| geneid | 6185 |
|---|---|
| ensemblid | ENSG00000118705.18 |
| hgncid | 10382 |
| symbol | RPN2 |
| name | ribophorin II |
| refseq_nuc | NM_002951.5 |
| refseq_prot | NP_002942.2 |
| ensembl_nuc | ENST00000237530.11 |
| ensembl_prot | ENSP00000237530.6 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 37179330 |
| end | 37241619 |
| strand | + |
| ver | v1.2 |
| region | chr20:37179330-37241619 |
| region5000 | chr20:37174330-37246619 |
| regionname0 | RPN2_chr20_37179330_37241619 |
| regionname5000 | RPN2_chr20_37174330_37246619 |
| 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 | 631 | 331 | 75 | 63 | 144 | 12 | 35 | 112 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0002 | 0/0 | 631 | 4 | 0 | 0 | 1 | 0 | 3 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0003 | 0/0 | 631 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0004 | 0/0 | 631 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0005 | 0/0 | 631 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0006 | 0/0 | 631 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0007 | 0/0 | 631 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0008 | 0/0 | 631 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0009 | 0/0 | 631 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| 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 | 0/1 | 1896 | 199 | 56 | 38 | 71 | 8 | 25 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0002 | 1/0 | 1896 | 129 | 19 | 25 | 70 | 4 | 10 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0003 | 0/0 | 1896 | 4 | 0 | 0 | 1 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0004 | 0/0 | 1896 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0005 | 0/0 | 1896 | 2 | 0 | 1 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0006 | 0/0 | 1896 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0007 | 0/0 | 1896 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0008 | 0/0 | 1896 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0009 | 0/0 | 1896 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0010 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| c0011 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| 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 | 332 | 345 | 78 | 64 | 150 | 11 | 40 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| t0002 | 0/0 | 332 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0002 | 0/0 | 9 | 1 | 5 | 2 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0003 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0004 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0005 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0007 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0020 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| 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 | 0/1 | 1896 | 199 | 56 | 38 | 71 | 8 | 25 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0001c0002 | 1/0 | 1896 | 129 | 19 | 25 | 70 | 4 | 10 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0001c0004 | 0/0 | 1896 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0002c0003 | 0/0 | 1896 | 4 | 0 | 0 | 1 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0003c0006 | 0/0 | 1896 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0004c0008 | 0/0 | 1896 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0005c0007 | 0/0 | 1896 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0006c0005 | 0/0 | 1896 | 2 | 0 | 1 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0007c0009 | 0/0 | 1896 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0008c0010 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0009c0011 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2227 | 198 | 56 | 38 | 71 | 7 | 25 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0001c0001t0002 | 0/0 | 2227 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0001c0002t0001 | 1/0 | 2227 | 129 | 19 | 25 | 70 | 4 | 10 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0001c0004t0001 | 0/0 | 2227 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0002c0003t0001 | 0/0 | 2227 | 4 | 0 | 0 | 1 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0003c0006t0001 | 0/0 | 2227 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0004c0008t0001 | 0/0 | 2227 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0005c0007t0001 | 0/0 | 2227 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0006c0005t0001 | 0/0 | 2227 | 2 | 0 | 1 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0007c0009t0001 | 0/0 | 2227 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0008c0010t0001 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| a0009c0011t0001 | 0/0 | 2227 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | copy fasta | chr20 | 37174330 | 37246619 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0002 | 0/0 | 9 | 1 | 5 | 2 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0002t0001g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0004t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0003c0006t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0004c0008t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0004c0008t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0005c0007t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0005c0007t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0006c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0006c0005t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0007c0009t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0008c0010t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| a0009c0011t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | FIN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0092 | EUR | FIN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00639 | hp2 | a0006 | c0005 | t0001 | g0236 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0040 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0166 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | CDX | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0135 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02615 | hp2 | a0005 | c0007 | t0001 | g0207 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02622 | hp1 | a0008 | c0010 | t0001 | g0124 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0137 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0132 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03579 | hp2 | a0005 | c0007 | t0001 | g0208 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04184 | hp1 | a0007 | c0009 | t0001 | g0243 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0133 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18747 | hp2 | a0004 | c0008 | t0001 | g0078 | EAS | CHB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18954 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19003 | hp2 | a0004 | c0008 | t0001 | g0089 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19012 | hp1 | a0009 | c0011 | t0001 | g0189 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19067 | hp1 | a0003 | c0006 | t0001 | g0026 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19076 | hp1 | a0001 | c0004 | t0001 | g0186 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19088 | hp2 | a0003 | c0006 | t0001 | g0026 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0069 | EUR | TSI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA20905 | hp1 | a0006 | c0005 | t0001 | g0235 | SAS | GIH | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | GIH | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | USA | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0155 | REF | REF | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0270 | REF | REF | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:37184332
|
G | A | 1 | a0007 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.166G>A | p.Val56Met | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/17 | 193/2227 | 166/1896 | 56/631 | chr20 | 37184332 | ||
| chr20:37199103
|
C | G | 1 | a0009 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.357C>G | p.Asp119Glu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/17 | 384/2227 | 357/1896 | 119/631 | chr20 | 37199103 | ||
| chr20:37207423
|
G | A | 1 | a0006 | 2 | HG00639.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.841G>A | p.Asp281Asn | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/17 | 868/2227 | 841/1896 | 281/631 | chr20 | 37207423 | ||
| chr20:37223906
|
G | A | 1 | a0002 | 4 | HG02523.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
missense_variant | MODERATE | c.1121G>A | p.Gly374Asp | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/17 | 1148/2227 | 1121/1896 | 374/631 | chr20 | 37223906 | ||
| chr20:37228577
|
A | T | 1 | a0003 | 2 | NA19067.hp1 NA19088.hp2 |
missense_variant | MODERATE | c.1327A>T | p.Thr443Ser | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/17 | 1354/2227 | 1327/1896 | 443/631 | chr20 | 37228577 | ||
| chr20:37228622
|
G | A | 1 | a0008 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1372G>A | p.Val458Met | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/17 | 1399/2227 | 1372/1896 | 458/631 | chr20 | 37228622 | ||
| chr20:37228622
|
G | T | 1 | a0004 | 2 | NA18747.hp2 NA19003.hp2 |
missense_variant | MODERATE | c.1372G>T | p.Val458Leu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/17 | 1399/2227 | 1372/1896 | 458/631 | chr20 | 37228622 | ||
| chr20:37229979
|
G | T | 1 | a0005 | 2 | HG02615.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.1501G>T | p.Val501Leu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/17 | 1528/2227 | 1501/1896 | 501/631 | chr20 | 37229979 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:37228576
|
G | A | 1 | a0003c0006 | 2 | NA19067.hp1 NA19088.hp2 |
synonymous_variant | LOW | c.1326G>A | p.Lys442Lys | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/17 | 1353/2227 | 1326/1896 | 442/631 | chr20 | 37228576 | ||
| chr20:37232377
|
C | T | 1 | a0001c0004 | 3 | HG02080.hp1 NA18954.hp2 NA19076.hp1 |
synonymous_variant | LOW | c.1663C>T | p.Leu555Leu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/17 | 1690/2227 | 1663/1896 | 555/631 | chr20 | 37232377 | ||
| chr20:37236651
|
C | T | 9 | a0001c0001a0001c0004a0002c0003others(6): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
synonymous_variant | LOW | c.1825C>T | p.Leu609Leu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/17 | 1852/2227 | 1825/1896 | 609/631 | chr20 | 37236651 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:37241413
|
A | G | 1 | a0001c0001t0002 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 17/17 | 98 | chr20 | 37241413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:37179387
|
G | GCTTACAG others(22): Show |
66 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0005others(63): Show | 96 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.13+21_13+22insACAG others(25): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37179387 | |||||
| chr20:37179387
|
G | GCTTATAG others(22): Show |
204 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(201): Show | 249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.13+21_13+22insATAG others(25): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37179387 | |||||
| chr20:37179394
|
GGA | G | 4 | a0001c0002t0001g0011a0001c0002t0001g0037a0001c0002t0001g0268others(1): Show | 7 | HG00609.hp2 HG02738.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+29_13+30delAG | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37179394 | |||||
| chr20:37179449
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.13+80C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179449 | ||||||
| chr20:37179610
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0255others(12): Show | 18 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+241C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179610 | ||||||
| chr20:37179804
|
C | T | 72 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(69): Show | 84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.13+435C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179804 | ||||||
| chr20:37179821
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.13+452G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179821 | ||||||
| chr20:37179882
|
A | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(20): Show | 28 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.13+513A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179882 | ||||||
| chr20:37180031
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.13+662G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180031 | ||||||
| chr20:37180151
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.13+782C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180151 | ||||||
| chr20:37180173
|
C | T | 8 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG00609.hp1 HG00738.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.13+804C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180173 | ||||||
| chr20:37180220
|
C | G | 74 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(71): Show | 86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.13+851C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180220 | ||||||
| chr20:37180410
|
T | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(6): Show | 10 | HG01361.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.13+1041T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180410 | ||||||
| chr20:37180576
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.13+1207G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180576 | ||||||
| chr20:37180614
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13+1245C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180614 | ||||||
| chr20:37180819
|
T | G | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.13+1450T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180819 | ||||||
| chr20:37180893
|
T | C | 3 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040 | 3 | HG01074.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.13+1524T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180893 | ||||||
| chr20:37180920
|
C | T | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.13+1551C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180920 | ||||||
| chr20:37181005
|
C | T | 72 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(69): Show | 84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.13+1636C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181005 | ||||||
| chr20:37181047
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.13+1678G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181047 | ||||||
| chr20:37181076
|
A | C | 1 | a0009c0011t0001g0189 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.13+1707A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181076 | ||||||
| chr20:37181099
|
C | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(65): Show | 80 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.13+1730C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181099 | ||||||
| chr20:37181178
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(69): Show | 84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.13+1809G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181178 | ||||||
| chr20:37181209
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.13+1840C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181209 | ||||||
| chr20:37181226
|
TA | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 11 | HG01361.hp2 HG01934.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.13+1871delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181226 | |||||
| chr20:37181380
|
T | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(71): Show | 86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.13+2011T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181380 | ||||||
| chr20:37181421
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13+2052T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181421 | ||||||
| chr20:37181431
|
C | CT | 10 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0103others(7): Show | 11 | HG00323.hp2 HG02280.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.13+2080dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181431 | |||||
| chr20:37181431
|
CT | C | 52 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0031others(49): Show | 61 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.13+2080delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181431 | |||||
| chr20:37181431
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.13+2069_13+2080del others(12): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181431 | |||||
| chr20:37181577
|
G | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(196): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.13+2208G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181577 | ||||||
| chr20:37181769
|
T | C | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.13+2400T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181769 | ||||||
| chr20:37181882
|
T | C | 2 | a0006c0005t0001g0235a0006c0005t0001g0236 | 2 | HG00639.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.14-2298T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181882 | ||||||
| chr20:37181912
|
G | GTTC | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(196): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.14-2266_14-2265ins others(3): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181912 | |||||
| chr20:37181943
|
A | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(113): Show | 147 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.14-2237A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181943 | ||||||
| chr20:37181969
|
T | C | 83 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(80): Show | 96 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.14-2211T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181969 | ||||||
| chr20:37182159
|
T | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-2021T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182159 | ||||||
| chr20:37182160
|
C | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-2020C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182160 | ||||||
| chr20:37182178
|
C | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0101others(8): Show | 12 | HG01361.hp2 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.14-2002C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182178 | ||||||
| chr20:37182362
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.14-1818G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182362 | ||||||
| chr20:37182550
|
C | T | 2 | a0001c0002t0001g0041a0001c0002t0001g0091 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.14-1630C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182550 | ||||||
| chr20:37182638
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(69): Show | 84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.14-1542G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182638 | ||||||
| chr20:37182664
|
G | A | 68 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(65): Show | 80 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.14-1516G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182664 | ||||||
| chr20:37182686
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.14-1494C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182686 | ||||||
| chr20:37182773
|
G | A | 6 | a0001c0002t0001g0028a0001c0002t0001g0042a0001c0002t0001g0179others(3): Show | 7 | HG00741.hp2 HG01167.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.14-1407G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182773 | ||||||
| chr20:37182971
|
T | C | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.14-1209T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182971 | ||||||
| chr20:37183083
|
G | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(196): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.14-1097G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183083 | ||||||
| chr20:37183219
|
A | AT | 83 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(80): Show | 96 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.14-948dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37183219 | |||||
| chr20:37183405
|
G | A | 83 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(80): Show | 96 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.14-775G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183405 | ||||||
| chr20:37183490
|
C | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(196): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.14-690C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183490 | ||||||
| chr20:37183558
|
T | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(197): Show | 244 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.14-622T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183558 | ||||||
| chr20:37183767
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.14-413G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183767 | ||||||
| chr20:37183769
|
A | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.14-411A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183769 | ||||||
| chr20:37183805
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-375G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183805 | ||||||
| chr20:37183845
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.14-335C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183845 | ||||||
| chr20:37184071
|
C | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0168a0001c0001t0001g0169others(10): Show | 14 | HG00408.hp2 HG00621.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.14-109C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37184071 | ||||||
| chr20:37184123
|
C | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(69): Show | 84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.14-57C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37184123 | ||||||
| chr20:37184424
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.207+51C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184424 | ||||||
| chr20:37184508
|
T | A | 1 | a0001c0002t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.207+135T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184508 | ||||||
| chr20:37184526
|
C | G | 7 | a0001c0001t0001g0106a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 8 | HG02080.hp1 NA18954.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+153C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184526 | ||||||
| chr20:37184626
|
G | A | 74 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(71): Show | 86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.207+253G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184626 | ||||||
| chr20:37184967
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.207+594T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184967 | ||||||
| chr20:37184971
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+598C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184971 | ||||||
| chr20:37185111
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.207+738T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185111 | ||||||
| chr20:37185144
|
CT | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(71): Show | 86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.207+788delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37185144 | |||||
| chr20:37185240
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.207+867A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185240 | ||||||
| chr20:37185576
|
T | G | 10 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(7): Show | 10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+1203T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185576 | ||||||
| chr20:37185599
|
C | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(71): Show | 86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.207+1226C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185599 | ||||||
| chr20:37185642
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.207+1269G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185642 | ||||||
| chr20:37185822
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.207+1449C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185822 | ||||||
| chr20:37185948
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.207+1575A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185948 | ||||||
| chr20:37186098
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.207+1725A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186098 | ||||||
| chr20:37186318
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+1945T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186318 | ||||||
| chr20:37186567
|
C | G | 1 | a0005c0007t0001g0208 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.207+2194C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186567 | ||||||
| chr20:37186765
|
C | T | 2 | a0006c0005t0001g0235a0006c0005t0001g0236 | 2 | HG00639.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.207+2392C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186765 | ||||||
| chr20:37186768
|
C | T | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.207+2395C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186768 | ||||||
| chr20:37186895
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.207+2522A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186895 | ||||||
| chr20:37187089
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.207+2716A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187089 | ||||||
| chr20:37187206
|
TAAGATCA others(305): Show |
T | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.207+2848_207+3159d others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187206 | |||||
| chr20:37187285
|
G | A | 2 | a0001c0002t0001g0012a0001c0002t0001g0048 | 3 | NA18948.hp2 NA18995.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.207+2912G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187285 | ||||||
| chr20:37187394
|
T | C | 1 | a0001c0002t0001g0049 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.207+3021T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187394 | ||||||
| chr20:37187501
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.207+3137_207+3147d others(13): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | |||||
| chr20:37187501
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.207+3134_207+3147d others(16): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | |||||
| chr20:37187501
|
C | CAAAAAAA others(10): Show |
1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.207+3131_207+3147d others(19): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | |||||
| chr20:37187501
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0001g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.207+3129_207+3147d others(21): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | |||||
| chr20:37187501
|
C | CAAAAAAA others(17): Show |
1 | a0001c0002t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.207+3147_207+3148i others(26): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | |||||
| chr20:37187501
|
C | CAAAAAAA others(18): Show |
1 | a0001c0002t0001g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.207+3147_207+3148i others(27): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | |||||
| chr20:37187501
|
C | CAAAAAAA others(29): Show |
1 | a0001c0002t0001g0109 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.207+3147_207+3148i others(38): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | |||||
| chr20:37187501
|
CAA | C | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+3146_207+3147d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | |||||
| chr20:37187635
|
A | T | 1 | a0001c0002t0001g0090 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.207+3262A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187635 | ||||||
| chr20:37187669
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.207+3296T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187669 | ||||||
| chr20:37187921
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.207+3548G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187921 | ||||||
| chr20:37187976
|
T | G | 1 | a0001c0002t0001g0090 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.207+3603T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187976 | ||||||
| chr20:37188208
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.207+3835T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188208 | ||||||
| chr20:37188209
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG00408.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.207+3836G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188209 | ||||||
| chr20:37188271
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3898C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188271 | ||||||
| chr20:37188303
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.207+3930C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188303 | ||||||
| chr20:37188320
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.207+3947G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188320 | ||||||
| chr20:37188331
|
T | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+3958T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188331 | ||||||
| chr20:37188414
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0196 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.207+4041A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188414 | ||||||
| chr20:37188420
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.207+4047T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188420 | ||||||
| chr20:37188448
|
C | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.207+4075C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188448 | ||||||
| chr20:37188574
|
T | C | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+4201T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188574 | ||||||
| chr20:37188594
|
G | A | 6 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(3): Show | 6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+4221G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188594 | ||||||
| chr20:37188620
|
C | CT | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(164): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.207+4260dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37188620 | |||||
| chr20:37188620
|
CT | C | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+4260delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37188620 | |||||
| chr20:37188663
|
G | A | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | HG02622.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.207+4290G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188663 | ||||||
| chr20:37188784
|
A | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.207+4411A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188784 | ||||||
| chr20:37188798
|
T | A | 30 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(27): Show | 34 | HG00741.hp1 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.207+4425T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188798 | ||||||
| chr20:37189025
|
G | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.207+4652G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189025 | ||||||
| chr20:37189114
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.207+4741T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189114 | ||||||
| chr20:37189209
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.207+4836A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189209 | ||||||
| chr20:37189311
|
CTGTGTGT others(5): Show |
C | 6 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0119others(3): Show | 6 | HG00438.hp1 HG01099.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+4950_207+4961d others(14): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189311 | |||||
| chr20:37189311
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG02040.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.207+4950_207+4963d others(16): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189311 | |||||
| chr20:37189311
|
CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0001g0116 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.207+4950_207+4967d others(20): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189311 | |||||
| chr20:37189311
|
CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0001g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.207+4950_207+4971d others(24): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189311 | |||||
| chr20:37189313
|
GTGTGTGT others(3): Show |
G | 29 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0030others(26): Show | 32 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.207+4950_207+4959d others(12): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189313 | |||||
| chr20:37189315
|
GTGTGTGT others(1): Show |
G | 28 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0031others(25): Show | 38 | HG00639.hp1 HG00741.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.207+4950_207+4957d others(10): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189315 | |||||
| chr20:37189317
|
GTGTGTA | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 57 | HG00099.hp1 HG00408.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.207+4950_207+4955d others(8): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189317 | |||||
| chr20:37189319
|
GTGTA | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0025others(16): Show | 24 | HG01943.hp1 HG02055.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.207+4950_207+4953d others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189319 | |||||
| chr20:37189321
|
GTA | G | 9 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(6): Show | 10 | HG01943.hp2 HG02027.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+4950_207+4951d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189321 | |||||
| chr20:37189323
|
A | ATG | 8 | a0001c0001t0001g0205a0001c0002t0001g0005a0001c0002t0001g0079others(5): Show | 12 | HG02602.hp1 HG02698.hp2 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+4987_207+4988d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | |||||
| chr20:37189323
|
A | ATGTG | 14 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0008others(11): Show | 30 | HG00408.hp1 HG00621.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.207+4985_207+4988d others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | |||||
| chr20:37189323
|
A | ATGTGTG | 2 | a0001c0002t0001g0015a0004c0008t0001g0089 | 3 | HG01952.hp1 NA18953.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.207+4983_207+4988d others(8): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | |||||
| chr20:37189323
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0117others(6): Show | 12 | HG01515.hp1 HG02080.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.207+4950A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189323 | ||||||
| chr20:37189323
|
ATG | A | 18 | a0001c0001t0001g0101a0001c0001t0001g0206a0001c0002t0001g0028others(15): Show | 19 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.207+4987_207+4988d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | |||||
| chr20:37189323
|
ATGTG | A | 6 | a0001c0001t0001g0250a0001c0002t0001g0051a0001c0002t0001g0052others(3): Show | 6 | HG01346.hp1 HG01358.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+4985_207+4988d others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | |||||
| chr20:37189323
|
ATGTGTG | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(14): Show | 22 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.207+4983_207+4988d others(8): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | |||||
| chr20:37189323
|
ATGTGTGT others(1): Show |
A | 5 | a0001c0001t0001g0238a0001c0001t0001g0252a0001c0002t0001g0098others(2): Show | 5 | HG01109.hp2 HG01361.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+4981_207+4988d others(10): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | |||||
| chr20:37189323
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0001g0237a0001c0002t0001g0097 | 2 | HG02976.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.207+4979_207+4988d others(12): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | |||||
| chr20:37189432
|
C | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01074.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.207+5059C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189432 | ||||||
| chr20:37189491
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG00738.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.207+5118G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189491 | ||||||
| chr20:37189554
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+5181A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189554 | ||||||
| chr20:37189595
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.207+5222G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189595 | ||||||
| chr20:37189672
|
G | A | 10 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(7): Show | 10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+5299G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189672 | ||||||
| chr20:37189838
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.207+5465T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189838 | ||||||
| chr20:37189922
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+5549C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189922 | ||||||
| chr20:37190005
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.207+5632T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190005 | ||||||
| chr20:37190104
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.207+5731T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190104 | ||||||
| chr20:37190119
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(20): Show | 28 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.207+5746C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190119 | ||||||
| chr20:37190547
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.207+6174T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190547 | ||||||
| chr20:37190572
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.207+6199C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190572 | ||||||
| chr20:37190726
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6353A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190726 | ||||||
| chr20:37190752
|
T | G | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+6379T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190752 | ||||||
| chr20:37190834
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0196 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.207+6461T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190834 | ||||||
| chr20:37191184
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.207+6811G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191184 | ||||||
| chr20:37191184
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.207+6811G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191184 | ||||||
| chr20:37191205
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6832G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191205 | ||||||
| chr20:37191258
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.207+6885C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191258 | ||||||
| chr20:37191295
|
G | A | 1 | a0004c0008t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.207+6922G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191295 | ||||||
| chr20:37191341
|
G | T | 1 | a0001c0002t0001g0077 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.207+6968G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191341 | ||||||
| chr20:37191658
|
CT | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 7 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-6726delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37191658 | |||||
| chr20:37191806
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.208-6591G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191806 | ||||||
| chr20:37192014
|
A | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6383A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192014 | ||||||
| chr20:37192073
|
G | T | 1 | a0001c0002t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.208-6324G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192073 | ||||||
| chr20:37192103
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0265 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.208-6294A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192103 | ||||||
| chr20:37192143
|
G | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.208-6254G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192143 | ||||||
| chr20:37192154
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208-6243A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192154 | ||||||
| chr20:37192291
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.208-6106C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192291 | ||||||
| chr20:37192339
|
A | C | 1 | a0001c0001t0001g0231 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.208-6058A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192339 | ||||||
| chr20:37192472
|
T | C | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208-5925T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192472 | ||||||
| chr20:37192580
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.208-5817G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192580 | ||||||
| chr20:37192698
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.208-5699T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192698 | ||||||
| chr20:37193067
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.208-5330G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193067 | ||||||
| chr20:37193165
|
A | G | 5 | a0001c0001t0001g0238a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01109.hp2 HG03225.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-5232A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193165 | ||||||
| chr20:37193340
|
C | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-5057C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193340 | ||||||
| chr20:37193341
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-5056G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193341 | ||||||
| chr20:37193662
|
C | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 27 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.208-4735C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193662 | ||||||
| chr20:37193692
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-4705G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193692 | ||||||
| chr20:37193706
|
T | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-4691T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193706 | ||||||
| chr20:37193848
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.208-4549G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193848 | ||||||
| chr20:37193880
|
A | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.208-4517A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193880 | ||||||
| chr20:37194032
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208-4365A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194032 | ||||||
| chr20:37194085
|
A | T | 1 | a0001c0002t0001g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.208-4312A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194085 | ||||||
| chr20:37194153
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.208-4244G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194153 | ||||||
| chr20:37194203
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.208-4194C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194203 | ||||||
| chr20:37194218
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.208-4179G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194218 | ||||||
| chr20:37194255
|
ATTG | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(168): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.208-4118_208-4116d others(5): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37194255 | |||||
| chr20:37194408
|
C | A | 1 | a0001c0001t0001g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.208-3989C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194408 | ||||||
| chr20:37194418
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.208-3979C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194418 | ||||||
| chr20:37194493
|
C | T | 1 | a0001c0002t0001g0269 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.208-3904C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194493 | ||||||
| chr20:37194509
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.208-3888G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194509 | ||||||
| chr20:37194621
|
A | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231 | 3 | HG02572.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.208-3776A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194621 | ||||||
| chr20:37194779
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-3618G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194779 | ||||||
| chr20:37194797
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0259 | 2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-3600G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194797 | ||||||
| chr20:37194891
|
G | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(156): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.208-3506G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194891 | ||||||
| chr20:37194985
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-3412G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194985 | ||||||
| chr20:37195035
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.208-3362C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195035 | ||||||
| chr20:37195066
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.208-3331C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195066 | ||||||
| chr20:37195085
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.208-3312G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195085 | ||||||
| chr20:37195172
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-3225A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195172 | ||||||
| chr20:37195186
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-3211C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195186 | ||||||
| chr20:37195265
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.208-3132C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195265 | ||||||
| chr20:37195287
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(160): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.208-3110G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195287 | ||||||
| chr20:37195317
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-3080C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195317 | ||||||
| chr20:37195388
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.208-3009T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195388 | ||||||
| chr20:37195518
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.208-2879A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195518 | ||||||
| chr20:37195519
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.208-2878T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195519 | ||||||
| chr20:37195551
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.208-2846G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195551 | ||||||
| chr20:37195693
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-2704G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195693 | ||||||
| chr20:37195694
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-2703G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195694 | ||||||
| chr20:37195802
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.208-2595T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195802 | ||||||
| chr20:37195827
|
A | T | 1 | a0001c0002t0001g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.208-2570A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195827 | ||||||
| chr20:37195968
|
A | G | 1 | a0001c0002t0001g0076 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.208-2429A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195968 | ||||||
| chr20:37196186
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(141): Show | 177 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.208-2211A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196186 | ||||||
| chr20:37196235
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(162): Show | 203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.208-2162C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196235 | ||||||
| chr20:37196239
|
T | G | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208-2158T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196239 | ||||||
| chr20:37196267
|
C | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(168): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.208-2130C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196267 | ||||||
| chr20:37196275
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-2122C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196275 | ||||||
| chr20:37196314
|
T | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(191): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.208-2083T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196314 | ||||||
| chr20:37196321
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.208-2076C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196321 | ||||||
| chr20:37196343
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.208-2054C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196343 | ||||||
| chr20:37196354
|
C | G | 6 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(3): Show | 6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-2043C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196354 | ||||||
| chr20:37196416
|
G | A | 1 | a0001c0002t0001g0079 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.208-1981G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196416 | ||||||
| chr20:37196434
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.208-1963C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196434 | ||||||
| chr20:37196437
|
G | C | 1 | a0001c0002t0001g0037 | 2 | NA18942.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.208-1960G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196437 | ||||||
| chr20:37196477
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0210 | 3 | HG02257.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.208-1920C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196477 | ||||||
| chr20:37196484
|
T | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(170): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.208-1913T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196484 | ||||||
| chr20:37196709
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1688A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196709 | ||||||
| chr20:37197001
|
C | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(95): Show | 124 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.208-1396C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197001 | ||||||
| chr20:37197090
|
C | T | 1 | a0001c0002t0001g0056 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.208-1307C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197090 | ||||||
| chr20:37197107
|
G | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1290G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197107 | ||||||
| chr20:37197190
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.208-1207G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197190 | ||||||
| chr20:37197557
|
G | A | 1 | a0005c0007t0001g0208 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.208-840G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197557 | ||||||
| chr20:37197638
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.208-759G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197638 | ||||||
| chr20:37197863
|
G | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-534G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197863 | ||||||
| chr20:37197917
|
A | C | 1 | a0001c0002t0001g0074 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.208-480A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197917 | ||||||
| chr20:37197984
|
A | G | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-413A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197984 | ||||||
| chr20:37198011
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.208-386G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37198011 | ||||||
| chr20:37198027
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.208-370G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37198027 | ||||||
| chr20:37198244
|
C | T | 4 | a0001c0002t0001g0011a0001c0002t0001g0037a0001c0002t0001g0268others(1): Show | 7 | HG00609.hp2 HG02738.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-153C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37198244 | ||||||
| chr20:37198280
|
T | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(141): Show | 177 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.208-117T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37198280 | ||||||
| chr20:37198506
|
C | T | 6 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(3): Show | 6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+14C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | chr20 | 37198506 | ||||||
| chr20:37198561
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.303+69A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | chr20 | 37198561 | ||||||
| chr20:37198625
|
A | AT | 13 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(10): Show | 17 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.303+143dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr20 | 37198625 | |||||
| chr20:37198625
|
A | ATT | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(170): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.303+142_303+143dup others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr20 | 37198625 | |||||
| chr20:37198663
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.303+171C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | chr20 | 37198663 | ||||||
| chr20:37199017
|
T | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0117a0001c0001t0001g0153 | 5 | NA18986.hp1 NA19058.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-33T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | chr20 | 37199017 | ||||||
| chr20:37199279
|
G | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.479+54G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199279 | ||||||
| chr20:37199439
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.479+214A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199439 | ||||||
| chr20:37199445
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.479+220C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199445 | ||||||
| chr20:37199725
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.479+500G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199725 | ||||||
| chr20:37199825
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.479+600A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199825 | ||||||
| chr20:37199997
|
AT | A | 14 | a0001c0001t0001g0172a0001c0001t0001g0205a0001c0001t0001g0206others(11): Show | 27 | HG00408.hp1 HG00621.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.479+787delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37199997 | |||||
| chr20:37200081
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.479+856G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200081 | ||||||
| chr20:37200199
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.479+974G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200199 | ||||||
| chr20:37200293
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.479+1068A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200293 | ||||||
| chr20:37200328
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.479+1103T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200328 | ||||||
| chr20:37200354
|
A | AT | 10 | a0001c0002t0001g0028a0001c0002t0001g0042a0001c0002t0001g0044others(7): Show | 11 | HG00741.hp2 HG01167.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+1142dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37200354 | |||||
| chr20:37200354
|
ATT | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.479+1141_479+1142d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37200354 | |||||
| chr20:37200463
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.479+1238G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200463 | ||||||
| chr20:37200535
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.479+1310T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200535 | ||||||
| chr20:37200734
|
C | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.479+1509C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200734 | ||||||
| chr20:37200846
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+1621C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200846 | ||||||
| chr20:37200848
|
G | A | 2 | a0001c0002t0001g0060a0001c0002t0001g0061 | 2 | HG00438.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.479+1623G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200848 | ||||||
| chr20:37201014
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.479+1789C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201014 | ||||||
| chr20:37201136
|
C | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0047others(2): Show | 8 | NA18951.hp1 NA18960.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.479+1911C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201136 | ||||||
| chr20:37201137
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.479+1912G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201137 | ||||||
| chr20:37201251
|
G | A | 1 | a0001c0002t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.479+2026G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201251 | ||||||
| chr20:37201281
|
C | CT | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(146): Show | 185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.479+2074dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37201281 | |||||
| chr20:37201281
|
C | CTT | 11 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0138others(8): Show | 13 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.479+2073_479+2074d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37201281 | |||||
| chr20:37201316
|
G | C | 1 | a0001c0002t0001g0062 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.479+2091G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201316 | ||||||
| chr20:37201376
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.479+2151T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201376 | ||||||
| chr20:37201391
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.479+2166T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201391 | ||||||
| chr20:37201452
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.479+2227A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201452 | ||||||
| chr20:37201541
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.479+2316T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201541 | ||||||
| chr20:37201578
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0131 | 2 | HG01099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.480-2307G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201578 | ||||||
| chr20:37201685
|
C | G | 1 | a0001c0002t0001g0182 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.480-2200C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201685 | ||||||
| chr20:37201698
|
C | T | 1 | a0001c0002t0001g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.480-2187C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201698 | ||||||
| chr20:37201898
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-1987G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201898 | ||||||
| chr20:37202222
|
G | A | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.480-1663G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37202222 | ||||||
| chr20:37202357
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480-1528G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37202357 | ||||||
| chr20:37202738
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-1147A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37202738 | ||||||
| chr20:37202909
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0103 | 4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-976A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37202909 | ||||||
| chr20:37203130
|
G | A | 1 | a0001c0002t0001g0192 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.480-755G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203130 | ||||||
| chr20:37203287
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.480-598A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203287 | ||||||
| chr20:37203361
|
CT | C | 19 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(16): Show | 21 | HG01070.hp2 HG01361.hp2 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.480-501delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37203361 | |||||
| chr20:37203361
|
CTT | C | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.480-502_480-501del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37203361 | |||||
| chr20:37203361
|
CTTTTTTT others(3): Show |
C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(165): Show | 206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.480-510_480-501del others(10): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37203361 | |||||
| chr20:37203361
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0172 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.480-511_480-501del others(11): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37203361 | |||||
| chr20:37203411
|
C | T | 1 | a0001c0002t0001g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.480-474C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203411 | ||||||
| chr20:37203461
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.480-424C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203461 | ||||||
| chr20:37203529
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.480-356G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203529 | ||||||
| chr20:37203538
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.480-347C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203538 | ||||||
| chr20:37203549
|
C | T | 30 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(27): Show | 34 | HG00741.hp1 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.480-336C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203549 | ||||||
| chr20:37203808
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.480-77A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203808 | ||||||
| chr20:37204055
|
G | T | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.555+95G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 5/16 | chr20 | 37204055 | ||||||
| chr20:37204078
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0250 | 2 | HG01346.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.555+118G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 5/16 | chr20 | 37204078 | ||||||
| chr20:37204500
|
A | G | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.556-267A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 5/16 | chr20 | 37204500 | ||||||
| chr20:37204550
|
C | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-217C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 5/16 | chr20 | 37204550 | ||||||
| chr20:37205047
|
A | G | 6 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(3): Show | 6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+146A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205047 | ||||||
| chr20:37205074
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+173G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205074 | ||||||
| chr20:37205265
|
T | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | HG02622.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.690+364T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205265 | ||||||
| chr20:37205380
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.690+479C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205380 | ||||||
| chr20:37205505
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.690+604A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205505 | ||||||
| chr20:37205590
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.690+689A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205590 | ||||||
| chr20:37205621
|
G | C | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(172): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.690+720G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205621 | ||||||
| chr20:37206048
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.690+1147A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37206048 | ||||||
| chr20:37206200
|
C | T | 1 | a0002c0003t0001g0137 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.691-1073C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37206200 | ||||||
| chr20:37206285
|
G | A | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.691-988G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37206285 | ||||||
| chr20:37206919
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.691-354C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37206919 | ||||||
| chr20:37207095
|
A | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.691-178A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37207095 | ||||||
| chr20:37207254
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.691-19C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37207254 | ||||||
| chr20:37207486
|
A | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.867+37A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37207486 | ||||||
| chr20:37207705
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+256A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37207705 | ||||||
| chr20:37208059
|
G | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.867+610G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208059 | ||||||
| chr20:37208185
|
G | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0253others(13): Show | 19 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.867+736G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208185 | ||||||
| chr20:37208267
|
T | TAA | 10 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(7): Show | 14 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.867+836_867+837dup others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr20 | 37208267 | |||||
| chr20:37208267
|
TAA | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0101others(7): Show | 11 | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.867+836_867+837del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr20 | 37208267 | |||||
| chr20:37208267
|
TAAA | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(160): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.867+835_867+837del others(3): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr20 | 37208267 | |||||
| chr20:37208444
|
A | G | 1 | a0001c0002t0001g0073 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.867+995A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208444 | ||||||
| chr20:37208448
|
C | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.867+999C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208448 | ||||||
| chr20:37208449
|
G | T | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.867+1000G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208449 | ||||||
| chr20:37208477
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.867+1028A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208477 | ||||||
| chr20:37208548
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.867+1099T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208548 | ||||||
| chr20:37208557
|
A | G | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+1108A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208557 | ||||||
| chr20:37208609
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.867+1160G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208609 | ||||||
| chr20:37208626
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.867+1177C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208626 | ||||||
| chr20:37208689
|
G | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.867+1240G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208689 | ||||||
| chr20:37208723
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.867+1274C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208723 | ||||||
| chr20:37208807
|
T | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.868-1240T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208807 | ||||||
| chr20:37208814
|
A | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.868-1233A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208814 | ||||||
| chr20:37208863
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.868-1184A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208863 | ||||||
| chr20:37208902
|
G | A | 2 | a0001c0002t0001g0041a0001c0002t0001g0091 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.868-1145G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208902 | ||||||
| chr20:37208919
|
A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0001g0177 | 3 | HG02155.hp2 NA18960.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.868-1128A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208919 | ||||||
| chr20:37209118
|
C | T | 3 | a0001c0001t0001g0167a0001c0004t0001g0166a0001c0004t0001g0186 | 3 | HG02080.hp1 NA18954.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.868-929C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209118 | ||||||
| chr20:37209469
|
A | AT | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.868-567dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr20 | 37209469 | |||||
| chr20:37209519
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0103 | 4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.868-528G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209519 | ||||||
| chr20:37209527
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.868-520G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209527 | ||||||
| chr20:37209626
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.868-421G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209626 | ||||||
| chr20:37209879
|
A | G | 1 | a0001c0001t0001g0019 | 2 | HG00544.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.868-168A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209879 | ||||||
| chr20:37209969
|
T | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.868-78T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209969 | ||||||
| chr20:37210188
|
T | C | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(264): Show | 342 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.986+23T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210188 | ||||||
| chr20:37210353
|
G | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.986+188G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210353 | ||||||
| chr20:37210377
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.986+212A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210377 | ||||||
| chr20:37210528
|
CT | C | 37 | a0001c0001t0001g0167a0001c0001t0001g0254a0001c0002t0001g0011others(34): Show | 43 | HG00609.hp2 HG00741.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.986+382delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37210528 | |||||
| chr20:37210528
|
CTT | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(168): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.986+381_986+382del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37210528 | |||||
| chr20:37210634
|
G | A | 1 | a0005c0007t0001g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.986+469G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210634 | ||||||
| chr20:37210771
|
G | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.986+606G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210771 | ||||||
| chr20:37210925
|
T | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.986+760T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210925 | ||||||
| chr20:37211064
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.986+899T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211064 | ||||||
| chr20:37211125
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.986+960C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211125 | ||||||
| chr20:37211313
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.986+1148G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211313 | ||||||
| chr20:37211397
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+1232G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211397 | ||||||
| chr20:37211455
|
A | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.986+1290A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211455 | ||||||
| chr20:37211628
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.986+1463C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211628 | ||||||
| chr20:37211645
|
TA | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.986+1497delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37211645 | |||||
| chr20:37211679
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.986+1514A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211679 | ||||||
| chr20:37211714
|
T | C | 1 | a0001c0002t0001g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.986+1549T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211714 | ||||||
| chr20:37211731
|
AT | A | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.986+1577delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37211731 | |||||
| chr20:37211881
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.986+1716G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211881 | ||||||
| chr20:37211898
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.986+1733C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211898 | ||||||
| chr20:37211918
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.986+1753G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211918 | ||||||
| chr20:37211994
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.987-1766C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211994 | ||||||
| chr20:37212025
|
C | T | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.987-1735C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212025 | ||||||
| chr20:37212131
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.987-1629A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212131 | ||||||
| chr20:37212132
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.987-1628G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212132 | ||||||
| chr20:37212193
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-1567C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212193 | ||||||
| chr20:37212320
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.987-1440A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212320 | ||||||
| chr20:37212391
|
A | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.987-1369A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212391 | ||||||
| chr20:37212485
|
AT | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.987-1260delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37212485 | |||||
| chr20:37212512
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.987-1248G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212512 | ||||||
| chr20:37212541
|
C | T | 4 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(1): Show | 4 | HG02886.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-1219C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212541 | ||||||
| chr20:37212701
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.987-1059G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212701 | ||||||
| chr20:37212745
|
G | T | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.987-1015G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212745 | ||||||
| chr20:37212840
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.987-920T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212840 | ||||||
| chr20:37212854
|
G | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.987-906G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212854 | ||||||
| chr20:37212917
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.987-843G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212917 | ||||||
| chr20:37213027
|
GAT | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-730_987-729del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37213027 | |||||
| chr20:37213028
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0101others(3): Show | 7 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.987-732A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213028 | ||||||
| chr20:37213252
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.987-508G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213252 | ||||||
| chr20:37213349
|
A | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.987-411A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213349 | ||||||
| chr20:37213456
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0131 | 2 | HG01099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.987-304G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213456 | ||||||
| chr20:37213712
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.987-48T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213712 | ||||||
| chr20:37213930
|
C | G | 1 | a0001c0001t0001g0216 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1092+65C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37213930 | ||||||
| chr20:37214173
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+308G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214173 | ||||||
| chr20:37214237
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1092+372C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214237 | ||||||
| chr20:37214431
|
G | A | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(164): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1092+566G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214431 | ||||||
| chr20:37214520
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(141): Show | 177 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1092+655A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214520 | ||||||
| chr20:37214598
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1092+733C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214598 | ||||||
| chr20:37215042
|
T | A | 1 | a0001c0001t0001g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1092+1177T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215042 | ||||||
| chr20:37215281
|
C | T | 2 | a0001c0002t0001g0058a0001c0002t0001g0080 | 2 | HG00597.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1092+1416C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215281 | ||||||
| chr20:37215324
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1092+1459G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215324 | ||||||
| chr20:37215401
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1092+1536G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215401 | ||||||
| chr20:37215426
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1092+1561A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215426 | ||||||
| chr20:37215462
|
T | C | 5 | a0001c0002t0001g0028a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 6 | HG00741.hp2 HG01167.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+1597T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215462 | ||||||
| chr20:37215531
|
CTTTTCTT others(3): Show |
C | 4 | a0001c0002t0001g0028a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 5 | HG00741.hp2 HG02145.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+1674_1092+168 others(14): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37215531 | |||||
| chr20:37215644
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1092+1779T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215644 | ||||||
| chr20:37215654
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0101others(3): Show | 7 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092+1789C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215654 | ||||||
| chr20:37215718
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1092+1853A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215718 | ||||||
| chr20:37215791
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1092+1926G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215791 | ||||||
| chr20:37215844
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1092+1979A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215844 | ||||||
| chr20:37215978
|
C | T | 2 | a0001c0002t0001g0069a0001c0002t0001g0074 | 2 | HG03834.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1092+2113C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215978 | ||||||
| chr20:37216002
|
T | C | 18 | a0001c0002t0001g0001a0001c0002t0001g0006a0001c0002t0001g0008others(15): Show | 35 | HG00408.hp1 HG00621.hp1 HG01952.hp1 others(32): Show |
intron_variant | MODIFIER | c.1092+2137T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216002 | ||||||
| chr20:37216229
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0175 | 2 | HG01070.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1092+2364C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216229 | ||||||
| chr20:37216231
|
C | T | 1 | a0005c0007t0001g0208 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1092+2366C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216231 | ||||||
| chr20:37216308
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1092+2443C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216308 | ||||||
| chr20:37216393
|
A | G | 4 | a0001c0002t0001g0045a0001c0002t0001g0054a0001c0002t0001g0055others(1): Show | 4 | NA18946.hp2 NA18998.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+2528A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216393 | ||||||
| chr20:37216425
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+2560A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216425 | ||||||
| chr20:37216465
|
T | TTTATTTT others(316): Show |
1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1092+2614_1092+261 others(327): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37216465 | |||||
| chr20:37216507
|
G | C | 1 | a0001c0001t0001g0035 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1092+2642G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216507 | ||||||
| chr20:37216544
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1092+2679C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216544 | ||||||
| chr20:37216564
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+2699C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216564 | ||||||
| chr20:37216627
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1092+2762A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216627 | ||||||
| chr20:37216704
|
C | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(125): Show | 158 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1092+2839C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216704 | ||||||
| chr20:37216808
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1092+2943T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216808 | ||||||
| chr20:37216907
|
A | G | 3 | a0001c0001t0001g0105a0001c0001t0001g0141a0001c0001t0001g0145 | 3 | HG00642.hp2 HG01516.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1092+3042A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216907 | ||||||
| chr20:37216939
|
C | CT | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1092+3083dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37216939 | |||||
| chr20:37217147
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1092+3282C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217147 | ||||||
| chr20:37217272
|
A | ATAT | 7 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0101others(4): Show | 8 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1092+3433_1092+343 others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217272 | |||||
| chr20:37217272
|
A | ATATTATT others(5): Show |
1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+3424_1092+343 others(16): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217272 | |||||
| chr20:37217272
|
ATAT | A | 33 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0002t0001g0011others(30): Show | 39 | HG00609.hp2 HG00741.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1092+3433_1092+343 others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217272 | |||||
| chr20:37217286
|
A | ATTG | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(162): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1092+3423_1092+342 others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217286 | |||||
| chr20:37217289
|
A | G | 1 | a0001c0001t0001g0022 | 2 | NA18981.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1092+3424A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217289 | ||||||
| chr20:37217301
|
C | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0101others(3): Show | 8 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+3436C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217301 | ||||||
| chr20:37217304
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+3439T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217304 | ||||||
| chr20:37217328
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1092+3463C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217328 | ||||||
| chr20:37217347
|
C | T | 1 | a0007c0009t0001g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1092+3482C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217347 | ||||||
| chr20:37217395
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1092+3530T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217395 | ||||||
| chr20:37217399
|
T | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1092+3534T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217399 | ||||||
| chr20:37217759
|
TTGC | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1092+3897_1092+389 others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217759 | |||||
| chr20:37217966
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0101others(3): Show | 7 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092+4101C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217966 | ||||||
| chr20:37218033
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1092+4168C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218033 | ||||||
| chr20:37218034
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1092+4169G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218034 | ||||||
| chr20:37218337
|
CA | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1092+4473delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218337 | ||||||
| chr20:37218341
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1092+4476A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218341 | ||||||
| chr20:37218464
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1092+4599T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218464 | ||||||
| chr20:37218545
|
T | TA | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(166): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1092+4691dupA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37218545 | |||||
| chr20:37218556
|
A | AAC | 5 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+4691_1092+469 others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218556 | ||||||
| chr20:37218557
|
C | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(6): Show | 10 | HG02280.hp2 HG02723.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1092+4692C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218557 | ||||||
| chr20:37218567
|
A | C | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1092+4702A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218567 | ||||||
| chr20:37218573
|
A | G | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1092+4708A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218573 | ||||||
| chr20:37218615
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+4750C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218615 | ||||||
| chr20:37218661
|
A | T | 2 | a0001c0002t0001g0180a0001c0002t0001g0182 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1092+4796A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218661 | ||||||
| chr20:37218668
|
T | A | 10 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(7): Show | 10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1092+4803T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218668 | ||||||
| chr20:37218739
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+4874G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218739 | ||||||
| chr20:37218821
|
A | T | 1 | a0001c0001t0001g0249 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1092+4956A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218821 | ||||||
| chr20:37219057
|
G | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1093-4821G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37219057 | ||||||
| chr20:37219311
|
C | G | 1 | a0001c0002t0001g0068 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1093-4567C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37219311 | ||||||
| chr20:37219814
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1093-4064T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37219814 | ||||||
| chr20:37219939
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-3939G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37219939 | ||||||
| chr20:37220183
|
T | TTG | 18 | a0001c0001t0001g0036a0001c0001t0001g0101a0001c0001t0001g0262others(15): Show | 23 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.1093-3674_1093-367 others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37220183 | |||||
| chr20:37220193
|
G | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0103 | 4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1093-3685G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220193 | ||||||
| chr20:37220297
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-3581A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220297 | ||||||
| chr20:37220404
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1093-3474G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220404 | ||||||
| chr20:37220496
|
A | G | 10 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(7): Show | 14 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1093-3382A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220496 | ||||||
| chr20:37220608
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1093-3270T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220608 | ||||||
| chr20:37220643
|
A | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01358.hp1 HG01993.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-3235A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220643 | ||||||
| chr20:37220908
|
G | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0117others(13): Show | 19 | HG00408.hp2 HG00621.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1093-2970G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220908 | ||||||
| chr20:37220980
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1093-2898G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220980 | ||||||
| chr20:37221035
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-2843T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221035 | ||||||
| chr20:37221059
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1093-2819G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221059 | ||||||
| chr20:37221195
|
C | CT | 39 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(36): Show | 43 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1093-2665dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37221195 | |||||
| chr20:37221195
|
CT | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0101others(5): Show | 9 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1093-2665delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37221195 | |||||
| chr20:37221219
|
G | A | 13 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(10): Show | 18 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1093-2659G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221219 | ||||||
| chr20:37221224
|
C | G | 1 | a0001c0002t0001g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1093-2654C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221224 | ||||||
| chr20:37221341
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1093-2537G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221341 | ||||||
| chr20:37221449
|
C | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(21): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1093-2429C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221449 | ||||||
| chr20:37221478
|
G | A | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1093-2400G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221478 | ||||||
| chr20:37221542
|
T | C | 2 | a0001c0002t0001g0041a0001c0002t0001g0091 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1093-2336T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221542 | ||||||
| chr20:37221842
|
G | A | 1 | a0009c0011t0001g0189 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1093-2036G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221842 | ||||||
| chr20:37222005
|
C | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1093-1873C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222005 | ||||||
| chr20:37222155
|
C | T | 1 | a0001c0002t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1093-1723C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222155 | ||||||
| chr20:37222273
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1093-1605C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222273 | ||||||
| chr20:37222397
|
GT | G | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1093-1470delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37222397 | |||||
| chr20:37222490
|
C | T | 1 | a0001c0001t0001g0033 | 2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1093-1388C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222490 | ||||||
| chr20:37222593
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(188): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1093-1285G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222593 | ||||||
| chr20:37222693
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1093-1185C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222693 | ||||||
| chr20:37222881
|
C | T | 1 | a0001c0002t0001g0067 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1093-997C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222881 | ||||||
| chr20:37222936
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093-942A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222936 | ||||||
| chr20:37223025
|
T | C | 7 | a0001c0001t0001g0238a0001c0001t0001g0246a0001c0001t0001g0247others(4): Show | 7 | HG01109.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-853T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223025 | ||||||
| chr20:37223063
|
C | T | 1 | a0001c0001t0001g0021 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1093-815C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223063 | ||||||
| chr20:37223324
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-554G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223324 | ||||||
| chr20:37223528
|
C | G | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1093-350C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223528 | ||||||
| chr20:37223603
|
G | T | 1 | a0001c0001t0001g0021 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1093-275G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223603 | ||||||
| chr20:37223635
|
C | CT | 90 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0030others(87): Show | 107 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1093-230dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37223635 | |||||
| chr20:37223985
|
C | T | 1 | a0001c0002t0001g0039 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1184+16C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37223985 | ||||||
| chr20:37223992
|
A | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.1184+23A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37223992 | ||||||
| chr20:37224035
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG00408.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1184+66G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224035 | ||||||
| chr20:37224047
|
G | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.1184+78G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224047 | ||||||
| chr20:37224083
|
A | G | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1184+114A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224083 | ||||||
| chr20:37224157
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+188G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224157 | ||||||
| chr20:37224201
|
TA | T | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1184+234delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr20 | 37224201 | |||||
| chr20:37224357
|
G | A | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1184+388G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224357 | ||||||
| chr20:37224440
|
T | G | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1184+471T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224440 | ||||||
| chr20:37224562
|
C | G | 1 | a0001c0001t0001g0216 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1184+593C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224562 | ||||||
| chr20:37224625
|
A | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1184+656A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224625 | ||||||
| chr20:37224693
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0255others(12): Show | 18 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1184+724C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224693 | ||||||
| chr20:37224816
|
G | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1184+847G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224816 | ||||||
| chr20:37224833
|
T | G | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1185-855T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224833 | ||||||
| chr20:37224875
|
G | C | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1185-813G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224875 | ||||||
| chr20:37224903
|
A | G | 1 | a0001c0002t0001g0054 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1185-785A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224903 | ||||||
| chr20:37225060
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1185-628T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37225060 | ||||||
| chr20:37225209
|
T | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1185-479T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37225209 | ||||||
| chr20:37225606
|
A | G | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1185-82A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37225606 | ||||||
| chr20:37225846
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1299+44T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37225846 | ||||||
| chr20:37225921
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0248 | 3 | HG00738.hp1 HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1299+119C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37225921 | ||||||
| chr20:37226028
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1299+226T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226028 | ||||||
| chr20:37226218
|
A | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1299+416A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226218 | ||||||
| chr20:37226254
|
G | A | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1299+452G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226254 | ||||||
| chr20:37226284
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+482G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226284 | ||||||
| chr20:37226386
|
T | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0140 | 3 | NA18971.hp1 NA18995.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1299+584T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226386 | ||||||
| chr20:37226423
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1299+621C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226423 | ||||||
| chr20:37226496
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1299+694G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226496 | ||||||
| chr20:37226621
|
T | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1299+819T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226621 | ||||||
| chr20:37227019
|
C | G | 2 | a0001c0001t0001g0241a0001c0001t0002g0242 | 2 | HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1299+1217C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227019 | ||||||
| chr20:37227084
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1299+1282A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227084 | ||||||
| chr20:37227269
|
G | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1300-1281G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227269 | ||||||
| chr20:37227359
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0103 | 4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-1191T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227359 | ||||||
| chr20:37227378
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1300-1172C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227378 | ||||||
| chr20:37227504
|
G | A | 10 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(7): Show | 10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1300-1046G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227504 | ||||||
| chr20:37227562
|
T | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-988T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227562 | ||||||
| chr20:37227610
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1300-940A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227610 | ||||||
| chr20:37227868
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-682T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227868 | ||||||
| chr20:37227898
|
A | G | 7 | a0001c0002t0001g0028a0001c0002t0001g0042a0001c0002t0001g0095others(4): Show | 8 | HG00741.hp2 HG01167.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-652A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227898 | ||||||
| chr20:37228091
|
C | G | 1 | a0001c0001t0001g0018 | 2 | HG01261.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1300-459C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228091 | ||||||
| chr20:37228091
|
C | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(172): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1300-459C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228091 | ||||||
| chr20:37228102
|
A | G | 4 | a0001c0002t0001g0045a0001c0002t0001g0054a0001c0002t0001g0055others(1): Show | 4 | NA18946.hp2 NA18998.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-448A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228102 | ||||||
| chr20:37228132
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1300-418G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228132 | ||||||
| chr20:37228266
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1300-284G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228266 | ||||||
| chr20:37228393
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-157G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228393 | ||||||
| chr20:37228444
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1300-106C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228444 | ||||||
| chr20:37228530
|
T | G | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1300-20T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228530 | ||||||
| chr20:37228881
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+137T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37228881 | ||||||
| chr20:37228976
|
A | ACTTAC | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1494+235_1494+236i others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr20 | 37228976 | |||||
| chr20:37229012
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1494+268C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229012 | ||||||
| chr20:37229013
|
A | G | 8 | a0001c0002t0001g0043a0001c0002t0001g0059a0001c0002t0001g0060others(5): Show | 8 | HG00438.hp2 HG02027.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1494+269A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229013 | ||||||
| chr20:37229029
|
G | A | 10 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(7): Show | 10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1494+285G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229029 | ||||||
| chr20:37229054
|
T | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1494+310T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229054 | ||||||
| chr20:37229063
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1494+319G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229063 | ||||||
| chr20:37229259
|
G | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0239others(5): Show | 12 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1494+515G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229259 | ||||||
| chr20:37229317
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1494+573G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229317 | ||||||
| chr20:37229546
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1495-427C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229546 | ||||||
| chr20:37229613
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1495-360C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229613 | ||||||
| chr20:37229710
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0001g0177 | 3 | HG02155.hp2 NA18960.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1495-263G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229710 | ||||||
| chr20:37229899
|
CAG | C | 3 | a0001c0002t0001g0051a0001c0002t0001g0064a0001c0002t0001g0075 | 3 | HG01975.hp1 HG02004.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1495-70_1495-69del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr20 | 37229899 | |||||
| chr20:37230099
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1581+40A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230099 | ||||||
| chr20:37230149
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1581+90G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230149 | ||||||
| chr20:37230205
|
C | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0266 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1581+146C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230205 | ||||||
| chr20:37230242
|
C | A | 1 | a0001c0002t0001g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1581+183C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230242 | ||||||
| chr20:37230346
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1581+287C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230346 | ||||||
| chr20:37230585
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1581+526A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230585 | ||||||
| chr20:37230673
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1581+614C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230673 | ||||||
| chr20:37231075
|
T | A | 4 | a0002c0003t0001g0132a0002c0003t0001g0133a0002c0003t0001g0135others(1): Show | 4 | HG02523.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1581+1016T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231075 | ||||||
| chr20:37231220
|
G | C | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1582-1076G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231220 | ||||||
| chr20:37231249
|
C | T | 1 | a0002c0003t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1582-1047C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231249 | ||||||
| chr20:37231333
|
G | A | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1582-963G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231333 | ||||||
| chr20:37231370
|
A | G | 1 | a0001c0002t0001g0049 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1582-926A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231370 | ||||||
| chr20:37231383
|
A | C | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1582-913A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231383 | ||||||
| chr20:37231386
|
A | C | 1 | a0001c0002t0001g0014 | 2 | NA18992.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1582-910A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231386 | ||||||
| chr20:37231387
|
C | A | 11 | a0001c0002t0001g0017a0001c0002t0001g0097a0001c0002t0001g0098others(8): Show | 12 | HG01361.hp2 HG02055.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1582-909C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231387 | ||||||
| chr20:37231397
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1582-899C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231397 | ||||||
| chr20:37231599
|
C | G | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1582-697C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231599 | ||||||
| chr20:37231711
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1582-585C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231711 | ||||||
| chr20:37231714
|
T | TAAAA | 14 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0123others(11): Show | 17 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1582-577_1582-574d others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr20 | 37231714 | |||||
| chr20:37231714
|
T | TAAAAAAA | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(126): Show | 159 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1582-580_1582-574d others(9): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr20 | 37231714 | |||||
| chr20:37231714
|
T | TAAAAAAA others(1): Show |
22 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 27 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1582-581_1582-574d others(10): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr20 | 37231714 | |||||
| chr20:37231723
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0123others(11): Show | 17 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1582-573G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231723 | ||||||
| chr20:37231734
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1582-562G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231734 | ||||||
| chr20:37231800
|
G | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1582-496G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231800 | ||||||
| chr20:37231816
|
G | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1582-480G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231816 | ||||||
| chr20:37231841
|
G | T | 1 | a0001c0002t0001g0043 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1582-455G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231841 | ||||||
| chr20:37231885
|
T | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1582-411T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231885 | ||||||
| chr20:37232027
|
G | A | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.1582-269G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37232027 | ||||||
| chr20:37232211
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1582-85C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37232211 | ||||||
| chr20:37232237
|
A | C | 1 | a0009c0011t0001g0189 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1582-59A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37232237 | ||||||
| chr20:37232704
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1677+313G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37232704 | ||||||
| chr20:37232921
|
G | C | 1 | a0001c0002t0001g0268 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1677+530G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37232921 | ||||||
| chr20:37233002
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0101others(3): Show | 7 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1677+611G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233002 | ||||||
| chr20:37233070
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(163): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1677+679A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233070 | ||||||
| chr20:37233097
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1677+706C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233097 | ||||||
| chr20:37233240
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1678-780C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233240 | ||||||
| chr20:37233261
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678-759A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233261 | ||||||
| chr20:37233273
|
T | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1678-747T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233273 | ||||||
| chr20:37233287
|
A | G | 10 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(7): Show | 10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1678-733A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233287 | ||||||
| chr20:37233374
|
A | G | 1 | a0001c0002t0001g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1678-646A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233374 | ||||||
| chr20:37233563
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1678-457C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233563 | ||||||
| chr20:37233570
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1678-450C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233570 | ||||||
| chr20:37233599
|
T | A | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.1678-421T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233599 | ||||||
| chr20:37233602
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1678-418C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233602 | ||||||
| chr20:37233641
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1678-379C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233641 | ||||||
| chr20:37233654
|
T | C | 22 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0029others(19): Show | 27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1678-366T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233654 | ||||||
| chr20:37233816
|
T | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678-204T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233816 | ||||||
| chr20:37233866
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1678-154T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233866 | ||||||
| chr20:37233964
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1678-56G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233964 | ||||||
| chr20:37234141
|
T | A | 4 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(1): Show | 4 | HG02886.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+46T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234141 | ||||||
| chr20:37234305
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.1753+210T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234305 | ||||||
| chr20:37234461
|
G | T | 1 | a0001c0002t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1753+366G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234461 | ||||||
| chr20:37234647
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1753+552G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234647 | ||||||
| chr20:37234685
|
G | GT | 27 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 32 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1753+603dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37234685 | |||||
| chr20:37234685
|
G | GTT | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(145): Show | 182 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.1753+602_1753+603d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37234685 | |||||
| chr20:37234902
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1753+807C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234902 | ||||||
| chr20:37234969
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1753+874C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234969 | ||||||
| chr20:37235008
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1753+913C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235008 | ||||||
| chr20:37235068
|
T | TAAGTCTC others(3): Show |
1 | a0001c0002t0001g0043 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1753+976_1753+985d others(12): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37235068 | |||||
| chr20:37235113
|
AAG | A | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+1025_1753+102 others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37235113 | |||||
| chr20:37235149
|
G | A | 1 | a0001c0002t0001g0054 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1753+1054G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235149 | ||||||
| chr20:37235303
|
A | G | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+1208A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235303 | ||||||
| chr20:37235354
|
G | A | 1 | a0008c0010t0001g0124 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1754-1226G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235354 | ||||||
| chr20:37235658
|
T | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(145): Show | 181 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.1754-922T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235658 | ||||||
| chr20:37235691
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1754-889C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235691 | ||||||
| chr20:37235811
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(199): Show | 247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1754-769T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235811 | ||||||
| chr20:37235875
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1754-705C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235875 | ||||||
| chr20:37235951
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0005c0007t0001g0207others(1): Show | 4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1754-629A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235951 | ||||||
| chr20:37236042
|
T | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1754-538T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236042 | ||||||
| chr20:37236086
|
C | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 27 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1754-494C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236086 | ||||||
| chr20:37236093
|
T | TTGTGGGT others(5): Show |
176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1754-482_1754-471d others(14): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37236093 | |||||
| chr20:37236192
|
A | T | 1 | a0001c0002t0001g0043 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1754-388A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236192 | ||||||
| chr20:37236322
|
A | T | 1 | a0001c0002t0001g0043 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1754-258A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236322 | ||||||
| chr20:37236326
|
A | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1754-254A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236326 | ||||||
| chr20:37236379
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1754-201G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236379 | ||||||
| chr20:37236867
|
A | C | 1 | a0001c0001t0001g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1883+158A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37236867 | ||||||
| chr20:37236948
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 27 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1883+239G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37236948 | ||||||
| chr20:37236958
|
TA | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1883+250delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37236958 | ||||||
| chr20:37237124
|
C | T | 10 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(7): Show | 10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+415C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237124 | ||||||
| chr20:37237138
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1883+429C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237138 | ||||||
| chr20:37237146
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1883+437T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237146 | ||||||
| chr20:37237389
|
G | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1883+680G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237389 | ||||||
| chr20:37237550
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1883+841G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237550 | ||||||
| chr20:37237588
|
G | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1883+879G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237588 | ||||||
| chr20:37237808
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1883+1099C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237808 | ||||||
| chr20:37237843
|
G | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+1134G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237843 | ||||||
| chr20:37237864
|
A | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1883+1155A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237864 | ||||||
| chr20:37237884
|
G | A | 2 | a0001c0002t0001g0060a0001c0002t0001g0061 | 2 | HG00438.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1883+1175G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237884 | ||||||
| chr20:37237915
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0128 | 2 | HG00735.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1883+1206G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237915 | ||||||
| chr20:37238337
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1883+1628T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37238337 | ||||||
| chr20:37238662
|
A | G | 6 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(3): Show | 6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1883+1953A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37238662 | ||||||
| chr20:37238731
|
G | T | 1 | a0001c0002t0001g0191 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1883+2022G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37238731 | ||||||
| chr20:37238981
|
C | G | 1 | a0001c0001t0001g0010 | 3 | HG02055.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1883+2272C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37238981 | ||||||
| chr20:37239137
|
G | A | 1 | a0001c0002t0001g0192 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1884-2166G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239137 | ||||||
| chr20:37239307
|
G | T | 1 | a0001c0002t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1884-1996G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239307 | ||||||
| chr20:37239573
|
ATTTG | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(197): Show | 245 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.1884-1698_1884-169 others(8): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr20 | 37239573 | |||||
| chr20:37239593
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1884-1710G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239593 | ||||||
| chr20:37239643
|
A | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(82): Show | 110 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1884-1660A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239643 | ||||||
| chr20:37239660
|
T | C | 1 | a0001c0002t0001g0080 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1884-1643T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239660 | ||||||
| chr20:37239816
|
C | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(143): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1884-1487C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239816 | ||||||
| chr20:37239834
|
C | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(12): Show | 20 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1884-1469C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239834 | ||||||
| chr20:37239907
|
G | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0239others(5): Show | 12 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1884-1396G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239907 | ||||||
| chr20:37239998
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1884-1305A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239998 | ||||||
| chr20:37240038
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1884-1265C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240038 | ||||||
| chr20:37240092
|
T | A | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1211T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240092 | ||||||
| chr20:37240113
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1190A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240113 | ||||||
| chr20:37240115
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1188G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240115 | ||||||
| chr20:37240118
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1185G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240118 | ||||||
| chr20:37240119
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1184A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240119 | ||||||
| chr20:37240123
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1180T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240123 | ||||||
| chr20:37240126
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1177C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240126 | ||||||
| chr20:37240127
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1176T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240127 | ||||||
| chr20:37240129
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1174G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240129 | ||||||
| chr20:37240131
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1172T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240131 | ||||||
| chr20:37240132
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1171C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240132 | ||||||
| chr20:37240135
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1168T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240135 | ||||||
| chr20:37240939
|
A | G | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1884-364A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240939 | ||||||
| chr20:37241012
|
A | C | 11 | a0001c0002t0001g0011a0001c0002t0001g0029a0001c0002t0001g0037others(8): Show | 15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1884-291A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37241012 | ||||||
| chr20:37241135
|
A | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(20): Show | 28 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1884-168A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37241135 | ||||||
| chr20:37241216
|
C | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1884-87C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37241216 |