| geneid | 55015 |
|---|---|
| ensemblid | ENSG00000185246.18 |
| hgncid | 20314 |
| symbol | PRPF39 |
| name | pre-mRNA processing factor 39 |
| refseq_nuc | NM_017922.4 |
| refseq_prot | NP_060392.3 |
| ensembl_nuc | ENST00000355765.11 |
| ensembl_prot | ENSP00000348010.6 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 45084116 |
| end | 45116282 |
| strand | + |
| ver | v1.2 |
| region | chr14:45084116-45116282 |
| region5000 | chr14:45079116-45121282 |
| regionname0 | PRPF39_chr14_45084116_45116282 |
| regionname5000 | PRPF39_chr14_45079116_45121282 |
| 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 | 669 | 239 | 87 | 34 | 87 | 15 | 14 | 63 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0002 | 0/0 | 669 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0003 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0004 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0005 | 0/0 | 669 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| 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 | 2010 | 239 | 87 | 34 | 87 | 15 | 14 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| c0002 | 0/0 | 2010 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| c0003 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| c0004 | 0/0 | 2010 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| c0005 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| 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 | 1/1 | 1523 | 158 | 53 | 28 | 53 | 12 | 10 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0002 | 0/0 | 1522 | 36 | 7 | 3 | 21 | 3 | 2 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0003 | 0/0 | 1522 | 26 | 24 | 2 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0004 | 0/0 | 1524 | 7 | 0 | 0 | 6 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0005 | 0/0 | 1521 | 6 | 5 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0006 | 0/0 | 1520 | 5 | 0 | 0 | 5 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0007 | 0/0 | 1521 | 2 | 0 | 1 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0008 | 0/0 | 1521 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0009 | 0/0 | 1522 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0010 | 0/0 | 1523 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| t0011 | 0/0 | 1522 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| 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 | 0/1 | 17 | 2 | 1 | 12 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0002 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0004 | 1/0 | 7 | 0 | 3 | 0 | 3 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0005 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0006 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| 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 | 2010 | 239 | 87 | 34 | 87 | 15 | 14 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0002c0002 | 0/0 | 2010 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0003c0005 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0004c0003 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0005c0004 | 0/0 | 2010 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3532 | 156 | 53 | 28 | 52 | 11 | 10 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0002 | 0/0 | 3531 | 35 | 6 | 3 | 21 | 3 | 2 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0003 | 0/0 | 3531 | 24 | 22 | 2 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0004 | 0/0 | 3533 | 7 | 0 | 0 | 6 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0005 | 0/0 | 3530 | 6 | 5 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0006 | 0/0 | 3529 | 5 | 0 | 0 | 5 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0007 | 0/0 | 3530 | 2 | 0 | 1 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0008 | 0/0 | 3530 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0009 | 0/0 | 3531 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0010 | 0/0 | 3532 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0001c0001t0011 | 0/0 | 3531 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0002c0002t0003 | 0/0 | 3531 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0003c0005t0001 | 0/0 | 3532 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0004c0003t0002 | 0/0 | 3531 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| a0005c0004t0001 | 0/0 | 3532 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | copy fasta | chr14 | 45079116 | 45121282 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 14 | 2 | 1 | 10 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0004 | 1/0 | 6 | 0 | 2 | 0 | 3 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 5 | 1 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0006g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0009g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0001c0001t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0002c0002t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0002c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0003c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0004c0003t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| a0005c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0056 | EAS | CHS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0132 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0133 | EUR | IBS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0115 | EAS | KHV | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02717 | hp2 | a0004 | c0003 | t0002 | g0141 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0134 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0005 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0131 | SAS | STU | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0137 | AFR | YRI | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18976 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | LWK | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19072 | hp2 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19074 | hp1 | a0003 | c0005 | t0001 | g0102 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | YRI | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ASW | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ASW | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20805 | hp2 | a0005 | c0004 | t0001 | g0054 | EUR | TSI | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | GIH | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | USA | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | USA | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | PRPF39_chr14_45079116_45121282 | PRPF39 | chr14 | 45079116 | 45121282 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:45095223
|
C | G | 1 | a0001 | 1 | HG00438.hp2 | splice_region_variant | LOW | c.-17C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/14 | chr14 | 45095223 | ||||||
| chr14:45095263
|
A | T | 1 | a0003 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.24A>T | p.Glu8Asp | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/14 | 177/3532 | 24/2010 | 8/669 | chr14 | 45095263 | ||
| chr14:45095277
|
G | A | 1 | a0004 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.38G>A | p.Ser13Asn | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/14 | 191/3532 | 38/2010 | 13/669 | chr14 | 45095277 | ||
| chr14:45095381
|
T | C | 1 | a0002 | 2 | HG02895.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.142T>C | p.Ser48Pro | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/14 | 295/3532 | 142/2010 | 48/669 | chr14 | 45095381 | ||
| chr14:45114899
|
C | T | 1 | a0005 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1996C>T | p.Pro666Ser | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 2149/3532 | 1996/2010 | 666/669 | chr14 | 45114899 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:45084189
|
C | T | 1 | a0001c0001t0011 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/14 | 11051 | chr14 | 45084189 | |||||
| chr14:45114918
|
A | C | 1 | a0001c0001t0009 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5A>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 5 | chr14 | 45114918 | |||||
| chr14:45115055
|
TA | T | 2 | a0001c0001t0007a0001c0001t0008 | 3 | HG01106.hp1 HG01516.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*143delA | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 143 | chr14 | 45115055 | |||||
| chr14:45115291
|
C | CT | 1 | a0001c0001t0004 | 7 | HG02015.hp1 HG02056.hp1 HG03017.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*396dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 397 | INFO_REALIGN_3_PRIME | chr14 | 45115291 | ||||
| chr14:45115291
|
CT | C | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(6): Show | 72 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*396delT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 396 | INFO_REALIGN_3_PRIME | chr14 | 45115291 | ||||
| chr14:45115291
|
CTT | C | 1 | a0001c0001t0005 | 6 | HG01884.hp1 HG01891.hp2 HG02132.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*395_*396delTT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 395 | INFO_REALIGN_3_PRIME | chr14 | 45115291 | ||||
| chr14:45115414
|
T | C | 4 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(1): Show | 29 | HG01106.hp1 HG01109.hp1 HG01358.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*501T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 501 | chr14 | 45115414 | |||||
| chr14:45115891
|
TCA | T | 1 | a0001c0001t0006 | 5 | NA18976.hp2 NA18979.hp1 NA19007.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*981_*982delCA | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 981 | INFO_REALIGN_3_PRIME | chr14 | 45115891 | ||||
| chr14:45115952
|
G | C | 1 | a0001c0001t0008 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1039G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 14/14 | 1039 | chr14 | 45115952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:45084331
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-20+82C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45084331 | ||||||
| chr14:45084662
|
A | AT | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+414dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45084662 | |||||
| chr14:45084691
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-20+442C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45084691 | ||||||
| chr14:45085122
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0167others(2): Show | 7 | HG01261.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+873A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45085122 | ||||||
| chr14:45085531
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG01978.hp1 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-20+1282A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45085531 | ||||||
| chr14:45085812
|
C | T | 23 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(20): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-20+1563C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45085812 | ||||||
| chr14:45085938
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(66): Show | 90 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-20+1689A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45085938 | ||||||
| chr14:45085948
|
A | G | 23 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(20): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-20+1699A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45085948 | ||||||
| chr14:45086473
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-20+2224T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45086473 | ||||||
| chr14:45086532
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-20+2283T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45086532 | ||||||
| chr14:45086778
|
T | G | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-20+2529T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45086778 | ||||||
| chr14:45086846
|
G | GT | 20 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0103others(17): Show | 25 | HG00741.hp1 HG00741.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.-20+2620dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45086846 | |||||
| chr14:45086846
|
GT | G | 62 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0028others(59): Show | 78 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.-20+2620delT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45086846 | |||||
| chr14:45086853
|
T | G | 1 | a0001c0001t0003g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-20+2604T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45086853 | ||||||
| chr14:45086854
|
T | G | 23 | a0001c0001t0003g0008a0001c0001t0003g0022a0001c0001t0003g0023others(20): Show | 27 | HG01106.hp1 HG01109.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+2605T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45086854 | ||||||
| chr14:45086855
|
T | G | 1 | a0002c0002t0003g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-20+2606T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45086855 | ||||||
| chr14:45087139
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-20+2890G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45087139 | ||||||
| chr14:45087562
|
G | GT | 23 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(20): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-20+3323dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45087562 | |||||
| chr14:45087568
|
T | TTTTTG | 4 | a0001c0001t0003g0008a0001c0001t0003g0128a0001c0001t0003g0129others(1): Show | 6 | HG02257.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+3334_-20+3338d others(7): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45087568 | |||||
| chr14:45087574
|
T | TTTTGC | 4 | a0001c0001t0003g0022a0001c0001t0003g0116a0001c0001t0003g0117others(1): Show | 5 | HG01358.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+3329_-20+3330i others(7): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45087574 | |||||
| chr14:45087588
|
T | G | 20 | a0001c0001t0003g0008a0001c0001t0003g0022a0001c0001t0003g0023others(17): Show | 24 | HG01109.hp1 HG01358.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-20+3339T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45087588 | ||||||
| chr14:45087678
|
A | G | 1 | a0003c0005t0001g0102 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-20+3429A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45087678 | ||||||
| chr14:45087717
|
G | T | 1 | a0001c0001t0002g0161 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-20+3468G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45087717 | ||||||
| chr14:45087740
|
A | AT | 11 | a0001c0001t0001g0028a0001c0001t0001g0101a0001c0001t0001g0173others(8): Show | 11 | HG01106.hp1 HG01516.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+3511dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45087740 | |||||
| chr14:45087740
|
AT | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 115 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-20+3511delT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45087740 | |||||
| chr14:45087759
|
T | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0114others(13): Show | 22 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20+3510T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45087759 | ||||||
| chr14:45088201
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-20+3952G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45088201 | ||||||
| chr14:45088399
|
A | C | 5 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0008g0133others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+4150A>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45088399 | ||||||
| chr14:45088482
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-20+4233A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45088482 | ||||||
| chr14:45088550
|
T | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0167others(2): Show | 7 | HG01261.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+4301T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45088550 | ||||||
| chr14:45088552
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-20+4303T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45088552 | ||||||
| chr14:45088689
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-20+4440G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45088689 | ||||||
| chr14:45088865
|
T | C | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-20+4616T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45088865 | ||||||
| chr14:45089330
|
C | T | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+5081C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45089330 | ||||||
| chr14:45089532
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+5283G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45089532 | ||||||
| chr14:45089670
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-20+5421T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45089670 | ||||||
| chr14:45090138
|
C | A | 2 | a0001c0001t0003g0119a0001c0001t0003g0120 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-19-5083C>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090138 | ||||||
| chr14:45090206
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(66): Show | 90 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-19-5015A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090206 | ||||||
| chr14:45090294
|
T | G | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-4927T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090294 | ||||||
| chr14:45090312
|
G | A | 2 | a0001c0001t0003g0119a0001c0001t0003g0120 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-19-4909G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090312 | ||||||
| chr14:45090394
|
T | G | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-4827T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090394 | ||||||
| chr14:45090409
|
G | A | 1 | a0001c0001t0002g0087 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-19-4812G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090409 | ||||||
| chr14:45090512
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-19-4709A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090512 | ||||||
| chr14:45090665
|
A | AT | 15 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0114others(12): Show | 21 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19-4550dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45090665 | |||||
| chr14:45090726
|
A | G | 52 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0156others(49): Show | 67 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19-4495A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090726 | ||||||
| chr14:45090966
|
C | G | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-19-4255C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45090966 | ||||||
| chr14:45091028
|
A | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-19-4193A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091028 | ||||||
| chr14:45091058
|
C | CT | 52 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0156others(49): Show | 67 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19-4158dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45091058 | |||||
| chr14:45091175
|
G | C | 7 | a0001c0001t0003g0023a0001c0001t0003g0121a0001c0001t0003g0122others(4): Show | 8 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-4046G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091175 | ||||||
| chr14:45091280
|
A | G | 3 | a0001c0001t0003g0119a0001c0001t0003g0120a0001c0001t0003g0127 | 3 | HG02486.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-19-3941A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091280 | ||||||
| chr14:45091352
|
G | A | 1 | a0001c0001t0005g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-19-3869G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091352 | ||||||
| chr14:45091402
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(67): Show | 91 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-19-3819G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091402 | ||||||
| chr14:45091527
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-3694G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091527 | ||||||
| chr14:45091544
|
T | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-3677T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091544 | ||||||
| chr14:45091612
|
T | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(66): Show | 90 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-19-3609T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091612 | ||||||
| chr14:45091643
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19-3578A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091643 | ||||||
| chr14:45091787
|
A | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-3434A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091787 | ||||||
| chr14:45091819
|
C | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG01433.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-19-3402C>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091819 | ||||||
| chr14:45091820
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19-3401T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091820 | ||||||
| chr14:45091824
|
G | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0150 | 3 | HG02056.hp2 NA18940.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-19-3397G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091824 | ||||||
| chr14:45091886
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-3335T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45091886 | ||||||
| chr14:45092066
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-19-3155G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45092066 | ||||||
| chr14:45092188
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19-3033A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45092188 | ||||||
| chr14:45092192
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-19-3029C>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45092192 | ||||||
| chr14:45092287
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0114others(13): Show | 22 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-2934A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45092287 | ||||||
| chr14:45092340
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0114others(13): Show | 22 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-2881C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45092340 | ||||||
| chr14:45092472
|
G | A | 5 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0008g0133others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-2749G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45092472 | ||||||
| chr14:45092600
|
C | CA | 37 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0030others(34): Show | 40 | HG00597.hp1 HG00673.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19-2597dupA | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45092600 | |||||
| chr14:45092600
|
CA | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0113others(16): Show | 26 | HG01358.hp1 HG01496.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19-2597delA | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45092600 | |||||
| chr14:45092909
|
T | TA | 65 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0113others(62): Show | 86 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.-19-2302dupA | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45092909 | |||||
| chr14:45092940
|
C | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-19-2281C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45092940 | ||||||
| chr14:45093001
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(66): Show | 90 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-19-2220G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093001 | ||||||
| chr14:45093062
|
C | T | 72 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(69): Show | 93 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-19-2159C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093062 | ||||||
| chr14:45093206
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0084 | 2 | NA18953.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-19-2015T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093206 | ||||||
| chr14:45093223
|
A | AT | 4 | a0001c0001t0003g0022a0001c0001t0003g0116a0001c0001t0003g0117others(1): Show | 5 | HG01358.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-1995dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45093223 | |||||
| chr14:45093227
|
A | AT | 59 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0113others(56): Show | 79 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-19-1981dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45093227 | |||||
| chr14:45093227
|
A | T | 4 | a0001c0001t0003g0022a0001c0001t0003g0116a0001c0001t0003g0117others(1): Show | 5 | HG01358.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-1994A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093227 | ||||||
| chr14:45093286
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-19-1935G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093286 | ||||||
| chr14:45093388
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19-1833A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093388 | ||||||
| chr14:45093559
|
C | CT | 44 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0156others(41): Show | 60 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19-1649dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45093559 | |||||
| chr14:45093559
|
C | CTT | 5 | a0001c0001t0003g0124a0001c0001t0003g0126a0001c0001t0003g0135others(2): Show | 5 | HG02258.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-1650_-19-1649d others(4): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 45093559 | |||||
| chr14:45093578
|
G | C | 1 | a0001c0001t0001g0021 | 2 | NA18952.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-19-1643G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093578 | ||||||
| chr14:45093668
|
G | T | 1 | a0001c0001t0001g0040 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-19-1553G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093668 | ||||||
| chr14:45093712
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-19-1509C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093712 | ||||||
| chr14:45093713
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-1508G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093713 | ||||||
| chr14:45093713
|
G | T | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-1508G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093713 | ||||||
| chr14:45093735
|
AGT | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1485_-19-1484d others(4): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093735 | ||||||
| chr14:45093738
|
A | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1483A>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093738 | ||||||
| chr14:45093739
|
G | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1482G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093739 | ||||||
| chr14:45093741
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1480G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093741 | ||||||
| chr14:45093743
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1478C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093743 | ||||||
| chr14:45093744
|
A | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1477A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093744 | ||||||
| chr14:45093745
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1476G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093745 | ||||||
| chr14:45093846
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0081 | 4 | HG00099.hp1 HG00140.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1375C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093846 | ||||||
| chr14:45093932
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19-1289A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093932 | ||||||
| chr14:45093984
|
T | C | 1 | a0001c0001t0003g0129 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-19-1237T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45093984 | ||||||
| chr14:45094204
|
T | A | 23 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(20): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-19-1017T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45094204 | ||||||
| chr14:45094219
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19-1002A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45094219 | ||||||
| chr14:45094301
|
T | C | 52 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0156others(49): Show | 67 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19-920T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45094301 | ||||||
| chr14:45094336
|
C | A | 1 | a0001c0001t0001g0013 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-19-885C>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45094336 | ||||||
| chr14:45094384
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19-837C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45094384 | ||||||
| chr14:45094704
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0103 | 4 | HG00438.hp1 HG00544.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-517T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45094704 | ||||||
| chr14:45094765
|
T | G | 1 | a0001c0001t0001g0012 | 2 | NA18961.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-19-456T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45094765 | ||||||
| chr14:45094880
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-341G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45094880 | ||||||
| chr14:45095007
|
A | C | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19-214A>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45095007 | ||||||
| chr14:45095209
|
G | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-12G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 1/13 | chr14 | 45095209 | ||||||
| chr14:45095837
|
T | G | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.325-266T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/13 | chr14 | 45095837 | ||||||
| chr14:45095889
|
G | GT | 12 | a0001c0001t0001g0034a0001c0001t0001g0078a0001c0001t0001g0079others(9): Show | 12 | HG00597.hp2 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.325-194dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 45095889 | |||||
| chr14:45095889
|
G | GTT | 41 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0148others(38): Show | 53 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.325-195_325-194dup others(2): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 45095889 | |||||
| chr14:45095889
|
G | GTTT | 22 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0114others(19): Show | 31 | HG01358.hp1 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.325-196_325-194dup others(3): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 45095889 | |||||
| chr14:45096011
|
T | C | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.325-92T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/13 | chr14 | 45096011 | ||||||
| chr14:45096050
|
AT | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0113others(14): Show | 23 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.325-46delT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 45096050 | |||||
| chr14:45096295
|
A | AT | 33 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0036others(30): Show | 41 | HG00741.hp1 HG01175.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.450+88dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 45096295 | |||||
| chr14:45096295
|
A | ATT | 32 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(29): Show | 45 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.450+87_450+88dupTT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 45096295 | |||||
| chr14:45096295
|
A | ATTT | 12 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0003g0117others(9): Show | 12 | HG01106.hp1 HG01516.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.450+86_450+88dupTT others(1): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 45096295 | |||||
| chr14:45096302
|
T | C | 1 | a0005c0004t0001g0054 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.450+74T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 3/13 | chr14 | 45096302 | ||||||
| chr14:45097135
|
ATAAACT | A | 20 | a0001c0001t0003g0008a0001c0001t0003g0022a0001c0001t0003g0023others(17): Show | 24 | HG01109.hp1 HG01358.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.569+134_569+139del others(6): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 45097135 | |||||
| chr14:45097464
|
T | C | 2 | a0001c0001t0002g0024a0001c0001t0002g0150 | 3 | HG02056.hp2 NA18940.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.569+459T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45097464 | ||||||
| chr14:45097818
|
A | G | 1 | a0001c0001t0001g0027 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.569+813A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45097818 | ||||||
| chr14:45097831
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.569+826G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45097831 | ||||||
| chr14:45097875
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.569+870A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45097875 | ||||||
| chr14:45098053
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0113others(10): Show | 17 | HG01496.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.569+1048A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098053 | ||||||
| chr14:45098238
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.569+1233C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098238 | ||||||
| chr14:45098438
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.569+1433C>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098438 | ||||||
| chr14:45098446
|
C | CA | 6 | a0001c0001t0001g0088a0001c0001t0003g0119a0001c0001t0003g0120others(3): Show | 6 | HG02486.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+1457dupA | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 45098446 | |||||
| chr14:45098461
|
AAGAG | A | 23 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(20): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.569+1464_569+1467d others(6): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 45098461 | |||||
| chr14:45098519
|
A | C | 23 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(20): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.569+1514A>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098519 | ||||||
| chr14:45098522
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.569+1517C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098522 | ||||||
| chr14:45098565
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.569+1560C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098565 | ||||||
| chr14:45098672
|
T | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+1667T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098672 | ||||||
| chr14:45098861
|
T | C | 25 | a0001c0001t0003g0008a0001c0001t0003g0022a0001c0001t0003g0023others(22): Show | 29 | HG01106.hp1 HG01109.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.569+1856T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098861 | ||||||
| chr14:45098891
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.569+1886A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45098891 | ||||||
| chr14:45099043
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0113others(13): Show | 22 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.569+2038A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45099043 | ||||||
| chr14:45099073
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.569+2068T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45099073 | ||||||
| chr14:45099441
|
GATT | G | 5 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0008g0133others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.569+2446_569+2448d others(5): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 45099441 | |||||
| chr14:45099451
|
A | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0100 | 3 | HG03239.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.569+2446A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45099451 | ||||||
| chr14:45099509
|
A | T | 1 | a0001c0001t0001g0067 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.569+2504A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45099509 | ||||||
| chr14:45099545
|
C | T | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.569+2540C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45099545 | ||||||
| chr14:45099586
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.569+2581A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45099586 | ||||||
| chr14:45099888
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.570-2641C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45099888 | ||||||
| chr14:45099972
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.570-2557A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45099972 | ||||||
| chr14:45100073
|
C | G | 2 | a0001c0001t0003g0119a0001c0001t0003g0120 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570-2456C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45100073 | ||||||
| chr14:45100207
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.570-2322G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45100207 | ||||||
| chr14:45100231
|
AAAAC | A | 47 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0156others(44): Show | 62 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.570-2270_570-2267d others(6): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 45100231 | |||||
| chr14:45100231
|
AAAACAAA others(1): Show |
A | 3 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0008g0133 | 3 | HG01106.hp1 HG01516.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.570-2274_570-2267d others(10): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 45100231 | |||||
| chr14:45100839
|
A | C | 1 | a0001c0001t0001g0064 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.570-1690A>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45100839 | ||||||
| chr14:45100910
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.570-1619A>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45100910 | ||||||
| chr14:45101130
|
T | C | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.570-1399T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101130 | ||||||
| chr14:45101254
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.570-1275G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101254 | ||||||
| chr14:45101460
|
C | CTT | 44 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(41): Show | 59 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.570-1059_570-1058d others(4): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 45101460 | |||||
| chr14:45101570
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.570-959A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101570 | ||||||
| chr14:45101623
|
G | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-906G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101623 | ||||||
| chr14:45101665
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065 | 3 | HG00544.hp1 NA18953.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.570-864C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101665 | ||||||
| chr14:45101689
|
C | G | 1 | a0001c0001t0002g0061 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.570-840C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101689 | ||||||
| chr14:45101732
|
C | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.570-797C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101732 | ||||||
| chr14:45101758
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.570-771T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101758 | ||||||
| chr14:45101809
|
C | CT | 6 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0173others(3): Show | 6 | HG01891.hp2 HG01981.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.570-705dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 45101809 | |||||
| chr14:45101871
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.570-658A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101871 | ||||||
| chr14:45101882
|
T | C | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.570-647T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101882 | ||||||
| chr14:45101938
|
C | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-591C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101938 | ||||||
| chr14:45101949
|
G | C | 2 | a0001c0001t0003g0119a0001c0001t0003g0120 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570-580G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45101949 | ||||||
| chr14:45102241
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.570-288A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 4/13 | chr14 | 45102241 | ||||||
| chr14:45102833
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.737+137A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45102833 | ||||||
| chr14:45102953
|
G | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0097 | 2 | HG01928.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.737+257G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45102953 | ||||||
| chr14:45103012
|
T | G | 1 | a0001c0001t0002g0011 | 3 | HG00280.hp2 HG00323.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.737+316T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103012 | ||||||
| chr14:45103014
|
T | G | 1 | a0001c0001t0002g0011 | 3 | HG00280.hp2 HG00323.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.737+318T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103014 | ||||||
| chr14:45103318
|
A | G | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.737+622A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103318 | ||||||
| chr14:45103319
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.737+623T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103319 | ||||||
| chr14:45103325
|
A | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0025others(79): Show | 108 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.737+629A>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103325 | ||||||
| chr14:45103340
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+644A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103340 | ||||||
| chr14:45103341
|
A | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+645A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103341 | ||||||
| chr14:45103363
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.737+667G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103363 | ||||||
| chr14:45103564
|
G | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.737+868G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103564 | ||||||
| chr14:45103613
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.737+917G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103613 | ||||||
| chr14:45103654
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.737+958C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103654 | ||||||
| chr14:45103797
|
T | C | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.737+1101T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45103797 | ||||||
| chr14:45104137
|
TCTC | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+1444_737+1446d others(5): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 45104137 | |||||
| chr14:45104173
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.737+1477C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45104173 | ||||||
| chr14:45104307
|
T | C | 2 | a0001c0001t0003g0119a0001c0001t0003g0120 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.737+1611T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45104307 | ||||||
| chr14:45104403
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.737+1707A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45104403 | ||||||
| chr14:45104590
|
G | A | 12 | a0001c0001t0003g0023a0001c0001t0003g0119a0001c0001t0003g0120others(9): Show | 13 | HG01109.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.737+1894G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45104590 | ||||||
| chr14:45104591
|
C | T | 25 | a0001c0001t0003g0008a0001c0001t0003g0022a0001c0001t0003g0023others(22): Show | 29 | HG01106.hp1 HG01109.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.737+1895C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45104591 | ||||||
| chr14:45105240
|
A | G | 2 | a0001c0001t0003g0128a0001c0001t0003g0130 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.738-2211A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45105240 | ||||||
| chr14:45105327
|
C | A | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.738-2124C>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45105327 | ||||||
| chr14:45105525
|
C | CT | 5 | a0001c0001t0001g0034a0001c0001t0001g0092a0001c0001t0001g0106others(2): Show | 5 | HG02145.hp1 HG02965.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-1907dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 45105525 | |||||
| chr14:45105525
|
CT | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0070a0001c0001t0001g0078others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.738-1907delT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 45105525 | |||||
| chr14:45105558
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0167 | 3 | HG01261.hp1 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.738-1893G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45105558 | ||||||
| chr14:45105806
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.738-1645G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45105806 | ||||||
| chr14:45106048
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.738-1403A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45106048 | ||||||
| chr14:45106119
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.738-1332G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45106119 | ||||||
| chr14:45106147
|
C | T | 50 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0160others(47): Show | 65 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.738-1304C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45106147 | ||||||
| chr14:45106148
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.738-1303G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45106148 | ||||||
| chr14:45106498
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.738-953G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45106498 | ||||||
| chr14:45106582
|
T | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-869T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45106582 | ||||||
| chr14:45106866
|
G | A | 52 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0156others(49): Show | 67 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.738-585G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45106866 | ||||||
| chr14:45106952
|
G | T | 2 | a0001c0001t0005g0138a0001c0001t0005g0139 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.738-499G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45106952 | ||||||
| chr14:45107090
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.738-361C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45107090 | ||||||
| chr14:45107238
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.738-213G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 5/13 | chr14 | 45107238 | ||||||
| chr14:45107632
|
C | G | 1 | a0001c0001t0005g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.903+16C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 6/13 | chr14 | 45107632 | ||||||
| chr14:45107805
|
T | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0114others(12): Show | 21 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.903+189T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 6/13 | chr14 | 45107805 | ||||||
| chr14:45107936
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.903+320A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 6/13 | chr14 | 45107936 | ||||||
| chr14:45108160
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.904-255A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 6/13 | chr14 | 45108160 | ||||||
| chr14:45108630
|
T | A | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1011+108T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45108630 | ||||||
| chr14:45108645
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1011+123A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45108645 | ||||||
| chr14:45108664
|
T | C | 1 | a0001c0001t0005g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1011+142T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45108664 | ||||||
| chr14:45108673
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1011+151T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45108673 | ||||||
| chr14:45108741
|
T | A | 1 | a0001c0001t0002g0158 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1011+219T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45108741 | ||||||
| chr14:45108840
|
A | G | 48 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0162others(45): Show | 63 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1011+318A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45108840 | ||||||
| chr14:45109038
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1011+516C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45109038 | ||||||
| chr14:45109055
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0129 | 4 | HG02257.hp2 HG02723.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+533C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45109055 | ||||||
| chr14:45109441
|
T | TC | 20 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0113others(17): Show | 26 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1012-175_1012-174i others(3): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45109441 | ||||||
| chr14:45109442
|
G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0113others(17): Show | 26 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1012-174G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | chr14 | 45109442 | ||||||
| chr14:45109499
|
TATG | T | 47 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0162others(44): Show | 62 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1012-114_1012-112d others(5): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 45109499 | |||||
| chr14:45110322
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0071 | 2 | HG02165.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1303+102A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 9/13 | chr14 | 45110322 | ||||||
| chr14:45110437
|
T | G | 1 | a0001c0001t0001g0040 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1304-112T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 9/13 | chr14 | 45110437 | ||||||
| chr14:45110926
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1572+109A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | chr14 | 45110926 | ||||||
| chr14:45111008
|
T | G | 47 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0162others(44): Show | 62 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1572+191T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | chr14 | 45111008 | ||||||
| chr14:45111353
|
C | CT | 8 | a0001c0001t0002g0143a0001c0001t0003g0023a0001c0001t0003g0121others(5): Show | 9 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1572+547dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 45111353 | |||||
| chr14:45111631
|
C | CT | 49 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0017others(46): Show | 67 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1573-660dupT | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 45111631 | |||||
| chr14:45111631
|
C | CTT | 19 | a0001c0001t0001g0019a0001c0001t0001g0081a0001c0001t0001g0113others(16): Show | 23 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1573-661_1573-660d others(4): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 45111631 | |||||
| chr14:45111631
|
C | CTTTT | 6 | a0001c0001t0001g0101a0001c0001t0003g0119a0001c0001t0003g0121others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1573-663_1573-660d others(6): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 45111631 | |||||
| chr14:45111631
|
C | CTTTTT | 4 | a0001c0001t0003g0023a0001c0001t0003g0120a0001c0001t0003g0125others(1): Show | 5 | HG01109.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1573-664_1573-660d others(7): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 45111631 | |||||
| chr14:45111631
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0055a0001c0001t0001g0089 | 2 | HG01109.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1573-670_1573-660d others(13): Show |
PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 45111631 | |||||
| chr14:45111658
|
T | C | 2 | a0001c0001t0002g0143a0004c0003t0002g0141 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1573-660T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | chr14 | 45111658 | ||||||
| chr14:45111834
|
T | TA | 5 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0008g0133others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1573-483dupA | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 45111834 | |||||
| chr14:45112002
|
G | A | 1 | a0001c0001t0010g0056 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1573-316G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | chr14 | 45112002 | ||||||
| chr14:45112081
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0103 | 4 | HG00438.hp1 HG00544.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573-237G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | chr14 | 45112081 | ||||||
| chr14:45112134
|
C | A | 1 | a0001c0001t0002g0009 | 3 | HG02717.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1573-184C>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 10/13 | chr14 | 45112134 | ||||||
| chr14:45112555
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0004g0018others(1): Show | 5 | HG02015.hp1 HG02071.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1757+53T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112555 | ||||||
| chr14:45112700
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1757+198T>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112700 | ||||||
| chr14:45112813
|
C | G | 20 | a0001c0001t0003g0008a0001c0001t0003g0022a0001c0001t0003g0023others(17): Show | 24 | HG01109.hp1 HG01358.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1757+311C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112813 | ||||||
| chr14:45112875
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+373G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112875 | ||||||
| chr14:45112876
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+374A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112876 | ||||||
| chr14:45112877
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+375G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112877 | ||||||
| chr14:45112879
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+377G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112879 | ||||||
| chr14:45112881
|
T | A | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+379T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112881 | ||||||
| chr14:45112882
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+380A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112882 | ||||||
| chr14:45112883
|
T | A | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+381T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112883 | ||||||
| chr14:45112884
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+382T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112884 | ||||||
| chr14:45112886
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+384T>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112886 | ||||||
| chr14:45112887
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+385C>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112887 | ||||||
| chr14:45112890
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+388A>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112890 | ||||||
| chr14:45112891
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1757+389G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112891 | ||||||
| chr14:45112916
|
C | G | 47 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0162others(44): Show | 62 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1757+414C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112916 | ||||||
| chr14:45112961
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0113others(17): Show | 26 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1757+459C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45112961 | ||||||
| chr14:45113074
|
G | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0005g0028others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1757+572G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45113074 | ||||||
| chr14:45113087
|
G | C | 47 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0001g0162others(44): Show | 62 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1757+585G>C | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45113087 | ||||||
| chr14:45113309
|
G | T | 1 | a0001c0001t0004g0108 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1757+807G>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45113309 | ||||||
| chr14:45113426
|
G | A | 8 | a0001c0001t0003g0008a0001c0001t0003g0022a0001c0001t0003g0116others(5): Show | 11 | HG01358.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1758-757G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45113426 | ||||||
| chr14:45113643
|
C | G | 1 | a0001c0001t0002g0009 | 3 | HG02717.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1758-540C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45113643 | ||||||
| chr14:45113665
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0057 | 2 | HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1758-518C>T | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45113665 | ||||||
| chr14:45113897
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1758-286A>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45113897 | ||||||
| chr14:45114078
|
G | A | 3 | a0001c0001t0006g0010a0001c0001t0006g0149a0001c0001t0006g0154 | 5 | NA18976.hp2 NA18979.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1758-105G>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 11/13 | chr14 | 45114078 | ||||||
| chr14:45114279
|
C | G | 1 | a0001c0001t0003g0130 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1832+22C>G | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 12/13 | chr14 | 45114279 | ||||||
| chr14:45114450
|
AC | A | 4 | a0001c0001t0003g0008a0001c0001t0003g0128a0001c0001t0003g0129others(1): Show | 6 | HG02257.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1833-42delC | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 45114450 | |||||
| chr14:45114686
|
T | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0084others(14): Show | 23 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1953+72T>A | PRPF39 | ENSG00000185246.18 | transcript | ENST00000355765.11 | protein_coding | 13/13 | chr14 | 45114686 |