Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 80196 |
|---|---|
| ensemblid | ENSG00000170633.17 |
| hgncid | 17297 |
| symbol | RNF34 |
| name | ring finger protein 34 |
| refseq_nuc | NM_025126.4 |
| refseq_prot | NP_079402.2 |
| ensembl_nuc | ENST00000361234.10 |
| ensembl_prot | ENSP00000355137.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 121400118 |
| end | 121424348 |
| strand | + |
| ver | v1.2 |
| region | chr12:121400118-121424348 |
| region5000 | chr12:121395118-121429348 |
| regionname0 | RNF34_chr12_121400118_121424348 |
| regionname5000 | RNF34_chr12_121395118_121429348 |
| 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 | 372 | 326 | 68 | 51 | 153 | 12 | 40 | 117 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0002 | 0/0 | 371 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0003 | 0/0 | 372 | 9 | 0 | 9 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0004 | 0/0 | 229 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1119 | 326 | 68 | 51 | 153 | 12 | 40 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| c0002 | 0/0 | 1116 | 14 | 14 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| c0003 | 0/0 | 1119 | 9 | 0 | 9 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| c0004 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| 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 | 868 | 261 | 37 | 45 | 134 | 11 | 32 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| t0002 | 0/0 | 868 | 83 | 41 | 14 | 20 | 1 | 7 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| t0003 | 0/0 | 868 | 4 | 4 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| t0004 | 0/0 | 868 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| t0005 | 0/0 | 868 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/1 | 13 | 1 | 4 | 3 | 1 | 3 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0002 | 0/0 | 7 | 0 | 2 | 3 | 2 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0003 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0004 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0008 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1119 | 326 | 68 | 51 | 153 | 12 | 40 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0002c0002 | 0/0 | 1116 | 14 | 14 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0003c0003 | 0/0 | 1119 | 9 | 0 | 9 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0004c0004 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1986 | 260 | 37 | 45 | 133 | 11 | 32 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0001c0001t0002 | 0/0 | 1986 | 60 | 27 | 5 | 20 | 1 | 7 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0001c0001t0003 | 0/0 | 1986 | 4 | 4 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0001c0001t0004 | 0/0 | 1986 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0001c0001t0005 | 0/0 | 1986 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0002c0002t0002 | 0/0 | 1983 | 14 | 14 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0003c0003t0002 | 0/0 | 1986 | 9 | 0 | 9 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| a0004c0004t0001 | 0/0 | 2024 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | copy fasta | chr12 | 121395118 | 121429348 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 13 | 1 | 4 | 3 | 1 | 3 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 2 | 3 | 2 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0004 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0003c0003t0002g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0003c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0003c0003t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0004c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0254 | EUR | GBR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01255 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01256 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01361 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01433 | hp1 | a0003 | c0003 | t0002 | g0221 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01496 | hp1 | a0003 | c0003 | t0002 | g0234 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02004 | hp1 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0243 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02300 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0258 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0209 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0219 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0240 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0242 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0264 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18950 | hp1 | a0004 | c0004 | t0001 | g0049 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0241 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0218 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | USA | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121417808
|
G | A | 1 | a0003 | 9 | HG01071.hp2 HG01255.hp2 HG01256.hp2 others(6): Show |
missense_variant | MODERATE | c.530G>A | p.Arg177His | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/6 | 625/1986 | 530/1119 | 177/372 | chr12 | 121417808 | ||
| chr12:121420261
|
C | CAGCAAAC others(31): Show |
1 | a0004 | 1 | NA18950.hp1 | frameshift_variant&stop_gained | HIGH | c.663_664insAAAAAAAA others(30): Show |
p.Glu222fs | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 4/6 | 759/1986 | 664/1119 | 222/372 | INFO_REALIGN_3_PRIME | chr12 | 121420261 | |
| chr12:121420274
|
AGAT | A | 1 | a0002 | 14 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
disruptive_inframe_deletion | MODERATE | c.675_677delTGA | p.Asp226del | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 4/6 | 770/1986 | 675/1119 | 225/372 | INFO_REALIGN_3_PRIME | chr12 | 121420274 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121400138
|
G | A | 1 | a0001c0001t0003 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-75G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/6 | 75 | chr12 | 121400138 | |||||
| chr12:121423621
|
C | A | 4 | a0001c0001t0002a0001c0001t0003a0002c0002t0002others(1): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*45C>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 6/6 | 45 | chr12 | 121423621 | |||||
| chr12:121423913
|
T | A | 1 | a0001c0001t0004 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*337T>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 6/6 | 337 | chr12 | 121423913 | |||||
| chr12:121424041
|
T | C | 1 | a0001c0001t0005 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 6/6 | 465 | chr12 | 121424041 | |||||
| chr12:121424268
|
T | C | 4 | a0001c0001t0002a0001c0001t0003a0002c0002t0002others(1): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*692T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 6/6 | 692 | chr12 | 121424268 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121400470
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6+252T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121400470 | ||||||
| chr12:121400475
|
G | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG00621.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.6+257G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121400475 | ||||||
| chr12:121400624
|
A | G | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02074.hp2 NA18963.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+406A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121400624 | ||||||
| chr12:121400725
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6+507G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121400725 | ||||||
| chr12:121400757
|
A | C | 67 | a0001c0001t0001g0206a0001c0001t0002g0004a0001c0001t0002g0016others(64): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.6+539A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121400757 | ||||||
| chr12:121400778
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.6+560C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121400778 | ||||||
| chr12:121400818
|
C | T | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+600C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121400818 | ||||||
| chr12:121400932
|
C | G | 1 | a0001c0001t0002g0262 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6+714C>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121400932 | ||||||
| chr12:121401051
|
T | C | 67 | a0001c0001t0001g0206a0001c0001t0002g0004a0001c0001t0002g0016others(64): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.6+833T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121401051 | ||||||
| chr12:121401122
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.6+904C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121401122 | ||||||
| chr12:121401153
|
A | G | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6+935A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121401153 | ||||||
| chr12:121401157
|
G | A | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+939G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121401157 | ||||||
| chr12:121401351
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6+1133T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121401351 | ||||||
| chr12:121401354
|
C | CA | 24 | a0001c0001t0001g0009a0001c0001t0001g0101a0001c0001t0001g0102others(21): Show | 27 | HG00140.hp2 HG00621.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.6+1156dupA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
C | CAAAAAAA | 21 | a0001c0001t0002g0004a0001c0001t0002g0245a0001c0001t0002g0246others(18): Show | 33 | HG00099.hp1 HG00558.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.6+1150_6+1156dupAA others(5): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
C | CAAAAAAA others(1): Show |
27 | a0001c0001t0001g0100a0001c0001t0002g0030a0001c0001t0002g0217others(24): Show | 31 | HG00423.hp1 HG00741.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.6+1149_6+1156dupAA others(6): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
C | CAAAAAAA others(2): Show |
21 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 28 | HG00438.hp2 HG00741.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+1148_6+1156dupAA others(7): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
C | CAAAAAAA others(3): Show |
53 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(50): Show | 70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.6+1147_6+1156dupAA others(8): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
C | CAAAAAAA others(4): Show |
22 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(19): Show | 22 | HG00642.hp1 HG01975.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.6+1146_6+1156dupAA others(9): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0037 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6+1145_6+1156dupAA others(10): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0036 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.6+1144_6+1156dupAA others(11): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0005g0035 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6+1143_6+1156dupAA others(12): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401354
|
CAA | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+1155_6+1156delAA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121401354 | |||||
| chr12:121401898
|
C | A | 170 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.6+1680C>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121401898 | ||||||
| chr12:121401921
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02015.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.6+1703T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121401921 | ||||||
| chr12:121402001
|
T | C | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6+1783T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402001 | ||||||
| chr12:121402254
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0201a0001c0001t0001g0202 | 5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+2036A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402254 | ||||||
| chr12:121402436
|
G | T | 67 | a0001c0001t0001g0206a0001c0001t0002g0004a0001c0001t0002g0016others(64): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.6+2218G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402436 | ||||||
| chr12:121402557
|
T | TA | 80 | a0001c0001t0001g0015a0001c0001t0001g0124a0001c0001t0001g0191others(77): Show | 103 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.6+2350dupA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121402557 | |||||
| chr12:121402577
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.6+2359G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402577 | ||||||
| chr12:121402670
|
G | T | 1 | a0001c0001t0002g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6+2452G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402670 | ||||||
| chr12:121402729
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6+2511T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402729 | ||||||
| chr12:121402831
|
T | C | 67 | a0001c0001t0001g0206a0001c0001t0002g0004a0001c0001t0002g0016others(64): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.6+2613T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402831 | ||||||
| chr12:121402836
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6+2618T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402836 | ||||||
| chr12:121402927
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02723.hp1 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6+2709A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402927 | ||||||
| chr12:121402951
|
G | A | 1 | a0001c0001t0001g0017 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.6+2733G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402951 | ||||||
| chr12:121402983
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG01175.hp1 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+2765C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121402983 | ||||||
| chr12:121403032
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.6+2814A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403032 | ||||||
| chr12:121403128
|
G | A | 12 | a0001c0001t0002g0217a0002c0002t0002g0010a0002c0002t0002g0209others(9): Show | 15 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.6+2910G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403128 | ||||||
| chr12:121403132
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.6+2914C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403132 | ||||||
| chr12:121403228
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6+3010C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403228 | ||||||
| chr12:121403245
|
A | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0089a0001c0001t0001g0099others(1): Show | 5 | HG00408.hp2 HG00438.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3027A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403245 | ||||||
| chr12:121403286
|
CTCTGGAG others(3): Show |
C | 1 | a0001c0001t0001g0093 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.6+3069_6+3078delTC others(8): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403286 | ||||||
| chr12:121403297
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+3079G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403297 | ||||||
| chr12:121403303
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6+3085G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403303 | ||||||
| chr12:121403321
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | HG01243.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+3103G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403321 | ||||||
| chr12:121403345
|
A | G | 83 | a0001c0001t0001g0015a0001c0001t0001g0124a0001c0001t0001g0125others(80): Show | 106 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.6+3127A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403345 | ||||||
| chr12:121403360
|
C | T | 1 | a0001c0001t0002g0216 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6+3142C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403360 | ||||||
| chr12:121403396
|
C | CA | 17 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0090others(14): Show | 24 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.6+3189dupA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121403396 | |||||
| chr12:121403414
|
CA | C | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6+3208delA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121403414 | |||||
| chr12:121403600
|
C | T | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6+3382C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403600 | ||||||
| chr12:121403614
|
G | C | 1 | a0001c0001t0001g0007 | 5 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3396G>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403614 | ||||||
| chr12:121403843
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6+3625A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121403843 | ||||||
| chr12:121403851
|
ATTGCTAT others(102): Show |
A | 1 | a0001c0001t0001g0189 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.6+3670_6+3778del | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121403851 | |||||
| chr12:121404019
|
C | CT | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0239others(4): Show | 13 | HG01071.hp2 HG01255.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.6+3815dupT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121404019 | |||||
| chr12:121404162
|
AT | A | 70 | a0001c0001t0001g0059a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 91 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.6+3958delT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121404162 | |||||
| chr12:121404249
|
C | T | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+4031C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121404249 | ||||||
| chr12:121404387
|
C | CT | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.6+4194dupT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121404387 | |||||
| chr12:121404387
|
C | CTT | 27 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(24): Show | 28 | HG00438.hp2 HG01069.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+4193_6+4194dupTT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121404387 | |||||
| chr12:121404387
|
CT | C | 19 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0106others(16): Show | 23 | HG00621.hp1 HG00673.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.6+4194delT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121404387 | |||||
| chr12:121404387
|
CTT | C | 60 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(57): Show | 80 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.6+4193_6+4194delTT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121404387 | |||||
| chr12:121404421
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | NA18982.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.6+4203G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121404421 | ||||||
| chr12:121404465
|
G | A | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(85): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.6+4247G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121404465 | ||||||
| chr12:121404481
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.6+4263G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121404481 | ||||||
| chr12:121404590
|
C | T | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6+4372C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121404590 | ||||||
| chr12:121404714
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6+4496C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121404714 | ||||||
| chr12:121404784
|
T | G | 67 | a0001c0001t0001g0206a0001c0001t0002g0004a0001c0001t0002g0016others(64): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.6+4566T>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121404784 | ||||||
| chr12:121404917
|
A | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(85): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.6+4699A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121404917 | ||||||
| chr12:121405109
|
T | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+4891T>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405109 | ||||||
| chr12:121405210
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0267 | 2 | NA18963.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.6+4992G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405210 | ||||||
| chr12:121405405
|
C | CTTG | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6+5188_6+5190dupTT others(1): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121405405 | |||||
| chr12:121405506
|
C | A | 23 | a0001c0001t0002g0016a0001c0001t0002g0028a0001c0001t0002g0029others(20): Show | 28 | HG00423.hp1 HG00558.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+5288C>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405506 | ||||||
| chr12:121405588
|
G | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6+5370G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405588 | ||||||
| chr12:121405617
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6+5399A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405617 | ||||||
| chr12:121405736
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6+5518G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405736 | ||||||
| chr12:121405807
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6+5589T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405807 | ||||||
| chr12:121405956
|
G | A | 2 | a0002c0002t0002g0240a0002c0002t0002g0241 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6+5738G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405956 | ||||||
| chr12:121405973
|
T | C | 4 | a0001c0001t0001g0191a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | HG01243.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+5755T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121405973 | ||||||
| chr12:121406096
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.6+5878T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406096 | ||||||
| chr12:121406283
|
A | AGTTGTTG others(2): Show |
18 | a0001c0001t0001g0015a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 27 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.6+6078_6+6086dupGT others(7): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406283 | |||||
| chr12:121406283
|
A | AGTTGTTG others(5): Show |
2 | a0001c0001t0001g0105a0001c0001t0005g0035 | 2 | HG02015.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6+6075_6+6086dupGT others(10): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406283 | |||||
| chr12:121406283
|
A | AGTTGTTG others(8): Show |
92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(89): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.6+6072_6+6086dupGT others(13): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406283 | |||||
| chr12:121406283
|
A | AGTTGTTG others(11): Show |
14 | a0001c0001t0001g0132a0001c0001t0002g0208a0001c0001t0002g0211others(11): Show | 14 | HG02055.hp1 HG02258.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+6069_6+6086dupGT others(16): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406283 | |||||
| chr12:121406283
|
A | AGTTGTTG others(14): Show |
19 | a0001c0001t0001g0040a0001c0001t0001g0111a0001c0001t0001g0112others(16): Show | 26 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+6066_6+6086dupGT others(19): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406283 | |||||
| chr12:121406283
|
A | AGTTGTTG others(17): Show |
32 | a0001c0001t0001g0009a0001c0001t0001g0103a0001c0001t0001g0104others(29): Show | 42 | HG00558.hp2 HG00673.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.6+6086_6+6087insGT others(22): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406283 | |||||
| chr12:121406283
|
A | AGTTGTTG others(20): Show |
5 | a0001c0001t0002g0212a0001c0001t0002g0224a0001c0001t0002g0237others(2): Show | 5 | HG02572.hp1 HG02735.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+6086_6+6087insGT others(25): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406283 | |||||
| chr12:121406283
|
A | AGTTGTTG others(23): Show |
3 | a0001c0001t0002g0220a0001c0001t0002g0223a0001c0001t0002g0260 | 3 | HG02074.hp1 HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.6+6086_6+6087insGT others(28): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406283 | |||||
| chr12:121406327
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6+6109G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406327 | ||||||
| chr12:121406348
|
C | T | 2 | a0002c0002t0002g0240a0002c0002t0002g0241 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6+6130C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406348 | ||||||
| chr12:121406356
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6+6138C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406356 | ||||||
| chr12:121406443
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 11 | HG01891.hp2 HG02055.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+6225C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406443 | ||||||
| chr12:121406453
|
A | AT | 23 | a0001c0001t0002g0016a0001c0001t0002g0028a0001c0001t0002g0029others(20): Show | 28 | HG00423.hp1 HG00558.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+6241dupT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406453 | |||||
| chr12:121406489
|
G | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(86): Show | 109 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.6+6271G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406489 | ||||||
| chr12:121406714
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6+6496C>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406714 | ||||||
| chr12:121406745
|
T | C | 63 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(60): Show | 83 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.6+6527T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406745 | ||||||
| chr12:121406869
|
CAAG | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0179a0001c0001t0001g0186others(1): Show | 4 | NA18940.hp2 NA19066.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6653_6+6655delAG others(1): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121406869 | |||||
| chr12:121406982
|
C | T | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6+6764C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406982 | ||||||
| chr12:121406983
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.6+6765G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121406983 | ||||||
| chr12:121407031
|
T | G | 1 | a0001c0001t0001g0018 | 2 | HG01516.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.6+6813T>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121407031 | ||||||
| chr12:121407197
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.6+6979G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121407197 | ||||||
| chr12:121407301
|
T | C | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0035 | 3 | HG02015.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6+7083T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121407301 | ||||||
| chr12:121407309
|
A | G | 6 | a0001c0001t0002g0004a0001c0001t0002g0222a0001c0001t0002g0245others(3): Show | 12 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+7091A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121407309 | ||||||
| chr12:121407445
|
T | TAGTATAC others(8): Show |
1 | a0001c0001t0001g0203 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.6+7231_6+7245dupAT others(13): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121407445 | |||||
| chr12:121407566
|
G | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6+7348G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121407566 | ||||||
| chr12:121408032
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0035 | 3 | HG02015.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6+7814G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121408032 | ||||||
| chr12:121408119
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6+7901A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121408119 | ||||||
| chr12:121408127
|
A | G | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.6+7909A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121408127 | ||||||
| chr12:121408206
|
T | C | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-7953T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121408206 | ||||||
| chr12:121408419
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7-7740G>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121408419 | ||||||
| chr12:121408434
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.7-7725C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121408434 | ||||||
| chr12:121408442
|
AAAAAAT | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-7695_7-7690delAA others(4): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121408442 | |||||
| chr12:121408814
|
G | A | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-7345G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121408814 | ||||||
| chr12:121409024
|
T | A | 1 | a0001c0001t0001g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7-7135T>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409024 | ||||||
| chr12:121409219
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 25 | HG01358.hp2 HG01952.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.7-6940A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409219 | ||||||
| chr12:121409331
|
C | T | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.7-6828C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409331 | ||||||
| chr12:121409332
|
A | G | 185 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.7-6827A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409332 | ||||||
| chr12:121409477
|
C | T | 82 | a0001c0001t0001g0015a0001c0001t0001g0124a0001c0001t0001g0125others(79): Show | 105 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.7-6682C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409477 | ||||||
| chr12:121409567
|
C | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-6592C>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409567 | ||||||
| chr12:121409582
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.7-6577A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409582 | ||||||
| chr12:121409696
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.7-6463A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409696 | ||||||
| chr12:121409776
|
A | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(85): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.7-6383A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409776 | ||||||
| chr12:121409814
|
C | T | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-6345C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409814 | ||||||
| chr12:121409918
|
A | G | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-6241A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121409918 | ||||||
| chr12:121410154
|
C | CA | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-5996dupA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121410154 | |||||
| chr12:121410253
|
C | G | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-5906C>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121410253 | ||||||
| chr12:121410383
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7-5776A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121410383 | ||||||
| chr12:121410445
|
G | A | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-5714G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121410445 | ||||||
| chr12:121410545
|
CA | C | 181 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.7-5601delA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121410545 | |||||
| chr12:121410569
|
G | GA | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(5): Show | 8 | HG01243.hp1 HG02015.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-5579dupA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121410569 | |||||
| chr12:121410670
|
AGAT | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0065others(1): Show | 4 | HG01123.hp2 HG01975.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-5485_7-5483delGA others(1): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121410670 | |||||
| chr12:121410687
|
G | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-5472G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121410687 | ||||||
| chr12:121410939
|
T | G | 1 | a0001c0001t0002g0225 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7-5220T>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121410939 | ||||||
| chr12:121410966
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0035 | 3 | HG02015.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.7-5193A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121410966 | ||||||
| chr12:121410971
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0064a0001c0001t0001g0067 | 3 | NA18978.hp2 NA19003.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.7-5188G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121410971 | ||||||
| chr12:121411278
|
CA | C | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-4880delA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121411278 | ||||||
| chr12:121411328
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.7-4831G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121411328 | ||||||
| chr12:121411388
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7-4771G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121411388 | ||||||
| chr12:121411503
|
T | C | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-4656T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121411503 | ||||||
| chr12:121411512
|
A | T | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(85): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.7-4647A>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121411512 | ||||||
| chr12:121411592
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02015.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.7-4567T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121411592 | ||||||
| chr12:121411756
|
A | G | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-4403A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121411756 | ||||||
| chr12:121412187
|
G | A | 20 | a0001c0001t0002g0208a0001c0001t0002g0211a0001c0001t0002g0216others(17): Show | 26 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.7-3972G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412187 | ||||||
| chr12:121412228
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.7-3931A>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412228 | ||||||
| chr12:121412229
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.7-3930T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412229 | ||||||
| chr12:121412230
|
C | CT | 14 | a0001c0001t0001g0088a0001c0001t0001g0109a0001c0001t0001g0110others(11): Show | 14 | HG00621.hp1 HG02027.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-3902dupT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121412230 | |||||
| chr12:121412230
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.7-3929C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412230 | ||||||
| chr12:121412230
|
CT | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(87): Show | 113 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.7-3902delT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121412230 | |||||
| chr12:121412230
|
CTT | C | 65 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0094others(62): Show | 86 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.7-3903_7-3902delTT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121412230 | |||||
| chr12:121412230
|
CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-3917_7-3902delTT others(14): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121412230 | |||||
| chr12:121412270
|
C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-3889C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412270 | ||||||
| chr12:121412388
|
C | T | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-3771C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412388 | ||||||
| chr12:121412396
|
C | T | 2 | a0001c0001t0002g0208a0001c0001t0002g0211 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-3763C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412396 | ||||||
| chr12:121412545
|
A | T | 1 | a0001c0001t0005g0035 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.7-3614A>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412545 | ||||||
| chr12:121412645
|
A | C | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-3514A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412645 | ||||||
| chr12:121412724
|
C | CT | 24 | a0001c0001t0001g0084a0001c0001t0001g0100a0001c0001t0001g0102others(21): Show | 25 | HG01243.hp1 HG01952.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.7-3417dupT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121412724 | |||||
| chr12:121412724
|
C | CTT | 13 | a0001c0001t0001g0015a0001c0001t0001g0087a0001c0001t0001g0192others(10): Show | 15 | HG01891.hp2 HG02055.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.7-3418_7-3417dupTT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121412724 | |||||
| chr12:121412725
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.7-3434T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412725 | ||||||
| chr12:121412850
|
A | G | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-3309A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121412850 | ||||||
| chr12:121413020
|
AT | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-3129delT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121413020 | |||||
| chr12:121413089
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0035 | 3 | HG02015.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.7-3070G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413089 | ||||||
| chr12:121413112
|
G | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-3047G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413112 | ||||||
| chr12:121413136
|
CT | C | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-3022delT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413136 | ||||||
| chr12:121413224
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-2935G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413224 | ||||||
| chr12:121413288
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0035 | 3 | HG02015.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.7-2871A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413288 | ||||||
| chr12:121413366
|
T | TGAGGTAT others(11): Show |
15 | a0001c0001t0001g0009a0001c0001t0001g0103a0001c0001t0001g0104others(12): Show | 18 | HG00621.hp1 HG00673.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.7-2792_7-2775dupGA others(16): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121413366 | |||||
| chr12:121413415
|
C | CT | 98 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(95): Show | 120 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.7-2730dupT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121413415 | |||||
| chr12:121413415
|
C | CTT | 17 | a0001c0001t0001g0009a0001c0001t0001g0077a0001c0001t0001g0089others(14): Show | 20 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.7-2731_7-2730dupTT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121413415 | |||||
| chr12:121413415
|
C | CTTTTTTT others(3): Show |
43 | a0001c0001t0002g0016a0001c0001t0002g0028a0001c0001t0002g0029others(40): Show | 57 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.7-2739_7-2730dupTT others(8): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121413415 | |||||
| chr12:121413415
|
C | CTTTTTTT others(4): Show |
18 | a0001c0001t0002g0004a0001c0001t0002g0208a0001c0001t0002g0211others(15): Show | 24 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-2740_7-2730dupTT others(9): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121413415 | |||||
| chr12:121413415
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7-2741_7-2730dupTT others(10): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121413415 | |||||
| chr12:121413428
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(51): Show | 74 | HG00140.hp2 HG00642.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.7-2731T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413428 | ||||||
| chr12:121413430
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.7-2729G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413430 | ||||||
| chr12:121413434
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.7-2725C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413434 | ||||||
| chr12:121413466
|
C | T | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(85): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.7-2693C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413466 | ||||||
| chr12:121413520
|
T | G | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.7-2639T>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413520 | ||||||
| chr12:121413575
|
C | CT | 45 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0032others(42): Show | 58 | HG00423.hp2 HG00621.hp2 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.7-2564dupT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121413575 | |||||
| chr12:121413641
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(239): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.7-2518T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413641 | ||||||
| chr12:121413702
|
C | T | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-2457C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413702 | ||||||
| chr12:121413864
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7-2295C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121413864 | ||||||
| chr12:121414167
|
A | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0062others(4): Show | 9 | HG01496.hp2 HG01978.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-1992A>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414167 | ||||||
| chr12:121414168
|
T | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0062others(4): Show | 9 | HG01496.hp2 HG01978.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-1991T>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414168 | ||||||
| chr12:121414248
|
A | G | 1 | a0001c0001t0001g0011 | 3 | HG01069.hp2 HG01071.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.7-1911A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414248 | ||||||
| chr12:121414270
|
A | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0103a0001c0001t0001g0104others(12): Show | 18 | HG00621.hp1 HG00673.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.7-1889A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414270 | ||||||
| chr12:121414327
|
G | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-1832G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414327 | ||||||
| chr12:121414457
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.7-1702A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414457 | ||||||
| chr12:121414669
|
CTGT | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 11 | HG01891.hp2 HG02055.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.7-1476_7-1474delGT others(1): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121414669 | |||||
| chr12:121414669
|
CTGTTGTT others(2): Show |
C | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0035 | 3 | HG02015.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.7-1482_7-1474delGT others(7): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121414669 | |||||
| chr12:121414758
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.7-1401C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414758 | ||||||
| chr12:121414797
|
C | T | 4 | a0001c0001t0002g0220a0003c0003t0002g0005a0003c0003t0002g0221others(1): Show | 10 | HG01071.hp2 HG01255.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.7-1362C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414797 | ||||||
| chr12:121414852
|
G | A | 1 | a0001c0001t0005g0035 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.7-1307G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414852 | ||||||
| chr12:121414875
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.7-1284C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121414875 | ||||||
| chr12:121415083
|
T | A | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(85): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.7-1076T>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121415083 | ||||||
| chr12:121415089
|
T | TC | 104 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(101): Show | 126 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.7-1068dupC | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121415089 | |||||
| chr12:121415248
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.7-911T>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121415248 | ||||||
| chr12:121415361
|
T | C | 104 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(101): Show | 126 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.7-798T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121415361 | ||||||
| chr12:121415405
|
G | C | 1 | a0001c0001t0002g0247 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7-754G>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121415405 | ||||||
| chr12:121415412
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.7-747C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121415412 | ||||||
| chr12:121415570
|
T | C | 186 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(183): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.7-589T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121415570 | ||||||
| chr12:121415840
|
C | CT | 34 | a0001c0001t0001g0015a0001c0001t0001g0125a0001c0001t0001g0191others(31): Show | 45 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.7-298dupT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121415840 | |||||
| chr12:121415840
|
C | CTT | 10 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(7): Show | 10 | HG01515.hp1 HG02074.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-299_7-298dupTT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121415840 | |||||
| chr12:121415840
|
C | CTTT | 71 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(68): Show | 91 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.7-300_7-298dupTTT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121415840 | |||||
| chr12:121415840
|
C | CTTTT | 6 | a0001c0001t0001g0048a0001c0001t0001g0080a0001c0001t0001g0087others(3): Show | 6 | HG01175.hp1 HG02080.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-301_7-298dupTTTT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121415840 | |||||
| chr12:121415840
|
CT | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0055others(23): Show | 29 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.7-298delT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 121415840 | |||||
| chr12:121415878
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7-281G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121415878 | ||||||
| chr12:121415896
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.7-263T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | chr12 | 121415896 | ||||||
| chr12:121416797
|
C | A | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.225+420C>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 2/5 | chr12 | 121416797 | ||||||
| chr12:121417092
|
C | T | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-412C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 2/5 | chr12 | 121417092 | ||||||
| chr12:121417138
|
A | G | 1 | a0002c0002t0002g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.226-366A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 2/5 | chr12 | 121417138 | ||||||
| chr12:121417234
|
A | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0200 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.226-270A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 2/5 | chr12 | 121417234 | ||||||
| chr12:121417246
|
A | T | 4 | a0001c0001t0002g0016a0001c0001t0002g0028a0001c0001t0002g0029others(1): Show | 8 | NA18952.hp2 NA18954.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-258A>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 2/5 | chr12 | 121417246 | ||||||
| chr12:121417267
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.226-237C>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 2/5 | chr12 | 121417267 | ||||||
| chr12:121417432
|
A | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0182 | 2 | NA18990.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.226-72A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 2/5 | chr12 | 121417432 | ||||||
| chr12:121417484
|
A | AT | 3 | a0002c0002t0002g0210a0002c0002t0002g0219a0002c0002t0002g0243 | 3 | HG02055.hp1 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.226-20_226-19insT | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 2/5 | chr12 | 121417484 | ||||||
| chr12:121418163
|
TTC | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0159a0001c0001t0001g0184 | 3 | NA19070.hp2 NA19075.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.633+256_633+257del others(2): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 121418163 | |||||
| chr12:121418279
|
A | ATC | 3 | a0001c0001t0002g0207a0001c0001t0002g0214a0001c0001t0002g0215 | 3 | HG02257.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.633+369_633+370dup others(2): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 121418279 | |||||
| chr12:121418360
|
GA | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0035 | 3 | HG02015.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.633+451delA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 121418360 | |||||
| chr12:121418414
|
G | A | 185 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.633+503G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121418414 | ||||||
| chr12:121418429
|
A | C | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0035 | 3 | HG02015.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.633+518A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121418429 | ||||||
| chr12:121418453
|
G | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0182 | 2 | NA18990.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.633+542G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121418453 | ||||||
| chr12:121418456
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02723.hp1 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.633+545T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121418456 | ||||||
| chr12:121418584
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0182 | 2 | NA18990.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.633+673G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121418584 | ||||||
| chr12:121418709
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.633+798G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121418709 | ||||||
| chr12:121418897
|
G | T | 1 | a0001c0001t0001g0007 | 5 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.633+986G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121418897 | ||||||
| chr12:121418926
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0097 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.633+1015C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121418926 | ||||||
| chr12:121419018
|
A | G | 67 | a0001c0001t0001g0206a0001c0001t0002g0004a0001c0001t0002g0016others(64): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.633+1107A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121419018 | ||||||
| chr12:121419085
|
CTAA | C | 4 | a0001c0001t0001g0147a0001c0001t0001g0165a0001c0001t0001g0204others(1): Show | 4 | HG02572.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-1152_634-1150d others(5): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 121419085 | |||||
| chr12:121419206
|
A | T | 1 | a0001c0001t0001g0184 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.634-1036A>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121419206 | ||||||
| chr12:121419547
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.634-695T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121419547 | ||||||
| chr12:121419576
|
C | CAGT | 171 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(168): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.634-664_634-663ins others(3): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 121419576 | |||||
| chr12:121419610
|
G | C | 20 | a0001c0001t0002g0208a0001c0001t0002g0211a0001c0001t0002g0216others(17): Show | 26 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.634-632G>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121419610 | ||||||
| chr12:121419701
|
G | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0036others(12): Show | 20 | HG00438.hp1 HG02071.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.634-541G>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 3/5 | chr12 | 121419701 | ||||||
| chr12:121420405
|
A | T | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.726+71A>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 4/5 | chr12 | 121420405 | ||||||
| chr12:121420409
|
G | T | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.726+75G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 4/5 | chr12 | 121420409 | ||||||
| chr12:121420542
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.727-35T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 4/5 | chr12 | 121420542 | ||||||
| chr12:121420929
|
G | A | 1 | a0003c0003t0002g0234 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928+151G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121420929 | ||||||
| chr12:121420940
|
G | T | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.928+162G>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121420940 | ||||||
| chr12:121421067
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0151 | 2 | HG02135.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.928+289G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421067 | ||||||
| chr12:121421197
|
A | G | 20 | a0001c0001t0002g0208a0001c0001t0002g0211a0001c0001t0002g0216others(17): Show | 26 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.928+419A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421197 | ||||||
| chr12:121421371
|
T | TA | 34 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0027others(31): Show | 42 | HG00642.hp2 HG00673.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.928+620dupA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421371 | |||||
| chr12:121421371
|
T | TAA | 55 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(52): Show | 69 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.928+619_928+620dup others(2): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421371 | |||||
| chr12:121421371
|
T | TAAA | 27 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(24): Show | 31 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.928+618_928+620dup others(3): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421371 | |||||
| chr12:121421371
|
T | TAAAA | 6 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0072others(3): Show | 6 | HG00621.hp2 HG03927.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+617_928+620dup others(4): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421371 | |||||
| chr12:121421371
|
T | TAC | 11 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0215others(8): Show | 13 | HG00423.hp1 HG02258.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.928+594_928+595ins others(2): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421371 | |||||
| chr12:121421371
|
T | TACAA | 7 | a0001c0001t0002g0235a0001c0001t0002g0253a0001c0001t0002g0254others(4): Show | 7 | HG00099.hp1 HG00741.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+594_928+595ins others(4): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421371 | |||||
| chr12:121421371
|
TA | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 24 | HG00621.hp1 HG00673.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.928+620delA | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421371 | |||||
| chr12:121421371
|
TAAAAAAA others(3): Show |
T | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.928+611_928+620del others(10): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421371 | |||||
| chr12:121421372
|
A | AC | 25 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0002g0016others(22): Show | 28 | HG00558.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.928+594_928+595ins others(1): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421372 | ||||||
| chr12:121421373
|
A | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0111a0001c0001t0001g0124others(18): Show | 38 | HG01071.hp2 HG01123.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.928+595A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421373 | ||||||
| chr12:121421374
|
A | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0103a0001c0001t0001g0104others(15): Show | 21 | HG00621.hp1 HG00673.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.928+596A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421374 | ||||||
| chr12:121421375
|
A | C | 6 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0002g0235others(3): Show | 6 | HG00099.hp1 HG00741.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.928+597A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421375 | ||||||
| chr12:121421376
|
A | C | 1 | a0001c0001t0002g0256 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.928+598A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421376 | ||||||
| chr12:121421379
|
A | C | 10 | a0001c0001t0002g0220a0001c0001t0002g0233a0001c0001t0002g0251others(7): Show | 16 | HG01071.hp2 HG01123.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.928+601A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421379 | ||||||
| chr12:121421382
|
A | C | 3 | a0001c0001t0002g0235a0001c0001t0002g0254a0001c0001t0002g0262 | 3 | HG00099.hp1 HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.928+604A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421382 | ||||||
| chr12:121421383
|
A | C | 4 | a0001c0001t0002g0256a0001c0001t0003g0031a0001c0001t0003g0263others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+605A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421383 | ||||||
| chr12:121421385
|
A | ACAAC | 9 | a0001c0001t0002g0220a0001c0001t0002g0233a0001c0001t0002g0251others(6): Show | 15 | HG01071.hp2 HG01123.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.928+607_928+608ins others(4): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421385 | ||||||
| chr12:121421386
|
A | C | 1 | a0001c0001t0002g0256 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.928+608A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421386 | ||||||
| chr12:121421388
|
A | C | 1 | a0001c0001t0002g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.928+610A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421388 | ||||||
| chr12:121421399
|
C | A | 15 | a0001c0001t0002g0220a0001c0001t0002g0233a0001c0001t0002g0235others(12): Show | 21 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.928+621C>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421399 | ||||||
| chr12:121421443
|
C | CTTGGGA | 5 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0061others(2): Show | 6 | HG00642.hp1 HG00733.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+666_928+671dup others(6): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421443 | |||||
| chr12:121421488
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0046others(1): Show | 6 | HG01516.hp2 HG02148.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+710G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421488 | ||||||
| chr12:121421535
|
TCAAAA | T | 3 | a0001c0001t0001g0058a0001c0001t0002g0227a0001c0001t0002g0231 | 3 | HG02622.hp1 NA18980.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.928+770_928+774del others(5): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121421535 | |||||
| chr12:121421602
|
T | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.928+824T>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421602 | ||||||
| chr12:121421619
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.928+841C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421619 | ||||||
| chr12:121421640
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.928+862A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421640 | ||||||
| chr12:121421844
|
C | T | 6 | a0001c0001t0002g0030a0001c0001t0002g0226a0001c0001t0002g0227others(3): Show | 7 | HG00423.hp1 HG00558.hp2 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+1066C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421844 | ||||||
| chr12:121421848
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.928+1070C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121421848 | ||||||
| chr12:121422024
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.928+1246G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422024 | ||||||
| chr12:121422041
|
A | C | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(85): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.928+1263A>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422041 | ||||||
| chr12:121422074
|
T | C | 3 | a0001c0001t0003g0031a0001c0001t0003g0263a0001c0001t0003g0264 | 4 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.928+1296T>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422074 | ||||||
| chr12:121422116
|
C | T | 66 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0028others(63): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.929-1270C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422116 | ||||||
| chr12:121422518
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.929-868G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422518 | ||||||
| chr12:121422544
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0097 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.929-842C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422544 | ||||||
| chr12:121422585
|
T | TTAAATCT others(31): Show |
1 | a0001c0001t0001g0153 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.929-799_929-762dup others(38): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 121422585 | |||||
| chr12:121422643
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0157 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.929-743A>G | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422643 | ||||||
| chr12:121422880
|
G | C | 1 | a0001c0001t0002g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.929-506G>C | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422880 | ||||||
| chr12:121422916
|
G | GA | 67 | a0001c0001t0001g0206a0001c0001t0002g0004a0001c0001t0002g0016others(64): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.929-470_929-469ins others(1): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121422916 | ||||||
| chr12:121423073
|
AG | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0156a0001c0001t0001g0179others(2): Show | 5 | NA18940.hp2 NA18952.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.929-312delG | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121423073 | ||||||
| chr12:121423335
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.929-51G>A | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121423335 | ||||||
| chr12:121423357
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.929-29C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121423357 |