Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1075 | 175 | 73 | 33 | 41 | 4 | 22 | 31 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0002 | 0/0 | 1075 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0003 | 0/0 | 1075 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0004 | 0/0 | 1075 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0005 | 0/0 | 1075 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0006 | 0/0 | 1075 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0007 | 0/0 | 1075 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0008 | 0/0 | 1075 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3228 | 171 | 72 | 30 | 41 | 4 | 22 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0002 | 0/0 | 3228 | 4 | 4 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0003 | 0/0 | 3228 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0004 | 0/0 | 3228 | 3 | 1 | 2 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0005 | 0/0 | 3228 | 2 | 0 | 0 | 2 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0006 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0007 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0008 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0009 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| c0010 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3101 | 48 | 23 | 8 | 10 | 0 | 6 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0002 | 0/0 | 3097 | 26 | 1 | 6 | 12 | 1 | 6 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0003 | 0/0 | 3102 | 14 | 8 | 1 | 4 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0004 | 0/0 | 3098 | 12 | 2 | 4 | 4 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0005 | 0/0 | 3102 | 10 | 8 | 0 | 0 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0006 | 0/0 | 3091 | 9 | 1 | 4 | 3 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0007 | 0/1 | 3100 | 8 | 2 | 3 | 0 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0008 | 0/0 | 3101 | 7 | 7 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0009 | 0/0 | 3094 | 7 | 1 | 4 | 1 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0010 | 0/0 | 3100 | 4 | 3 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0011 | 0/0 | 3105 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0012 | 0/0 | 3103 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0013 | 0/0 | 3100 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0014 | 0/0 | 3101 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0015 | 0/0 | 3102 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0016 | 0/0 | 3106 | 2 | 2 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0017 | 0/0 | 3101 | 2 | 2 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0018 | 0/0 | 3101 | 2 | 0 | 0 | 2 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0019 | 0/0 | 3098 | 2 | 1 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0020 | 0/0 | 3103 | 2 | 1 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0021 | 0/0 | 3101 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0022 | 0/0 | 3101 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0023 | 0/0 | 3098 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0024 | 0/0 | 3061 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0025 | 0/0 | 3097 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0026 | 0/0 | 3083 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0027 | 0/0 | 3101 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0028 | 0/0 | 3101 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0029 | 0/0 | 3101 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0030 | 0/0 | 3101 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0031 | 0/0 | 3101 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0032 | 0/0 | 3101 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0033 | 0/0 | 3094 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0034 | 0/0 | 3101 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0035 | 0/0 | 3091 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0036 | 0/0 | 3100 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0037 | 0/0 | 3101 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| t0038 | 0/0 | 3103 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3228 | 171 | 72 | 30 | 41 | 4 | 22 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0004 | 0/0 | 3228 | 3 | 1 | 2 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0008 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0002c0002 | 0/0 | 3228 | 4 | 4 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0003c0003 | 0/0 | 3228 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0004c0005 | 0/0 | 3228 | 2 | 0 | 0 | 2 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0005c0006 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0006c0009 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0007c0010 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0008c0007 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6328 | 42 | 20 | 5 | 10 | 0 | 6 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0002 | 0/0 | 6324 | 26 | 1 | 6 | 12 | 1 | 6 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0003 | 0/0 | 6329 | 14 | 8 | 1 | 4 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0004 | 0/0 | 6325 | 11 | 2 | 4 | 3 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0005 | 0/0 | 6329 | 10 | 8 | 0 | 0 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0006 | 0/0 | 6318 | 9 | 1 | 4 | 3 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0007 | 0/1 | 6327 | 8 | 2 | 3 | 0 | 0 | 2 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0008 | 0/0 | 6328 | 7 | 7 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0009 | 0/0 | 6321 | 7 | 1 | 4 | 1 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0010 | 0/0 | 6327 | 4 | 3 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0012 | 0/0 | 6330 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0013 | 0/0 | 6327 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0015 | 0/0 | 6329 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0016 | 0/0 | 6333 | 2 | 2 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0017 | 0/0 | 6328 | 2 | 2 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0018 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0019 | 0/0 | 6325 | 2 | 1 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0020 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0021 | 0/0 | 6328 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0023 | 0/0 | 6325 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0024 | 0/0 | 6288 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0025 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0026 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0027 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0028 | 0/0 | 6328 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0029 | 0/0 | 6328 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0030 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0031 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0032 | 0/0 | 6328 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0033 | 0/0 | 6321 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0034 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0035 | 0/0 | 6318 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0037 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0001t0038 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0004t0001 | 0/0 | 6328 | 3 | 1 | 2 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0001c0008t0001 | 0/0 | 6328 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0002c0002t0014 | 0/0 | 6328 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0002c0002t0036 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0003c0003t0011 | 0/0 | 6332 | 3 | 3 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0004c0005t0004 | 0/0 | 6325 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0004c0005t0022 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0005c0006t0018 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0006c0009t0020 | 0/0 | 6330 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0007c0010t0001 | 0/0 | 6328 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| a0008c0007t0001 | 0/0 | 6328 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | copy fasta | chr16 | 68080370 | 68234259 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0086 | 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 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0001g0119 | 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 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0156 | 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 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0003g0085 | 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 |
| a0001c0001t0003g0116 | 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 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0142 | 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 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0004g0155 | 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 |
| a0001c0001t0005g0026 | 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 |
| a0001c0001t0005g0058 | 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 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 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 |
| 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 |
| a0001c0001t0009g0074 | 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 |
| a0001c0001t0015g0025 | 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 |
| a0001c0001t0018g0096 | 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 |
| a0001c0001t0020g0030 | 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 |
| a0001c0001t0023g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0024g0168 | 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 |
| a0001c0001t0027g0066 | 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 |
| a0001c0001t0030g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0031g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0032g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0033g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0034g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0035g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0037g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0001c0001t0038g0029 | 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 |
| a0001c0008t0001g0107 | 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 |
| a0002c0002t0036g0179 | 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 |
| a0004c0005t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0004c0005t0022g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0005c0006t0018g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| a0006c0009t0020g0028 | 0/0 | 1 | 0 | 1 | 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 |
| a0008c0007t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0120 | EAS | CHS | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | CHS | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0075 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0082 | 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 | g0107 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0091 | 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 | t0032 | g0050 | AMR | PUR | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01109 | hp2 | a0006 | 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 | g0118 | 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 | g0061 | 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 | g0169 | 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 | g0145 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0105 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0060 | AMR | CLM | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0146 | 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 | g0110 | AMR | PEL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0064 | 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 | g0116 | AFR | ACB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02071 | hp2 | a0001 | c0001 | t0024 | g0168 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02080 | hp1 | a0001 | c0001 | t0037 | g0108 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02080 | hp2 | a0001 | c0001 | t0031 | g0054 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0074 | EAS | KHV | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02132 | hp2 | a0001 | c0001 | t0023 | g0134 | 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 | g0113 | 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 | a0008 | 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 | g0085 | 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 | g0077 | 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 | g0030 | 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 | g0065 | 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 | g0078 | 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 | g0058 | 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 | g0069 | 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 | g0056 | AFR | GWD | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0017 | 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 | g0086 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02976 | hp1 | a0002 | c0002 | t0036 | g0179 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0070 | 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 | g0084 | 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 | g0059 | 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 | t0033 | 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 | t0035 | 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 | t0038 | g0029 | 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 | g0051 | 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 | g0132 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0062 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0151 | 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 | g0111 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0063 | 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 | g0057 | SAS | BEB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0080 | 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 | g0154 | 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 | g0115 | 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 | g0025 | 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 | g0083 | 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 | g0143 | 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 | g0153 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18952 | hp1 | a0001 | c0001 | t0018 | g0096 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0052 | 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 | g0138 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0112 | 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 | g0068 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18978 | hp2 | a0001 | c0001 | t0034 | g0053 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0135 | 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 | g0148 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA18995 | hp2 | a0005 | c0006 | t0018 | g0097 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0155 | 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 | g0144 | 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 | g0026 | AFR | LWK | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0081 | 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 | g0071 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0136 | 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 | g0117 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0090 | 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 | g0106 | 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 | g0066 | 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 | g0016 | 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 | hp1 | a0001 | c0001 | t0007 | g0076 | REF | REF | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0102 | REF | REF | NFATC3_chr16_68080370_68234259 | NFATC3 | chr16 | 68080370 | 68234259 |
| 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 | a0005 | 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 | a0008 | 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 | a0007a0008 | 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 | a0006 | 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 |
| 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 | a0007c0010a0008c0007 | 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 |
| 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 | a0001c0001t0005a0001c0001t0015a0001c0001t0019others(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 | a0001c0001t0037 | 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 | a0001c0001t0002a0001c0001t0004a0001c0001t0019others(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 | a0002c0002t0014a0002c0002t0036 | 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 | a0001c0001t0035 | 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 | a0001c0001t0003a0001c0001t0020a0001c0001t0038others(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 | a0001c0001t0016a0003c0003t0011 | 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 | a0001c0001t0007a0001c0001t0010a0001c0001t0013others(1): Show | 16 | HG00639.hp1 HG01192.hp1 HG01258.hp1 others(13): 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 | a0001c0001t0004a0004c0005t0004 | 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 | a0001c0001t0002a0001c0001t0019a0001c0001t0023others(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 | a0001c0001t0009a0001c0001t0033 | 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 | a0001c0001t0006a0001c0001t0035 | 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 | a0001c0001t0034 | 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 | a0001c0001t0032 | 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 | a0001c0001t0012a0001c0001t0016a0003c0003t0011 | 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 | a0001c0001t0012a0001c0001t0016a0003c0003t0011 | 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 | a0001c0001t0012a0001c0001t0016a0003c0003t0011 | 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 | a0001c0001t0008a0001c0001t0010a0001c0001t0033 | 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 | a0001c0001t0012a0001c0001t0016a0001c0001t0023 | 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 | a0001c0001t0013a0001c0001t0029 | 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 | a0001c0001t0018a0005c0006t0018 | 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 | a0001c0001t0015a0001c0001t0038 | 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 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(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 |
| 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0033g0007 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0001g0008a0002c0002t0014g0177a0002c0002t0014g0178others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0033a0001c0001t0012g0185a0001c0001t0012g0187others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | 138 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0043others(135): Show | 138 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(135): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0001g0098a0001c0001t0003g0100a0001c0001t0005g0099 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0017g0005a0001c0001t0025g0130 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0005g0021a0001c0001t0005g0175 | 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 | 185 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0035others(182): Show | 185 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(182): 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0001g0098a0001c0001t0003g0100a0001c0001t0005g0099 | 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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0001c0001t0001g0045a0001c0001t0003g0044a0001c0001t0003g0046others(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 | a0001c0001t0002g0161a0001c0001t0013g0001a0001c0001t0013g0003others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0004g0162a0001c0001t0004g0163a0001c0001t0004g0164others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0016g0184others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0103a0001c0001t0003g0100a0001c0001t0008g0018others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0001g0048a0001c0001t0001g0090a0001c0001t0001g0091others(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 | a0001c0001t0002g0129a0001c0001t0002g0153a0001c0001t0002g0156others(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 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0132 | 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 | a0001c0004t0001g0034a0001c0004t0001g0088a0001c0004t0001g0089 | 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 | a0001c0001t0035g0047 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0003g0041a0001c0001t0033g0007 | 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 | a0001c0001t0001g0087a0001c0001t0001g0104a0001c0001t0005g0021others(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 | a0001c0001t0009g0125a0001c0001t0009g0126a0001c0001t0009g0127 | 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 | a0001c0001t0006g0114a0001c0001t0035g0047a0008c0007t0001g0093 | 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 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0005g0022others(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 | a0001c0001t0008g0012a0001c0001t0008g0017a0001c0001t0008g0018 | 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 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0037others(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 | a0001c0001t0006g0106a0001c0001t0006g0117a0001c0008t0001g0107 | 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 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(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 | 99 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0035others(96): Show | 99 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(96): 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0003g0042a0001c0001t0032g0050 | 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 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0006g0113 | 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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0161others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0006g0114 | 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 | a0001c0001t0006g0105 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0006g0120 | 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 | a0001c0001t0015g0025a0001c0001t0015g0031a0001c0001t0015g0032others(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 | a0001c0001t0001g0048a0001c0001t0001g0079a0001c0001t0001g0082others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0169 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0004g0142a0001c0001t0005g0024a0004c0005t0004g0144others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0148a0001c0001t0002g0156 | 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 | a0001c0001t0005g0026 | 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 | a0001c0001t0005g0027a0001c0001t0008g0012a0001c0001t0008g0013others(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 | a0001c0001t0007g0077a0001c0001t0007g0078a0003c0003t0011g0182others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0101a0001c0001t0031g0054 | 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 | a0001c0001t0024g0168 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0037g0108 | 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 | a0001c0001t0004g0142a0001c0001t0033g0007a0002c0002t0014g0178others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0015g0025a0001c0001t0015g0031a0001c0001t0015g0032others(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 | a0001c0001t0002g0151 | 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 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0086others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0082others(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 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0012g0185others(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 | a0001c0001t0030g0115 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0006g0110 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0141 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0111 | 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 | 2 | a0001c0001t0007g0075a0001c0001t0007g0076 | 2 | HG00639.hp1 homoSapiens_chm13v2.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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0016g0184others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0140a0001c0001t0002g0167a0001c0001t0004g0152others(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 | a0001c0001t0010g0010a0001c0001t0010g0011 | 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 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0015 | 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 | a0001c0001t0008g0012a0001c0001t0008g0016a0001c0001t0008g0017others(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 | a0001c0001t0009g0123a0001c0001t0009g0127 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0004t0001g0034a0001c0004t0001g0088a0001c0004t0001g0089 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0092a0001c0001t0002g0139a0001c0001t0010g0011others(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 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0020g0030 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0020g0030 | 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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0026others(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 | a0001c0001t0015g0025a0001c0001t0015g0032a0001c0001t0038g0029 | 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 | a0001c0001t0032g0050 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0043a0001c0001t0001g0104a0001c0001t0001g0109others(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 | a0001c0001t0001g0048a0001c0001t0008g0012a0001c0001t0008g0013others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0009g0074 | 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 | a0001c0001t0003g0071 | 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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0026others(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 | a0001c0001t0002g0139a0001c0001t0002g0167a0001c0001t0004g0142others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0006c0009t0020g0028 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0057a0001c0001t0001g0176 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0008c0007t0001g0093 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0137a0001c0001t0002g0148a0001c0001t0002g0156others(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 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0012g0185others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0004g0138 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0008a0001c0001t0001g0056a0001c0001t0001g0069others(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 | a0001c0001t0015g0025a0001c0001t0038g0029 | 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 | a0001c0001t0004g0162a0001c0001t0004g0163a0001c0001t0004g0164 | 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 | a0006c0009t0020g0028 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0004g0154 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0010g0020a0001c0001t0012g0185a0001c0001t0012g0187others(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 | a0001c0001t0001g0049a0001c0001t0001g0080a0001c0001t0001g0104others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0141a0001c0001t0002g0146a0001c0001t0002g0147others(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 | a0001c0001t0012g0185a0001c0001t0012g0188a0001c0001t0016g0186 | 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 | a0001c0001t0007g0075a0001c0001t0010g0011a0001c0001t0010g0019others(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 | a0002c0002t0014g0178a0002c0002t0014g0180a0002c0002t0036g0179 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0006c0009t0020g0028 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0166a0001c0001t0004g0155a0001c0001t0024g0168others(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 | a0001c0001t0002g0173a0001c0001t0010g0010a0001c0001t0010g0011others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0092others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0082a0001c0001t0003g0085 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0035g0047 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0007g0077a0001c0001t0007g0078 | 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 | a0001c0001t0001g0083a0001c0001t0003g0084 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | ||||||
| chr16:68114340
|
C | T | 187 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0035others(184): Show | 187 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(184): Show |
intron_variant | MODIFIER | c.104-7647C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | chr16 | 68114340 | ||||||
| chr16:68114354
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0004g0152 | 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 | a0001c0001t0006g0118 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0003g0085 | 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 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0051others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0136a0001c0001t0004g0138 | 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 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0003g0044 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0007g0060 | 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 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0003g0044 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0006g0114 | 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 | a0001c0001t0010g0020a0001c0001t0028g0040 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0101a0001c0001t0031g0054 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0010g0020a0001c0001t0028g0040 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0010g0010a0001c0001t0010g0011 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0006g0110 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0013g0003a0001c0001t0029g0002 | 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 | a0001c0001t0006g0114 | 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 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0080others(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 | a0001c0001t0006g0120a0001c0001t0012g0185a0001c0001t0012g0187others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0080a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0001g0043a0001c0001t0007g0077a0001c0001t0008g0012others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0002g0139a0001c0001t0002g0160a0001c0001t0008g0012others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0043a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0007g0075a0001c0001t0013g0001a0001c0001t0013g0004others(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 | a0001c0001t0001g0091a0001c0001t0001g0109a0001c0001t0006g0105others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0004g0155a0001c0001t0005g0099a0001c0001t0006g0113others(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 | 17 | a0001c0001t0002g0147a0001c0001t0007g0076a0001c0001t0009g0123others(14): Show | 17 | HG00741.hp2 HG01071.hp2 HG01346.hp1 others(14): 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 | a0001c0001t0003g0044a0001c0001t0003g0067a0001c0001t0003g0094others(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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0002g0132a0001c0001t0002g0139a0001c0001t0002g0141others(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 | a0001c0001t0015g0025a0001c0001t0015g0032a0001c0001t0038g0029 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0003g0055others(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 | a0001c0001t0001g0035a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0004t0001g0034a0001c0004t0001g0088a0001c0004t0001g0089 | 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 | a0001c0001t0027g0066 | 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 | a0001c0001t0005g0024a0003c0003t0011g0181a0003c0003t0011g0182others(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 | a0001c0001t0010g0020a0001c0001t0028g0040 | 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 | a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0140 | 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 | 184 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0035others(181): Show | 184 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(181): 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0010g0020a0001c0001t0028g0040 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0002g0141 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0091a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0015g0025a0001c0001t0015g0031a0001c0001t0015g0032others(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 | a0008c0007t0001g0093 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0001g0065a0001c0001t0001g0104a0001c0001t0003g0067others(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 | a0001c0001t0001g0109a0001c0001t0002g0139a0001c0001t0002g0167others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0005g0021a0001c0001t0005g0175 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0010g0020a0001c0001t0028g0040 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0015g0025a0001c0001t0015g0031a0001c0001t0015g0032others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0167 | 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 | a0001c0001t0010g0020a0001c0001t0028g0040 | 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 | a0001c0001t0002g0141 | 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 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0001c0001t0005g0026 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0153a0001c0001t0004g0152a0001c0001t0009g0124others(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 | a0006c0009t0020g0028 | 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 | a0001c0001t0009g0123a0001c0001t0009g0125a0001c0001t0009g0127others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0056others(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 | |||||
| chr16:68133968
|
A | G | 1 | a0001c0001t0007g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1401+7358A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68133968 | ||||||
| chr16:68133973
|
C | G | 4 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0002g0151 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0051others(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 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0080others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0023others(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 | a0001c0001t0002g0160a0001c0001t0005g0022a0001c0001t0012g0185others(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 | a0001c0001t0002g0148a0001c0001t0009g0123a0001c0001t0009g0124others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0109a0001c0001t0006g0105a0001c0001t0006g0106others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | ||||||
| chr16:68136348
|
A | G | 1 | a0001c0001t0007g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1401+9738A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 3/9 | chr16 | 68136348 | ||||||
| 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0005g0021a0001c0001t0005g0175 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0091a0001c0001t0003g0100a0001c0001t0005g0023others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0037g0108 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0004c0005t0022g0143 | 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 | a0004c0005t0022g0143 | 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 | a0004c0005t0022g0143 | 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 | a0004c0005t0022g0143 | 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 | a0004c0005t0022g0143 | 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 | a0004c0005t0022g0143 | 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 | a0004c0005t0022g0143 | 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 | a0004c0005t0022g0143 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0104others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0030g0115 | 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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0064a0001c0001t0003g0068 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0004g0131a0001c0001t0004g0150a0001c0001t0019g0170 | 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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0002g0148a0001c0001t0002g0156 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0015g0025a0001c0001t0015g0032a0001c0001t0038g0029 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0003g0070 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0119a0001c0001t0002g0129a0001c0001t0002g0136others(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 | a0001c0001t0008g0018a0001c0001t0013g0001a0001c0001t0013g0003others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0030g0115 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0024g0168 | 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 | a0001c0001t0010g0020a0001c0001t0028g0040 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0010g0020a0001c0001t0028g0040 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0104a0001c0001t0004g0142a0001c0001t0021g0158others(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 | a0001c0004t0001g0034a0001c0004t0001g0088a0001c0004t0001g0089 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0002g0151 | 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 | a0001c0001t0018g0096 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0004g0162a0001c0001t0004g0163a0001c0001t0004g0164 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0125a0001c0001t0009g0126 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0125a0001c0001t0009g0126 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0033a0001c0001t0012g0185a0001c0001t0012g0187others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0125a0001c0001t0009g0126 | 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 | a0001c0001t0027g0066 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0080a0001c0001t0003g0067a0001c0001t0005g0058others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0013g0003a0001c0001t0029g0002 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0020g0030 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0032g0050 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0043a0001c0001t0001g0111a0001c0001t0001g0119others(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 | a0001c0001t0002g0132a0001c0001t0002g0149a0001c0001t0002g0151others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0037a0001c0001t0003g0068a0002c0002t0014g0177others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | 97 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0045others(94): Show | 97 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(94): 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0003g0070 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0008c0007t0001g0093 | 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 | a0001c0001t0002g0149a0001c0001t0013g0001a0001c0001t0013g0003others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0036others(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 | a0001c0001t0033g0007 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0004g0138others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0033g0007 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0090a0001c0001t0005g0058 | 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 | a0002c0002t0036g0179 | 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 | a0001c0001t0002g0147 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0001g0008a0001c0001t0001g0056a0001c0001t0001g0069 | 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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0125a0001c0001t0009g0126others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0002g0160others(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 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0111others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0001g0065a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0004g0162a0001c0001t0004g0163a0001c0001t0004g0164 | 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 | a0001c0001t0015g0025a0001c0001t0015g0031a0001c0001t0015g0032others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(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 | a0001c0001t0001g0065a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0009g0123a0001c0001t0009g0125a0001c0001t0009g0126others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0002g0137a0001c0001t0002g0173 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0004g0163a0001c0001t0004g0164 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0001g0065a0001c0001t0002g0137a0001c0001t0009g0123others(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 | a0001c0001t0001g0065a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0079a0001c0001t0001g0090a0001c0001t0005g0058 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0065a0001c0001t0009g0123a0001c0001t0009g0124others(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 | a0001c0001t0001g0086a0001c0001t0001g0087 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0052a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0009g0074 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0001g0065a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0020g0030 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0015g0025a0001c0001t0038g0029 | 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 | a0001c0001t0007g0060 | 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 | a0001c0001t0007g0060 | 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 | a0001c0001t0027g0066 | 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 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(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 | a0001c0001t0006g0117 | 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 | a0001c0001t0001g0073 | 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 | 16 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0057others(13): Show | 16 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(13): 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 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0063others(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 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0104others(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 | a0001c0001t0001g0064a0001c0001t0001g0087a0001c0001t0003g0067others(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 | a0001c0001t0001g0036a0001c0001t0001g0092a0001c0001t0006g0105others(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 | a0001c0001t0001g0039a0001c0001t0016g0184 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0002g0132a0001c0001t0004g0152a0001c0001t0004g0157others(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 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0151others(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 | a0001c0001t0001g0037a0001c0001t0002g0129a0001c0001t0002g0137others(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 | a0001c0001t0002g0133a0001c0001t0002g0135a0001c0001t0002g0136others(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 | a0001c0001t0005g0009a0001c0001t0005g0058 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0012g0185a0001c0001t0028g0040 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0008c0007t0001g0093 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0023g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1774+1033G>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168048 | ||||||
| chr16:68168128
|
C | T | 1 | a0001c0001t0007g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1774+1113C>T | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | chr16 | 68168128 | ||||||
| chr16:68168471
|
TTTA | T | 67 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0003g0084 | 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 | a0001c0001t0003g0046a0001c0001t0003g0084 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0151 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0032g0050 | 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 | a0001c0001t0002g0148a0001c0001t0002g0156 | 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 | a0001c0001t0006g0120 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0051others(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 | a0001c0001t0002g0151a0001c0001t0002g0156a0001c0001t0002g0167others(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 | a0001c0001t0003g0055a0001c0001t0008g0012a0001c0001t0008g0013others(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 | a0001c0001t0004g0154 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0007g0078 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0141 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0004g0155a0001c0001t0013g0001a0001c0001t0013g0003others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0091 | 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 | a0004c0005t0004g0144a0004c0005t0022g0143 | 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 | a0001c0001t0009g0125a0001c0001t0009g0126 | 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 | a0001c0001t0006g0120 | 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 | a0001c0001t0001g0080a0001c0001t0001g0092 | 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 | a0001c0001t0004g0154 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0007g0077a0001c0001t0007g0078 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0023g0134 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0063 | 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 | a0001c0001t0003g0116 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0140 | 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 | a0001c0001t0033g0007 | 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 | a0001c0001t0032g0050 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0051others(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 | a0001c0001t0006g0106 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0016 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0029g0002 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0004g0131a0001c0001t0004g0150a0001c0001t0019g0170 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0052a0001c0001t0002g0129a0001c0001t0002g0132others(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 | a0001c0001t0004g0131a0001c0001t0004g0150a0001c0001t0019g0170others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0027g0066 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0052a0001c0001t0003g0067a0001c0008t0001g0107 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0007c0010t0001g0121a0008c0007t0001g0093 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0083others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0002g0156a0001c0001t0004g0142a0001c0001t0004g0155others(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 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0176others(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 | a0001c0001t0001g0111a0001c0001t0030g0115 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0036others(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 | a0001c0001t0009g0074 | 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 | a0001c0001t0001g0090a0001c0001t0005g0058 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0007g0062 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0052a0001c0001t0003g0067a0001c0001t0034g0053others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0064others(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 | a0001c0001t0002g0160a0001c0001t0004g0150a0001c0001t0009g0123others(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 | a0001c0001t0002g0132a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0004g0154 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0125a0001c0001t0009g0126 | 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 | 6 | a0001c0001t0007g0060a0001c0001t0007g0061a0001c0001t0007g0062others(3): Show | 6 | HG00639.hp1 HG01192.hp1 HG01258.hp1 others(3): 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 | a0001c0001t0030g0115 | 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 | a0001c0001t0006g0120 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0003g0046a0001c0001t0003g0084 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0003g0055 | 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 | a0001c0001t0009g0125a0001c0001t0009g0126 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0001g0057a0001c0001t0001g0176 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0004g0142a0004c0005t0004g0144a0004c0005t0022g0143 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0079others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180 | 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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0002g0141a0001c0001t0002g0145a0001c0001t0002g0147others(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 | a0001c0001t0003g0041a0007c0010t0001g0121 | 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 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0056others(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 | AATATAT | 5 | a0001c0001t0001g0057a0001c0001t0007g0061a0001c0001t0007g0076others(2): Show | 5 | HG01192.hp1 HG03942.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.3106+452_3106+453i others(8): 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0035a0001c0001t0004g0162a0001c0001t0006g0113others(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 | a0001c0001t0001g0033a0001c0001t0009g0074 | 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 | a0001c0001t0007g0075a0001c0001t0028g0040 | 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 | a0001c0001t0001g0049a0001c0001t0003g0041a0007c0010t0001g0121 | 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 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0001g0073others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0007g0060 | 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 | a0001c0001t0001g0091a0001c0001t0001g0109a0001c0001t0003g0044others(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 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0082others(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 | a0001c0001t0001g0079a0001c0001t0001g0087 | 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 | 46 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0035others(43): Show | 46 | HG00639.hp1 HG01099.hp1 HG01169.hp1 others(43): 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 | a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0005g0009a0001c0001t0009g0125a0001c0001t0009g0126others(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 | a0001c0001t0005g0023a0001c0001t0009g0123a0001c0001t0013g0004others(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 | a0001c0001t0001g0051a0001c0001t0002g0165a0001c0001t0004g0154 | 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 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0003g0046others(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 | a0001c0001t0001g0086a0001c0001t0010g0010 | 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 | 93 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0035others(90): Show | 93 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(90): 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 | a0001c0001t0002g0132a0001c0001t0002g0151a0001c0001t0002g0160others(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 | a0001c0001t0002g0136a0001c0001t0002g0139a0001c0001t0002g0140others(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 | a0001c0001t0005g0021a0001c0001t0005g0175a0001c0001t0012g0185others(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 | a0001c0001t0002g0132a0001c0001t0004g0142a0001c0001t0012g0187others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | 36 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0052others(33): Show | 36 | HG00639.hp1 HG01070.hp2 HG01109.hp1 others(33): 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 | a0001c0001t0001g0098a0001c0001t0005g0099 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0123a0001c0001t0009g0125a0001c0001t0009g0126others(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 | a0001c0001t0009g0124a0001c0001t0013g0004 | 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 | a0001c0001t0002g0132a0001c0001t0002g0135a0001c0001t0002g0136others(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 | a0001c0001t0002g0149a0001c0001t0012g0185a0001c0001t0012g0187others(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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0001g0049a0001c0001t0001g0065a0001c0001t0001g0098others(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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0139others(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 | a0001c0001t0002g0141a0001c0001t0002g0165 | 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 | a0001c0001t0001g0101a0001c0001t0021g0158a0001c0001t0031g0054others(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 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0057others(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 | a0001c0001t0005g0009a0001c0001t0005g0022a0001c0001t0005g0023others(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 | a0001c0001t0005g0023a0001c0001t0005g0027a0001c0001t0006g0114others(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 | a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0030g0115 | 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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0006g0113 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0003g0071 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0141 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | 3 | a0001c0001t0007g0061a0001c0001t0007g0075a0001c0001t0007g0076 | 3 | HG00639.hp1 HG01192.hp1 homoSapiens_chm13v2.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 | a0001c0001t0002g0137 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0125a0001c0001t0009g0126 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0052 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0003g0071 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0003g0116 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0028g0040 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0002g0136a0001c0001t0004g0138 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0015g0025 | 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 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0024 | 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 | a0001c0001t0004g0154 | 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 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0051others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0008a0001c0001t0001g0056a0001c0001t0001g0069 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0145a0001c0001t0002g0147a0001c0001t0002g0165others(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 | a0001c0001t0002g0137 | 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 | a0001c0001t0002g0165a0001c0001t0017g0006 | 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 | a0001c0001t0037g0108 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0063 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0059others(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 | a0001c0001t0001g0048a0001c0001t0002g0132a0001c0001t0002g0145others(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 | a0001c0001t0009g0124a0001c0001t0009g0125a0001c0001t0009g0126others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0004g0154 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0002c0002t0036g0179 | 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 | a0002c0002t0036g0179 | 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 | a0002c0002t0036g0179 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0004g0142a0004c0005t0004g0144a0004c0005t0022g0143 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0051others(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 | a0001c0001t0002g0135a0001c0001t0003g0116a0001c0001t0010g0011others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0079others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0004g0142a0004c0005t0004g0144a0004c0005t0022g0143 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0001g0045a0001c0001t0001g0073a0001c0001t0002g0145others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0008g0015a0001c0001t0008g0016 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0003g0084 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0007g0060a0001c0001t0008g0012others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0033g0007 | 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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0002g0132a0001c0001t0002g0137a0001c0001t0002g0139others(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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0161others(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 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0004g0138others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0057a0001c0001t0001g0176 | 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 | a0001c0001t0003g0067 | 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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0004t0001g0034a0001c0004t0001g0088a0001c0004t0001g0089 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0004t0001g0034a0001c0004t0001g0088a0001c0004t0001g0089 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0051others(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 | a0001c0001t0006g0105a0001c0001t0008g0017a0001c0001t0009g0126others(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 | a0001c0001t0005g0026a0001c0001t0020g0030 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0083others(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 | a0001c0001t0001g0033a0001c0001t0003g0071 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0004g0142 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0161 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0045a0001c0001t0001g0083 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0001g0033a0001c0001t0001g0073a0001c0001t0001g0080others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0015others(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 | a0001c0001t0004g0142a0001c0001t0009g0123a0001c0001t0009g0124others(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 | a0001c0001t0002g0132a0001c0001t0002g0165a0001c0001t0002g0171others(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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0002g0136a0001c0001t0002g0156a0001c0001t0002g0167others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0001g0051a0001c0001t0001g0059 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0004g0131a0001c0001t0004g0150a0001c0001t0019g0170 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0135others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0002g0148a0001c0001t0002g0156 | 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 | a0001c0004t0001g0034a0001c0004t0001g0088a0001c0004t0001g0089 | 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 | 19 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0104others(16): Show | 19 | HG01258.hp1 HG01346.hp1 HG01934.hp2 others(16): 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0167others(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 | a0001c0001t0009g0124a0001c0001t0012g0185a0001c0001t0012g0188others(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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0020g0030 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187 | 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 | a0001c0001t0012g0188a0001c0001t0016g0184a0001c0001t0016g0186 | 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 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0129others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0005g0009a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | ||||||
| chr16:68218841
|
A | G | 187 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0035others(184): Show | 187 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(184): Show |
intron_variant | MODIFIER | c.3107-7509A>G | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68218841 | ||||||
| chr16:68219025
|
A | G | 6 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0003g0046a0001c0001t0003g0084 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0004g0162a0001c0001t0004g0163a0001c0001t0004g0164 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0034g0053 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0018g0096a0005c0006t0018g0097 | 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 | a0001c0001t0002g0139a0001c0001t0002g0167 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0024 | 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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0087 | 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 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0065others(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 | a0001c0001t0001g0035a0001c0001t0003g0042a0001c0001t0003g0116others(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 | a0001c0001t0027g0066 | 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 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0082others(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 | 18 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0057others(15): Show | 18 | HG00438.hp1 HG00639.hp1 HG01070.hp2 others(15): 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 | a0001c0001t0002g0133a0001c0001t0002g0135a0001c0001t0002g0136others(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 | a0001c0001t0002g0132a0001c0001t0002g0137a0001c0001t0002g0139others(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 | a0001c0001t0002g0129a0001c0001t0002g0140a0001c0001t0005g0021others(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 | a0001c0001t0001g0038a0001c0001t0003g0094a0001c0001t0005g0009others(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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039 | 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 | a0001c0001t0033g0007 | 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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0002c0002t0014g0177a0002c0002t0014g0180a0002c0002t0036g0179 | 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 | a0001c0001t0013g0001a0001c0001t0013g0003a0001c0001t0013g0004others(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 | a0001c0001t0002g0145a0001c0001t0002g0146 | 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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0001c0001t0002g0167 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0005g0058 | 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 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0092others(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 | a0001c0001t0002g0161a0001c0001t0012g0185a0001c0001t0012g0187others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0004g0142a0001c0001t0013g0001a0001c0001t0013g0003others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0111others(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 | a0001c0001t0001g0065a0001c0001t0001g0101a0001c0001t0009g0123others(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 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0052others(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 | a0001c0001t0009g0123a0001c0001t0009g0124a0001c0001t0009g0125others(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 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(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 | a0001c0001t0010g0010a0001c0001t0010g0011a0001c0001t0010g0019 | 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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0001g0039a0001c0001t0001g0064a0001c0001t0001g0069others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0012g0188others(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 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0014others(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 | a0001c0001t0003g0084 | 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 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(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 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 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 | a0001c0001t0006g0110a0001c0001t0006g0113 | 2 | HG01934.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.3107-131G>A | NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | chr16 | 68226219 |