Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 152006 |
|---|---|
| ensemblid | ENSG00000137075.18 |
| hgncid | 18052 |
| symbol | RNF38 |
| name | ring finger protein 38 |
| refseq_nuc | NM_022781.5 |
| refseq_prot | NP_073618.3 |
| ensembl_nuc | ENST00000259605.11 |
| ensembl_prot | ENSP00000259605.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 36336400 |
| end | 36400269 |
| strand | - |
| ver | v1.2 |
| region | chr9:36336400-36400269 |
| region5000 | chr9:36331400-36405269 |
| regionname0 | RNF38_chr9_36336400_36400269 |
| regionname5000 | RNF38_chr9_36331400_36405269 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 515 | 402 | 90 | 76 | 178 | 14 | 42 | 136 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1548 | 400 | 88 | 76 | 178 | 14 | 42 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| c0002 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| c0003 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3514 | 269 | 60 | 43 | 133 | 3 | 29 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0002 | 0/0 | 3515 | 56 | 1 | 13 | 27 | 7 | 8 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0003 | 0/0 | 3515 | 29 | 0 | 17 | 7 | 2 | 3 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0004 | 0/0 | 3515 | 9 | 8 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0005 | 0/0 | 3514 | 8 | 8 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0006 | 0/0 | 3514 | 4 | 4 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0007 | 0/0 | 3514 | 4 | 0 | 0 | 4 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0008 | 0/0 | 3511 | 3 | 3 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0009 | 0/0 | 3515 | 3 | 0 | 0 | 0 | 2 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0010 | 0/0 | 3514 | 2 | 2 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0011 | 0/0 | 3514 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0012 | 0/0 | 3514 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0013 | 0/0 | 3514 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0014 | 0/0 | 3515 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0015 | 0/0 | 3514 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0016 | 0/0 | 3514 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0017 | 0/0 | 3514 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0018 | 0/0 | 3514 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0019 | 0/0 | 3514 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0020 | 0/0 | 3515 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0021 | 0/0 | 3515 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0022 | 0/0 | 3515 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0023 | 1/0 | 3514 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| t0024 | 0/0 | 3514 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1548 | 400 | 88 | 76 | 178 | 14 | 42 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0002 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0003 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5061 | 268 | 59 | 43 | 133 | 3 | 29 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0002 | 0/0 | 5062 | 56 | 1 | 13 | 27 | 7 | 8 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0003 | 0/0 | 5062 | 29 | 0 | 17 | 7 | 2 | 3 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0004 | 0/0 | 5062 | 9 | 8 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0005 | 0/0 | 5061 | 7 | 7 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0006 | 0/0 | 5061 | 4 | 4 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0007 | 0/0 | 5061 | 4 | 0 | 0 | 4 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0008 | 0/0 | 5058 | 3 | 3 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0009 | 0/0 | 5062 | 3 | 0 | 0 | 0 | 2 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0010 | 0/0 | 5061 | 2 | 2 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0011 | 0/0 | 5061 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0012 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0013 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0014 | 0/0 | 5062 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0015 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0016 | 0/0 | 5061 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0017 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0018 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0019 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0020 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0021 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0022 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0023 | 1/0 | 5061 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0001t0024 | 0/0 | 5061 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0002t0001 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| a0001c0003t0005 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | copy fasta | chr9 | 36331400 | 36405269 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0007g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0008g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0008g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0008g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0014g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0016g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0017g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0018g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0019g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0020g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0021g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0022g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0023g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0024g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0003t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0155 | EUR | GBR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | GBR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | GBR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0154 | EUR | FIN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | FIN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00408 | hp1 | a0001 | c0001 | t0020 | g0108 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0391 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0392 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0375 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0383 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0384 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01346 | hp2 | a0001 | c0001 | t0024 | g0313 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01515 | hp1 | a0001 | c0001 | t0009 | g0087 | EUR | IBS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | IBS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0147 | EUR | IBS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0085 | EUR | IBS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01891 | hp2 | a0001 | c0001 | t0015 | g0042 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0372 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0374 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0377 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02027 | hp1 | a0001 | c0001 | t0018 | g0056 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0385 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0382 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02293 | hp2 | a0001 | c0001 | t0016 | g0318 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0376 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0351 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02738 | hp1 | a0001 | c0001 | t0009 | g0092 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02965 | hp1 | a0001 | c0003 | t0005 | g0018 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0352 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0386 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0373 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0387 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0353 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0378 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04228 | hp1 | a0001 | c0001 | t0014 | g0036 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0367 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0388 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | CHB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0012 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18943 | hp2 | a0001 | c0001 | t0022 | g0097 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0078 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18966 | hp1 | a0001 | c0001 | t0019 | g0216 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0079 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18990 | hp1 | a0001 | c0001 | t0017 | g0178 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19002 | hp2 | a0001 | c0001 | t0011 | g0238 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0011 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19054 | hp1 | a0001 | c0001 | t0011 | g0241 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19086 | hp2 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | ASW | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0390 | AFR | ASW | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | TSI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | TSI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | TSI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | TSI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | GIH | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0389 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0381 | AFR | USA | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | USA | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | USA | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | USA | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA21309 | hp1 | a0001 | c0001 | t0021 | g0038 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0287 | REF | REF | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0023 | g0261 | REF | REF | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36344867
|
C | T | 1 | a0001c0002 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1350G>A | p.Arg450Arg | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/12 | 1511/5061 | 1350/1548 | 450/515 | chr9 | 36344867 | ||
| chr9:36353221
|
G | A | 1 | a0001c0003 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1020C>T | p.Pro340Pro | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 7/12 | 1181/5061 | 1020/1548 | 340/515 | chr9 | 36353221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36336677
|
C | A | 1 | a0001c0001t0007 | 4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3075G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 3075 | chr9 | 36336677 | |||||
| chr9:36337073
|
A | G | 2 | a0001c0001t0013a0001c0001t0020 | 2 | HG00408.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2679T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2679 | chr9 | 36337073 | |||||
| chr9:36337183
|
C | T | 1 | a0001c0001t0007 | 4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2569G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2569 | chr9 | 36337183 | |||||
| chr9:36337191
|
A | G | 2 | a0001c0001t0005a0001c0003t0005 | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2561T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2561 | chr9 | 36337191 | |||||
| chr9:36337256
|
T | G | 1 | a0001c0001t0009 | 3 | HG00099.hp2 HG01515.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2496A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2496 | chr9 | 36337256 | |||||
| chr9:36337395
|
T | C | 1 | a0001c0001t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2357A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2357 | chr9 | 36337395 | |||||
| chr9:36337470
|
T | C | 1 | a0001c0001t0017 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2282 | chr9 | 36337470 | |||||
| chr9:36337503
|
T | C | 1 | a0001c0001t0022 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2249A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2249 | chr9 | 36337503 | |||||
| chr9:36337649
|
A | AT | 2 | a0001c0001t0003a0001c0001t0014 | 30 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2102dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2102 | chr9 | 36337649 | |||||
| chr9:36337775
|
A | G | 1 | a0001c0001t0014 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1977T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1977 | chr9 | 36337775 | |||||
| chr9:36337790
|
A | T | 1 | a0001c0001t0014 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1962T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1962 | chr9 | 36337790 | |||||
| chr9:36337961
|
G | A | 1 | a0001c0001t0018 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1791 | chr9 | 36337961 | |||||
| chr9:36338025
|
A | G | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
3_prime_UTR_variant | MODIFIER | c.*1727T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1727 | chr9 | 36338025 | |||||
| chr9:36338488
|
C | T | 1 | a0001c0001t0019 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1264 | chr9 | 36338488 | |||||
| chr9:36338512
|
G | T | 1 | a0001c0001t0011 | 2 | NA19002.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1240C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1240 | chr9 | 36338512 | |||||
| chr9:36338570
|
T | TA | 1 | a0001c0001t0004 | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1181dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1181 | chr9 | 36338570 | |||||
| chr9:36338589
|
T | C | 1 | a0001c0001t0019 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1163A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1163 | chr9 | 36338589 | |||||
| chr9:36338760
|
T | TA | 5 | a0001c0001t0002a0001c0001t0009a0001c0001t0020others(2): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*991dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 991 | chr9 | 36338760 | |||||
| chr9:36338958
|
C | T | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
3_prime_UTR_variant | MODIFIER | c.*794G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 794 | chr9 | 36338958 | |||||
| chr9:36339133
|
C | T | 1 | a0001c0001t0016 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 619 | chr9 | 36339133 | |||||
| chr9:36339396
|
TATC | T | 1 | a0001c0001t0008 | 3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*353_*355delGAT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 353 | chr9 | 36339396 | |||||
| chr9:36339643
|
C | T | 1 | a0001c0001t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 109 | chr9 | 36339643 | |||||
| chr9:36339699
|
G | A | 1 | a0001c0001t0024 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 53 | chr9 | 36339699 | |||||
| chr9:36400159
|
C | T | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(4): Show | 25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-51G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/12 | 51 | chr9 | 36400159 | |||||
| chr9:36400220
|
C | T | 1 | a0001c0001t0012 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-112G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/12 | 112 | chr9 | 36400220 | |||||
| chr9:36400242
|
A | G | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(5): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-134T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/12 | 134 | chr9 | 36400242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36339823
|
C | A | 1 | a0001c0001t0001g0073 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1486-9G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36339823 | ||||||
| chr9:36339880
|
G | C | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1486-66C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36339880 | ||||||
| chr9:36339986
|
AT | A | 384 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(381): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1486-173delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36339986 | ||||||
| chr9:36340092
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1486-278C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340092 | ||||||
| chr9:36340138
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1486-324G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340138 | ||||||
| chr9:36340168
|
G | A | 1 | a0001c0001t0003g0142 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1486-354C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340168 | ||||||
| chr9:36340248
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1486-434C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340248 | ||||||
| chr9:36340296
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1486-482C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340296 | ||||||
| chr9:36340393
|
C | T | 2 | a0001c0001t0001g0326a0001c0001t0001g0329 | 2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1486-579G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340393 | ||||||
| chr9:36340452
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0338 | 2 | NA18974.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1486-638G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340452 | ||||||
| chr9:36340464
|
G | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0369a0001c0001t0001g0370others(1): Show | 4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1486-650C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340464 | ||||||
| chr9:36340503
|
C | G | 1 | a0001c0001t0008g0353 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1486-689G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340503 | ||||||
| chr9:36340638
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1486-824A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340638 | ||||||
| chr9:36340721
|
C | T | 2 | a0001c0001t0010g0012a0001c0001t0014g0036 | 2 | HG04228.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1486-907G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340721 | ||||||
| chr9:36340914
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1486-1100G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340914 | ||||||
| chr9:36340943
|
T | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0107 | 3 | HG03491.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1486-1129A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340943 | ||||||
| chr9:36341092
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0186 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1485+1233C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341092 | ||||||
| chr9:36341120
|
CGCTTCAG others(4): Show |
C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1485+1194_1485+120 others(15): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341120 | ||||||
| chr9:36341201
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | HG00609.hp1 HG02083.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+1124G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341201 | ||||||
| chr9:36341217
|
G | A | 1 | a0001c0001t0001g0366 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1485+1108C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341217 | ||||||
| chr9:36341227
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0194 | 3 | HG03654.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1485+1098C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341227 | ||||||
| chr9:36341249
|
C | T | 1 | a0001c0001t0001g0368 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1485+1076G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341249 | ||||||
| chr9:36341250
|
G | A | 13 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0124others(10): Show | 13 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1485+1075C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341250 | ||||||
| chr9:36341384
|
T | G | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1485+941A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341384 | ||||||
| chr9:36341387
|
T | G | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1485+938A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341387 | ||||||
| chr9:36341391
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1485+934C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341391 | ||||||
| chr9:36341393
|
T | A | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1485+932A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341393 | ||||||
| chr9:36341455
|
T | G | 1 | a0001c0001t0015g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1485+870A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341455 | ||||||
| chr9:36341514
|
A | G | 1 | a0001c0001t0015g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1485+811T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341514 | ||||||
| chr9:36341521
|
T | C | 1 | a0001c0001t0001g0350 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1485+804A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341521 | ||||||
| chr9:36341679
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0290a0001c0001t0001g0301 | 3 | HG03688.hp1 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1485+646G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341679 | ||||||
| chr9:36341721
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1485+604C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341721 | ||||||
| chr9:36341751
|
G | A | 2 | a0001c0001t0002g0391a0001c0001t0002g0392 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1485+574C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341751 | ||||||
| chr9:36341793
|
A | AATATATA others(15): Show |
1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1485+510_1485+531d others(24): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1485+522_1485+531d others(12): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(9): Show |
A | 1 | a0001c0001t0006g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1485+516_1485+531d others(18): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0006g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1485+510_1485+531d others(24): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(17): Show |
A | 3 | a0001c0001t0001g0369a0001c0001t0006g0033a0001c0001t0013g0034 | 3 | HG03209.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1485+508_1485+531d others(26): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(19): Show |
A | 2 | a0001c0001t0001g0347a0001c0001t0001g0381 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1485+506_1485+531d others(28): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(21): Show |
A | 1 | a0001c0001t0005g0016 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1485+504_1485+531d others(30): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(25): Show |
A | 2 | a0001c0001t0005g0013a0001c0001t0010g0012 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1485+500_1485+531d others(34): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(29): Show |
A | 1 | a0001c0001t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1485+496_1485+531d others(38): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(31): Show |
A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0025others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+494_1485+531d others(40): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(35): Show |
A | 4 | a0001c0001t0004g0026a0001c0001t0005g0017a0001c0001t0005g0019others(1): Show | 4 | HG01496.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+490_1485+531d others(44): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(37): Show |
A | 6 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0027others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1485+488_1485+531d others(46): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341793
|
AATATATA others(49): Show |
A | 1 | a0001c0001t0001g0370 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1485+476_1485+531d others(58): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | ||||||
| chr9:36341807
|
TATATATA others(53): Show |
T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1485+458_1485+517d others(62): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341807 | ||||||
| chr9:36341809
|
TATATATA others(51): Show |
T | 150 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(147): Show | 153 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1485+458_1485+515d others(60): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341809 | ||||||
| chr9:36341811
|
TATATATA others(49): Show |
T | 1 | a0001c0001t0001g0307 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1485+458_1485+513d others(58): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341811 | ||||||
| chr9:36341815
|
TATATATA others(45): Show |
T | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(34): Show | 39 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1485+458_1485+509d others(54): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341815 | ||||||
| chr9:36341817
|
TATATATA others(43): Show |
T | 1 | a0001c0001t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1485+458_1485+507d others(52): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341817 | ||||||
| chr9:36341823
|
TATATATA others(37): Show |
T | 1 | a0001c0001t0015g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1485+458_1485+501d others(46): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341823 | ||||||
| chr9:36341825
|
T | C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1485+500A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341825 | ||||||
| chr9:36341827
|
TATATATA others(33): Show |
T | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1485+458_1485+497d others(42): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341827 | ||||||
| chr9:36341829
|
TATATATA others(31): Show |
T | 1 | a0001c0001t0005g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1485+458_1485+495d others(40): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341829 | ||||||
| chr9:36341867
|
A | T | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1485+458T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341867 | ||||||
| chr9:36341986
|
AT | A | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1485+338delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341986 | ||||||
| chr9:36342046
|
A | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0369a0001c0001t0001g0370others(1): Show | 4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+279T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36342046 | ||||||
| chr9:36342178
|
G | T | 1 | a0001c0001t0001g0366 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1485+147C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36342178 | ||||||
| chr9:36342184
|
T | TCTC | 386 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(383): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1485+138_1485+140d others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36342184 | ||||||
| chr9:36342306
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1485+19T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36342306 | ||||||
| chr9:36342668
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1386-244A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342668 | ||||||
| chr9:36342673
|
A | T | 362 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(359): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1386-249T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342673 | ||||||
| chr9:36342674
|
A | T | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1386-250T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342674 | ||||||
| chr9:36342683
|
G | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0369a0001c0001t0001g0370others(1): Show | 4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386-259C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342683 | ||||||
| chr9:36342699
|
G | T | 1 | a0001c0001t0001g0306 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1386-275C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342699 | ||||||
| chr9:36342742
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1386-318A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342742 | ||||||
| chr9:36342825
|
T | G | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1386-401A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342825 | ||||||
| chr9:36342889
|
G | C | 362 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(359): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1386-465C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342889 | ||||||
| chr9:36343095
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1386-671T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343095 | ||||||
| chr9:36343167
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1386-743A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343167 | ||||||
| chr9:36343489
|
G | A | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1386-1065C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343489 | ||||||
| chr9:36343568
|
T | C | 367 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(364): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1386-1144A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343568 | ||||||
| chr9:36343585
|
A | G | 1 | a0001c0001t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1386-1161T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343585 | ||||||
| chr9:36343646
|
A | G | 63 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1385+1186T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343646 | ||||||
| chr9:36343677
|
T | C | 375 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(372): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1385+1155A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343677 | ||||||
| chr9:36343767
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1385+1065C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343767 | ||||||
| chr9:36343876
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1385+956T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343876 | ||||||
| chr9:36343895
|
A | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1385+937T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343895 | ||||||
| chr9:36343996
|
C | A | 1 | a0001c0001t0012g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1385+836G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343996 | ||||||
| chr9:36344104
|
C | A | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1385+728G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344104 | ||||||
| chr9:36344235
|
A | C | 1 | a0001c0001t0003g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1385+597T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344235 | ||||||
| chr9:36344331
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1385+501T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344331 | ||||||
| chr9:36344387
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1385+445T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344387 | ||||||
| chr9:36344503
|
A | G | 2 | a0001c0001t0001g0369a0001c0001t0001g0381 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1385+329T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344503 | ||||||
| chr9:36344633
|
A | G | 1 | a0001c0001t0003g0199 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1385+199T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344633 | ||||||
| chr9:36344715
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1385+117C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344715 | ||||||
| chr9:36344961
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG00544.hp1 | splice_region_variant&intron_variant | LOW | c.1264-8C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36344961 | ||||||
| chr9:36344971
|
G | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(2): Show | 5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-18C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36344971 | ||||||
| chr9:36345010
|
CT | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(35): Show | 40 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1264-58delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345010 | ||||||
| chr9:36345154
|
C | T | 142 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 145 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1264-201G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345154 | ||||||
| chr9:36345160
|
T | C | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1264-207A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345160 | ||||||
| chr9:36345349
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1264-396C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345349 | ||||||
| chr9:36345357
|
G | A | 4 | a0001c0001t0001g0347a0001c0001t0001g0369a0001c0001t0001g0370others(1): Show | 4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-404C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345357 | ||||||
| chr9:36345399
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1264-446T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345399 | ||||||
| chr9:36345438
|
C | T | 4 | a0001c0001t0001g0350a0001c0001t0001g0379a0001c0001t0001g0380others(1): Show | 4 | HG00642.hp2 NA18951.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-485G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345438 | ||||||
| chr9:36345514
|
C | G | 1 | a0001c0001t0003g0159 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1264-561G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345514 | ||||||
| chr9:36345774
|
TGGCCTAA others(8): Show |
T | 2 | a0001c0001t0001g0006a0001c0001t0001g0194 | 3 | HG03654.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1264-836_1264-822d others(17): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345774 | ||||||
| chr9:36345799
|
T | C | 1 | a0001c0001t0008g0351 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1264-846A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345799 | ||||||
| chr9:36345837
|
G | A | 1 | a0001c0001t0010g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1264-884C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345837 | ||||||
| chr9:36345962
|
C | T | 3 | a0001c0001t0004g0024a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02572.hp2 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1264-1009G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345962 | ||||||
| chr9:36346013
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0222 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1264-1060A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346013 | ||||||
| chr9:36346019
|
C | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(2): Show | 5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-1066G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346019 | ||||||
| chr9:36346104
|
T | C | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1264-1151A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346104 | ||||||
| chr9:36346108
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1264-1155C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346108 | ||||||
| chr9:36346284
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0174 | 2 | HG02056.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1264-1331G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346284 | ||||||
| chr9:36346308
|
C | T | 142 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 145 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1264-1355G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346308 | ||||||
| chr9:36346384
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1264-1431A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346384 | ||||||
| chr9:36346530
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1264-1577G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346530 | ||||||
| chr9:36346692
|
T | TGTG | 385 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(382): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1264-1740_1264-173 others(7): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346692 | ||||||
| chr9:36347120
|
CGGGGGGG others(3): Show |
C | 17 | a0001c0001t0001g0073a0001c0001t0001g0181a0001c0001t0001g0251others(14): Show | 17 | HG00408.hp1 HG01192.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1264-2177_1264-216 others(14): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(4): Show |
C | 29 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0248others(26): Show | 29 | HG00673.hp2 HG01109.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.1264-2178_1264-216 others(15): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(5): Show |
C | 38 | a0001c0001t0001g0249a0001c0001t0001g0255a0001c0001t0001g0257others(35): Show | 38 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1264-2179_1264-216 others(16): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(6): Show |
C | 27 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0247others(24): Show | 27 | HG01071.hp2 HG01074.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1264-2180_1264-216 others(17): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(7): Show |
C | 41 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0144others(38): Show | 41 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1264-2181_1264-216 others(18): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(8): Show |
C | 56 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0048others(53): Show | 57 | HG00099.hp2 HG00408.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1264-2182_1264-216 others(19): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(9): Show |
C | 73 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(70): Show | 76 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1264-2183_1264-216 others(20): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(10): Show |
C | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(64): Show | 70 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1264-2184_1264-216 others(21): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(11): Show |
C | 2 | a0001c0001t0001g0045a0001c0001t0006g0030 | 2 | NA19012.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1264-2185_1264-216 others(22): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347120
|
CGGGGGGG others(14): Show |
C | 1 | a0001c0001t0001g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1264-2188_1264-216 others(25): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | ||||||
| chr9:36347136
|
GGGGGGGG others(7): Show |
G | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1264-2197_1264-218 others(18): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347136 | ||||||
| chr9:36347138
|
G | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0127a0001c0001t0002g0129 | 3 | HG00741.hp1 HG01433.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1264-2185C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347138 | ||||||
| chr9:36347138
|
GGGGGGGG others(5): Show |
G | 1 | a0001c0001t0001g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1264-2197_1264-218 others(16): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347138 | ||||||
| chr9:36347139
|
G | T | 1 | a0001c0001t0015g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1264-2186C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347139 | ||||||
| chr9:36347139
|
GGGGGGGG others(4): Show |
G | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0341others(1): Show | 4 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-2197_1264-218 others(15): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347139 | ||||||
| chr9:36347183
|
TATAAAAT others(4): Show |
T | 1 | a0001c0001t0002g0100 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1264-2241_1264-223 others(15): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347183 | ||||||
| chr9:36347213
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1264-2260A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347213 | ||||||
| chr9:36347218
|
A | C | 326 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(323): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1264-2265T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347218 | ||||||
| chr9:36347645
|
C | T | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0332others(1): Show | 4 | HG01243.hp2 HG01261.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-2692G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347645 | ||||||
| chr9:36347904
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1264-2951C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347904 | ||||||
| chr9:36347932
|
C | T | 1 | a0001c0001t0001g0389 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1264-2979G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347932 | ||||||
| chr9:36347946
|
G | A | 2 | a0001c0001t0001g0371a0001c0001t0001g0373 | 2 | HG02071.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1264-2993C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347946 | ||||||
| chr9:36348008
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1264-3055C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348008 | ||||||
| chr9:36348025
|
G | A | 366 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(363): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1264-3072C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348025 | ||||||
| chr9:36348129
|
A | G | 2 | a0001c0001t0001g0357a0001c0001t0001g0367 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1263+2986T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348129 | ||||||
| chr9:36348182
|
T | C | 2 | a0001c0001t0009g0092a0001c0001t0009g0155 | 2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1263+2933A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348182 | ||||||
| chr9:36348285
|
A | C | 1 | a0001c0001t0001g0305 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1263+2830T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348285 | ||||||
| chr9:36348828
|
T | C | 2 | a0001c0001t0001g0344a0001c0001t0001g0345 | 2 | HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1263+2287A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348828 | ||||||
| chr9:36348848
|
A | C | 1 | a0001c0001t0001g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1263+2267T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348848 | ||||||
| chr9:36348958
|
GCTGA | G | 25 | a0001c0001t0001g0348a0001c0001t0001g0350a0001c0001t0001g0355others(22): Show | 25 | HG00609.hp2 HG00642.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1263+2153_1263+215 others(8): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348958 | ||||||
| chr9:36349376
|
G | A | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1263+1739C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349376 | ||||||
| chr9:36349384
|
G | A | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1263+1731C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349384 | ||||||
| chr9:36349564
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1263+1551G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349564 | ||||||
| chr9:36349589
|
G | A | 3 | a0001c0001t0008g0351a0001c0001t0008g0352a0001c0001t0008g0353 | 3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1263+1526C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349589 | ||||||
| chr9:36349663
|
A | G | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1263+1452T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349663 | ||||||
| chr9:36349720
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1263+1395G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349720 | ||||||
| chr9:36349876
|
A | G | 1 | a0001c0001t0015g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1263+1239T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349876 | ||||||
| chr9:36349921
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1263+1194C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349921 | ||||||
| chr9:36349975
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1263+1140G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349975 | ||||||
| chr9:36349980
|
C | T | 365 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(362): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1263+1135G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349980 | ||||||
| chr9:36350007
|
G | A | 3 | a0001c0001t0001g0347a0001c0001t0001g0369a0001c0001t0001g0381 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1263+1108C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350007 | ||||||
| chr9:36350023
|
G | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1263+1092C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350023 | ||||||
| chr9:36350037
|
C | T | 1 | a0001c0001t0010g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1263+1078G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350037 | ||||||
| chr9:36350108
|
C | T | 8 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1263+1007G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350108 | ||||||
| chr9:36350267
|
T | A | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1263+848A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350267 | ||||||
| chr9:36350315
|
T | A | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1263+800A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350315 | ||||||
| chr9:36350552
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1263+563T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350552 | ||||||
| chr9:36350567
|
A | T | 1 | a0001c0001t0001g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1263+548T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350567 | ||||||
| chr9:36351077
|
C | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0187a0001c0001t0001g0188others(28): Show | 32 | HG00438.hp1 HG00544.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263+38G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36351077 | ||||||
| chr9:36351084
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1263+31G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36351084 | ||||||
| chr9:36351229
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0234a0001c0001t0001g0235others(8): Show | 12 | HG02071.hp1 HG02523.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.1179-30T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351229 | ||||||
| chr9:36351638
|
G | A | 1 | a0001c0001t0006g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1179-439C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351638 | ||||||
| chr9:36351662
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0068 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1179-463C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351662 | ||||||
| chr9:36351697
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(180): Show | 188 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.1179-498C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351697 | ||||||
| chr9:36351803
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(179): Show | 187 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.1179-604G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351803 | ||||||
| chr9:36352026
|
G | A | 4 | a0001c0001t0005g0017a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02965.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1178+716C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352026 | ||||||
| chr9:36352070
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1178+672A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352070 | ||||||
| chr9:36352320
|
A | C | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1178+422T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352320 | ||||||
| chr9:36352356
|
C | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1178+386G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352356 | ||||||
| chr9:36352584
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1178+158G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352584 | ||||||
| chr9:36352690
|
G | T | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1178+52C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352690 | ||||||
| chr9:36352916
|
T | C | 1 | a0001c0001t0003g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1072-68A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 7/11 | chr9 | 36352916 | ||||||
| chr9:36353130
|
C | T | 2 | a0001c0001t0001g0385a0001c0001t0003g0384 | 2 | HG01255.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1071+40G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 7/11 | chr9 | 36353130 | ||||||
| chr9:36353139
|
G | C | 2 | a0001c0001t0002g0104a0001c0001t0002g0106 | 2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1071+31C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 7/11 | chr9 | 36353139 | ||||||
| chr9:36353343
|
GA | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(2): Show | 5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-13delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353343 | ||||||
| chr9:36353344
|
A | G | 2 | a0001c0001t0001g0357a0001c0001t0001g0367 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.910-13T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353344 | ||||||
| chr9:36353405
|
A | C | 1 | a0001c0001t0001g0383 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.910-74T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353405 | ||||||
| chr9:36353462
|
T | G | 3 | a0001c0001t0008g0351a0001c0001t0008g0352a0001c0001t0008g0353 | 3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.910-131A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353462 | ||||||
| chr9:36353625
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA18965.hp2 NA19060.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.910-294G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353625 | ||||||
| chr9:36353670
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.910-339T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353670 | ||||||
| chr9:36353677
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG01891.hp1 HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.910-346A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353677 | ||||||
| chr9:36353698
|
A | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0043others(21): Show | 26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-367T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353698 | ||||||
| chr9:36353859
|
G | C | 1 | a0001c0001t0001g0323 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.910-528C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353859 | ||||||
| chr9:36353879
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.910-548G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353879 | ||||||
| chr9:36354047
|
A | C | 1 | a0001c0001t0002g0096 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.910-716T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354047 | ||||||
| chr9:36354074
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.910-743A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354074 | ||||||
| chr9:36354116
|
T | C | 138 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(135): Show | 141 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.910-785A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354116 | ||||||
| chr9:36354187
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0222 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.910-856G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354187 | ||||||
| chr9:36354215
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.910-884T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354215 | ||||||
| chr9:36354253
|
C | T | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-922G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354253 | ||||||
| chr9:36354255
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.910-924G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354255 | ||||||
| chr9:36354448
|
C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0043others(21): Show | 26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-1117G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354448 | ||||||
| chr9:36354493
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0016g0318 | 2 | HG02293.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.910-1162C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354493 | ||||||
| chr9:36354502
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.910-1171T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354502 | ||||||
| chr9:36354599
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00558.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.910-1268T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354599 | ||||||
| chr9:36354616
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.910-1285T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354616 | ||||||
| chr9:36354721
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.910-1390A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354721 | ||||||
| chr9:36354754
|
T | C | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-1423A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354754 | ||||||
| chr9:36354832
|
T | C | 11 | a0001c0001t0003g0148a0001c0001t0003g0149a0001c0001t0003g0150others(8): Show | 11 | HG00741.hp2 HG01099.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+1471A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354832 | ||||||
| chr9:36354938
|
T | C | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.909+1365A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354938 | ||||||
| chr9:36355107
|
C | T | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.909+1196G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355107 | ||||||
| chr9:36355149
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.909+1154T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355149 | ||||||
| chr9:36355274
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.909+1029G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355274 | ||||||
| chr9:36355338
|
C | T | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(91): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.909+965G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355338 | ||||||
| chr9:36355385
|
T | C | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.909+918A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355385 | ||||||
| chr9:36355387
|
T | C | 1 | a0001c0001t0006g0033 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.909+916A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355387 | ||||||
| chr9:36355499
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.909+804A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355499 | ||||||
| chr9:36355563
|
A | G | 1 | a0001c0001t0004g0025 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.909+740T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355563 | ||||||
| chr9:36355565
|
G | T | 1 | a0001c0001t0002g0114 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.909+738C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355565 | ||||||
| chr9:36355853
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.909+450A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355853 | ||||||
| chr9:36355865
|
G | A | 29 | a0001c0001t0001g0315a0001c0001t0001g0348a0001c0001t0001g0350others(26): Show | 29 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.909+438C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355865 | ||||||
| chr9:36355943
|
T | G | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+360A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355943 | ||||||
| chr9:36356022
|
C | T | 366 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(363): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.909+281G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36356022 | ||||||
| chr9:36356045
|
C | T | 366 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(363): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.909+258G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36356045 | ||||||
| chr9:36356135
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.909+168G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36356135 | ||||||
| chr9:36356625
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.739-152T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36356625 | ||||||
| chr9:36356747
|
T | TG | 166 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(163): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.739-275dupC | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36356747 | ||||||
| chr9:36356756
|
C | G | 2 | a0001c0001t0001g0341a0001c0001t0002g0100 | 2 | HG00423.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.739-283G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36356756 | ||||||
| chr9:36356883
|
A | G | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-410T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36356883 | ||||||
| chr9:36357135
|
T | A | 1 | a0001c0001t0001g0244 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.738+640A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357135 | ||||||
| chr9:36357158
|
G | A | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.738+617C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357158 | ||||||
| chr9:36357436
|
C | G | 2 | a0001c0001t0001g0283a0001c0001t0001g0327 | 2 | NA18944.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.738+339G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357436 | ||||||
| chr9:36357537
|
C | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.738+238G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357537 | ||||||
| chr9:36357541
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.738+234A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357541 | ||||||
| chr9:36357570
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.738+205T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357570 | ||||||
| chr9:36357582
|
T | C | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.738+193A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357582 | ||||||
| chr9:36357609
|
C | A | 14 | a0001c0001t0001g0258a0001c0001t0001g0268a0001c0001t0001g0279others(11): Show | 14 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+166G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357609 | ||||||
| chr9:36357678
|
C | A | 7 | a0001c0001t0001g0249a0001c0001t0001g0260a0001c0001t0001g0337others(4): Show | 7 | HG00423.hp2 NA18946.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+97G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357678 | ||||||
| chr9:36357713
|
A | C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.738+62T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357713 | ||||||
| chr9:36357962
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.571-20A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36357962 | ||||||
| chr9:36358055
|
C | CA | 24 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0043others(21): Show | 26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-114dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358055 | ||||||
| chr9:36358246
|
G | C | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-304C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358246 | ||||||
| chr9:36358332
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.571-390A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358332 | ||||||
| chr9:36358535
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.571-593A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358535 | ||||||
| chr9:36358566
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.571-624A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358566 | ||||||
| chr9:36358632
|
A | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.571-690T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358632 | ||||||
| chr9:36358705
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571-763G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358705 | ||||||
| chr9:36358811
|
G | A | 367 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(364): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.571-869C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358811 | ||||||
| chr9:36358839
|
G | A | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-897C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358839 | ||||||
| chr9:36358852
|
A | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG01891.hp2 HG04115.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-910T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358852 | ||||||
| chr9:36358855
|
C | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.571-913G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358855 | ||||||
| chr9:36358867
|
T | A | 138 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(135): Show | 141 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.571-925A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358867 | ||||||
| chr9:36358930
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0290a0001c0001t0001g0301 | 3 | HG03688.hp1 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.571-988C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358930 | ||||||
| chr9:36359161
|
T | A | 1 | a0001c0001t0003g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.571-1219A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359161 | ||||||
| chr9:36359279
|
AT | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(35): Show | 40 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.571-1338delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359279 | ||||||
| chr9:36359314
|
G | C | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.571-1372C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359314 | ||||||
| chr9:36359379
|
G | A | 62 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.571-1437C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359379 | ||||||
| chr9:36359550
|
C | T | 386 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(383): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.571-1608G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359550 | ||||||
| chr9:36359624
|
T | C | 1 | a0001c0001t0005g0016 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.571-1682A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359624 | ||||||
| chr9:36359644
|
C | T | 46 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0080others(43): Show | 46 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.571-1702G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359644 | ||||||
| chr9:36359737
|
A | AT | 375 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(372): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.571-1796dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359737 | ||||||
| chr9:36359737
|
A | ATT | 8 | a0001c0001t0001g0191a0001c0001t0001g0270a0001c0001t0001g0378others(5): Show | 8 | HG00280.hp1 HG02055.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-1797_571-1796d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359737 | ||||||
| chr9:36359912
|
C | CT | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.571-1971dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359912 | ||||||
| chr9:36360035
|
G | A | 1 | a0001c0001t0007g0076 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.571-2093C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360035 | ||||||
| chr9:36360097
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(35): Show | 40 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.571-2155G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360097 | ||||||
| chr9:36360153
|
GA | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(179): Show | 187 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.571-2212delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360153 | ||||||
| chr9:36360165
|
T | C | 1 | a0001c0001t0001g0327 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.571-2223A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360165 | ||||||
| chr9:36360336
|
A | T | 1 | a0001c0001t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.571-2394T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360336 | ||||||
| chr9:36360461
|
G | T | 1 | a0001c0001t0008g0351 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.571-2519C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360461 | ||||||
| chr9:36360504
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG04115.hp1 NA18612.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-2562G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360504 | ||||||
| chr9:36360612
|
G | A | 365 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(362): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.571-2670C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360612 | ||||||
| chr9:36360848
|
T | C | 14 | a0001c0001t0001g0258a0001c0001t0001g0268a0001c0001t0001g0279others(11): Show | 14 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-2906A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360848 | ||||||
| chr9:36360891
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.571-2949C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360891 | ||||||
| chr9:36361007
|
G | C | 1 | a0001c0001t0002g0117 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.571-3065C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361007 | ||||||
| chr9:36361059
|
T | C | 367 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(364): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.571-3117A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361059 | ||||||
| chr9:36361138
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.571-3196G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361138 | ||||||
| chr9:36361151
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.571-3209A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361151 | ||||||
| chr9:36361298
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.571-3356G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361298 | ||||||
| chr9:36361306
|
C | A | 138 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(135): Show | 141 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.571-3364G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361306 | ||||||
| chr9:36361339
|
T | TTTTTTTT others(174): Show |
1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3398_571-3397i others(183): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361339 | ||||||
| chr9:36361354
|
A | G | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3412T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361354 | ||||||
| chr9:36361364
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.571-3422G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361364 | ||||||
| chr9:36361367
|
G | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3425C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361367 | ||||||
| chr9:36361374
|
A | G | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3432T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361374 | ||||||
| chr9:36361399
|
G | A | 3 | a0001c0001t0008g0351a0001c0001t0008g0352a0001c0001t0008g0353 | 3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.571-3457C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361399 | ||||||
| chr9:36361438
|
T | C | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3496A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361438 | ||||||
| chr9:36361441
|
A | G | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3499T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361441 | ||||||
| chr9:36361442
|
CG | C | 365 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(362): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.571-3501delC | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361442 | ||||||
| chr9:36361454
|
C | T | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.571-3512G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361454 | ||||||
| chr9:36361538
|
A | G | 1 | a0001c0001t0003g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.571-3596T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361538 | ||||||
| chr9:36361745
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0003g0288 | 2 | NA18747.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.571-3803G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361745 | ||||||
| chr9:36361907
|
ATG | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0194 | 3 | HG03654.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.571-3967_571-3966d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361907 | ||||||
| chr9:36362005
|
C | T | 384 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(381): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.571-4063G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362005 | ||||||
| chr9:36362018
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.571-4076A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362018 | ||||||
| chr9:36362078
|
C | T | 1 | a0001c0001t0001g0387 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.571-4136G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362078 | ||||||
| chr9:36362095
|
G | A | 10 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0214others(7): Show | 10 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-4153C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362095 | ||||||
| chr9:36362301
|
T | A | 1 | a0001c0001t0002g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.571-4359A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362301 | ||||||
| chr9:36362312
|
C | T | 1 | a0001c0001t0001g0362 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.571-4370G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362312 | ||||||
| chr9:36362319
|
T | C | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-4377A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362319 | ||||||
| chr9:36362354
|
G | A | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-4412C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362354 | ||||||
| chr9:36362470
|
CA | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(365): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.571-4529delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362470 | ||||||
| chr9:36362627
|
T | C | 1 | a0001c0001t0002g0123 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-4685A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362627 | ||||||
| chr9:36362653
|
A | AT | 6 | a0001c0001t0001g0045a0001c0001t0001g0141a0001c0001t0001g0195others(3): Show | 6 | HG01109.hp2 HG03225.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-4712dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362653 | ||||||
| chr9:36362660
|
T | A | 1 | a0001c0001t0012g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.571-4718A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362660 | ||||||
| chr9:36362884
|
GGCCTCCC others(1191): Show |
G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.570+5637_571-4943d others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362884 | ||||||
| chr9:36362904
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(180): Show | 188 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.571-4962A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362904 | ||||||
| chr9:36362934
|
A | C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.571-4992T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362934 | ||||||
| chr9:36363020
|
G | A | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-5078C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363020 | ||||||
| chr9:36363162
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.571-5220G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363162 | ||||||
| chr9:36363302
|
A | AT | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0262others(7): Show | 12 | NA18950.hp1 NA18955.hp1 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-5361dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363302 | ||||||
| chr9:36363356
|
T | C | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571-5414A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363356 | ||||||
| chr9:36363487
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571-5545C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363487 | ||||||
| chr9:36363859
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.570+5860G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363859 | ||||||
| chr9:36363873
|
A | AT | 24 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0063others(21): Show | 24 | HG00597.hp2 HG01175.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.570+5845dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363873 | ||||||
| chr9:36363873
|
AT | A | 6 | a0001c0001t0001g0252a0001c0001t0001g0258a0001c0001t0001g0291others(3): Show | 6 | HG00140.hp2 HG01168.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+5845delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363873 | ||||||
| chr9:36363980
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(181): Show | 189 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.570+5739T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363980 | ||||||
| chr9:36364021
|
G | A | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.570+5698C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364021 | ||||||
| chr9:36364119
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570+5600G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364119 | ||||||
| chr9:36364164
|
C | T | 142 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 145 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.570+5555G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364164 | ||||||
| chr9:36364188
|
A | G | 375 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(372): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.570+5531T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364188 | ||||||
| chr9:36364423
|
G | A | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.570+5296C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364423 | ||||||
| chr9:36364516
|
T | C | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+5203A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364516 | ||||||
| chr9:36364567
|
G | T | 102 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(99): Show | 105 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.570+5152C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364567 | ||||||
| chr9:36364786
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.570+4933G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364786 | ||||||
| chr9:36364826
|
G | A | 4 | a0001c0001t0007g0076a0001c0001t0007g0077a0001c0001t0007g0078others(1): Show | 4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+4893C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364826 | ||||||
| chr9:36364873
|
C | A | 1 | a0001c0001t0003g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.570+4846G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364873 | ||||||
| chr9:36365149
|
C | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0226 | 2 | HG02027.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.570+4570G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365149 | ||||||
| chr9:36365152
|
G | GT | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+4566dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365152 | ||||||
| chr9:36365202
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.570+4517A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365202 | ||||||
| chr9:36365231
|
TA | T | 386 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(383): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.570+4487delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365231 | ||||||
| chr9:36365268
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.570+4451A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365268 | ||||||
| chr9:36365493
|
G | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0110 | 2 | HG00544.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.570+4226C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365493 | ||||||
| chr9:36365537
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0107 | 3 | HG03491.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.570+4182G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365537 | ||||||
| chr9:36365551
|
C | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.570+4168G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365551 | ||||||
| chr9:36365662
|
G | GT | 16 | a0001c0001t0001g0074a0001c0001t0001g0183a0001c0001t0001g0184others(13): Show | 16 | HG02074.hp1 HG02723.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+4056dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | ||||||
| chr9:36365662
|
G | GTT | 278 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.570+4055_570+4056d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | ||||||
| chr9:36365662
|
G | GTTT | 48 | a0001c0001t0001g0072a0001c0001t0001g0140a0001c0001t0001g0180others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.570+4054_570+4056d others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | ||||||
| chr9:36365662
|
G | GTTTT | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0043others(24): Show | 29 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.570+4053_570+4056d others(6): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | ||||||
| chr9:36365662
|
G | GTTTTT | 14 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0054others(11): Show | 14 | HG00597.hp2 HG01934.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.570+4052_570+4056d others(7): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | ||||||
| chr9:36365752
|
G | A | 3 | a0001c0001t0008g0351a0001c0001t0008g0352a0001c0001t0008g0353 | 3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.570+3967C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365752 | ||||||
| chr9:36365815
|
G | A | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.570+3904C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365815 | ||||||
| chr9:36365815
|
G | GCCA | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+3901_570+3903d others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365815 | ||||||
| chr9:36365832
|
A | C | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.570+3887T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365832 | ||||||
| chr9:36365933
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.570+3786C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365933 | ||||||
| chr9:36366067
|
G | A | 1 | a0001c0001t0009g0087 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.570+3652C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366067 | ||||||
| chr9:36366068
|
C | G | 384 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(381): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.570+3651G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366068 | ||||||
| chr9:36366132
|
T | C | 4 | a0001c0001t0005g0017a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02965.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+3587A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366132 | ||||||
| chr9:36366260
|
A | G | 3 | a0001c0001t0001g0347a0001c0001t0001g0369a0001c0001t0001g0381 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.570+3459T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366260 | ||||||
| chr9:36366700
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.570+3019C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366700 | ||||||
| chr9:36366838
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570+2881A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366838 | ||||||
| chr9:36367004
|
T | A | 1 | a0001c0001t0002g0119 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.570+2715A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367004 | ||||||
| chr9:36367125
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.570+2594G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367125 | ||||||
| chr9:36367256
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.570+2463A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367256 | ||||||
| chr9:36367340
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.570+2379G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367340 | ||||||
| chr9:36367341
|
G | A | 62 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.570+2378C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367341 | ||||||
| chr9:36367559
|
C | T | 1 | a0001c0001t0012g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570+2160G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367559 | ||||||
| chr9:36367579
|
CT | C | 14 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0124others(11): Show | 14 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.570+2139delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367579 | ||||||
| chr9:36367656
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.570+2063C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367656 | ||||||
| chr9:36367659
|
T | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.570+2060A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367659 | ||||||
| chr9:36367673
|
T | C | 1 | a0001c0001t0012g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570+2046A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367673 | ||||||
| chr9:36367716
|
T | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(29): Show | 34 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.570+2003A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367716 | ||||||
| chr9:36367883
|
G | A | 2 | a0001c0001t0001g0344a0001c0001t0001g0345 | 2 | HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.570+1836C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367883 | ||||||
| chr9:36367885
|
T | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(2): Show | 5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+1834A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367885 | ||||||
| chr9:36367927
|
C | A | 1 | a0001c0001t0001g0347 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.570+1792G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367927 | ||||||
| chr9:36367939
|
C | T | 1 | a0001c0001t0001g0354 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.570+1780G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367939 | ||||||
| chr9:36367954
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.570+1765G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367954 | ||||||
| chr9:36367980
|
T | C | 1 | a0001c0001t0002g0104 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.570+1739A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367980 | ||||||
| chr9:36368477
|
A | T | 1 | a0001c0001t0001g0380 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.570+1242T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368477 | ||||||
| chr9:36368674
|
T | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0305a0001c0001t0001g0307 | 3 | HG00140.hp2 HG01168.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.570+1045A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368674 | ||||||
| chr9:36368763
|
G | GA | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+955dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368763 | ||||||
| chr9:36368768
|
T | C | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+951A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368768 | ||||||
| chr9:36368810
|
G | T | 3 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0079 | 3 | NA18949.hp1 NA18983.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.570+909C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368810 | ||||||
| chr9:36368857
|
T | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0058 | 2 | HG00673.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.570+862A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368857 | ||||||
| chr9:36368867
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.570+852C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368867 | ||||||
| chr9:36368886
|
C | CT | 24 | a0001c0001t0001g0006a0001c0001t0001g0187a0001c0001t0001g0188others(21): Show | 25 | HG00438.hp1 HG00544.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.570+832dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368886 | ||||||
| chr9:36369029
|
T | A | 5 | a0001c0001t0006g0030a0001c0001t0006g0031a0001c0001t0006g0032others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+690A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369029 | ||||||
| chr9:36369262
|
C | T | 3 | a0001c0001t0008g0351a0001c0001t0008g0352a0001c0001t0008g0353 | 3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.570+457G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369262 | ||||||
| chr9:36369295
|
C | T | 1 | a0001c0001t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.570+424G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369295 | ||||||
| chr9:36369377
|
C | CA | 3 | a0001c0001t0001g0269a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG02109.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.570+341dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369377 | ||||||
| chr9:36369437
|
G | A | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0158others(1): Show | 4 | HG00741.hp2 HG01255.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+282C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369437 | ||||||
| chr9:36369490
|
T | C | 62 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.570+229A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369490 | ||||||
| chr9:36369498
|
T | C | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+221A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369498 | ||||||
| chr9:36369516
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.570+203G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369516 | ||||||
| chr9:36369610
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.570+109T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369610 | ||||||
| chr9:36369649
|
CA | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.570+69delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369649 | ||||||
| chr9:36369649
|
CAA | C | 20 | a0001c0001t0001g0046a0001c0001t0001g0227a0001c0001t0001g0228others(17): Show | 20 | HG00741.hp2 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+68_570+69delTT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369649 | ||||||
| chr9:36369935
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.357-3C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36369935 | ||||||
| chr9:36370008
|
T | A | 1 | a0001c0001t0001g0316 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.357-76A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370008 | ||||||
| chr9:36370386
|
C | T | 2 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | HG01167.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.357-454G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370386 | ||||||
| chr9:36370568
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.357-636C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370568 | ||||||
| chr9:36370576
|
C | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0369a0001c0001t0001g0370others(1): Show | 4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.357-644G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370576 | ||||||
| chr9:36370580
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357-648C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370580 | ||||||
| chr9:36370646
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.357-714G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370646 | ||||||
| chr9:36370675
|
G | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(2): Show | 5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.357-743C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370675 | ||||||
| chr9:36370685
|
C | T | 1 | a0001c0001t0006g0033 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.357-753G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370685 | ||||||
| chr9:36370849
|
T | TA | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(33): Show | 38 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.357-918dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370849 | ||||||
| chr9:36370905
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0174 | 2 | HG02056.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.357-973A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370905 | ||||||
| chr9:36370919
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.357-987C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370919 | ||||||
| chr9:36370969
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.357-1037T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370969 | ||||||
| chr9:36371259
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.357-1327G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371259 | ||||||
| chr9:36371358
|
A | G | 1 | a0001c0001t0002g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.357-1426T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371358 | ||||||
| chr9:36371436
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.357-1504G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371436 | ||||||
| chr9:36371443
|
C | CT | 13 | a0001c0001t0001g0045a0001c0001t0001g0163a0001c0001t0001g0172others(10): Show | 13 | HG02056.hp2 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.357-1512dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371443 | ||||||
| chr9:36371443
|
CT | C | 13 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0174others(10): Show | 13 | HG01496.hp2 HG01975.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.357-1512delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371443 | ||||||
| chr9:36371516
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.357-1584C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371516 | ||||||
| chr9:36371728
|
A | G | 1 | a0001c0001t0003g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.357-1796T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371728 | ||||||
| chr9:36371760
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.357-1828A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371760 | ||||||
| chr9:36371834
|
C | G | 1 | a0001c0001t0002g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.357-1902G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371834 | ||||||
| chr9:36371934
|
C | CT | 12 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(9): Show | 12 | HG01106.hp2 HG01243.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.357-2003dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371934 | ||||||
| chr9:36371934
|
C | CTT | 7 | a0001c0001t0006g0030a0001c0001t0006g0031a0001c0001t0006g0032others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.357-2004_357-2003d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371934 | ||||||
| chr9:36371971
|
G | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.357-2039C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371971 | ||||||
| chr9:36372183
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.357-2251G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372183 | ||||||
| chr9:36372419
|
T | C | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG01891.hp2 HG04115.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.357-2487A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372419 | ||||||
| chr9:36372465
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.357-2533C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372465 | ||||||
| chr9:36372651
|
C | A | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.357-2719G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372651 | ||||||
| chr9:36372740
|
C | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.357-2808G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372740 | ||||||
| chr9:36372762
|
A | G | 4 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(1): Show | 4 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357-2830T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372762 | ||||||
| chr9:36372808
|
C | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 18 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.357-2876G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372808 | ||||||
| chr9:36372846
|
T | C | 1 | a0001c0001t0016g0318 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.357-2914A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372846 | ||||||
| chr9:36373082
|
C | CT | 7 | a0001c0001t0001g0004a0001c0001t0001g0175a0001c0001t0001g0176others(4): Show | 8 | HG00408.hp2 HG02602.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.356+2851dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373082 | ||||||
| chr9:36373084
|
G | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0175a0001c0001t0001g0176others(4): Show | 8 | HG00408.hp2 HG02602.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.356+2850C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373084 | ||||||
| chr9:36373142
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.356+2792C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373142 | ||||||
| chr9:36373332
|
T | C | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.356+2602A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373332 | ||||||
| chr9:36373342
|
A | G | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.356+2592T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373342 | ||||||
| chr9:36373410
|
C | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(286): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.356+2524G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373410 | ||||||
| chr9:36373489
|
C | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.356+2445G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373489 | ||||||
| chr9:36373513
|
C | T | 1 | a0001c0001t0002g0106 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.356+2421G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373513 | ||||||
| chr9:36373544
|
A | C | 2 | a0001c0001t0005g0013a0001c0001t0005g0016 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.356+2390T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373544 | ||||||
| chr9:36373589
|
C | CT | 18 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0253others(15): Show | 18 | HG00438.hp2 HG02615.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.356+2344dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373589 | ||||||
| chr9:36373589
|
CT | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.356+2344delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373589 | ||||||
| chr9:36373590
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.356+2344A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373590 | ||||||
| chr9:36373591
|
T | C | 1 | a0001c0001t0013g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.356+2343A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373591 | ||||||
| chr9:36373608
|
T | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | NA18949.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.356+2326A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373608 | ||||||
| chr9:36373638
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.356+2296G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373638 | ||||||
| chr9:36373658
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0220 | 2 | HG02132.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.356+2276G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373658 | ||||||
| chr9:36373695
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.356+2239C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373695 | ||||||
| chr9:36373739
|
C | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.356+2195G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373739 | ||||||
| chr9:36373817
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.356+2117C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373817 | ||||||
| chr9:36373853
|
G | A | 1 | a0001c0001t0003g0142 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.356+2081C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373853 | ||||||
| chr9:36373982
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.356+1952G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373982 | ||||||
| chr9:36374159
|
G | T | 6 | a0001c0001t0001g0385a0001c0001t0001g0386a0001c0001t0001g0387others(3): Show | 6 | HG01255.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+1775C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374159 | ||||||
| chr9:36374171
|
T | C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.356+1763A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374171 | ||||||
| chr9:36374207
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.356+1727T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374207 | ||||||
| chr9:36374216
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.356+1718T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374216 | ||||||
| chr9:36374621
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.356+1313G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374621 | ||||||
| chr9:36374678
|
C | A | 5 | a0001c0001t0006g0030a0001c0001t0006g0031a0001c0001t0006g0032others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.356+1256G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374678 | ||||||
| chr9:36374724
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(29): Show | 34 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.356+1210G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374724 | ||||||
| chr9:36374835
|
A | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(35): Show | 40 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.356+1099T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374835 | ||||||
| chr9:36374943
|
A | G | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.356+991T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374943 | ||||||
| chr9:36375340
|
G | A | 1 | a0001c0001t0001g0368 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.356+594C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375340 | ||||||
| chr9:36375412
|
G | A | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.356+522C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375412 | ||||||
| chr9:36375462
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.356+472C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375462 | ||||||
| chr9:36375650
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.356+284C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375650 | ||||||
| chr9:36375686
|
T | G | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.356+248A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375686 | ||||||
| chr9:36375712
|
G | C | 62 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.356+222C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375712 | ||||||
| chr9:36375878
|
T | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG01074.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.356+56A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375878 | ||||||
| chr9:36376204
|
G | C | 1 | a0001c0001t0001g0387 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-77C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376204 | ||||||
| chr9:36376335
|
G | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.163-208C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376335 | ||||||
| chr9:36376385
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.163-258C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376385 | ||||||
| chr9:36376398
|
G | A | 1 | a0001c0001t0003g0204 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.163-271C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376398 | ||||||
| chr9:36376595
|
C | G | 25 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(22): Show | 25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-468G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376595 | ||||||
| chr9:36376648
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-521C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376648 | ||||||
| chr9:36376674
|
C | T | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163-547G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376674 | ||||||
| chr9:36376760
|
T | C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163-633A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376760 | ||||||
| chr9:36376790
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.163-663C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376790 | ||||||
| chr9:36376877
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.163-750C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376877 | ||||||
| chr9:36376888
|
G | T | 26 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-761C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376888 | ||||||
| chr9:36376912
|
G | GT | 4 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0095others(1): Show | 4 | HG02074.hp2 NA18944.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-786dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376912 | ||||||
| chr9:36376926
|
C | CA | 14 | a0001c0001t0001g0267a0001c0001t0001g0278a0001c0001t0001g0302others(11): Show | 14 | HG01261.hp2 HG01934.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.163-800dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376926 | ||||||
| chr9:36376926
|
CA | C | 79 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0066others(76): Show | 79 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.163-800delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376926 | ||||||
| chr9:36376926
|
CAA | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.163-801_163-800del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376926 | ||||||
| chr9:36376926
|
CAAA | C | 7 | a0001c0001t0001g0060a0001c0001t0001g0181a0001c0001t0001g0189others(4): Show | 7 | HG01975.hp1 HG02976.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-802_163-800del others(3): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376926 | ||||||
| chr9:36376996
|
G | T | 28 | a0001c0001t0001g0348a0001c0001t0001g0350a0001c0001t0001g0354others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.163-869C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376996 | ||||||
| chr9:36377070
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.163-943T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377070 | ||||||
| chr9:36377300
|
T | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0306 | 2 | NA18747.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.163-1173A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377300 | ||||||
| chr9:36377625
|
A | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(2): Show | 5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-1498T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377625 | ||||||
| chr9:36377733
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.163-1606G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377733 | ||||||
| chr9:36377760
|
A | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.163-1633T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377760 | ||||||
| chr9:36377802
|
A | G | 2 | a0001c0001t0002g0082a0001c0001t0002g0086 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.163-1675T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377802 | ||||||
| chr9:36377824
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.163-1697T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377824 | ||||||
| chr9:36377933
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.163-1806G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377933 | ||||||
| chr9:36377983
|
GAAAGTTA others(19): Show |
G | 8 | a0001c0001t0001g0383a0001c0001t0001g0385a0001c0001t0001g0386others(5): Show | 8 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-1882_163-1857d others(28): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377983 | ||||||
| chr9:36378012
|
AACTTAAA others(25): Show |
A | 1 | a0001c0001t0005g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-1917_163-1886d others(34): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378012 | ||||||
| chr9:36378016
|
T | TA | 7 | a0001c0001t0006g0030a0001c0001t0006g0031a0001c0001t0006g0032others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-1890dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378016 | ||||||
| chr9:36378057
|
A | AT | 7 | a0001c0001t0006g0030a0001c0001t0006g0031a0001c0001t0006g0032others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-1931dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378057 | ||||||
| chr9:36378169
|
C | CT | 70 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0185others(67): Show | 71 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-2043dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378169 | ||||||
| chr9:36378169
|
CT | C | 37 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0071others(34): Show | 37 | HG00609.hp1 HG01123.hp2 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.163-2043delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378169 | ||||||
| chr9:36378169
|
CTT | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(39): Show | 44 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.163-2044_163-2043d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378169 | ||||||
| chr9:36378192
|
T | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0068others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2065A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378192 | ||||||
| chr9:36378192
|
T | TG | 4 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0115others(1): Show | 4 | NA18965.hp1 NA18978.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2066dupC | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378192 | ||||||
| chr9:36378200
|
G | T | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163-2073C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378200 | ||||||
| chr9:36378413
|
T | C | 1 | a0001c0001t0010g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.163-2286A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378413 | ||||||
| chr9:36378643
|
T | C | 7 | a0001c0001t0006g0030a0001c0001t0006g0031a0001c0001t0006g0032others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2516A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378643 | ||||||
| chr9:36378856
|
G | A | 62 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.163-2729C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378856 | ||||||
| chr9:36378904
|
C | CT | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.163-2778dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378904 | ||||||
| chr9:36379086
|
G | C | 1 | a0001c0001t0001g0324 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.163-2959C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379086 | ||||||
| chr9:36379143
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.163-3016C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379143 | ||||||
| chr9:36379147
|
G | A | 2 | a0001c0001t0008g0352a0001c0001t0008g0353 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.163-3020C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379147 | ||||||
| chr9:36379201
|
A | G | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.163-3074T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379201 | ||||||
| chr9:36379652
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.163-3525G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379652 | ||||||
| chr9:36380359
|
CCTG | C | 5 | a0001c0001t0001g0347a0001c0001t0001g0368a0001c0001t0001g0369others(2): Show | 5 | HG03098.hp1 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-4235_163-4233d others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380359 | ||||||
| chr9:36380501
|
G | GT | 12 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0001g0292others(9): Show | 12 | HG00639.hp2 HG00738.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-4375dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380501 | ||||||
| chr9:36380519
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.163-4392C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380519 | ||||||
| chr9:36380694
|
A | G | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-4567T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380694 | ||||||
| chr9:36380866
|
G | C | 12 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(9): Show | 12 | HG00733.hp2 HG00741.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-4739C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380866 | ||||||
| chr9:36380941
|
C | T | 1 | a0001c0001t0005g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-4814G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380941 | ||||||
| chr9:36381028
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.163-4901G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381028 | ||||||
| chr9:36381034
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(40): Show | 45 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.163-4907A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381034 | ||||||
| chr9:36381118
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA18965.hp2 NA19060.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.163-4991G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381118 | ||||||
| chr9:36381141
|
G | A | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-5014C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381141 | ||||||
| chr9:36381229
|
T | C | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-5102A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381229 | ||||||
| chr9:36381583
|
G | A | 1 | a0001c0001t0006g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-5456C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381583 | ||||||
| chr9:36381740
|
G | C | 1 | a0001c0001t0019g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.163-5613C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381740 | ||||||
| chr9:36381801
|
T | A | 28 | a0001c0001t0001g0348a0001c0001t0001g0350a0001c0001t0001g0354others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.163-5674A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381801 | ||||||
| chr9:36381905
|
C | T | 367 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(364): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.163-5778G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381905 | ||||||
| chr9:36381918
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-5791G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381918 | ||||||
| chr9:36382074
|
G | C | 28 | a0001c0001t0001g0348a0001c0001t0001g0350a0001c0001t0001g0354others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.163-5947C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382074 | ||||||
| chr9:36382079
|
T | C | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-5952A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382079 | ||||||
| chr9:36382240
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.163-6113A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382240 | ||||||
| chr9:36382311
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-6184G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382311 | ||||||
| chr9:36382392
|
T | C | 6 | a0001c0001t0001g0264a0001c0001t0001g0308a0001c0001t0001g0326others(3): Show | 6 | NA18962.hp1 NA18971.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-6265A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382392 | ||||||
| chr9:36382427
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0225 | 2 | NA18977.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.163-6300G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382427 | ||||||
| chr9:36382793
|
A | G | 28 | a0001c0001t0003g0142a0001c0001t0003g0143a0001c0001t0003g0145others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.163-6666T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382793 | ||||||
| chr9:36382857
|
C | T | 4 | a0001c0001t0001g0347a0001c0001t0001g0369a0001c0001t0001g0370others(1): Show | 4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-6730G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382857 | ||||||
| chr9:36382865
|
C | T | 26 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-6738G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382865 | ||||||
| chr9:36383069
|
G | A | 1 | a0001c0001t0012g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163-6942C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383069 | ||||||
| chr9:36383195
|
A | T | 1 | a0001c0001t0007g0076 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.163-7068T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383195 | ||||||
| chr9:36383196
|
C | A | 1 | a0001c0001t0007g0076 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.163-7069G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383196 | ||||||
| chr9:36383296
|
G | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0222 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-7169C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383296 | ||||||
| chr9:36383372
|
T | C | 1 | a0001c0001t0021g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.162+7095A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383372 | ||||||
| chr9:36383433
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162+7034C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383433 | ||||||
| chr9:36383445
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.162+7022G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383445 | ||||||
| chr9:36383499
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.162+6968A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383499 | ||||||
| chr9:36383718
|
AATGTTGT others(14): Show |
A | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+6728_162+6748d others(23): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383718 | ||||||
| chr9:36383738
|
C | A | 25 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(22): Show | 25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+6729G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383738 | ||||||
| chr9:36383892
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.162+6575C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383892 | ||||||
| chr9:36384057
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162+6410T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384057 | ||||||
| chr9:36384505
|
T | C | 1 | a0001c0001t0003g0157 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.162+5962A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384505 | ||||||
| chr9:36384565
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.162+5902T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384565 | ||||||
| chr9:36384649
|
T | C | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+5818A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384649 | ||||||
| chr9:36384658
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.162+5809C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384658 | ||||||
| chr9:36384684
|
TA | T | 6 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(3): Show | 6 | HG00621.hp1 NA18949.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+5782delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384684 | ||||||
| chr9:36385083
|
A | G | 1 | a0001c0001t0001g0368 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.162+5384T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385083 | ||||||
| chr9:36385144
|
T | TA | 8 | a0001c0001t0001g0188a0001c0001t0001g0211a0001c0001t0001g0212others(5): Show | 8 | HG00438.hp1 HG00544.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+5322_162+5323i others(3): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385144 | ||||||
| chr9:36385145
|
T | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.162+5322A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385145 | ||||||
| chr9:36385145
|
T | TA | 25 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(22): Show | 25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+5321dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385145 | ||||||
| chr9:36385380
|
C | CT | 92 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(89): Show | 92 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.162+5086dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385380 | ||||||
| chr9:36385380
|
C | CTT | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0043others(27): Show | 32 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+5085_162+5086d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385380 | ||||||
| chr9:36385439
|
C | T | 1 | a0001c0001t0001g0337 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.162+5028G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385439 | ||||||
| chr9:36385442
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.162+5025C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385442 | ||||||
| chr9:36385536
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.162+4931T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385536 | ||||||
| chr9:36385885
|
A | C | 2 | a0001c0001t0005g0017a0001c0003t0005g0018 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.162+4582T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385885 | ||||||
| chr9:36385903
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0222 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.162+4564C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385903 | ||||||
| chr9:36386039
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.162+4428C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386039 | ||||||
| chr9:36386060
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162+4407C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386060 | ||||||
| chr9:36386086
|
G | C | 4 | a0001c0001t0007g0076a0001c0001t0007g0077a0001c0001t0007g0078others(1): Show | 4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+4381C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386086 | ||||||
| chr9:36386145
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.162+4322G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386145 | ||||||
| chr9:36386170
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162+4297G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386170 | ||||||
| chr9:36386221
|
T | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0234a0001c0001t0001g0235others(11): Show | 15 | HG01106.hp1 HG02071.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.162+4246A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386221 | ||||||
| chr9:36386296
|
A | G | 1 | a0001c0001t0001g0346 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+4171T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386296 | ||||||
| chr9:36386413
|
C | T | 1 | a0001c0001t0008g0352 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.162+4054G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386413 | ||||||
| chr9:36386585
|
C | T | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG00609.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.162+3882G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386585 | ||||||
| chr9:36386590
|
C | A | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.162+3877G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386590 | ||||||
| chr9:36386604
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162+3863T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386604 | ||||||
| chr9:36386844
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.162+3623G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386844 | ||||||
| chr9:36386868
|
T | G | 14 | a0001c0001t0001g0258a0001c0001t0001g0268a0001c0001t0001g0279others(11): Show | 14 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.162+3599A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386868 | ||||||
| chr9:36387018
|
A | G | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.162+3449T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387018 | ||||||
| chr9:36387045
|
C | T | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.162+3422G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387045 | ||||||
| chr9:36387052
|
T | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+3415A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387052 | ||||||
| chr9:36387058
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.162+3409G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387058 | ||||||
| chr9:36387154
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.162+3313T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387154 | ||||||
| chr9:36387198
|
G | C | 1 | a0001c0001t0001g0277 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.162+3269C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387198 | ||||||
| chr9:36387242
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.162+3225A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387242 | ||||||
| chr9:36387286
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.162+3181G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387286 | ||||||
| chr9:36387342
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.162+3125T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387342 | ||||||
| chr9:36387384
|
TA | T | 4 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(1): Show | 4 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3082delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387384 | ||||||
| chr9:36387386
|
A | G | 4 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(1): Show | 4 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3081T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387386 | ||||||
| chr9:36387388
|
G | T | 4 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(1): Show | 4 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3079C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387388 | ||||||
| chr9:36387683
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0256 | 3 | HG02257.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.162+2784C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387683 | ||||||
| chr9:36387750
|
C | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+2717G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387750 | ||||||
| chr9:36387891
|
CA | C | 11 | a0001c0001t0001g0258a0001c0001t0001g0268a0001c0001t0001g0279others(8): Show | 11 | HG01433.hp1 HG01981.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+2575delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387891 | ||||||
| chr9:36388146
|
C | A | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+2321G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388146 | ||||||
| chr9:36388246
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.162+2221C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388246 | ||||||
| chr9:36388353
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.162+2114T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388353 | ||||||
| chr9:36388470
|
G | T | 1 | a0001c0001t0001g0381 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.162+1997C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388470 | ||||||
| chr9:36388587
|
T | C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.162+1880A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388587 | ||||||
| chr9:36388616
|
C | T | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1851G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388616 | ||||||
| chr9:36388719
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162+1748C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388719 | ||||||
| chr9:36388729
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.162+1738A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388729 | ||||||
| chr9:36389107
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG04115.hp1 NA18612.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+1360A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389107 | ||||||
| chr9:36389210
|
C | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.162+1257G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389210 | ||||||
| chr9:36389328
|
T | G | 1 | a0001c0001t0004g0028 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.162+1139A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389328 | ||||||
| chr9:36389344
|
C | CA | 35 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0304others(32): Show | 35 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.162+1122dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389344 | ||||||
| chr9:36389344
|
CA | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.162+1122delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389344 | ||||||
| chr9:36389344
|
CAA | C | 6 | a0001c0001t0001g0237a0001c0001t0007g0076a0001c0001t0007g0077others(3): Show | 6 | HG02071.hp1 NA18906.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1121_162+1122d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389344 | ||||||
| chr9:36389356
|
A | C | 62 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.162+1111T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389356 | ||||||
| chr9:36389368
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.162+1099A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389368 | ||||||
| chr9:36389386
|
G | A | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+1081C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389386 | ||||||
| chr9:36389556
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.162+911C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389556 | ||||||
| chr9:36389596
|
C | G | 1 | a0001c0001t0001g0344 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162+871G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389596 | ||||||
| chr9:36389676
|
A | G | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG00609.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.162+791T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389676 | ||||||
| chr9:36389872
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.162+595G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389872 | ||||||
| chr9:36390009
|
T | A | 4 | a0001c0001t0001g0237a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG02071.hp1 HG02523.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+458A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36390009 | ||||||
| chr9:36390751
|
T | C | 2 | a0001c0001t0001g0344a0001c0001t0001g0345 | 2 | HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.13-135A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36390751 | ||||||
| chr9:36390828
|
C | T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.13-212G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36390828 | ||||||
| chr9:36390912
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.13-296T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36390912 | ||||||
| chr9:36391274
|
A | C | 1 | a0001c0001t0001g0309 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.13-658T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391274 | ||||||
| chr9:36391297
|
T | C | 9 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.13-681A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391297 | ||||||
| chr9:36391328
|
T | C | 1 | a0001c0001t0019g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.13-712A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391328 | ||||||
| chr9:36391361
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.13-745T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391361 | ||||||
| chr9:36391462
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.13-846C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391462 | ||||||
| chr9:36391540
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG00099.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.13-924A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391540 | ||||||
| chr9:36391548
|
A | G | 1 | a0001c0001t0001g0327 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.13-932T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391548 | ||||||
| chr9:36391587
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00558.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.13-971G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391587 | ||||||
| chr9:36391612
|
C | CT | 12 | a0001c0001t0001g0093a0001c0001t0001g0166a0001c0001t0001g0189others(9): Show | 12 | HG00738.hp1 HG01934.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-997dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391612 | ||||||
| chr9:36391612
|
CT | C | 10 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0184others(7): Show | 10 | HG00140.hp2 HG02559.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-997delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391612 | ||||||
| chr9:36391613
|
T | C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13-997A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391613 | ||||||
| chr9:36391637
|
T | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.13-1021A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391637 | ||||||
| chr9:36391673
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.13-1057A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391673 | ||||||
| chr9:36391751
|
C | T | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13-1135G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391751 | ||||||
| chr9:36391771
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0068 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.13-1155C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391771 | ||||||
| chr9:36391860
|
G | A | 6 | a0001c0001t0001g0264a0001c0001t0001g0308a0001c0001t0001g0326others(3): Show | 6 | NA18962.hp1 NA18971.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.13-1244C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391860 | ||||||
| chr9:36391873
|
G | A | 26 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.13-1257C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391873 | ||||||
| chr9:36392090
|
C | A | 4 | a0001c0001t0007g0076a0001c0001t0007g0077a0001c0001t0007g0078others(1): Show | 4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-1474G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392090 | ||||||
| chr9:36392098
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.13-1482G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392098 | ||||||
| chr9:36392690
|
A | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0019g0216 | 3 | HG00438.hp1 HG00544.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.13-2074T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392690 | ||||||
| chr9:36392748
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.13-2132A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392748 | ||||||
| chr9:36392806
|
G | A | 2 | a0001c0001t0008g0352a0001c0001t0008g0353 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.13-2190C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392806 | ||||||
| chr9:36392892
|
A | C | 62 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.13-2276T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392892 | ||||||
| chr9:36392908
|
A | C | 24 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(21): Show | 24 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.13-2292T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392908 | ||||||
| chr9:36393082
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.13-2466G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393082 | ||||||
| chr9:36393110
|
C | T | 1 | a0001c0001t0010g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13-2494G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393110 | ||||||
| chr9:36393433
|
G | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.13-2817C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393433 | ||||||
| chr9:36393473
|
CACATTGT others(4): Show |
C | 1 | a0001c0001t0003g0210 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.13-2868_13-2858del others(11): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393473 | ||||||
| chr9:36393475
|
CA | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 19 | HG00558.hp1 HG01175.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.13-2860delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | ||||||
| chr9:36393475
|
CATT | C | 27 | a0001c0001t0001g0138a0001c0001t0001g0169a0001c0001t0001g0170others(24): Show | 27 | HG00099.hp1 HG00544.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.13-2862_13-2860del others(3): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | ||||||
| chr9:36393475
|
CATTGT | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0206a0001c0001t0001g0207others(42): Show | 46 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.13-2864_13-2860del others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | ||||||
| chr9:36393475
|
CATTGTGT | C | 8 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(5): Show | 8 | HG00639.hp1 HG01255.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.13-2866_13-2860del others(7): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | ||||||
| chr9:36393475
|
CATTGTGT others(2): Show |
C | 6 | a0001c0001t0001g0004a0001c0001t0001g0175a0001c0001t0001g0176others(3): Show | 7 | HG00408.hp2 NA18943.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.13-2868_13-2860del others(9): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | ||||||
| chr9:36393476
|
A | G | 18 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(15): Show | 18 | HG00438.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.13-2860T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393476 | ||||||
| chr9:36393477
|
T | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 19 | HG00558.hp1 HG01175.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.13-2861A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TG | 12 | a0001c0001t0001g0144a0001c0001t0001g0162a0001c0001t0001g0163others(9): Show | 12 | HG00438.hp1 HG01255.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-2862_13-2861ins others(1): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.13-2862_13-2861ins others(11): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTG | 34 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0232others(31): Show | 34 | HG00673.hp2 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.13-2863_13-2862dup others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTGTG | 52 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(49): Show | 55 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.13-2865_13-2862dup others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTGTGTG | 32 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0063others(29): Show | 32 | HG00558.hp2 HG00642.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.13-2867_13-2862dup others(6): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTGTGTGT others(1): Show |
30 | a0001c0001t0001g0044a0001c0001t0001g0320a0001c0001t0001g0321others(27): Show | 30 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.13-2869_13-2862dup others(8): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTGTGTGT others(3): Show |
12 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329others(9): Show | 12 | HG00609.hp2 HG01993.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.13-2871_13-2862dup others(10): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTGTGTGT others(5): Show |
8 | a0001c0001t0001g0068a0001c0001t0001g0348a0001c0001t0001g0378others(5): Show | 8 | HG01981.hp1 HG02040.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.13-2873_13-2862dup others(12): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTGTGTGT others(7): Show |
5 | a0001c0001t0001g0379a0001c0001t0001g0380a0001c0001t0002g0116others(2): Show | 5 | HG00423.hp1 NA18951.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-2875_13-2862dup others(14): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTGTGTGT others(9): Show |
3 | a0001c0001t0001g0264a0001c0001t0002g0119a0001c0001t0002g0120 | 3 | NA18969.hp1 NA18971.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.13-2877_13-2862dup others(16): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
T | TTGTGTGT others(11): Show |
2 | a0001c0001t0001g0066a0001c0001t0002g0121 | 2 | NA18972.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.13-2879_13-2862dup others(18): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0029 | 3 | HG02896.hp2 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.13-2869_13-2862del others(8): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
TTGTGTGT others(3): Show |
T | 6 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(3): Show | 6 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.13-2871_13-2862del others(10): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0258a0001c0002t0001g0075 | 2 | HG01981.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.13-2873_13-2862del others(12): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393477
|
TTGTGTGT others(7): Show |
T | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02615.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-2875_13-2862del others(14): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | ||||||
| chr9:36393485
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.13-2869C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393485 | ||||||
| chr9:36393512
|
TGTGTGTG others(5): Show |
T | 4 | a0001c0001t0002g0124a0001c0001t0005g0013a0001c0001t0005g0014others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-2908_13-2897del others(12): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393512 | ||||||
| chr9:36393514
|
TGTGTGTG others(3): Show |
T | 5 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0019others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-2908_13-2899del others(10): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393514 | ||||||
| chr9:36393520
|
TGTGG | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0069a0001c0001t0001g0070others(2): Show | 5 | HG01433.hp2 HG02559.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-2908_13-2905del others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393520 | ||||||
| chr9:36393522
|
T | G | 1 | a0001c0001t0001g0332 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.13-2906A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393522 | ||||||
| chr9:36393522
|
TGG | T | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 10 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-2908_13-2907del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393522 | ||||||
| chr9:36393523
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0367 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.13-2908_13-2907ins others(11): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393523 | ||||||
| chr9:36393523
|
G | GTGTGTGT others(10): Show |
1 | a0001c0001t0001g0350 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.13-2908_13-2907ins others(17): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393523 | ||||||
| chr9:36393524
|
G | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.13-2908C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393524 | ||||||
| chr9:36393539
|
T | C | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.13-2923A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393539 | ||||||
| chr9:36393577
|
C | T | 5 | a0001c0001t0006g0030a0001c0001t0006g0031a0001c0001t0006g0032others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-2961G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393577 | ||||||
| chr9:36393580
|
T | G | 2 | a0001c0001t0001g0333a0001c0001t0001g0334 | 2 | HG00438.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.13-2964A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393580 | ||||||
| chr9:36393747
|
A | G | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.13-3131T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393747 | ||||||
| chr9:36393976
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.13-3360C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393976 | ||||||
| chr9:36394009
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.13-3393C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394009 | ||||||
| chr9:36394010
|
C | A | 1 | a0001c0001t0001g0180 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.13-3394G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394010 | ||||||
| chr9:36394042
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0165others(15): Show | 20 | HG00408.hp2 HG00558.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.13-3426G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394042 | ||||||
| chr9:36394231
|
T | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(286): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.13-3615A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394231 | ||||||
| chr9:36394523
|
G | C | 1 | a0001c0001t0002g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.13-3907C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394523 | ||||||
| chr9:36394594
|
C | T | 1 | a0001c0001t0021g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.13-3978G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394594 | ||||||
| chr9:36394716
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.13-4100C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394716 | ||||||
| chr9:36394971
|
G | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.13-4355C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394971 | ||||||
| chr9:36395105
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.13-4489C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395105 | ||||||
| chr9:36395164
|
C | G | 3 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.13-4548G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395164 | ||||||
| chr9:36395228
|
T | C | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.13-4612A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395228 | ||||||
| chr9:36395241
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.13-4625G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395241 | ||||||
| chr9:36395396
|
T | C | 8 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+4701A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395396 | ||||||
| chr9:36395400
|
G | A | 1 | a0001c0001t0001g0380 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.12+4697C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395400 | ||||||
| chr9:36395429
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.12+4668C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395429 | ||||||
| chr9:36395678
|
AATCTCTA others(18): Show |
A | 1 | a0001c0001t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.12+4394_12+4418del others(25): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395678 | ||||||
| chr9:36395754
|
C | A | 1 | a0001c0001t0003g0161 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.12+4343G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395754 | ||||||
| chr9:36395892
|
T | C | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | HG00621.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.12+4205A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395892 | ||||||
| chr9:36395949
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.12+4148C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395949 | ||||||
| chr9:36395960
|
C | A | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.12+4137G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395960 | ||||||
| chr9:36396197
|
T | C | 1 | a0001c0001t0003g0143 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.12+3900A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396197 | ||||||
| chr9:36396198
|
G | GT | 6 | a0001c0001t0001g0249a0001c0001t0001g0260a0001c0001t0001g0337others(3): Show | 6 | NA18946.hp2 NA18974.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3898dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396198 | ||||||
| chr9:36396229
|
A | C | 1 | a0001c0001t0001g0262 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.12+3868T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396229 | ||||||
| chr9:36396422
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.12+3675A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396422 | ||||||
| chr9:36396551
|
G | A | 25 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(22): Show | 25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+3546C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396551 | ||||||
| chr9:36396772
|
T | C | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.12+3325A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396772 | ||||||
| chr9:36396775
|
T | C | 2 | a0001c0001t0006g0033a0001c0001t0013g0034 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.12+3322A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396775 | ||||||
| chr9:36396786
|
T | TAAAAAAA others(2734): Show |
1 | a0001c0001t0001g0044 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12+3310_12+3311ins others(2741): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396786 | ||||||
| chr9:36396786
|
T | TAAAAAAA others(2760): Show |
1 | a0001c0001t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.12+3310_12+3311ins others(2767): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396786 | ||||||
| chr9:36396835
|
T | C | 7 | a0001c0001t0001g0249a0001c0001t0001g0260a0001c0001t0001g0337others(4): Show | 7 | HG00423.hp2 NA18946.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3262A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396835 | ||||||
| chr9:36396919
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.12+3178C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396919 | ||||||
| chr9:36396979
|
TCACTA | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02055.hp2 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.12+3113_12+3117del others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396979 | ||||||
| chr9:36397011
|
ATG | A | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.12+3084_12+3085del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397011 | ||||||
| chr9:36397013
|
GTGTGTGT others(51): Show |
G | 1 | a0001c0001t0001g0383 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.12+3026_12+3083del others(58): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397013 | ||||||
| chr9:36397019
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.12+3078C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397019 | ||||||
| chr9:36397021
|
G | GTGTATAT others(21): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01358.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.12+3075_12+3076ins others(28): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397021 | ||||||
| chr9:36397021
|
G | GTGTATAT others(21): Show |
1 | a0001c0001t0001g0223 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.12+3075_12+3076ins others(28): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397021 | ||||||
| chr9:36397022
|
TGTGTATA others(3): Show |
T | 1 | a0001c0001t0010g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.12+3065_12+3074del others(10): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397022 | ||||||
| chr9:36397025
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG01358.hp1 NA18977.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.12+3072C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397025 | ||||||
| chr9:36397071
|
A | ATG | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.12+3024_12+3025dup others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397071 | ||||||
| chr9:36397081
|
G | GTA | 7 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+3014_12+3015dup others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | ||||||
| chr9:36397081
|
G | GTGTA | 13 | a0001c0001t0001g0226a0001c0001t0002g0124a0001c0001t0002g0125others(10): Show | 13 | HG00733.hp2 HG00741.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.12+3015_12+3016ins others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | ||||||
| chr9:36397081
|
G | GTGTATA | 48 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0037others(45): Show | 48 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.12+3015_12+3016ins others(6): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | ||||||
| chr9:36397081
|
GTA | G | 3 | a0001c0001t0008g0351a0001c0001t0008g0352a0001c0001t0008g0353 | 3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.12+3014_12+3015del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | ||||||
| chr9:36397081
|
GTATA | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.12+3012_12+3015del others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | ||||||
| chr9:36397083
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(37): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.12+3014T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397083 | ||||||
| chr9:36397085
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01192.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.12+3012T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397085 | ||||||
| chr9:36397104
|
G | GT | 6 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(3): Show | 6 | HG01891.hp2 HG01981.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.12+2992dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397104 | ||||||
| chr9:36397104
|
G | T | 1 | a0001c0001t0001g0257 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.12+2993C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397104 | ||||||
| chr9:36397104
|
GT | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.12+2992delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397104 | ||||||
| chr9:36397104
|
GTT | G | 24 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(21): Show | 24 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.12+2991_12+2992del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397104 | ||||||
| chr9:36397106
|
T | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.12+2991A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397106 | ||||||
| chr9:36397236
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.12+2861G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397236 | ||||||
| chr9:36397240
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.12+2857T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397240 | ||||||
| chr9:36397287
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.12+2810A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397287 | ||||||
| chr9:36397424
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.12+2673A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397424 | ||||||
| chr9:36397461
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.12+2636T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397461 | ||||||
| chr9:36397543
|
T | C | 1 | a0001c0001t0014g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.12+2554A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397543 | ||||||
| chr9:36397578
|
T | A | 1 | a0001c0001t0001g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.12+2519A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397578 | ||||||
| chr9:36397579
|
C | A | 2 | a0001c0001t0001g0344a0001c0001t0001g0345 | 2 | HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.12+2518G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397579 | ||||||
| chr9:36397612
|
C | T | 25 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(22): Show | 25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+2485G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397612 | ||||||
| chr9:36397701
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.12+2396G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397701 | ||||||
| chr9:36397781
|
CTT | C | 46 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0002g0080others(43): Show | 46 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.12+2314_12+2315del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397781 | ||||||
| chr9:36397874
|
G | T | 1 | a0001c0001t0010g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+2223C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397874 | ||||||
| chr9:36397889
|
T | G | 1 | a0001c0001t0010g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+2208A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397889 | ||||||
| chr9:36397938
|
A | T | 8 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+2159T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397938 | ||||||
| chr9:36398248
|
G | A | 25 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(22): Show | 25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+1849C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398248 | ||||||
| chr9:36398426
|
A | T | 1 | a0001c0001t0001g0249 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.12+1671T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398426 | ||||||
| chr9:36398427
|
T | A | 6 | a0001c0001t0001g0382a0001c0001t0006g0030a0001c0001t0006g0031others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+1670A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398427 | ||||||
| chr9:36398566
|
G | C | 1 | a0001c0001t0003g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.12+1531C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398566 | ||||||
| chr9:36398577
|
C | T | 2 | a0001c0001t0003g0142a0001c0001t0003g0143 | 2 | NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.12+1520G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398577 | ||||||
| chr9:36398706
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.12+1391A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398706 | ||||||
| chr9:36398751
|
T | C | 12 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(9): Show | 12 | HG00733.hp2 HG00741.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.12+1346A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398751 | ||||||
| chr9:36398935
|
T | C | 16 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(13): Show | 16 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+1162A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398935 | ||||||
| chr9:36399023
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.12+1074A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399023 | ||||||
| chr9:36399039
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.12+1058C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399039 | ||||||
| chr9:36399213
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.12+884C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399213 | ||||||
| chr9:36399295
|
T | C | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG00609.hp1 HG02083.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.12+802A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399295 | ||||||
| chr9:36399442
|
A | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+655T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399442 | ||||||
| chr9:36399493
|
A | AAC | 14 | a0001c0001t0001g0007a0001c0001t0001g0234a0001c0001t0001g0235others(11): Show | 15 | HG01106.hp1 HG02071.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.12+603_12+604insGT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399493 | ||||||
| chr9:36399493
|
A | AAT | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.12+602_12+603dupAT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399493 | ||||||
| chr9:36399493
|
A | AATATATA others(32): Show |
1 | a0001c0001t0010g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+603_12+604insAT others(37): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399493 | ||||||
| chr9:36399529
|
T | C | 25 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(22): Show | 25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+568A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399529 | ||||||
| chr9:36399536
|
T | C | 2 | a0001c0001t0001g0389a0001c0001t0001g0390 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.12+561A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399536 | ||||||
| chr9:36399542
|
T | G | 8 | a0001c0001t0001g0383a0001c0001t0001g0385a0001c0001t0001g0386others(5): Show | 8 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+555A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399542 | ||||||
| chr9:36399563
|
A | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.12+534T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399563 | ||||||
| chr9:36399751
|
T | C | 2 | a0001c0001t0002g0391a0001c0001t0002g0392 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.12+346A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399751 | ||||||
| chr9:36399826
|
C | T | 26 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.12+271G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399826 | ||||||
| chr9:36400026
|
G | A | 1 | a0001c0001t0010g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+71C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36400026 |