Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MKAGA others(367): Show |
chr12 | 121395118 | 121429348 |
| a0002 | 0/0 | 371 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | MKAGA others(366): Show |
chr12 | 121395118 | 121429348 |
| a0003 | 0/0 | 372 | 9 | 0 | 9 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | MKAGA others(367): Show |
chr12 | 121395118 | 121429348 |
| a0004 | 0/0 | 229 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | MKAGA others(224): Show |
chr12 | 121395118 | 121429348 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1116 | 326 | 68 | 51 | 153 | 12 | 40 | RNF34_chr12_121395118_121429348 | RNF34 | ATGAA others(1111): Show |
chr12 | 121395118 | 121429348 | ||
| a0002c0002 | 0/0 | 1113 | 14 | 14 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | ATGAA others(1108): Show |
chr12 | 121395118 | 121429348 | ||
| a0003c0003 | 0/0 | 1116 | 9 | 0 | 9 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | ATGAA others(1111): Show |
chr12 | 121395118 | 121429348 | ||
| a0004c0004 | 0/0 | 1154 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | ATGAA others(1149): Show |
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 | AATCA others(1981): Show |
chr12 | 121395118 | 121429348 |
| a0001c0001t0002 | 0/0 | 1986 | 60 | 27 | 5 | 20 | 1 | 7 | RNF34_chr12_121395118_121429348 | RNF34 | AATCA others(1981): Show |
chr12 | 121395118 | 121429348 |
| a0001c0001t0003 | 0/0 | 1986 | 4 | 4 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | AATCA others(1981): Show |
chr12 | 121395118 | 121429348 |
| a0001c0001t0004 | 0/0 | 1986 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | AATCA others(1981): Show |
chr12 | 121395118 | 121429348 |
| a0001c0001t0005 | 0/0 | 1986 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | AATCA others(1981): Show |
chr12 | 121395118 | 121429348 |
| a0002c0002t0002 | 0/0 | 1983 | 14 | 14 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | AATCA others(1978): Show |
chr12 | 121395118 | 121429348 |
| a0003c0003t0002 | 0/0 | 1986 | 9 | 0 | 9 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | AATCA others(1981): Show |
chr12 | 121395118 | 121429348 |
| a0004c0004t0001 | 0/0 | 2024 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | AATCA others(2019): Show |
chr12 | 121395118 | 121429348 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 16 | 1 | 5 | 5 | 1 | 3 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 5 | 0 | 3 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 2 | 3 | 2 | 0 | 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 | 0 | 1 | 3 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 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 | 3 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | 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 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 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 | 0 | 0 | 1 | 0 | 1 | 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 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0049 | 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 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0001g0259 | 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 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0001c0001t0005g0041 | 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 |
| a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0002c0002t0002g0247 | 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 |
| a0003c0003t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0003c0003t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| a0004c0004t0001g0055 | 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 | g0243 | EUR | GBR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | 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 | g0011 | 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 | g0224 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | 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 | g0115 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | 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 | g0027 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0065 | 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 | g0092 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0077 | 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 | g0012 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0140 | 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 | g0210 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01496 | hp1 | a0003 | c0003 | t0002 | g0223 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | 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 | g0007 | EUR | IBS | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0236 | 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 | g0011 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0031 | 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 | g0011 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0172 | 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 | g0013 | 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 | g0121 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0050 | 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 | g0169 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | 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 | g0181 | EAS | CDX | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0232 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0037 | 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 | g0100 | AMR | PEL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0158 | 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 | g0252 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0073 | 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 | g0213 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0233 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0041 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0186 | 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 | g0211 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0193 | 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 | g0227 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0247 | 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 | g0198 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0203 | 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 | g0008 | 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 | g0191 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0229 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0231 | 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 | g0147 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0253 | 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 | g0033 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0246 | 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 | g0244 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0094 | 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 | g0240 | 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 | g0248 | SAS | PJL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | 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 | g0018 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18950 | hp1 | a0004 | c0004 | t0001 | g0055 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | 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 | g0063 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0217 | 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 | g0025 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0030 | 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 | g0078 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0220 | 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 | g0152 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0230 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0051 | 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 | g0003 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | 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 | g0215 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0177 | 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 | g0110 | 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 | g0102 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0021 | 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 | g0002 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | 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 | g0126 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | 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 | g0095 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0025 | 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 | g0036 | 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 | g0174 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0122 | 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 | g0083 | EUR | TSI | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0207 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ACB | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0008 | 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 | g0200 | AFR | MSL | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | USA | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | USA | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | USA | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | LWK | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0132 | REF | REF | RNF34_chr12_121395118_121429348 | RNF34 | chr12 | 121395118 | 121429348 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0002 a0001c0001t0003 a0002c0002t0002 others(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 | a0001c0001t0002 a0001c0001t0003 a0002c0002t0002 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121400470 | T | C | 1 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
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 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0195 a0001c0001t0002g0004 a0001c0001t0002g0016 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | a0001c0001t0002g0251 | 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 | a0001c0001t0001g0195 a0001c0001t0002g0004 a0001c0001t0002g0016 others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | a0001c0001t0001g0040 | 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 | 21 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): 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 | a0001c0001t0002g0004 a0001c0001t0002g0234 a0001c0001t0002g0235 others(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 | a0001c0001t0001g0102 a0001c0001t0002g0036 a0001c0001t0002g0206 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 |
51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(48): 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 |
21 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0045 others(18): 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0005g0041 | 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 | 12 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0182 others(9): 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 | 166 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(163): 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0190 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0195 a0001c0001t0002g0004 a0001c0001t0002g0016 others(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 | 79 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0120 others(76): 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0002g0197 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0195 a0001c0001t0002g0004 a0001c0001t0002g0016 others(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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0092 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0060 | 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 | a0001c0001t0002g0206 a0002c0002t0002g0010 a0002c0002t0002g0198 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0095 | 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 | 12 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0182 others(9): 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | 82 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0120 others(79): 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 | a0001c0001t0002g0205 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0092 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0228 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0120 a0001c0001t0001g0121 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): 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 | 26 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): 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 | 17 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): 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 | 59 | a0001c0001t0001g0024 a0001c0001t0001g0105 a0001c0001t0002g0004 others(56): 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 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
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 | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(82): 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0195 a0001c0001t0002g0004 a0001c0001t0002g0016 others(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 | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(82): 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 | 12 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0182 others(9): 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 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0035 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0182 | 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 | a0002c0002t0002g0229 a0002c0002t0002g0230 |
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 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0086 | 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 |
17 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0183 others(14): 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 | a0001c0001t0001g0105 a0001c0001t0005g0041 |
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 |
89 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(86): 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 | a0001c0001t0001g0128 a0001c0001t0002g0197 a0001c0001t0002g0200 others(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 |
18 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0109 others(15): 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 |
30 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(27): 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 | a0001c0001t0002g0201 a0001c0001t0002g0213 a0001c0001t0002g0226 others(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 | a0001c0001t0002g0209 a0001c0001t0002g0212 a0001c0001t0002g0249 |
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 | a0001c0001t0001g0047 | 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 | a0002c0002t0002g0229 a0002c0002t0002g0230 |
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 | a0001c0001t0001g0085 | 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 | 8 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0183 others(5): 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 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0035 others(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 | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(83): 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0170 a0001c0001t0001g0177 others(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 | a0001c0001t0002g0226 a0001c0001t0002g0227 |
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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0002g0218 | 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0041 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0211 a0001c0001t0002g0234 others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0041 |
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 | a0001c0001t0001g0040 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | a0001c0001t0001g0190 | 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 | 15 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(12): 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 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
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 | 178 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(175): 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 | 81 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0120 others(78): 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0094 | 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 | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(82): 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0237 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | 174 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(171): 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0069 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0214 | 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0041 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0001g0071 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | a0001c0001t0001g0040 | 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 | a0001c0001t0002g0225 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(82): 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0200 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0071 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | 12 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0182 others(9): 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0200 |
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 | a0001c0001t0005g0041 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | 23 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0001t0001g0102 others(20): 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 | 12 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0090 others(9): 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0041 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | 12 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0182 others(9): 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0041 |
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 |
12 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(9): 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 | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(91): 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 | 14 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): 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 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0035 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0197 a0001c0001t0002g0200 others(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 | a0001c0001t0002g0211 | 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 | 52 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0027 others(49): Show |
73 | HG00140.hp2 HG00642.hp2 HG00673.hp1 others(70): 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0157 | 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 | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(82): 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 | a0001c0001t0002g0245 a0001c0001t0002g0246 |
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 | 44 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(41): 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 | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(230): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0012 | 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 | 12 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(9): 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0166 | 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 | 8 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0183 others(5): 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0041 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0002g0209 a0003c0003t0002g0005 a0003c0003t0002g0210 others(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 | a0001c0001t0005g0041 | 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 | a0001c0001t0001g0167 | 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 | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(82): 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 | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(97): 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 | a0001c0001t0001g0040 | 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 | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(97): 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 | a0001c0001t0002g0234 | 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 | a0001c0001t0001g0161 | 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 | 179 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(176): 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 | 33 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0121 others(30): 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 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(65): 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 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0090 others(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 | 23 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(20): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | a0002c0002t0002g0230 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 |
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 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0035 others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0175 |
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 | a0002c0002t0002g0199 a0002c0002t0002g0208 a0002c0002t0002g0232 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0151 a0001c0001t0001g0174 |
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 | a0001c0001t0002g0196 a0001c0001t0002g0203 a0001c0001t0002g0204 |
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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0041 |
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 | 178 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(175): 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0041 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0099 |
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 | a0001c0001t0001g0195 a0001c0001t0002g0004 a0001c0001t0002g0016 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0075 | 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 | 167 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(164): 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 | a0001c0001t0002g0197 a0001c0001t0002g0200 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0042 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0141 | 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 | a0003c0003t0002g0223 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0144 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0200 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0032 others(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 | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(48): 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0076 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0204 others(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 | a0001c0001t0002g0224 a0001c0001t0002g0242 a0001c0001t0002g0243 others(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 | 16 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): 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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0002g0016 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0109 a0001c0001t0001g0120 others(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 | 14 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0002g0224 others(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 | a0001c0001t0002g0245 | 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 | a0001c0001t0002g0209 a0001c0001t0002g0222 a0001c0001t0002g0240 others(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 | a0001c0001t0002g0224 a0001c0001t0002g0243 a0001c0001t0002g0251 |
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 | a0001c0001t0002g0245 a0001c0001t0003g0037 a0001c0001t0003g0252 others(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 | a0001c0001t0002g0209 a0001c0001t0002g0222 a0001c0001t0002g0240 others(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 | a0001c0001t0002g0245 | 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 | a0001c0001t0002g0241 | 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 | a0001c0001t0002g0209 a0001c0001t0002g0222 a0001c0001t0002g0224 others(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 | 4 | a0001c0001t0001g0011 a0001c0001t0001g0053 a0001c0001t0001g0065 others(1): 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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0062 a0001c0001t0002g0216 a0001c0001t0002g0220 |
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 | 12 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0182 others(9): 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 | a0001c0001t0002g0236 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0002g0036 a0001c0001t0002g0215 a0001c0001t0002g0216 others(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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0131 | 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 | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(82): 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 | a0001c0001t0003g0037 a0001c0001t0003g0252 a0001c0001t0003g0253 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(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 | 12 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0182 others(9): 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 | a0001c0001t0001g0062 a0001c0001t0001g0099 |
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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0147 a0001c0001t0001g0150 |
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 | a0001c0001t0002g0241 | 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 | a0001c0001t0001g0195 a0001c0001t0002g0004 a0001c0001t0002g0016 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0149 a0001c0001t0001g0170 others(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 | a0001c0001t0002g0201 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.929-29C>T | RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 5/5 | chr12 | 121423357 |