G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68167095 | |||||||
| chr16:68167282 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1774+267A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68167282 | |||||||
| chr16:68167810 | C | CT | 15 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0058 others(12): Show |
15 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1774+834dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTT | 24 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0062 others(21): Show |
24 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1774+833_1774+834d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTT | 8 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0051 others(5): Show |
8 | HG02109.hp1 HG02572.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1774+832_1774+834d others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTTT | 5 | a0001c0001t0001g0063 a0001c0001t0001g0087 a0001c0001t0003g0069 others(2): Show |
5 | HG02027.hp2 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1774+831_1774+834d others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0036 a0001c0001t0001g0092 a0001c0001t0006g0112 others(2): Show |
5 | HG01256.hp2 HG01433.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1774+826_1774+834d others(11): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0039 a0001c0001t0016g0184 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1774+825_1774+834d others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0074 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1774+824_1774+834d others(13): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1774+822_1774+834d others(15): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0070 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1774+820_1774+834d others(17): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0091 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1774+819_1774+834d others(18): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | C | CTTTTTTT others(14): Show |
1 | a0003c0003t0011g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1774+814_1774+834d others(23): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0001c0001t0004g0157 others(3): Show |
6 | HG01175.hp2 HG02572.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1774+826_1774+834d others(11): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0002g0135 a0001c0001t0002g0148 a0001c0001t0002g0149 others(5): Show |
8 | HG00741.hp1 HG03486.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+825_1774+834d others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(4): Show |
C | 31 | a0001c0001t0001g0037 a0001c0001t0002g0129 a0001c0001t0002g0132 others(28): Show |
31 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1774+824_1774+834d others(13): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0002g0136 a0001c0001t0002g0138 a0001c0001t0002g0139 others(12): Show |
15 | HG01109.hp2 HG02132.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.1774+823_1774+834d others(14): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0005g0009 a0001c0001t0005g0065 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1774+822_1774+834d others(15): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1774+819_1774+834d others(18): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(10): Show |
C | 2 | a0001c0001t0012g0185 a0001c0001t0028g0040 |
2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1774+818_1774+834d others(19): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(15): Show |
C | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1774+813_1774+834d others(24): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167810 | CTTTTTTT others(20): Show |
C | 1 | a0006c0007t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1774+808_1774+834d others(29): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68167810 | ||||||
| chr16:68167892 | T | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+877T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68167892 | |||||||
| chr16:68167975 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1774+960G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68167975 | |||||||
| chr16:68168048 | G | T | 1 | a0001c0001t0023g0137 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1774+1033G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168048 | |||||||
| chr16:68168471 | TTTA | T | 67 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(64): Show |
67 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1774+1483_1774+148 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68168471 | ||||||
| chr16:68168471 | TTTATTA | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+1480_1774+148 others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68168471 | ||||||
| chr16:68168472 | T | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1774+1457T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168472 | |||||||
| chr16:68168495 | A | T | 1 | a0001c0001t0003g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1774+1480A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168495 | |||||||
| chr16:68168498 | A | T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0082 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1774+1483A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168498 | |||||||
| chr16:68168554 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+1539T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168554 | |||||||
| chr16:68168585 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1774+1570A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168585 | |||||||
| chr16:68168652 | A | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+1637A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168652 | |||||||
| chr16:68168783 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1774+1768C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168783 | |||||||
| chr16:68168844 | C | T | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1774+1829C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168844 | |||||||
| chr16:68169010 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+1995C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169010 | |||||||
| chr16:68169325 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1774+2310A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169325 | |||||||
| chr16:68169457 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1774+2442T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169457 | |||||||
| chr16:68169531 | G | C | 1 | a0002c0002t0014g0177 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1774+2516G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169531 | |||||||
| chr16:68169613 | C | T | 2 | a0001c0001t0002g0135 a0001c0001t0002g0153 |
2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1774+2598C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169613 | |||||||
| chr16:68169666 | C | T | 1 | a0001c0001t0006g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1774+2651C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169666 | |||||||
| chr16:68169668 | C | G | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1774+2653C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169668 | |||||||
| chr16:68169762 | G | A | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1774+2747G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169762 | |||||||
| chr16:68169811 | C | T | 1 | a0001c0001t0004g0157 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1774+2796C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68169811 | |||||||
| chr16:68170140 | C | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1774+3125C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68170140 | |||||||
| chr16:68170386 | C | CA | 81 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0058 others(78): Show |
81 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.1774+3388dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68170386 | ||||||
| chr16:68170386 | C | CAA | 15 | a0001c0001t0002g0148 a0001c0001t0002g0153 a0001c0001t0002g0168 others(12): Show |
15 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1774+3387_1774+338 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68170386 | ||||||
| chr16:68170494 | C | CT | 8 | a0001c0001t0001g0051 a0001c0001t0003g0053 a0001c0001t0008g0012 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+3495dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68170494 | ||||||
| chr16:68170880 | T | G | 1 | a0001c0001t0004g0155 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1775-3494T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68170880 | |||||||
| chr16:68170886 | C | CTT | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1775-3488_1775-348 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68170886 | |||||||
| chr16:68171121 | G | A | 1 | a0001c0001t0007g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1775-3253G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171121 | |||||||
| chr16:68171151 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1775-3223G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171151 | |||||||
| chr16:68171209 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1775-3165A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171209 | |||||||
| chr16:68171311 | T | A | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1775-3063T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171311 | |||||||
| chr16:68171325 | TTACTTAG others(4): Show |
T | 1 | a0001c0001t0001g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1775-3045_1775-303 others(15): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68171325 | ||||||
| chr16:68171406 | T | C | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1775-2968T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171406 | |||||||
| chr16:68171473 | C | CT | 10 | a0001c0001t0004g0156 a0001c0001t0013g0001 a0001c0001t0013g0003 others(7): Show |
10 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1775-2886dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68171473 | ||||||
| chr16:68171519 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1775-2855G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171519 | |||||||
| chr16:68171665 | G | A | 1 | a0001c0001t0005g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1775-2709G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171665 | |||||||
| chr16:68171750 | C | T | 1 | a0001c0001t0008g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1775-2624C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171750 | |||||||
| chr16:68171753 | A | G | 58 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(55): Show |
58 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1775-2621A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171753 | |||||||
| chr16:68171769 | C | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-2605C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68171769 | |||||||
| chr16:68172001 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1775-2373A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172001 | |||||||
| chr16:68172008 | C | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-2366C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172008 | |||||||
| chr16:68172068 | C | T | 7 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1775-2306C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172068 | |||||||
| chr16:68172077 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1775-2297C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172077 | |||||||
| chr16:68172124 | C | T | 2 | a0004c0005t0004g0147 a0004c0005t0022g0146 |
2 | NA18940.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1775-2250C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172124 | |||||||
| chr16:68172532 | C | T | 2 | a0001c0001t0009g0125 a0001c0001t0009g0126 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1775-1842C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172532 | |||||||
| chr16:68172680 | G | A | 1 | a0001c0001t0006g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1775-1694G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172680 | |||||||
| chr16:68172820 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0092 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1775-1554A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172820 | |||||||
| chr16:68172872 | A | G | 1 | a0001c0001t0004g0155 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1775-1502A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172872 | |||||||
| chr16:68172936 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-1438G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172936 | |||||||
| chr16:68172940 | C | T | 2 | a0001c0001t0007g0078 a0001c0001t0007g0079 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1775-1434C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172940 | |||||||
| chr16:68172941 | G | A | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1775-1433G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68172941 | |||||||
| chr16:68173063 | C | T | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1775-1311C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173063 | |||||||
| chr16:68173064 | C | G | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1775-1310C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173064 | |||||||
| chr16:68173124 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1775-1250C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173124 | |||||||
| chr16:68173292 | C | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1775-1082C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173292 | |||||||
| chr16:68173410 | T | TA | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-957dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 68173410 | ||||||
| chr16:68173545 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1775-829C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173545 | |||||||
| chr16:68173549 | A | G | 1 | a0001c0001t0013g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1775-825A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173549 | |||||||
| chr16:68173663 | G | A | 1 | a0001c0001t0023g0137 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1775-711G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173663 | |||||||
| chr16:68173724 | C | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1775-650C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173724 | |||||||
| chr16:68173748 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1775-626A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173748 | |||||||
| chr16:68173838 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1775-536C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173838 | |||||||
| chr16:68173868 | G | C | 1 | a0001c0001t0003g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1775-506G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68173868 | |||||||
| chr16:68174054 | G | A | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1775-320G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68174054 | |||||||
| chr16:68174140 | C | G | 1 | a0001c0001t0002g0143 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1775-234C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68174140 | |||||||
| chr16:68174245 | A | T | 1 | a0001c0001t0032g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1775-129A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68174245 | |||||||
| chr16:68174646 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1915+132A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68174646 | |||||||
| chr16:68174728 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1915+214G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68174728 | |||||||
| chr16:68174888 | A | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1915+374A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68174888 | |||||||
| chr16:68175053 | A | C | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1915+539A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68175053 | |||||||
| chr16:68175596 | G | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0055 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1915+1082G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68175596 | |||||||
| chr16:68175701 | C | T | 1 | a0001c0001t0006g0113 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1915+1187C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68175701 | |||||||
| chr16:68175838 | G | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1915+1324G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68175838 | |||||||
| chr16:68175853 | G | A | 1 | a0001c0001t0008g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1915+1339G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68175853 | |||||||
| chr16:68175874 | A | G | 3 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0029g0002 |
3 | HG01891.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1915+1360A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68175874 | |||||||
| chr16:68175969 | T | C | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1915+1455T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68175969 | |||||||
| chr16:68176007 | C | G | 3 | a0001c0001t0004g0131 a0001c0001t0004g0150 a0001c0001t0019g0170 |
3 | HG02055.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1915+1493C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68176007 | |||||||
| chr16:68176087 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1915+1573C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68176087 | |||||||
| chr16:68176262 | T | C | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1915+1748T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68176262 | |||||||
| chr16:68176350 | C | CTT | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1915+1849_1915+185 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 68176350 | ||||||
| chr16:68176617 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1915+2103A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68176617 | |||||||
| chr16:68176701 | A | G | 83 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.1915+2187A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68176701 | |||||||
| chr16:68176706 | A | G | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1915+2192A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68176706 | |||||||
| chr16:68176965 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1915+2451C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68176965 | |||||||
| chr16:68177032 | C | CT | 48 | a0001c0001t0001g0060 a0001c0001t0002g0129 a0001c0001t0002g0133 others(45): Show |
48 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.1915+2532dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 68177032 | ||||||
| chr16:68177032 | C | CTT | 5 | a0001c0001t0004g0131 a0001c0001t0004g0150 a0001c0001t0019g0170 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1915+2531_1915+253 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 68177032 | ||||||
| chr16:68177044 | T | G | 1 | a0001c0001t0005g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1915+2530T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68177044 | |||||||
| chr16:68177047 | G | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1915+2533G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68177047 | |||||||
| chr16:68177254 | T | C | 50 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(47): Show |
50 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1915+2740T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68177254 | |||||||
| chr16:68177340 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1915+2826T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68177340 | |||||||
| chr16:68177418 | A | G | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1915+2904A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68177418 | |||||||
| chr16:68177579 | ACTT | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1915+3069_1915+307 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 68177579 | ||||||
| chr16:68177751 | TTA | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1915+3239_1915+324 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 68177751 | ||||||
| chr16:68177843 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1915+3329C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68177843 | |||||||
| chr16:68177860 | A | G | 1 | a0001c0001t0027g0068 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1915+3346A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68177860 | |||||||
| chr16:68178221 | C | G | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1916-3254C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68178221 | |||||||
| chr16:68178274 | T | G | 7 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1916-3201T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68178274 | |||||||
| chr16:68178640 | G | A | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1916-2835G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68178640 | |||||||
| chr16:68178711 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0003g0069 a0001c0008t0001g0114 |
3 | HG01070.hp2 NA18953.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1916-2764C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68178711 | |||||||
| chr16:68178738 | C | G | 1 | a0001c0001t0021g0158 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1916-2737C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68178738 | |||||||
| chr16:68178917 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1916-2558C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68178917 | |||||||
| chr16:68179056 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1916-2419A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179056 | |||||||
| chr16:68179117 | C | T | 1 | a0001c0001t0013g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1916-2358C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179117 | |||||||
| chr16:68179173 | C | T | 1 | a0001c0001t0005g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1916-2302C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179173 | |||||||
| chr16:68179222 | C | T | 1 | a0001c0001t0006g0122 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1916-2253C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179222 | |||||||
| chr16:68179285 | T | C | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1916-2190T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179285 | |||||||
| chr16:68179447 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1916-2028A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179447 | |||||||
| chr16:68179696 | T | G | 1 | a0003c0003t0011g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1916-1779T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179696 | |||||||
| chr16:68179718 | G | C | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1916-1757G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179718 | |||||||
| chr16:68179777 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1916-1698C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68179777 | |||||||
| chr16:68180032 | G | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1916-1443G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68180032 | |||||||
| chr16:68180040 | G | A | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1916-1435G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68180040 | |||||||
| chr16:68180237 | T | G | 7 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1916-1238T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68180237 | |||||||
| chr16:68180628 | C | T | 2 | a0006c0007t0001g0093 a0007c0010t0001g0121 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1916-847C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68180628 | |||||||
| chr16:68180750 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1916-725C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68180750 | |||||||
| chr16:68181389 | A | T | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1916-86A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 6/9 | chr16 | 68181389 | |||||||
| chr16:68181869 | G | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00738.hp1 HG02572.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1971+339G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68181869 | |||||||
| chr16:68182083 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1971+553C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68182083 | |||||||
| chr16:68182169 | A | G | 58 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(55): Show |
58 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1971+639A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68182169 | |||||||
| chr16:68182192 | T | A | 1 | a0001c0001t0010g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1971+662T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68182192 | |||||||
| chr16:68182625 | A | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972-615A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68182625 | |||||||
| chr16:68182799 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1972-441A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68182799 | |||||||
| chr16:68182836 | G | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1972-404G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68182836 | |||||||
| chr16:68183031 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972-209A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68183031 | |||||||
| chr16:68183153 | A | G | 1 | a0001c0001t0015g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1972-87A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 7/9 | chr16 | 68183153 | |||||||
| chr16:68183779 | G | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2098+413G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68183779 | |||||||
| chr16:68183785 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2098+419C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68183785 | |||||||
| chr16:68184004 | C | CA | 66 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(63): Show |
66 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.2098+659dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68184004 | ||||||
| chr16:68184004 | C | CAA | 7 | a0001c0001t0002g0153 a0001c0001t0004g0145 a0001c0001t0004g0156 others(4): Show |
7 | HG00438.hp2 HG01891.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.2098+658_2098+659d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68184004 | ||||||
| chr16:68184004 | CA | C | 11 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0176 others(8): Show |
11 | HG01346.hp2 HG01884.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.2098+659delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68184004 | ||||||
| chr16:68184022 | A | G | 1 | a0001c0001t0005g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2098+656A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184022 | |||||||
| chr16:68184062 | T | A | 2 | a0001c0001t0001g0110 a0001c0001t0030g0109 |
2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2098+696T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184062 | |||||||
| chr16:68184076 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2098+710C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184076 | |||||||
| chr16:68184406 | A | G | 1 | a0001c0001t0016g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2098+1040A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184406 | |||||||
| chr16:68184420 | T | C | 1 | a0001c0001t0003g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2098+1054T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184420 | |||||||
| chr16:68184433 | G | A | 145 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(142): Show |
145 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(142): Show |
intron_variant | MODIFIER | c.2098+1067G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184433 | |||||||
| chr16:68184566 | G | C | 1 | a0001c0001t0009g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2098+1200G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184566 | |||||||
| chr16:68184585 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0005g0065 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2098+1219C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184585 | |||||||
| chr16:68184599 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2098+1233C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184599 | |||||||
| chr16:68184783 | A | C | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.2098+1417A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184783 | |||||||
| chr16:68184787 | G | C | 1 | a0001c0001t0007g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2098+1421G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184787 | |||||||
| chr16:68184790 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2098+1424C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184790 | |||||||
| chr16:68184806 | A | AAAAC | 4 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0003g0069 others(1): Show |
4 | HG01070.hp2 NA18953.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2098+1468_2098+147 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68184806 | ||||||
| chr16:68184806 | AAAAC | A | 52 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(49): Show |
52 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2098+1468_2098+147 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68184806 | ||||||
| chr16:68184845 | C | CAG | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.2098+1480_2098+148 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68184845 | ||||||
| chr16:68184924 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2098+1558A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184924 | |||||||
| chr16:68184991 | T | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.2098+1625T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68184991 | |||||||
| chr16:68185000 | G | T | 9 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(6): Show |
9 | HG01109.hp2 HG02622.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2098+1634G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185000 | |||||||
| chr16:68185001 | A | T | 9 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(6): Show |
9 | HG01109.hp2 HG02622.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2098+1635A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185001 | |||||||
| chr16:68185179 | G | A | 1 | a0001c0001t0019g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2098+1813G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185179 | |||||||
| chr16:68185220 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2098+1854G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185220 | |||||||
| chr16:68185412 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2098+2046G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185412 | |||||||
| chr16:68185604 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2098+2238G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185604 | |||||||
| chr16:68185661 | G | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2098+2295G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185661 | |||||||
| chr16:68185811 | C | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2098+2445C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185811 | |||||||
| chr16:68185862 | C | CA | 33 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0060 others(30): Show |
33 | HG00438.hp2 HG00639.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.2098+2518dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68185862 | ||||||
| chr16:68185862 | C | CAA | 8 | a0001c0001t0002g0160 a0001c0001t0004g0150 a0001c0001t0009g0123 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.2098+2517_2098+251 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68185862 | ||||||
| chr16:68185862 | CA | C | 11 | a0001c0001t0002g0151 a0001c0001t0008g0013 a0001c0001t0008g0014 others(8): Show |
11 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.2098+2518delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68185862 | ||||||
| chr16:68185914 | G | A | 1 | a0001c0001t0004g0155 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2098+2548G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185914 | |||||||
| chr16:68185959 | A | G | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2098+2593A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185959 | |||||||
| chr16:68185989 | T | C | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2098+2623T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68185989 | |||||||
| chr16:68186035 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2098+2669G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68186035 | |||||||
| chr16:68186066 | A | G | 97 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(94): Show |
97 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.2098+2700A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68186066 | |||||||
| chr16:68186667 | G | A | 2 | a0001c0001t0009g0125 a0001c0001t0009g0126 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2098+3301G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68186667 | |||||||
| chr16:68186778 | CTGTTATG others(4): Show |
C | 5 | a0001c0001t0007g0057 a0001c0001t0007g0059 a0001c0001t0007g0061 others(2): Show |
5 | HG00639.hp1 HG01192.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2098+3419_2098+342 others(15): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68186778 | ||||||
| chr16:68186856 | G | A | 1 | a0001c0001t0030g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2098+3490G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68186856 | |||||||
| chr16:68186929 | C | T | 1 | a0001c0001t0015g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2098+3563C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68186929 | |||||||
| chr16:68187065 | G | A | 1 | a0001c0001t0006g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2098+3699G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68187065 | |||||||
| chr16:68187095 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2099-3673A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68187095 | |||||||
| chr16:68187199 | C | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.2099-3569C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68187199 | |||||||
| chr16:68187414 | G | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0082 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2099-3354G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68187414 | |||||||
| chr16:68187520 | AAG | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2099-3246_2099-324 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 68187520 | ||||||
| chr16:68188065 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2099-2703C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188065 | |||||||
| chr16:68188108 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2099-2660A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188108 | |||||||
| chr16:68188229 | G | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2099-2539G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188229 | |||||||
| chr16:68188347 | C | A | 1 | a0001c0001t0003g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2099-2421C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188347 | |||||||
| chr16:68188387 | G | A | 1 | a0001c0001t0009g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2099-2381G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188387 | |||||||
| chr16:68188419 | G | C | 2 | a0001c0001t0009g0125 a0001c0001t0009g0126 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2099-2349G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188419 | |||||||
| chr16:68188672 | T | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2099-2096T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188672 | |||||||
| chr16:68188730 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0176 |
2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2099-2038C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188730 | |||||||
| chr16:68188745 | G | C | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2099-2023G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188745 | |||||||
| chr16:68188979 | A | T | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2099-1789A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68188979 | |||||||
| chr16:68189053 | A | G | 3 | a0001c0001t0004g0145 a0004c0005t0004g0147 a0004c0005t0022g0146 |
3 | HG00438.hp2 NA18940.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2099-1715A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68189053 | |||||||
| chr16:68189496 | G | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2099-1272G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68189496 | |||||||
| chr16:68189632 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2099-1136A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68189632 | |||||||
| chr16:68190013 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2099-755T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68190013 | |||||||
| chr16:68190115 | C | T | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.2099-653C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68190115 | |||||||
| chr16:68190274 | A | T | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2099-494A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68190274 | |||||||
| chr16:68190546 | C | T | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2099-222C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68190546 | |||||||
| chr16:68190626 | C | T | 8 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0080 others(5): Show |
8 | HG00738.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2099-142C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68190626 | |||||||
| chr16:68190679 | C | T | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.2099-89C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 8/9 | chr16 | 68190679 | |||||||
| chr16:68192115 | G | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3106+340G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192115 | |||||||
| chr16:68192210 | G | GGAAAA | 3 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 |
3 | HG02572.hp2 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3106+435_3106+436i others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192210 | |||||||
| chr16:68192210 | GA | G | 17 | a0001c0001t0002g0129 a0001c0001t0002g0133 a0001c0001t0002g0135 others(14): Show |
17 | HG01099.hp2 HG01255.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.3106+456delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192210 | ||||||
| chr16:68192210 | GAA | G | 7 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0144 others(4): Show |
7 | HG00639.hp2 HG01256.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3106+455_3106+456d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192210 | ||||||
| chr16:68192224 | A | AT | 2 | a0001c0001t0003g0041 a0007c0010t0001g0121 |
2 | HG02486.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.3106+449_3106+450i others(3): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192224 | |||||||
| chr16:68192226 | A | AAT | 13 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0055 others(10): Show |
13 | HG02886.hp1 HG02895.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.3106+452_3106+453i others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192226 | ||||||
| chr16:68192226 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3106+452_3106+453i others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192226 | ||||||
| chr16:68192226 | A | AATATATA others(31): Show |
1 | a0001c0001t0001g0117 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3106+452_3106+453i others(40): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192226 | ||||||
| chr16:68192226 | A | AT | 5 | a0001c0001t0001g0035 a0001c0001t0004g0162 a0001c0001t0006g0105 others(2): Show |
5 | HG01175.hp1 HG01192.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.3106+451_3106+452i others(3): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192226 | |||||||
| chr16:68192226 | A | ATAT | 2 | a0001c0001t0001g0033 a0001c0001t0009g0076 |
2 | HG02132.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.3106+451_3106+452i others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192226 | |||||||
| chr16:68192226 | A | ATATAT | 2 | a0001c0001t0007g0077 a0001c0001t0028g0040 |
2 | HG00639.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3106+451_3106+452i others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192226 | |||||||
| chr16:68192226 | A | T | 3 | a0001c0001t0001g0049 a0001c0001t0003g0041 a0007c0010t0001g0121 |
3 | HG02109.hp1 HG02486.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.3106+451A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192226 | |||||||
| chr16:68192228 | A | AAT | 7 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0063 others(4): Show |
7 | HG02027.hp2 HG02809.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.3106+454_3106+455i others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192228 | ||||||
| chr16:68192228 | A | AATAT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+454_3106+455i others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192228 | ||||||
| chr16:68192228 | A | AATATATA others(3): Show |
1 | a0001c0001t0007g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3106+454_3106+455i others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192228 | ||||||
| chr16:68192228 | A | AT | 7 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0003g0044 others(4): Show |
7 | HG00438.hp1 HG01071.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.3106+453_3106+454i others(3): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192228 | |||||||
| chr16:68192228 | A | ATAT | 9 | a0001c0001t0001g0045 a0001c0001t0001g0066 a0001c0001t0001g0080 others(6): Show |
9 | HG00738.hp1 HG01256.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.3106+453_3106+454i others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192228 | |||||||
| chr16:68192228 | A | ATATAT | 2 | a0001c0001t0001g0084 a0001c0001t0001g0087 |
2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3106+453_3106+454i others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192228 | |||||||
| chr16:68192228 | A | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0035 others(42): Show |
45 | HG00639.hp1 HG01099.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.3106+453A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192228 | |||||||
| chr16:68192230 | A | AAAAAAAA others(10): Show |
2 | a0003c0003t0011g0182 a0003c0003t0011g0183 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3106+456_3106+457i others(19): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192230 | ||||||
| chr16:68192230 | A | AAAAAAAT others(20): Show |
1 | a0003c0003t0011g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3106+456_3106+457i others(29): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192230 | ||||||
| chr16:68192230 | A | AAAAAT | 5 | a0001c0001t0005g0009 a0001c0001t0009g0125 a0001c0001t0009g0126 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3106+456_3106+457i others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192230 | ||||||
| chr16:68192230 | A | AAATAT | 6 | a0001c0001t0005g0023 a0001c0001t0009g0123 a0001c0001t0013g0004 others(3): Show |
6 | HG01346.hp1 HG02818.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+456_3106+457i others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192230 | ||||||
| chr16:68192230 | A | AAATATAT others(10): Show |
1 | a0001c0001t0008g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3106+456_3106+457i others(19): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192230 | ||||||
| chr16:68192230 | A | AT | 3 | a0001c0001t0001g0058 a0001c0001t0002g0165 a0001c0001t0004g0155 |
3 | HG03491.hp2 HG03579.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3106+455_3106+456i others(3): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192230 | |||||||
| chr16:68192230 | A | ATAT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0081 others(3): Show |
6 | HG01109.hp1 HG02630.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3106+455_3106+456i others(5): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192230 | |||||||
| chr16:68192230 | A | ATATAT | 2 | a0001c0001t0001g0085 a0001c0001t0010g0010 |
2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3106+455_3106+456i others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192230 | |||||||
| chr16:68192230 | A | T | 92 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0035 others(89): Show |
92 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.3106+455A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192230 | |||||||
| chr16:68192230 | AAT | A | 10 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0160 others(7): Show |
10 | HG00438.hp2 HG01175.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.3106+478_3106+479d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192230 | ||||||
| chr16:68192231 | AT | A | 4 | a0001c0001t0002g0139 a0001c0001t0002g0142 a0001c0001t0002g0143 others(1): Show |
4 | HG03704.hp2 HG03942.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+457delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192231 | |||||||
| chr16:68192232 | T | A | 7 | a0001c0001t0005g0021 a0001c0001t0005g0175 a0001c0001t0012g0185 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3106+457T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192232 | |||||||
| chr16:68192234 | T | A | 6 | a0001c0001t0002g0151 a0001c0001t0004g0145 a0001c0001t0012g0187 others(3): Show |
6 | HG00438.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+459T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192234 | |||||||
| chr16:68192243 | A | ATATATAT others(33): Show |
1 | a0001c0001t0008g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3106+479_3106+480i others(42): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192243 | ||||||
| chr16:68192247 | A | G | 6 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+472A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192247 | |||||||
| chr16:68192251 | A | ATGTATG | 2 | a0003c0003t0011g0182 a0003c0003t0011g0183 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3106+477_3106+478i others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192251 | ||||||
| chr16:68192251 | A | G | 6 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+476A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192251 | |||||||
| chr16:68192261 | G | GTA | 35 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0050 others(32): Show |
35 | HG00639.hp1 HG01070.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.3106+496_3106+497d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192261 | ||||||
| chr16:68192263 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0005g0099 |
2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3106+488A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192263 | |||||||
| chr16:68192267 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+492A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192267 | |||||||
| chr16:68192279 | G | GTA | 5 | a0001c0001t0009g0123 a0001c0001t0009g0125 a0001c0001t0009g0126 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.3106+514_3106+515d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192279 | ||||||
| chr16:68192291 | G | A | 1 | a0001c0001t0009g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3106+516G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192291 | |||||||
| chr16:68192293 | A | G | 1 | a0001c0001t0009g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3106+518A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192293 | |||||||
| chr16:68192295 | G | A | 1 | a0001c0001t0009g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3106+520G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192295 | |||||||
| chr16:68192301 | A | G | 2 | a0001c0001t0009g0124 a0001c0001t0013g0004 |
2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3106+526A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192301 | |||||||
| chr16:68192319 | G | GTA | 38 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(35): Show |
38 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.3106+557_3106+558d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192319 | ||||||
| chr16:68192319 | G | GTATA | 6 | a0001c0001t0002g0149 a0001c0001t0012g0185 a0001c0001t0012g0187 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+555_3106+558d others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192319 | ||||||
| chr16:68192321 | A | G | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3106+546A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192321 | |||||||
| chr16:68192332 | T | G | 7 | a0001c0001t0001g0049 a0001c0001t0001g0067 a0001c0001t0001g0098 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3106+557T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192332 | |||||||
| chr16:68192332 | T | TAG | 8 | a0001c0001t0002g0129 a0001c0001t0002g0136 a0001c0001t0002g0142 others(5): Show |
8 | HG03669.hp2 HG03704.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+579_3106+580d others(4): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192332 | ||||||
| chr16:68192332 | T | TATAG | 2 | a0001c0001t0002g0144 a0001c0001t0002g0165 |
2 | HG00639.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.3106+558_3106+559i others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192332 | ||||||
| chr16:68192332 | TAGAG | T | 6 | a0001c0001t0001g0101 a0001c0001t0021g0158 a0001c0001t0031g0052 others(3): Show |
6 | HG01169.hp2 HG02080.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+577_3106+580d others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192332 | ||||||
| chr16:68192332 | TAGAGAGA others(3): Show |
T | 1 | a0001c0001t0008g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3106+571_3106+580d others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68192332 | ||||||
| chr16:68192334 | G | T | 69 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0056 others(66): Show |
69 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.3106+559G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192334 | |||||||
| chr16:68192336 | G | T | 27 | a0001c0001t0005g0009 a0001c0001t0005g0022 a0001c0001t0005g0023 others(24): Show |
27 | HG00741.hp2 HG01109.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.3106+561G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192336 | |||||||
| chr16:68192338 | G | T | 13 | a0001c0001t0005g0023 a0001c0001t0005g0027 a0001c0001t0006g0115 others(10): Show |
13 | HG01109.hp2 HG01169.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3106+563G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192338 | |||||||
| chr16:68192340 | G | T | 2 | a0003c0003t0011g0182 a0003c0003t0011g0183 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3106+565G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192340 | |||||||
| chr16:68192342 | G | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3106+567G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192342 | |||||||
| chr16:68192344 | G | T | 1 | a0001c0001t0008g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3106+569G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68192344 | |||||||
| chr16:68193114 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+1339A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193114 | |||||||
| chr16:68193225 | A | G | 1 | a0001c0001t0030g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3106+1450A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193225 | |||||||
| chr16:68193247 | C | T | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3106+1472C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193247 | |||||||
| chr16:68193280 | TG | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+1507delG | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68193280 | ||||||
| chr16:68193282 | G | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+1507G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193282 | |||||||
| chr16:68193283 | T | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+1508T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193283 | |||||||
| chr16:68193367 | C | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3106+1592C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193367 | |||||||
| chr16:68193629 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3106+1854A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193629 | |||||||
| chr16:68193663 | C | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3106+1888C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193663 | |||||||
| chr16:68193773 | C | CA | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+1999dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68193773 | ||||||
| chr16:68193877 | A | G | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3106+2102A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193877 | |||||||
| chr16:68193931 | G | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+2156G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68193931 | |||||||
| chr16:68194048 | C | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+2273C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68194048 | |||||||
| chr16:68194070 | T | C | 1 | a0001c0001t0006g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3106+2295T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68194070 | |||||||
| chr16:68194197 | G | C | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3106+2422G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68194197 | |||||||
| chr16:68194216 | T | C | 75 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(72): Show |
75 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.3106+2441T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68194216 | |||||||
| chr16:68194270 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3106+2495C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68194270 | |||||||
| chr16:68194284 | A | G | 1 | a0001c0001t0008g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3106+2509A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68194284 | |||||||
| chr16:68194326 | C | T | 1 | a0001c0001t0009g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3106+2551C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68194326 | |||||||
| chr16:68194524 | C | T | 57 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(54): Show |
57 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.3106+2749C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68194524 | |||||||
| chr16:68194852 | ATATAT | A | 9 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(6): Show |
9 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.3106+3080_3106+308 others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68194852 | ||||||
| chr16:68195164 | A | T | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3106+3389A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195164 | |||||||
| chr16:68195210 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3106+3435G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195210 | |||||||
| chr16:68195220 | A | G | 2 | a0001c0001t0007g0059 a0001c0001t0007g0077 |
2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.3106+3445A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195220 | |||||||
| chr16:68195242 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3106+3467C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195242 | |||||||
| chr16:68195345 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3106+3570A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195345 | |||||||
| chr16:68195399 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3106+3624A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195399 | |||||||
| chr16:68195499 | G | A | 1 | a0001c0001t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3106+3724G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195499 | |||||||
| chr16:68195676 | T | TGGTCGC | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3106+3902_3106+390 others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68195676 | ||||||
| chr16:68195679 | T | A | 2 | a0001c0001t0009g0125 a0001c0001t0009g0126 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3106+3904T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195679 | |||||||
| chr16:68195733 | A | G | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3106+3958A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195733 | |||||||
| chr16:68195734 | A | G | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3106+3959A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195734 | |||||||
| chr16:68195757 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3106+3982G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68195757 | |||||||
| chr16:68196170 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3106+4395A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68196170 | |||||||
| chr16:68196229 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3106+4454C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68196229 | |||||||
| chr16:68196619 | G | A | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3106+4844G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68196619 | |||||||
| chr16:68196659 | G | A | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+4884G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68196659 | |||||||
| chr16:68196860 | G | A | 1 | a0001c0001t0003g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3106+5085G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68196860 | |||||||
| chr16:68196926 | A | T | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+5151A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68196926 | |||||||
| chr16:68196945 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3106+5170G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68196945 | |||||||
| chr16:68196971 | G | C | 1 | a0001c0001t0003g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3106+5196G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68196971 | |||||||
| chr16:68197034 | A | AAAAT | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0028g0040 |
3 | HG02486.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3106+5283_3106+528 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68197034 | ||||||
| chr16:68197034 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+5279_3106+528 others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68197034 | ||||||
| chr16:68197100 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3106+5325C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68197100 | |||||||
| chr16:68197108 | A | AT | 8 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(5): Show |
8 | HG01891.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+5342dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68197108 | ||||||
| chr16:68197318 | C | G | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3106+5543C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68197318 | |||||||
| chr16:68197602 | AGTCATAG others(3): Show |
A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3106+5828_3106+583 others(14): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68197602 | |||||||
| chr16:68198058 | G | A | 2 | a0001c0001t0002g0139 a0001c0001t0004g0141 |
2 | NA18973.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.3106+6283G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68198058 | |||||||
| chr16:68198314 | G | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+6539G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68198314 | |||||||
| chr16:68198396 | C | A | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+6621C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68198396 | |||||||
| chr16:68198804 | T | G | 1 | a0001c0001t0015g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3106+7029T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68198804 | |||||||
| chr16:68198876 | G | A | 3 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 |
3 | HG02922.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3106+7101G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68198876 | |||||||
| chr16:68199108 | C | T | 1 | a0001c0001t0004g0155 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3106+7333C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199108 | |||||||
| chr16:68199164 | T | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0055 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.3106+7389T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199164 | |||||||
| chr16:68199219 | T | A | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3106+7444T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199219 | |||||||
| chr16:68199226 | A | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3106+7451A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199226 | |||||||
| chr16:68199227 | T | TTTA | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3106+7454_3106+745 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68199227 | ||||||
| chr16:68199232 | TA | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3106+7458delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199232 | |||||||
| chr16:68199233 | A | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3106+7458A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199233 | |||||||
| chr16:68199247 | A | G | 83 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.3106+7472A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199247 | |||||||
| chr16:68199324 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0072 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3106+7549C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199324 | |||||||
| chr16:68199369 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3106+7594G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199369 | |||||||
| chr16:68199513 | C | T | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.3106+7738C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199513 | |||||||
| chr16:68199517 | C | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+7742C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199517 | |||||||
| chr16:68199520 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3106+7745G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199520 | |||||||
| chr16:68199537 | TA | T | 5 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0165 others(2): Show |
5 | HG01256.hp1 HG01975.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3106+7778delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68199537 | ||||||
| chr16:68199813 | C | T | 1 | a0001c0001t0007g0095 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3106+8038C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199813 | |||||||
| chr16:68199881 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3106+8106C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68199881 | |||||||
| chr16:68200402 | T | TTA | 2 | a0001c0001t0002g0165 a0001c0001t0017g0006 |
2 | HG02965.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.3106+8643_3106+864 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68200402 | ||||||
| chr16:68201006 | A | C | 1 | a0001c0001t0035g0106 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3106+9231A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201006 | |||||||
| chr16:68201149 | A | C | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.3106+9374A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201149 | |||||||
| chr16:68201368 | A | C | 1 | a0001c0001t0012g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3106+9593A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201368 | |||||||
| chr16:68201397 | G | A | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+9622G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201397 | |||||||
| chr16:68201419 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3106+9644T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201419 | |||||||
| chr16:68201648 | A | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+9873A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201648 | |||||||
| chr16:68201713 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3106+9938G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201713 | |||||||
| chr16:68201802 | A | AG | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+10028dupG | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68201802 | ||||||
| chr16:68201820 | CGATGGTG others(42): Show |
C | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3106+10046_3106+10 others(55): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201820 | |||||||
| chr16:68201861 | C | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+10086C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201861 | |||||||
| chr16:68201870 | A | C | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3106+10095A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201870 | |||||||
| chr16:68201957 | C | CA | 20 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0056 others(17): Show |
20 | HG00738.hp2 HG00741.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.3106+10209dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68201957 | ||||||
| chr16:68201957 | CA | C | 29 | a0001c0001t0001g0048 a0001c0001t0002g0132 a0001c0001t0002g0148 others(26): Show |
29 | HG00438.hp2 HG00741.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.3106+10209delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68201957 | ||||||
| chr16:68201957 | CAA | C | 7 | a0001c0001t0009g0124 a0001c0001t0009g0125 a0001c0001t0009g0126 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.3106+10208_3106+10 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68201957 | ||||||
| chr16:68201957 | CAAA | C | 16 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(13): Show |
16 | HG01346.hp1 HG01433.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3106+10207_3106+10 others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68201957 | ||||||
| chr16:68201977 | A | C | 1 | a0001c0001t0004g0155 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3106+10202A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68201977 | |||||||
| chr16:68202745 | G | T | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+10970G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68202745 | |||||||
| chr16:68202766 | C | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.3106+10991C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68202766 | |||||||
| chr16:68202832 | T | A | 1 | a0002c0002t0034g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3106+11057T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68202832 | |||||||
| chr16:68202833 | A | T | 1 | a0002c0002t0034g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3106+11058A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68202833 | |||||||
| chr16:68202836 | A | T | 1 | a0002c0002t0034g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3106+11061A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68202836 | |||||||
| chr16:68202838 | A | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3106+11063A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68202838 | |||||||
| chr16:68203118 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3106+11343A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68203118 | |||||||
| chr16:68203273 | G | A | 1 | a0001c0001t0005g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3106+11498G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68203273 | |||||||
| chr16:68203817 | G | A | 3 | a0001c0001t0004g0145 a0004c0005t0004g0147 a0004c0005t0022g0146 |
3 | HG00438.hp2 NA18940.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.3106+12042G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68203817 | |||||||
| chr16:68203857 | C | T | 1 | a0001c0001t0019g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3106+12082C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68203857 | |||||||
| chr16:68204294 | A | G | 83 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.3106+12519A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68204294 | |||||||
| chr16:68204491 | A | G | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+12716A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68204491 | |||||||
| chr16:68204608 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+12833C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68204608 | |||||||
| chr16:68204673 | TA | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+12901delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68204673 | ||||||
| chr16:68204749 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0055 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.3106+12974A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68204749 | |||||||
| chr16:68204993 | C | CT | 8 | a0001c0001t0002g0138 a0001c0001t0003g0118 a0001c0001t0010g0011 others(5): Show |
8 | HG02055.hp2 HG02071.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+13236dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68204993 | ||||||
| chr16:68204993 | CT | C | 9 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0084 others(6): Show |
9 | HG00741.hp1 HG01070.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.3106+13236delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68204993 | ||||||
| chr16:68205062 | A | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3106+13287A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68205062 | |||||||
| chr16:68205255 | G | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+13480G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68205255 | |||||||
| chr16:68205557 | T | C | 83 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.3106+13782T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68205557 | |||||||
| chr16:68205904 | C | CT | 15 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(12): Show |
15 | HG01891.hp1 HG02622.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.3106+14140dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68205904 | ||||||
| chr16:68205922 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3106+14147G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68205922 | |||||||
| chr16:68206282 | G | A | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.3106+14507G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68206282 | |||||||
| chr16:68206313 | A | G | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3106+14538A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68206313 | |||||||
| chr16:68206467 | G | A | 3 | a0001c0001t0004g0145 a0004c0005t0004g0147 a0004c0005t0022g0146 |
3 | HG00438.hp2 NA18940.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.3106+14692G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68206467 | |||||||
| chr16:68206567 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3106+14792C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68206567 | |||||||
| chr16:68206731 | C | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.3106+14956C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68206731 | |||||||
| chr16:68206778 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+15003A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68206778 | |||||||
| chr16:68206786 | C | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3106+15011C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68206786 | |||||||
| chr16:68207005 | TA | T | 12 | a0001c0001t0001g0045 a0001c0001t0001g0075 a0001c0001t0002g0132 others(9): Show |
12 | HG01256.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3106+15249delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68207005 | ||||||
| chr16:68207048 | C | T | 1 | a0001c0001t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3106+15273C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68207048 | |||||||
| chr16:68207110 | GA | G | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3106+15336delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68207110 | |||||||
| chr16:68207309 | TC | T | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+15535delC | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68207309 | |||||||
| chr16:68207310 | C | CA | 6 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+15549dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68207310 | ||||||
| chr16:68207310 | CA | C | 10 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 others(7): Show |
10 | HG01433.hp1 HG01891.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.3106+15549delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68207310 | ||||||
| chr16:68207311 | A | T | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+15536A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68207311 | |||||||
| chr16:68207428 | C | T | 2 | a0001c0001t0008g0015 a0001c0001t0008g0017 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3106+15653C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68207428 | |||||||
| chr16:68207705 | A | G | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.3106+15930A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68207705 | |||||||
| chr16:68207926 | T | TC | 83 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.3106+16151_3106+16 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68207926 | |||||||
| chr16:68207952 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3106+16177C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68207952 | |||||||
| chr16:68208031 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3106+16256A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68208031 | |||||||
| chr16:68208092 | G | A | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+16317G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68208092 | |||||||
| chr16:68208192 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3106+16417C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68208192 | |||||||
| chr16:68208408 | A | G | 50 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(47): Show |
50 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.3106+16633A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68208408 | |||||||
| chr16:68208488 | A | G | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3106+16713A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68208488 | |||||||
| chr16:68208670 | G | C | 58 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(55): Show |
58 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.3106+16895G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68208670 | |||||||
| chr16:68208728 | C | CA | 23 | a0001c0001t0001g0050 a0001c0001t0002g0129 a0001c0001t0007g0057 others(20): Show |
23 | HG01109.hp1 HG01258.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.3106+16964dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68208728 | ||||||
| chr16:68209151 | A | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3107-17199A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68209151 | |||||||
| chr16:68209362 | C | G | 1 | a0001c0001t0032g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3107-16988C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68209362 | |||||||
| chr16:68209362 | C | T | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3107-16988C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68209362 | |||||||
| chr16:68209583 | G | T | 102 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(99): Show |
102 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(99): Show |
intron_variant | MODIFIER | c.3107-16767G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68209583 | |||||||
| chr16:68209850 | G | GAC | 34 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(31): Show |
34 | HG00438.hp2 HG00639.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.3107-16483_3107-16 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68209850 | ||||||
| chr16:68209850 | G | GACAC | 8 | a0001c0001t0002g0129 a0001c0001t0002g0136 a0001c0001t0002g0161 others(5): Show |
8 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-16485_3107-16 others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68209850 | ||||||
| chr16:68209850 | GAC | G | 4 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0004g0141 others(1): Show |
4 | HG02132.hp2 NA18973.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.3107-16483_3107-16 others(8): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68209850 | ||||||
| chr16:68209981 | C | CATG | 97 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(94): Show |
97 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.3107-16367_3107-16 others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68209981 | ||||||
| chr16:68210063 | C | A | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-16287C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210063 | |||||||
| chr16:68210167 | G | A | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-16183G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210167 | |||||||
| chr16:68210256 | C | T | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3107-16094C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210256 | |||||||
| chr16:68210297 | CA | C | 89 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.3107-16040delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68210297 | ||||||
| chr16:68210298 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3107-16040_3107-16 others(19): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68210298 | ||||||
| chr16:68210309 | A | G | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3107-16041A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210309 | |||||||
| chr16:68210310 | A | G | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3107-16040A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210310 | |||||||
| chr16:68210310 | AG | A | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3107-16039delG | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210310 | |||||||
| chr16:68210311 | G | A | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3107-16039G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210311 | |||||||
| chr16:68210439 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-15911C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210439 | |||||||
| chr16:68210444 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3107-15906C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210444 | |||||||
| chr16:68210474 | AAAAAT | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-15871_3107-15 others(11): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68210474 | ||||||
| chr16:68210790 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3107-15560T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68210790 | |||||||
| chr16:68211046 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0176 |
2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3107-15304G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211046 | |||||||
| chr16:68211142 | T | G | 1 | a0001c0001t0003g0069 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3107-15208T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211142 | |||||||
| chr16:68211292 | A | G | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.3107-15058A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211292 | |||||||
| chr16:68211350 | G | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-15000G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211350 | |||||||
| chr16:68211428 | C | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3107-14922C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211428 | |||||||
| chr16:68211432 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-14918C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211432 | |||||||
| chr16:68211460 | A | G | 3 | a0001c0004t0001g0034 a0001c0004t0001g0088 a0001c0004t0001g0089 |
3 | HG01433.hp2 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3107-14890A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211460 | |||||||
| chr16:68211481 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3107-14869C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211481 | |||||||
| chr16:68211482 | G | A | 76 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(73): Show |
76 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.3107-14868G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211482 | |||||||
| chr16:68211510 | T | TTTG | 3 | a0001c0004t0001g0034 a0001c0004t0001g0088 a0001c0004t0001g0089 |
3 | HG01433.hp2 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3107-14813_3107-14 others(9): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68211510 | ||||||
| chr16:68211510 | TTTGTTG | T | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3107-14816_3107-14 others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68211510 | ||||||
| chr16:68211635 | GC | G | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3107-14713delC | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68211635 | ||||||
| chr16:68211695 | T | C | 46 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3107-14655T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211695 | |||||||
| chr16:68211802 | A | G | 1 | a0001c0001t0005g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3107-14548A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68211802 | |||||||
| chr16:68212172 | A | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3107-14178A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68212172 | |||||||
| chr16:68212525 | C | T | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-13825C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68212525 | |||||||
| chr16:68212589 | T | C | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3107-13761T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68212589 | |||||||
| chr16:68212597 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3107-13753C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68212597 | |||||||
| chr16:68212785 | C | CT | 66 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0055 others(63): Show |
66 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.3107-13543dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68212785 | ||||||
| chr16:68212785 | CT | C | 10 | a0001c0001t0006g0112 a0001c0001t0008g0016 a0001c0001t0009g0126 others(7): Show |
10 | HG01070.hp1 HG01256.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.3107-13543delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68212785 | ||||||
| chr16:68212787 | T | C | 2 | a0001c0001t0005g0025 a0001c0001t0020g0029 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3107-13563T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68212787 | |||||||
| chr16:68212851 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3107-13499G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68212851 | |||||||
| chr16:68212956 | A | AT | 23 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0051 others(20): Show |
23 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.3107-13378dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68212956 | ||||||
| chr16:68213044 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0003g0073 |
2 | NA18961.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.3107-13306C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213044 | |||||||
| chr16:68213095 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3107-13255G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213095 | |||||||
| chr16:68213102 | T | C | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3107-13248T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213102 | |||||||
| chr16:68213212 | A | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-13138A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213212 | |||||||
| chr16:68213275 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3107-13075C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213275 | |||||||
| chr16:68213292 | G | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-13058G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213292 | |||||||
| chr16:68213393 | C | T | 1 | a0001c0001t0004g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3107-12957C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213393 | |||||||
| chr16:68213460 | T | TA | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.3107-12880dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68213460 | ||||||
| chr16:68213460 | TA | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-12880delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68213460 | ||||||
| chr16:68213553 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3107-12797C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213553 | |||||||
| chr16:68213863 | C | G | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-12487C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68213863 | |||||||
| chr16:68214283 | C | G | 2 | a0001c0001t0002g0129 a0001c0001t0002g0161 |
2 | NA18953.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.3107-12067C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68214283 | |||||||
| chr16:68214704 | G | A | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-11646G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68214704 | |||||||
| chr16:68214885 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0081 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3107-11465T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68214885 | |||||||
| chr16:68215034 | T | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-11316T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68215034 | |||||||
| chr16:68215040 | G | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-11310G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68215040 | |||||||
| chr16:68215611 | A | T | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3107-10739A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68215611 | |||||||
| chr16:68215722 | C | CT | 6 | a0001c0001t0001g0033 a0001c0001t0001g0070 a0001c0001t0001g0075 others(3): Show |
6 | HG01175.hp1 HG02055.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.3107-10605dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68215722 | ||||||
| chr16:68215722 | C | CTTTT | 16 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0015 others(13): Show |
16 | HG01070.hp1 HG01433.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3107-10608_3107-10 others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68215722 | ||||||
| chr16:68215722 | C | CTTTTT | 19 | a0001c0001t0004g0145 a0001c0001t0009g0123 a0001c0001t0009g0124 others(16): Show |
19 | HG00438.hp2 HG00741.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.3107-10609_3107-10 others(11): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68215722 | ||||||
| chr16:68215722 | C | CTTTTTT | 6 | a0001c0001t0002g0151 a0001c0001t0002g0165 a0001c0001t0002g0171 others(3): Show |
6 | HG03209.hp2 HG03486.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-10610_3107-10 others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68215722 | ||||||
| chr16:68215722 | C | CTTTTTTT | 33 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(30): Show |
33 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.3107-10611_3107-10 others(13): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68215722 | ||||||
| chr16:68215722 | C | CTTTTTTT others(1): Show |
5 | a0001c0001t0002g0139 a0001c0001t0002g0153 a0001c0001t0002g0168 others(2): Show |
5 | HG02027.hp1 HG03942.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.3107-10612_3107-10 others(14): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68215722 | ||||||
| chr16:68215813 | C | T | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3107-10537C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68215813 | |||||||
| chr16:68215854 | A | G | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-10496A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68215854 | |||||||
| chr16:68215879 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3107-10471C>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68215879 | |||||||
| chr16:68215918 | T | C | 1 | a0001c0001t0021g0158 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3107-10432T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68215918 | |||||||
| chr16:68215989 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0066 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3107-10361A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68215989 | |||||||
| chr16:68216001 | G | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-10349G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68216001 | |||||||
| chr16:68216020 | G | A | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-10330G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68216020 | |||||||
| chr16:68216036 | A | G | 3 | a0001c0001t0004g0131 a0001c0001t0004g0150 a0001c0001t0019g0170 |
3 | HG02055.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3107-10314A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68216036 | |||||||
| chr16:68216291 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3107-10059A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68216291 | |||||||
| chr16:68216489 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3107-9861A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68216489 | |||||||
| chr16:68216562 | C | T | 1 | a0001c0001t0008g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3107-9788C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68216562 | |||||||
| chr16:68216664 | T | TG | 33 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(30): Show |
33 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.3107-9685dupG | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68216664 | ||||||
| chr16:68216688 | C | T | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.3107-9662C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68216688 | |||||||
| chr16:68217036 | C | G | 2 | a0001c0001t0002g0135 a0001c0001t0002g0153 |
2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.3107-9314C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68217036 | |||||||
| chr16:68217396 | A | G | 3 | a0001c0004t0001g0034 a0001c0004t0001g0088 a0001c0004t0001g0089 |
3 | HG01433.hp2 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3107-8954A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68217396 | |||||||
| chr16:68217464 | C | CA | 18 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0104 others(15): Show |
18 | HG01258.hp1 HG01346.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.3107-8860dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68217464 | ||||||
| chr16:68217464 | C | CAA | 37 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(34): Show |
37 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.3107-8861_3107-886 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68217464 | ||||||
| chr16:68217464 | C | CAAA | 8 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0168 others(5): Show |
8 | HG02132.hp2 HG03486.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-8862_3107-886 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68217464 | ||||||
| chr16:68217464 | CA | C | 12 | a0001c0001t0009g0124 a0001c0001t0012g0185 a0001c0001t0012g0188 others(9): Show |
12 | HG02257.hp2 HG02280.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.3107-8860delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68217464 | ||||||
| chr16:68217699 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3107-8651C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68217699 | |||||||
| chr16:68217733 | A | G | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3107-8617A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68217733 | |||||||
| chr16:68217779 | G | A | 3 | a0001c0001t0005g0009 a0001c0001t0005g0025 a0001c0001t0020g0029 |
3 | HG02451.hp2 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3107-8571G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68217779 | |||||||
| chr16:68217851 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3107-8499A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68217851 | |||||||
| chr16:68217881 | C | G | 81 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(78): Show |
81 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.3107-8469C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68217881 | |||||||
| chr16:68218103 | A | T | 4 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-8247A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218103 | |||||||
| chr16:68218176 | T | C | 96 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(93): Show |
96 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(93): Show |
intron_variant | MODIFIER | c.3107-8174T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218176 | |||||||
| chr16:68218514 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0012g0185 a0001c0001t0012g0187 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3107-7828_3107-781 others(16): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68218514 | ||||||
| chr16:68218514 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0012g0188 a0001c0001t0016g0184 a0001c0001t0016g0186 |
3 | HG02257.hp2 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3107-7829_3107-781 others(17): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68218514 | ||||||
| chr16:68218514 | CA | C | 71 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0002g0129 others(68): Show |
71 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.3107-7817delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68218514 | ||||||
| chr16:68218575 | C | CT | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-7764dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68218575 | ||||||
| chr16:68218575 | CT | C | 14 | a0001c0001t0005g0009 a0001c0001t0005g0021 a0001c0001t0005g0022 others(11): Show |
14 | HG01109.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.3107-7764delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68218575 | ||||||
| chr16:68218586 | T | C | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-7764T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218586 | |||||||
| chr16:68218613 | A | G | 96 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(93): Show |
96 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(93): Show |
intron_variant | MODIFIER | c.3107-7737A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218613 | |||||||
| chr16:68218620 | C | G | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3107-7730C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218620 | |||||||
| chr16:68218660 | C | T | 1 | a0001c0001t0009g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3107-7690C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218660 | |||||||
| chr16:68218661 | C | T | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-7689C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218661 | |||||||
| chr16:68218792 | C | G | 1 | a0001c0001t0002g0160 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3107-7558C>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218792 | |||||||
| chr16:68219025 | A | G | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-7325A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219025 | |||||||
| chr16:68219105 | A | G | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.3107-7245A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219105 | |||||||
| chr16:68219124 | G | A | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3107-7226G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219124 | |||||||
| chr16:68219157 | G | A | 7 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.3107-7193G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219157 | |||||||
| chr16:68219323 | C | T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0082 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3107-7027C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219323 | |||||||
| chr16:68219421 | T | G | 101 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(98): Show |
101 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(98): Show |
intron_variant | MODIFIER | c.3107-6929T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219421 | |||||||
| chr16:68219423 | T | A | 101 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(98): Show |
101 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(98): Show |
intron_variant | MODIFIER | c.3107-6927T>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219423 | |||||||
| chr16:68219473 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3107-6877G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219473 | |||||||
| chr16:68219474 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3107-6876G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219474 | |||||||
| chr16:68219486 | G | A | 1 | a0001c0001t0009g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3107-6864G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219486 | |||||||
| chr16:68219580 | A | G | 1 | a0001c0001t0017g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3107-6770A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219580 | |||||||
| chr16:68219605 | T | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-6745T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219605 | |||||||
| chr16:68219979 | C | T | 3 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 |
3 | HG00738.hp2 HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.3107-6371C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219979 | |||||||
| chr16:68219980 | A | T | 1 | a0001c0001t0002g0171 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3107-6370A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68219980 | |||||||
| chr16:68220155 | C | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.3107-6195C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68220155 | |||||||
| chr16:68220293 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3107-6057G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68220293 | |||||||
| chr16:68220427 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3107-5923C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68220427 | |||||||
| chr16:68220456 | A | G | 8 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(5): Show |
8 | HG02622.hp2 HG02896.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-5894A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68220456 | |||||||
| chr16:68220501 | A | C | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3107-5849A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68220501 | |||||||
| chr16:68220511 | A | T | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3107-5839A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68220511 | |||||||
| chr16:68220594 | C | CTT | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-5743_3107-574 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68220594 | ||||||
| chr16:68220734 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3107-5616C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68220734 | |||||||
| chr16:68220743 | T | TA | 13 | a0001c0001t0001g0051 a0001c0001t0008g0012 a0001c0001t0008g0013 others(10): Show |
13 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.3107-5596dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68220743 | ||||||
| chr16:68220757 | C | CA | 89 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.3107-5580dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68220757 | ||||||
| chr16:68220971 | T | G | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.3107-5379T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68220971 | |||||||
| chr16:68221070 | G | A | 2 | a0001c0001t0018g0097 a0008c0006t0018g0096 |
2 | NA18952.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3107-5280G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68221070 | |||||||
| chr16:68221134 | T | G | 2 | a0001c0001t0002g0142 a0001c0001t0002g0168 |
2 | HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3107-5216T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68221134 | |||||||
| chr16:68221230 | G | A | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3107-5120G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68221230 | |||||||
| chr16:68221301 | A | C | 1 | a0001c0001t0005g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3107-5049A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68221301 | |||||||
| chr16:68221317 | G | A | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-5033G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68221317 | |||||||
| chr16:68221365 | C | T | 3 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 |
3 | HG02922.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3107-4985C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68221365 | |||||||
| chr16:68221548 | A | G | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-4802A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68221548 | |||||||
| chr16:68221964 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3107-4386A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68221964 | |||||||
| chr16:68222056 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3107-4294G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68222056 | |||||||
| chr16:68222060 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3107-4290C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68222060 | |||||||
| chr16:68222218 | A | ATCACCTG others(11): Show |
8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-4129_3107-412 others(22): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222218 | ||||||
| chr16:68222267 | C | T | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3107-4083C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68222267 | |||||||
| chr16:68222287 | G | GC | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0087 |
3 | HG02280.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3107-4061dupC | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222287 | ||||||
| chr16:68222289 | C | CA | 25 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
25 | HG01169.hp1 HG01175.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.3107-4024dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | C | CAA | 6 | a0001c0001t0001g0035 a0001c0001t0003g0042 a0001c0001t0003g0118 others(3): Show |
6 | HG01099.hp1 HG02055.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-4025_3107-402 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0027g0068 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3107-4035_3107-402 others(16): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | C | CCA | 5 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0080 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3107-4061_3107-406 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68222289 | |||||||
| chr16:68222289 | CA | C | 17 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0054 others(14): Show |
17 | HG00438.hp1 HG00639.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.3107-4024delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA | C | 16 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(13): Show |
16 | HG01099.hp2 HG01175.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.3107-4030_3107-402 others(11): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(1): Show |
C | 24 | a0001c0001t0002g0140 a0001c0001t0002g0142 a0001c0001t0002g0144 others(21): Show |
24 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.3107-4031_3107-402 others(12): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(2): Show |
C | 11 | a0001c0001t0002g0129 a0001c0001t0002g0143 a0001c0001t0005g0021 others(8): Show |
11 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.3107-4032_3107-402 others(13): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(3): Show |
C | 14 | a0001c0001t0001g0038 a0001c0001t0003g0094 a0001c0001t0005g0009 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3107-4033_3107-402 others(14): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0039 |
3 | HG02647.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3107-4034_3107-402 others(15): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0032g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3107-4036_3107-402 others(17): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(7): Show |
C | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.3107-4037_3107-402 others(18): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(8): Show |
C | 3 | a0002c0002t0014g0177 a0002c0002t0014g0180 a0002c0002t0034g0179 |
3 | HG02717.hp2 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3107-4038_3107-402 others(19): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0013g0001 a0001c0001t0013g0003 a0001c0001t0013g0004 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-4039_3107-402 others(20): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3107-4040_3107-402 others(21): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(11): Show |
C | 6 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3107-4041_3107-402 others(22): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222289 | CAAAAAAA others(17): Show |
C | 1 | a0001c0001t0002g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3107-4047_3107-402 others(28): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68222289 | ||||||
| chr16:68222576 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3107-3774C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68222576 | |||||||
| chr16:68222736 | G | A | 75 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(72): Show |
75 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.3107-3614G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68222736 | |||||||
| chr16:68222896 | C | T | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-3454C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68222896 | |||||||
| chr16:68222926 | G | A | 1 | a0001c0001t0010g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3107-3424G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68222926 | |||||||
| chr16:68223372 | A | T | 1 | a0001c0001t0019g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3107-2978A>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68223372 | |||||||
| chr16:68223490 | C | T | 1 | a0001c0001t0005g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3107-2860C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68223490 | |||||||
| chr16:68223894 | C | CA | 25 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(22): Show |
25 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.3107-2435dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68223894 | ||||||
| chr16:68223894 | CA | C | 12 | a0001c0001t0002g0161 a0001c0001t0012g0185 a0001c0001t0012g0187 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3107-2435delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68223894 | ||||||
| chr16:68224028 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3107-2322T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224028 | |||||||
| chr16:68224125 | TTA | T | 15 | a0001c0001t0004g0145 a0001c0001t0013g0001 a0001c0001t0013g0003 others(12): Show |
15 | HG00438.hp2 HG01891.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.3107-2224_3107-222 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224125 | |||||||
| chr16:68224125 | TTAA | T | 48 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(45): Show |
48 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.3107-2224_3107-222 others(7): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224125 | |||||||
| chr16:68224125 | TTAAAAA | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(9): Show |
12 | HG01433.hp1 HG02622.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.3107-2224_3107-221 others(10): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224125 | |||||||
| chr16:68224126 | T | TA | 11 | a0001c0001t0001g0036 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
11 | HG00438.hp1 HG01109.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.3107-2204dupA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68224126 | ||||||
| chr16:68224126 | TA | T | 8 | a0001c0001t0001g0067 a0001c0001t0001g0101 a0001c0001t0009g0123 others(5): Show |
8 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-2204delA | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68224126 | ||||||
| chr16:68224129 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3107-2221A>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224129 | |||||||
| chr16:68224274 | C | CT | 38 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0051 others(35): Show |
38 | HG00639.hp1 HG01109.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.3107-2056dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68224274 | ||||||
| chr16:68224274 | C | CTT | 11 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(8): Show |
11 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3107-2057_3107-205 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68224274 | ||||||
| chr16:68224305 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3107-2045C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224305 | |||||||
| chr16:68224347 | G | A | 4 | a0002c0002t0014g0177 a0002c0002t0014g0178 a0002c0002t0014g0180 others(1): Show |
4 | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-2003G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224347 | |||||||
| chr16:68224418 | C | T | 3 | a0001c0001t0010g0010 a0001c0001t0010g0011 a0001c0001t0010g0019 |
3 | HG01433.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3107-1932C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224418 | |||||||
| chr16:68224469 | T | G | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-1881T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224469 | |||||||
| chr16:68224549 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3107-1801A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224549 | |||||||
| chr16:68224573 | C | CT | 21 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0063 others(18): Show |
21 | HG01109.hp1 HG01175.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.3107-1755dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68224573 | ||||||
| chr16:68224573 | CT | C | 49 | a0001c0001t0002g0129 a0001c0001t0002g0133 a0001c0001t0002g0134 others(46): Show |
49 | HG00639.hp2 HG00741.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.3107-1755delT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68224573 | ||||||
| chr16:68224573 | CTT | C | 5 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3107-1756_3107-175 others(6): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68224573 | ||||||
| chr16:68224604 | G | A | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3107-1746G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224604 | |||||||
| chr16:68224720 | A | AT | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-1629dupT | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 68224720 | ||||||
| chr16:68224949 | T | G | 45 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(42): Show |
45 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3107-1401T>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68224949 | |||||||
| chr16:68225078 | G | A | 82 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.3107-1272G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68225078 | |||||||
| chr16:68225369 | G | C | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.3107-981G>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68225369 | |||||||
| chr16:68225417 | T | C | 8 | a0001c0001t0012g0185 a0001c0001t0012g0187 a0001c0001t0012g0188 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3107-933T>C | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68225417 | |||||||
| chr16:68225534 | C | T | 18 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.3107-816C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68225534 | |||||||
| chr16:68225692 | G | A | 1 | a0001c0001t0017g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3107-658G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68225692 | |||||||
| chr16:68225836 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3107-514G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68225836 | |||||||
| chr16:68226180 | C | T | 75 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(72): Show |
75 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.3107-170C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68226180 | |||||||
| chr16:68226184 | G | A | 3 | a0003c0003t0011g0181 a0003c0003t0011g0182 a0003c0003t0011g0183 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3107-166G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68226184 | |||||||
| chr16:68226219 | G | A | 2 | a0001c0001t0006g0105 a0001c0001t0006g0108 |
2 | HG01934.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.3107-131G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68226219 |