Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 257160 |
|---|---|
| ensemblid | ENSG00000167257.11 |
| hgncid | 25335 |
| symbol | RNF214 |
| name | ring finger protein 214 |
| refseq_nuc | NM_207343.4 |
| refseq_prot | NP_997226.2 |
| ensembl_nuc | ENST00000300650.9 |
| ensembl_prot | ENSP00000300650.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 117232671 |
| end | 117286454 |
| strand | + |
| ver | v1.2 |
| region | chr11:117232671-117286454 |
| region5000 | chr11:117227671-117291454 |
| regionname0 | RNF214_chr11_117232671_117286454 |
| regionname5000 | RNF214_chr11_117227671_117291454 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 703 | 359 | 82 | 63 | 152 | 16 | 44 | 108 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0002 | 0/0 | 645 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2112 | 353 | 78 | 63 | 150 | 16 | 44 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| c0002 | 0/0 | 2112 | 4 | 4 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| c0003 | 0/0 | 2112 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| c0004 | 0/0 | 2083 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1366 | 283 | 65 | 45 | 127 | 10 | 35 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0002 | 1/0 | 1366 | 41 | 11 | 14 | 10 | 5 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0003 | 0/0 | 1366 | 18 | 0 | 0 | 12 | 0 | 6 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0004 | 0/0 | 1366 | 6 | 2 | 3 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0005 | 0/0 | 1366 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0006 | 0/0 | 1366 | 2 | 0 | 1 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0007 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0008 | 0/0 | 1366 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0009 | 0/0 | 1366 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0010 | 0/0 | 1366 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0011 | 0/0 | 1366 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0012 | 0/0 | 1366 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0013 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| t0014 | 0/0 | 1366 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2112 | 353 | 78 | 63 | 150 | 16 | 44 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0002 | 0/0 | 2112 | 4 | 4 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0003 | 0/0 | 2112 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0002c0004 | 0/0 | 2083 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3477 | 278 | 62 | 45 | 125 | 10 | 35 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0002 | 1/0 | 3477 | 40 | 11 | 13 | 10 | 5 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0003 | 0/0 | 3477 | 18 | 0 | 0 | 12 | 0 | 6 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0004 | 0/0 | 3477 | 5 | 1 | 3 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0005 | 0/0 | 3477 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0006 | 0/0 | 3477 | 2 | 0 | 1 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0007 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0008 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0009 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0010 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0011 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0012 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0013 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0001t0014 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0002t0001 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0002t0004 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0001c0003t0001 | 0/0 | 3477 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| a0002c0004t0002 | 0/0 | 3448 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | copy fasta | chr11 | 117227671 | 117291454 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0010g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0013g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0001t0014g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| a0002c0004t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0146 | EUR | GBR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | GBR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | FIN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0229 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0076 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01257 | hp2 | a0002 | c0004 | t0002 | g0007 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0096 | EUR | IBS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0119 | EUR | IBS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0337 | EUR | IBS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0336 | EUR | IBS | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CDX | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CDX | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0144 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02602 | hp1 | a0001 | c0001 | t0011 | g0033 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02735 | hp2 | a0001 | c0001 | t0010 | g0303 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02738 | hp2 | a0001 | c0001 | t0014 | g0101 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0072 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0309 | SAS | PJL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | BEB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0317 | SAS | BEB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0319 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | YRI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18612 | hp2 | a0001 | c0001 | t0013 | g0130 | EAS | CHB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | CHB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0265 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | LWK | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | LWK | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ASW | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | TSI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | TSI | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0318 | SAS | GIH | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | USA | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | LWK | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0110 | REF | REF | RNF214_chr11_117227671_117291454 | RNF214 | chr11 | 117227671 | 117291454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:117282758
|
ATCCGGGC others(22): Show |
A | 1 | a0002 | 1 | HG01257.hp2 | frameshift_variant | HIGH | c.1859_1887delTCCGGG others(23): Show |
p.Ile620fs | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 13/15 | 1921/3477 | 1859/2112 | 620/703 | chr11 | 117282758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:117281686
|
A | G | 1 | a0001c0002 | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.1323A>G | p.Pro441Pro | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 10/15 | 1385/3477 | 1323/2112 | 441/703 | chr11 | 117281686 | ||
| chr11:117283174
|
G | A | 1 | a0001c0003 | 2 | NA18965.hp2 NA18994.hp1 |
synonymous_variant | LOW | c.2010G>A | p.Leu670Leu | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/15 | 2072/3477 | 2010/2112 | 670/703 | chr11 | 117283174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:117232681
|
T | C | 1 | a0001c0001t0007 | 1 | NA19001.hp2 | 5_prime_UTR_variant | MODIFIER | c.-52T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/15 | 1592 | chr11 | 117232681 | |||||
| chr11:117232703
|
C | T | 1 | a0001c0001t0014 | 1 | HG02738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/15 | 1570 | chr11 | 117232703 | |||||
| chr11:117232712
|
G | T | 1 | a0001c0001t0003 | 18 | HG03710.hp2 HG03831.hp2 HG03834.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-21G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/15 | 1561 | chr11 | 117232712 | |||||
| chr11:117285252
|
T | C | 1 | a0001c0001t0008 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 101 | chr11 | 117285252 | |||||
| chr11:117285352
|
C | T | 1 | a0001c0001t0013 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*201C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 201 | chr11 | 117285352 | |||||
| chr11:117285564
|
C | T | 1 | a0001c0001t0012 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 413 | chr11 | 117285564 | |||||
| chr11:117285699
|
T | G | 1 | a0001c0001t0009 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*548T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 548 | chr11 | 117285699 | |||||
| chr11:117285836
|
T | C | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*685T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 685 | chr11 | 117285836 | |||||
| chr11:117285904
|
G | A | 2 | a0001c0001t0005a0001c0001t0008 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*753G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 753 | chr11 | 117285904 | |||||
| chr11:117286171
|
A | G | 1 | a0001c0001t0011 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1020A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 1020 | chr11 | 117286171 | |||||
| chr11:117286177
|
G | C | 3 | a0001c0001t0004a0001c0001t0009a0001c0002t0004 | 7 | HG01070.hp2 HG01106.hp2 HG01167.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1026G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 1026 | chr11 | 117286177 | |||||
| chr11:117286177
|
G | T | 1 | a0001c0001t0006 | 2 | HG00099.hp2 HG01167.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1026G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 1026 | chr11 | 117286177 | |||||
| chr11:117286204
|
A | G | 1 | a0001c0001t0010 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1053A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 1053 | chr11 | 117286204 | |||||
| chr11:117286308
|
T | C | 2 | a0001c0001t0005a0001c0001t0008 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1157T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 15/15 | 1157 | chr11 | 117286308 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:117232764
|
G | T | 4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 4 | HG01346.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+38G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117232764 | ||||||
| chr11:117232788
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0330a0001c0001t0001g0331others(4): Show | 8 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+62C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117232788 | ||||||
| chr11:117232875
|
TC | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 16 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7+152delC | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 117232875 | |||||
| chr11:117232882
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7+156C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117232882 | ||||||
| chr11:117232955
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-7+229C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117232955 | ||||||
| chr11:117232956
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7+230C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117232956 | ||||||
| chr11:117232964
|
C | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 16 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7+238C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117232964 | ||||||
| chr11:117232966
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7+240G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117232966 | ||||||
| chr11:117233065
|
C | T | 1 | a0001c0001t0003g0322 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-7+339C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117233065 | ||||||
| chr11:117233360
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-7+634G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117233360 | ||||||
| chr11:117233423
|
C | CG | 17 | a0001c0001t0001g0306a0001c0001t0003g0307a0001c0001t0003g0308others(14): Show | 17 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7+704dupG | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 117233423 | |||||
| chr11:117233432
|
A | G | 138 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(135): Show | 144 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-7+706A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117233432 | ||||||
| chr11:117233705
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | HG03579.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-6-562G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117233705 | ||||||
| chr11:117233776
|
T | G | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 28 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.-6-491T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117233776 | ||||||
| chr11:117233820
|
C | A | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(223): Show | 237 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-6-447C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117233820 | ||||||
| chr11:117233879
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-6-388G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117233879 | ||||||
| chr11:117233935
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-6-332A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117233935 | ||||||
| chr11:117234141
|
C | T | 1 | a0001c0001t0003g0321 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-6-126C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117234141 | ||||||
| chr11:117234184
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6-83G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117234184 | ||||||
| chr11:117234201
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-6-66G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 1/14 | chr11 | 117234201 | ||||||
| chr11:117234697
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+318G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117234697 | ||||||
| chr11:117234716
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.107+337A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117234716 | ||||||
| chr11:117234840
|
A | G | 1 | a0001c0001t0003g0320 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.107+461A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117234840 | ||||||
| chr11:117234856
|
T | G | 146 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(143): Show | 152 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.107+477T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117234856 | ||||||
| chr11:117235010
|
A | G | 45 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(42): Show | 48 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.107+631A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235010 | ||||||
| chr11:117235157
|
A | T | 1 | a0001c0001t0002g0175 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.107+778A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235157 | ||||||
| chr11:117235244
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.107+865T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235244 | ||||||
| chr11:117235319
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+940C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235319 | ||||||
| chr11:117235335
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.107+956T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235335 | ||||||
| chr11:117235351
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+972T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235351 | ||||||
| chr11:117235353
|
C | T | 35 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(32): Show | 37 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.107+974C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235353 | ||||||
| chr11:117235357
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 48 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.107+978C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235357 | ||||||
| chr11:117235358
|
G | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0324a0001c0001t0005g0080others(2): Show | 5 | HG02055.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+979G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235358 | ||||||
| chr11:117235384
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+1005A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235384 | ||||||
| chr11:117235385
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+1006A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235385 | ||||||
| chr11:117235400
|
G | A | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(165): Show | 176 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.107+1021G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235400 | ||||||
| chr11:117235495
|
C | CT | 37 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0087others(34): Show | 37 | HG00673.hp2 HG00741.hp1 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.107+1137dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 117235495 | |||||
| chr11:117235495
|
CT | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0022others(31): Show | 37 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.107+1137delT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 117235495 | |||||
| chr11:117235522
|
G | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG02698.hp2 HG03239.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+1143G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235522 | ||||||
| chr11:117235564
|
A | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.107+1185A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235564 | ||||||
| chr11:117235566
|
C | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.107+1187C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235566 | ||||||
| chr11:117235584
|
C | T | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.107+1205C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235584 | ||||||
| chr11:117235616
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.107+1237C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235616 | ||||||
| chr11:117235633
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.107+1254A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235633 | ||||||
| chr11:117235742
|
T | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 21 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.107+1363T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235742 | ||||||
| chr11:117235787
|
A | G | 1 | a0001c0001t0002g0090 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.107+1408A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235787 | ||||||
| chr11:117235931
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.107+1552A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117235931 | ||||||
| chr11:117236121
|
C | T | 3 | a0001c0001t0003g0317a0001c0001t0003g0318a0001c0001t0003g0319 | 3 | HG03834.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.107+1742C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236121 | ||||||
| chr11:117236186
|
C | G | 1 | a0001c0001t0001g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+1807C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236186 | ||||||
| chr11:117236198
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+1819T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236198 | ||||||
| chr11:117236263
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.107+1884G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236263 | ||||||
| chr11:117236804
|
C | G | 19 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 21 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.108-1797C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236804 | ||||||
| chr11:117236814
|
T | C | 1 | a0001c0001t0001g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-1787T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236814 | ||||||
| chr11:117236843
|
A | C | 1 | a0001c0001t0003g0307 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.108-1758A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236843 | ||||||
| chr11:117236869
|
T | G | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-1732T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236869 | ||||||
| chr11:117236909
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.108-1692T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236909 | ||||||
| chr11:117236954
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.108-1647G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117236954 | ||||||
| chr11:117237059
|
A | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.108-1542A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237059 | ||||||
| chr11:117237262
|
G | A | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.108-1339G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237262 | ||||||
| chr11:117237270
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-1331A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237270 | ||||||
| chr11:117237436
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.108-1165G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237436 | ||||||
| chr11:117237452
|
C | G | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.108-1149C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237452 | ||||||
| chr11:117237453
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.108-1148C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237453 | ||||||
| chr11:117237500
|
A | T | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.108-1101A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237500 | ||||||
| chr11:117237602
|
T | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.108-999T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237602 | ||||||
| chr11:117237620
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.108-981A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117237620 | ||||||
| chr11:117238161
|
C | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.108-440C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117238161 | ||||||
| chr11:117238172
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.108-429T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117238172 | ||||||
| chr11:117238363
|
G | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-238G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117238363 | ||||||
| chr11:117238423
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.108-178A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117238423 | ||||||
| chr11:117238439
|
A | G | 19 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 21 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.108-162A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117238439 | ||||||
| chr11:117238554
|
G | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.108-47G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 2/14 | chr11 | 117238554 | ||||||
| chr11:117239246
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.618+135A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 3/14 | chr11 | 117239246 | ||||||
| chr11:117239312
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.618+201C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 3/14 | chr11 | 117239312 | ||||||
| chr11:117239334
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.618+223T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 3/14 | chr11 | 117239334 | ||||||
| chr11:117239415
|
TTGACCTT others(7): Show |
T | 1 | a0001c0001t0001g0181 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.618+305_618+318del others(14): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 3/14 | chr11 | 117239415 | ||||||
| chr11:117239504
|
G | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.619-297G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 3/14 | chr11 | 117239504 | ||||||
| chr11:117239548
|
G | A | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.619-253G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 3/14 | chr11 | 117239548 | ||||||
| chr11:117239701
|
T | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 44 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.619-100T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 3/14 | chr11 | 117239701 | ||||||
| chr11:117239892
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.678+32G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117239892 | ||||||
| chr11:117239979
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.678+119C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117239979 | ||||||
| chr11:117240011
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 5 | HG01074.hp2 HG01243.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.678+151G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240011 | ||||||
| chr11:117240024
|
C | T | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(210): Show | 224 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.678+164C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240024 | ||||||
| chr11:117240048
|
TA | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 44 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.678+199delA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117240048 | |||||
| chr11:117240205
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.678+345T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240205 | ||||||
| chr11:117240216
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.678+356G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240216 | ||||||
| chr11:117240383
|
T | A | 1 | a0001c0001t0003g0307 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.678+523T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240383 | ||||||
| chr11:117240384
|
T | TA | 34 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0025others(31): Show | 36 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.678+545dupA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117240384 | |||||
| chr11:117240384
|
TA | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0066others(9): Show | 13 | HG01069.hp1 HG01069.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.678+545delA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117240384 | |||||
| chr11:117240385
|
A | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(35): Show | 42 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.678+525A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240385 | ||||||
| chr11:117240386
|
A | T | 1 | a0001c0001t0001g0155 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.678+526A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240386 | ||||||
| chr11:117240462
|
T | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 44 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.678+602T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240462 | ||||||
| chr11:117240498
|
G | A | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(167): Show | 178 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.678+638G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240498 | ||||||
| chr11:117240549
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0008g0079 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.678+689G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240549 | ||||||
| chr11:117240652
|
C | T | 2 | a0001c0001t0006g0145a0001c0001t0006g0146 | 2 | HG00099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.678+792C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240652 | ||||||
| chr11:117240780
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.678+920G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240780 | ||||||
| chr11:117240800
|
C | G | 1 | a0001c0001t0004g0077 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.678+940C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117240800 | ||||||
| chr11:117241054
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.678+1194C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241054 | ||||||
| chr11:117241175
|
C | T | 1 | a0001c0001t0012g0144 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.678+1315C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241175 | ||||||
| chr11:117241197
|
C | A | 46 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 49 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.678+1337C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241197 | ||||||
| chr11:117241301
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.678+1441G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241301 | ||||||
| chr11:117241348
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.678+1488G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241348 | ||||||
| chr11:117241409
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.678+1549A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241409 | ||||||
| chr11:117241422
|
A | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 44 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.678+1562A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241422 | ||||||
| chr11:117241427
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.678+1567A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241427 | ||||||
| chr11:117241486
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.678+1626A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241486 | ||||||
| chr11:117241578
|
C | CA | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 54 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.678+1735dupA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117241578 | |||||
| chr11:117241578
|
CA | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0173others(32): Show | 37 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.678+1735delA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117241578 | |||||
| chr11:117241810
|
G | T | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(164): Show | 175 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.678+1950G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241810 | ||||||
| chr11:117241859
|
A | C | 1 | a0001c0001t0001g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.678+1999A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241859 | ||||||
| chr11:117241882
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.678+2022A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241882 | ||||||
| chr11:117241903
|
T | C | 1 | a0001c0001t0003g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.678+2043T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241903 | ||||||
| chr11:117241914
|
A | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(211): Show | 225 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.678+2054A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241914 | ||||||
| chr11:117241936
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG00738.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+2076C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117241936 | ||||||
| chr11:117242384
|
T | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0178 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.679-2061T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242384 | ||||||
| chr11:117242462
|
G | A | 6 | a0001c0001t0002g0006a0001c0001t0002g0094a0001c0001t0002g0102others(3): Show | 7 | HG02027.hp1 HG02056.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.679-1983G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242462 | ||||||
| chr11:117242545
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.679-1900T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242545 | ||||||
| chr11:117242557
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.679-1888T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242557 | ||||||
| chr11:117242619
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 44 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.679-1826A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242619 | ||||||
| chr11:117242705
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.679-1740T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242705 | ||||||
| chr11:117242706
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 44 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.679-1739A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242706 | ||||||
| chr11:117242714
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.679-1731G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242714 | ||||||
| chr11:117242721
|
C | T | 2 | a0001c0002t0001g0070a0001c0002t0001g0074 | 2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.679-1724C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242721 | ||||||
| chr11:117242762
|
G | C | 2 | a0001c0001t0002g0007a0002c0004t0002g0007 | 2 | HG00639.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.679-1683G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242762 | ||||||
| chr11:117242836
|
AGAGT | A | 4 | a0001c0001t0001g0078a0001c0001t0004g0075a0001c0001t0004g0077others(1): Show | 4 | HG01167.hp2 HG01175.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-1605_679-1602d others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117242836 | |||||
| chr11:117242950
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | NA18983.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.679-1495A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117242950 | ||||||
| chr11:117243035
|
A | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.679-1410A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243035 | ||||||
| chr11:117243076
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.679-1369A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243076 | ||||||
| chr11:117243119
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.679-1326G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243119 | ||||||
| chr11:117243131
|
T | TATTA | 10 | a0001c0001t0001g0016a0001c0001t0001g0193a0001c0001t0001g0194others(7): Show | 11 | HG00597.hp2 HG02300.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.679-1298_679-1295d others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117243131 | |||||
| chr11:117243143
|
A | AATTT | 111 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0022others(108): Show | 113 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.679-1299_679-1298i others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117243143 | |||||
| chr11:117243143
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.679-1302A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243143 | ||||||
| chr11:117243147
|
A | AATTT | 100 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(97): Show | 108 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.679-1285_679-1282d others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 117243147 | |||||
| chr11:117243147
|
A | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(181): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.679-1298A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243147 | ||||||
| chr11:117243151
|
T | A | 1 | a0001c0001t0002g0095 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.679-1294T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243151 | ||||||
| chr11:117243173
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.679-1272G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243173 | ||||||
| chr11:117243177
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.679-1268C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243177 | ||||||
| chr11:117243392
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.679-1053C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243392 | ||||||
| chr11:117243397
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.679-1048C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243397 | ||||||
| chr11:117243457
|
T | C | 1 | a0001c0001t0003g0321 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.679-988T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243457 | ||||||
| chr11:117243698
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.679-747G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243698 | ||||||
| chr11:117243716
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.679-729T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243716 | ||||||
| chr11:117243742
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.679-703A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243742 | ||||||
| chr11:117243909
|
T | C | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG00738.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-536T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117243909 | ||||||
| chr11:117244085
|
G | A | 1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.679-360G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117244085 | ||||||
| chr11:117244223
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0005g0080a0001c0001t0005g0081others(1): Show | 4 | HG02055.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.679-222C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117244223 | ||||||
| chr11:117244348
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.679-97C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117244348 | ||||||
| chr11:117244367
|
A | G | 1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.679-78A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 4/14 | chr11 | 117244367 | ||||||
| chr11:117244635
|
T | TCAAACTT others(308): Show |
3 | a0001c0001t0001g0082a0001c0001t0005g0080a0001c0001t0008g0079 | 3 | HG02976.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.819+66_819+67insTT others(313): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117244635 | |||||
| chr11:117244635
|
T | TCAAACTT others(309): Show |
2 | a0001c0001t0001g0044a0001c0001t0005g0081 | 2 | HG00642.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.819+66_819+67insTT others(314): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117244635 | |||||
| chr11:117244635
|
T | TCAAACTT others(310): Show |
1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.819+66_819+67insTT others(315): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117244635 | |||||
| chr11:117244658
|
C | CTTTA | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+93_819+96dupAT others(2): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117244658 | |||||
| chr11:117244658
|
CTT | C | 3 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338 | 3 | HG01346.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.819+75_819+76delTT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117244658 | |||||
| chr11:117244658
|
CTTTA | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG00673.hp1 NA18979.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.819+93_819+96delAT others(2): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117244658 | |||||
| chr11:117244848
|
G | T | 1 | a0001c0001t0005g0080 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.819+263G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117244848 | ||||||
| chr11:117244864
|
G | T | 1 | a0001c0001t0014g0101 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.819+279G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117244864 | ||||||
| chr11:117244912
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.819+327C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117244912 | ||||||
| chr11:117245020
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.819+435T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245020 | ||||||
| chr11:117245047
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0125others(20): Show | 26 | HG02293.hp1 NA18612.hp2 NA18943.hp2 others(23): Show |
intron_variant | MODIFIER | c.819+462G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245047 | ||||||
| chr11:117245210
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.819+625A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245210 | ||||||
| chr11:117245343
|
C | CT | 31 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(28): Show | 35 | HG00642.hp1 HG01168.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.819+772dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117245343 | |||||
| chr11:117245440
|
C | T | 1 | a0001c0001t0003g0322 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.819+855C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245440 | ||||||
| chr11:117245465
|
A | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(3): Show | 6 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+880A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245465 | ||||||
| chr11:117245484
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.819+899C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245484 | ||||||
| chr11:117245488
|
C | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 18 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.819+903C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245488 | ||||||
| chr11:117245489
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.819+904G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245489 | ||||||
| chr11:117245596
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0062others(7): Show | 11 | HG01069.hp1 HG01168.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.819+1011C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245596 | ||||||
| chr11:117245642
|
A | G | 1 | a0001c0001t0002g0115 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.819+1057A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245642 | ||||||
| chr11:117245728
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.820-1081T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245728 | ||||||
| chr11:117245734
|
A | G | 132 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(129): Show | 137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.820-1075A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245734 | ||||||
| chr11:117245838
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.820-971A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245838 | ||||||
| chr11:117245994
|
T | G | 2 | a0001c0001t0001g0228a0001c0001t0004g0229 | 2 | HG01106.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.820-815T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117245994 | ||||||
| chr11:117246042
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.820-767C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117246042 | ||||||
| chr11:117246065
|
G | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.820-744G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117246065 | ||||||
| chr11:117246193
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.820-616G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117246193 | ||||||
| chr11:117246280
|
T | TA | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 28 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.820-515dupA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117246280 | |||||
| chr11:117246280
|
TA | T | 6 | a0001c0001t0001g0131a0001c0001t0001g0155a0001c0001t0001g0197others(3): Show | 6 | HG02897.hp1 NA18612.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-515delA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 117246280 | |||||
| chr11:117246301
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.820-508G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117246301 | ||||||
| chr11:117246510
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.820-299A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117246510 | ||||||
| chr11:117246620
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.820-189A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 5/14 | chr11 | 117246620 | ||||||
| chr11:117247031
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.959+83C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247031 | ||||||
| chr11:117247150
|
A | G | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 18 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.959+202A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247150 | ||||||
| chr11:117247180
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.959+232T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247180 | ||||||
| chr11:117247197
|
AGTTCGAT others(16): Show |
A | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.959+251_959+273del others(23): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117247197 | |||||
| chr11:117247201
|
C | A | 1 | a0001c0001t0001g0083 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.959+253C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247201 | ||||||
| chr11:117247202
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.959+254G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247202 | ||||||
| chr11:117247222
|
G | C | 1 | a0001c0001t0001g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.959+274G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247222 | ||||||
| chr11:117247223
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.959+275C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247223 | ||||||
| chr11:117247257
|
A | G | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 28 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.959+309A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247257 | ||||||
| chr11:117247321
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.959+373C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247321 | ||||||
| chr11:117247322
|
T | G | 131 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(128): Show | 136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.959+374T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247322 | ||||||
| chr11:117247367
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.959+419T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247367 | ||||||
| chr11:117247488
|
T | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 56 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.959+540T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247488 | ||||||
| chr11:117247504
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.959+556A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247504 | ||||||
| chr11:117247557
|
A | G | 2 | a0001c0001t0005g0080a0001c0001t0005g0081 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.959+609A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247557 | ||||||
| chr11:117247583
|
T | TGTAATTA others(2): Show |
132 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(129): Show | 137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.959+636_959+637ins others(9): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117247583 | |||||
| chr11:117247667
|
A | G | 2 | a0001c0001t0005g0080a0001c0001t0005g0081 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.959+719A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247667 | ||||||
| chr11:117247765
|
C | T | 131 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(128): Show | 136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.959+817C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247765 | ||||||
| chr11:117247828
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+880A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247828 | ||||||
| chr11:117247856
|
C | CA | 50 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0027others(47): Show | 52 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.959+923dupA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117247856 | |||||
| chr11:117247863
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0169 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.959+924_959+937del others(14): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117247863 | |||||
| chr11:117247867
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+919A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247867 | ||||||
| chr11:117247877
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.959+929C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247877 | ||||||
| chr11:117247977
|
T | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG00423.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.959+1029T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247977 | ||||||
| chr11:117247996
|
A | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(95): Show | 106 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.959+1048A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117247996 | ||||||
| chr11:117248244
|
A | ATTTTTTT others(182): Show |
1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+1301_959+1302i others(191): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117248244 | |||||
| chr11:117248313
|
T | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02258.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+1365T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117248313 | ||||||
| chr11:117248423
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.959+1475G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117248423 | ||||||
| chr11:117248513
|
G | A | 13 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 16 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+1565G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117248513 | ||||||
| chr11:117248574
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.959+1626C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117248574 | ||||||
| chr11:117248752
|
A | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 16 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+1804A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117248752 | ||||||
| chr11:117248836
|
A | G | 305 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(302): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.959+1888A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117248836 | ||||||
| chr11:117248868
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.959+1920A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117248868 | ||||||
| chr11:117249080
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+2132G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249080 | ||||||
| chr11:117249098
|
A | T | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.959+2150A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249098 | ||||||
| chr11:117249120
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+2172C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249120 | ||||||
| chr11:117249178
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.959+2230G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249178 | ||||||
| chr11:117249311
|
T | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(160): Show | 170 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.959+2363T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249311 | ||||||
| chr11:117249314
|
C | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+2366C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249314 | ||||||
| chr11:117249536
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.959+2588A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249536 | ||||||
| chr11:117249757
|
T | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.959+2809T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249757 | ||||||
| chr11:117249812
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0005g0080a0001c0001t0005g0081 | 3 | HG02055.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.959+2864T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117249812 | ||||||
| chr11:117250066
|
G | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0189a0001c0001t0001g0200others(7): Show | 11 | HG01123.hp2 HG01255.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.959+3118G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250066 | ||||||
| chr11:117250198
|
A | C | 1 | a0001c0001t0001g0283 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.959+3250A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250198 | ||||||
| chr11:117250198
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0131a0001c0001t0001g0150others(7): Show | 11 | NA18953.hp1 NA18959.hp1 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.959+3250A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250198 | ||||||
| chr11:117250282
|
T | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(96): Show | 107 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.959+3334T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250282 | ||||||
| chr11:117250327
|
T | G | 1 | a0001c0001t0010g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.959+3379T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250327 | ||||||
| chr11:117250331
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.959+3383A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250331 | ||||||
| chr11:117250449
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.959+3501G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250449 | ||||||
| chr11:117250458
|
T | G | 1 | a0001c0001t0001g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.959+3510T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250458 | ||||||
| chr11:117250491
|
TG | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 27 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.959+3544delG | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250491 | ||||||
| chr11:117250493
|
C | A | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 27 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.959+3545C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250493 | ||||||
| chr11:117250556
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.959+3608A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250556 | ||||||
| chr11:117250558
|
T | C | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+3610T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250558 | ||||||
| chr11:117250607
|
T | TA | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(38): Show | 44 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.959+3659_959+3660i others(3): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250607 | ||||||
| chr11:117250608
|
T | A | 1 | a0001c0001t0001g0326 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.959+3660T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250608 | ||||||
| chr11:117250609
|
A | AT | 30 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0007others(27): Show | 33 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.959+3671dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117250609 | |||||
| chr11:117250609
|
A | T | 45 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(42): Show | 48 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.959+3661A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250609 | ||||||
| chr11:117250610
|
T | A | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 45 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.959+3662T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250610 | ||||||
| chr11:117250610
|
T | TTA | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.959+3663_959+3664i others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117250610 | |||||
| chr11:117250610
|
T | TTATTA | 56 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 61 | HG00099.hp2 HG00642.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.959+3663_959+3664i others(7): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117250610 | |||||
| chr11:117250611
|
T | A | 1 | a0001c0001t0001g0326 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.959+3663T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250611 | ||||||
| chr11:117250701
|
A | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 55 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.959+3753A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250701 | ||||||
| chr11:117250759
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+3811C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250759 | ||||||
| chr11:117250859
|
A | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0196others(8): Show | 13 | HG00408.hp1 HG03704.hp2 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.959+3911A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250859 | ||||||
| chr11:117250930
|
G | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0141 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.959+3982G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250930 | ||||||
| chr11:117250936
|
G | A | 4 | a0001c0001t0002g0106a0001c0001t0002g0109a0001c0001t0002g0111others(1): Show | 4 | HG03540.hp1 NA20129.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+3988G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250936 | ||||||
| chr11:117250962
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.959+4014A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117250962 | ||||||
| chr11:117250992
|
GAA | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0142a0001c0001t0001g0147 | 3 | NA18964.hp1 NA18984.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.959+4047_959+4048d others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117250992 | |||||
| chr11:117251029
|
C | T | 1 | a0001c0001t0003g0307 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.959+4081C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251029 | ||||||
| chr11:117251059
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG00738.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+4111C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251059 | ||||||
| chr11:117251071
|
C | G | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 45 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.959+4123C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251071 | ||||||
| chr11:117251106
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.959+4158G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251106 | ||||||
| chr11:117251191
|
C | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0066 | 2 | HG01069.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.959+4243C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251191 | ||||||
| chr11:117251225
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.959+4277C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251225 | ||||||
| chr11:117251242
|
GGCTGACC others(2): Show |
G | 149 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(146): Show | 160 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.959+4304_959+4312d others(11): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251242 | |||||
| chr11:117251251
|
C | CCCCACCT others(33): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0162 | 2 | HG01070.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.959+4303_959+4304i others(42): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251251 | ||||||
| chr11:117251251
|
C | CCCCACCT others(82): Show |
1 | a0001c0001t0001g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.959+4303_959+4304i others(91): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251251 | ||||||
| chr11:117251251
|
C | CCCCACCT others(82): Show |
184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.959+4303_959+4304i others(91): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251251 | ||||||
| chr11:117251251
|
C | CCCCACCT others(82): Show |
1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.959+4303_959+4304i others(91): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251251 | ||||||
| chr11:117251251
|
C | CCCCACCT others(86): Show |
1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.959+4303_959+4304i others(95): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251251 | ||||||
| chr11:117251251
|
C | CCCCACCT others(82): Show |
1 | a0001c0001t0004g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.959+4303_959+4304i others(91): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251251 | ||||||
| chr11:117251256
|
A | AC | 22 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0044others(19): Show | 24 | HG00642.hp1 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.959+4315dupC | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251256 | |||||
| chr11:117251257
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.959+4309C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251257 | ||||||
| chr11:117251263
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0162 | 2 | HG01070.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.959+4315C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251263 | ||||||
| chr11:117251265
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.959+4317C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251265 | ||||||
| chr11:117251274
|
G | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 121 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.959+4326G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251274 | ||||||
| chr11:117251298
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(109): Show | 120 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.959+4350A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251298 | ||||||
| chr11:117251301
|
GGCTC | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 119 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.959+4354_959+4357d others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251301 | ||||||
| chr11:117251304
|
T | TGACCCCC others(3): Show |
1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+4356_959+4357i others(12): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251304 | ||||||
| chr11:117251308
|
C | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 119 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.959+4360C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251308 | ||||||
| chr11:117251311
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(109): Show | 120 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.959+4363T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251311 | ||||||
| chr11:117251312
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 119 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.959+4364T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251312 | ||||||
| chr11:117251316
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+4368A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251316 | ||||||
| chr11:117251316
|
AGTAGGGG others(17): Show |
A | 111 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 119 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.959+4369_959+4392d others(26): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251316 | ||||||
| chr11:117251318
|
T | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+4370T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251318 | ||||||
| chr11:117251319
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+4371A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251319 | ||||||
| chr11:117251325
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.959+4377G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251325 | ||||||
| chr11:117251335
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+4387A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251335 | ||||||
| chr11:117251338
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+4390C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251338 | ||||||
| chr11:117251338
|
C | T | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(1): Show | 4 | HG00642.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+4390C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251338 | ||||||
| chr11:117251339
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+4391G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251339 | ||||||
| chr11:117251341
|
C | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 119 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.959+4393C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251341 | ||||||
| chr11:117251344
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+4396T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251344 | ||||||
| chr11:117251345
|
CA | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 119 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.959+4398delA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251345 | ||||||
| chr11:117251346
|
ACCTCCCG others(91): Show |
A | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.959+4471_959+4568d others(100): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251346 | |||||
| chr11:117251370
|
GGGCGGGG others(42): Show |
G | 19 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0158others(16): Show | 21 | HG00140.hp1 HG01070.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.959+4471_959+4519d others(51): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251370 | |||||
| chr11:117251373
|
CGGGGGGC others(39): Show |
C | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.959+4428_959+4473d others(48): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251373 | |||||
| chr11:117251401
|
C | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(109): Show | 120 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.959+4453C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251401 | ||||||
| chr11:117251419
|
T | G | 61 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(58): Show | 64 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.959+4471T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251419 | ||||||
| chr11:117251419
|
TGGCGGGG others(42): Show |
T | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0046others(29): Show | 34 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.959+4572_959+4620d others(51): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251419 | |||||
| chr11:117251422
|
C | CA | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4474_959+4475i others(3): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251422 | ||||||
| chr11:117251423
|
G | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 38 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.959+4475G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251423 | ||||||
| chr11:117251424
|
G | A | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4476G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251424 | ||||||
| chr11:117251425
|
G | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 38 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.959+4477G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251425 | ||||||
| chr11:117251428
|
G | GGCTC | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 38 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.959+4480_959+4481i others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251428 | ||||||
| chr11:117251430
|
TGACCC | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+4483_959+4487d others(7): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251430 | ||||||
| chr11:117251430
|
TGACCCCC others(3): Show |
T | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028 | 3 | HG01256.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.959+4483_959+4492d others(12): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251430 | ||||||
| chr11:117251431
|
G | C | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 38 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.959+4483G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251431 | ||||||
| chr11:117251434
|
C | T | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 38 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.959+4486C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251434 | ||||||
| chr11:117251435
|
C | T | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 38 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.959+4487C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251435 | ||||||
| chr11:117251438
|
C | CAGTAGGG others(17): Show |
33 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 36 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(33): Show |
intron_variant | MODIFIER | c.959+4490_959+4491i others(26): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251438 | ||||||
| chr11:117251438
|
C | CAGTAGGG others(17): Show |
2 | a0001c0001t0005g0080a0001c0001t0005g0081 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.959+4490_959+4491i others(26): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251438 | ||||||
| chr11:117251438
|
C | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+4490C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251438 | ||||||
| chr11:117251440
|
A | C | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 38 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.959+4492A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251440 | ||||||
| chr11:117251440
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.959+4492A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251440 | ||||||
| chr11:117251440
|
ACCTC | A | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+4499_959+4502d others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251440 | |||||
| chr11:117251444
|
C | CA | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 38 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.959+4496_959+4497i others(3): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251444 | ||||||
| chr11:117251445
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028 | 3 | HG01256.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.959+4497C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251445 | ||||||
| chr11:117251446
|
C | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+4498C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251446 | ||||||
| chr11:117251448
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028 | 3 | HG01256.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.959+4500C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251448 | ||||||
| chr11:117251451
|
G | A | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+4503G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251451 | ||||||
| chr11:117251451
|
G | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028 | 3 | HG01256.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.959+4503G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251451 | ||||||
| chr11:117251452
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028 | 3 | HG01256.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.959+4504G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251452 | ||||||
| chr11:117251453
|
A | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+4505A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251453 | ||||||
| chr11:117251454
|
C | A | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+4506C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251454 | ||||||
| chr11:117251454
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028 | 3 | HG01256.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.959+4506C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251454 | ||||||
| chr11:117251455
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028 | 3 | HG01256.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.959+4507G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251455 | ||||||
| chr11:117251459
|
CGGCT | C | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+4515_959+4518d others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251459 | |||||
| chr11:117251460
|
G | T | 9 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0203others(6): Show | 9 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.959+4512G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251460 | ||||||
| chr11:117251462
|
CT | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028 | 3 | HG01256.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.959+4515delT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251462 | ||||||
| chr11:117251467
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0212a0001c0001t0001g0285others(1): Show | 4 | HG00609.hp1 NA18947.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+4519C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251467 | ||||||
| chr11:117251468
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(9): Show | 14 | NA18939.hp2 NA18945.hp1 NA18954.hp2 others(11): Show |
intron_variant | MODIFIER | c.959+4520G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251468 | ||||||
| chr11:117251472
|
G | A | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4524G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251472 | ||||||
| chr11:117251474
|
G | A | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4526G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251474 | ||||||
| chr11:117251476
|
GGCTGAC | G | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4529_959+4534d others(8): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251476 | ||||||
| chr11:117251481
|
ACCCCCCC others(43): Show |
A | 130 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(127): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.959+4540_959+4589d others(52): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251481 | |||||
| chr11:117251484
|
C | G | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4536C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251484 | ||||||
| chr11:117251489
|
A | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4541A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251489 | ||||||
| chr11:117251490
|
CCT | C | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4544_959+4545d others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117251490 | |||||
| chr11:117251493
|
C | A | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.959+4545C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251493 | ||||||
| chr11:117251517
|
G | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 18 | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.959+4569G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251517 | ||||||
| chr11:117251536
|
C | G | 135 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 140 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.959+4588C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251536 | ||||||
| chr11:117251540
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.959+4592C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251540 | ||||||
| chr11:117251584
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+4636A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251584 | ||||||
| chr11:117251733
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.959+4785G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251733 | ||||||
| chr11:117251891
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.959+4943C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251891 | ||||||
| chr11:117251918
|
G | C | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+4970G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117251918 | ||||||
| chr11:117252069
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.959+5121A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252069 | ||||||
| chr11:117252115
|
C | G | 19 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 21 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.959+5167C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252115 | ||||||
| chr11:117252315
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.959+5367A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252315 | ||||||
| chr11:117252457
|
T | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.959+5509T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252457 | ||||||
| chr11:117252502
|
C | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0062others(7): Show | 11 | HG01069.hp1 HG01168.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.959+5554C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252502 | ||||||
| chr11:117252581
|
C | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 56 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.959+5633C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252581 | ||||||
| chr11:117252591
|
G | T | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.959+5643G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252591 | ||||||
| chr11:117252645
|
C | G | 1 | a0001c0001t0001g0300 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.959+5697C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252645 | ||||||
| chr11:117252695
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.959+5747T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252695 | ||||||
| chr11:117252741
|
CG | C | 3 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0008g0079 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.959+5794delG | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252741 | ||||||
| chr11:117252742
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.959+5794G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252742 | ||||||
| chr11:117252743
|
C | A | 4 | a0001c0001t0001g0282a0001c0001t0005g0080a0001c0001t0005g0081others(1): Show | 4 | HG01099.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+5795C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252743 | ||||||
| chr11:117252771
|
T | C | 2 | a0001c0001t0005g0080a0001c0001t0005g0081 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.959+5823T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252771 | ||||||
| chr11:117252800
|
A | G | 5 | a0001c0001t0001g0200a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02055.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+5852A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252800 | ||||||
| chr11:117252807
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0232a0001c0001t0001g0255 | 3 | HG02080.hp1 HG02132.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.959+5859G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252807 | ||||||
| chr11:117252824
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.959+5876A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117252824 | ||||||
| chr11:117253066
|
G | A | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.959+6118G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253066 | ||||||
| chr11:117253274
|
G | A | 2 | a0001c0001t0002g0093a0001c0001t0002g0112 | 2 | HG00639.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.959+6326G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253274 | ||||||
| chr11:117253315
|
A | G | 1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.959+6367A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253315 | ||||||
| chr11:117253323
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.959+6375A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253323 | ||||||
| chr11:117253334
|
G | A | 1 | a0001c0001t0004g0060 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.959+6386G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253334 | ||||||
| chr11:117253467
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+6519A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253467 | ||||||
| chr11:117253569
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.959+6621C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253569 | ||||||
| chr11:117253590
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0005g0080a0001c0001t0005g0081 | 3 | HG02055.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.959+6642C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253590 | ||||||
| chr11:117253702
|
GACA | G | 8 | a0001c0001t0001g0128a0001c0001t0001g0277a0001c0001t0001g0278others(5): Show | 8 | HG02040.hp1 HG02080.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.959+6765_959+6767d others(5): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117253702 | |||||
| chr11:117253710
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0039others(1): Show | 4 | HG02071.hp1 NA18972.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+6762C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253710 | ||||||
| chr11:117253756
|
G | A | 1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.959+6808G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253756 | ||||||
| chr11:117253763
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.959+6815C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253763 | ||||||
| chr11:117253980
|
G | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(169): Show | 181 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.959+7032G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117253980 | ||||||
| chr11:117254063
|
G | C | 1 | a0001c0001t0002g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.959+7115G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254063 | ||||||
| chr11:117254174
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0031others(2): Show | 6 | HG00621.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.959+7226G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254174 | ||||||
| chr11:117254203
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.959+7255C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254203 | ||||||
| chr11:117254259
|
A | G | 1 | a0001c0001t0003g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.959+7311A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254259 | ||||||
| chr11:117254456
|
T | A | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.959+7508T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254456 | ||||||
| chr11:117254500
|
T | C | 144 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.959+7552T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254500 | ||||||
| chr11:117254629
|
C | CT | 20 | a0001c0001t0001g0262a0001c0001t0001g0306a0001c0001t0002g0092others(17): Show | 20 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(17): Show |
intron_variant | MODIFIER | c.959+7693dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117254629 | |||||
| chr11:117254632
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.959+7684T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254632 | ||||||
| chr11:117254654
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0295 | 2 | NA18967.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.959+7706C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254654 | ||||||
| chr11:117254655
|
G | C | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+7707G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254655 | ||||||
| chr11:117254710
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.959+7762G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254710 | ||||||
| chr11:117254942
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.959+7994C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254942 | ||||||
| chr11:117254959
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.959+8011G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254959 | ||||||
| chr11:117254986
|
T | G | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG00738.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+8038T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117254986 | ||||||
| chr11:117255053
|
A | G | 1 | a0001c0001t0004g0060 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.959+8105A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117255053 | ||||||
| chr11:117255243
|
C | T | 1 | a0001c0001t0013g0130 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.959+8295C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117255243 | ||||||
| chr11:117255605
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.959+8657A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117255605 | ||||||
| chr11:117255686
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.959+8738C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117255686 | ||||||
| chr11:117255777
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0179others(8): Show | 12 | HG00099.hp1 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.959+8829G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117255777 | ||||||
| chr11:117255994
|
A | G | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.959+9046A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117255994 | ||||||
| chr11:117256076
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+9128T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117256076 | ||||||
| chr11:117256396
|
A | T | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+9448A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117256396 | ||||||
| chr11:117256420
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.959+9472G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117256420 | ||||||
| chr11:117256443
|
G | A | 63 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(60): Show | 67 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.959+9495G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117256443 | ||||||
| chr11:117256465
|
C | T | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+9517C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117256465 | ||||||
| chr11:117256488
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.959+9540C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117256488 | ||||||
| chr11:117256664
|
AG | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(15): Show | 20 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.959+9717delG | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117256664 | ||||||
| chr11:117256904
|
C | T | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.959+9956C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117256904 | ||||||
| chr11:117257524
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.959+10576G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117257524 | ||||||
| chr11:117257532
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.959+10584T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117257532 | ||||||
| chr11:117257555
|
A | G | 147 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 154 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.959+10607A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117257555 | ||||||
| chr11:117257673
|
C | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0212a0001c0001t0001g0285others(1): Show | 4 | HG00609.hp1 NA18947.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+10725C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117257673 | ||||||
| chr11:117257674
|
A | G | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+10726A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117257674 | ||||||
| chr11:117258126
|
G | A | 3 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097 | 3 | HG00738.hp1 HG01123.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.959+11178G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258126 | ||||||
| chr11:117258248
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.959+11300T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258248 | ||||||
| chr11:117258255
|
A | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.959+11307A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258255 | ||||||
| chr11:117258256
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.959+11308A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258256 | ||||||
| chr11:117258342
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.959+11394C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258342 | ||||||
| chr11:117258344
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.959+11396G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258344 | ||||||
| chr11:117258367
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(31): Show | 36 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.959+11419C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258367 | ||||||
| chr11:117258392
|
A | G | 2 | a0001c0001t0001g0257a0001c0001t0010g0303 | 2 | HG01358.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.959+11444A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258392 | ||||||
| chr11:117258431
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.959+11483T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258431 | ||||||
| chr11:117258516
|
A | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(31): Show | 36 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.959+11568A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258516 | ||||||
| chr11:117258588
|
T | A | 1 | a0001c0001t0001g0332 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.959+11640T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258588 | ||||||
| chr11:117258670
|
A | G | 3 | a0001c0001t0001g0305a0001c0003t0001g0127a0001c0003t0001g0149 | 3 | NA18965.hp2 NA18994.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.959+11722A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258670 | ||||||
| chr11:117258711
|
T | C | 1 | a0001c0001t0011g0033 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.959+11763T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258711 | ||||||
| chr11:117258795
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.959+11847A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258795 | ||||||
| chr11:117258801
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0010g0303 | 2 | HG01358.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.959+11853G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258801 | ||||||
| chr11:117258880
|
T | C | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+11932T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258880 | ||||||
| chr11:117258921
|
C | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(44): Show | 51 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.959+11973C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258921 | ||||||
| chr11:117258935
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.959+11987T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117258935 | ||||||
| chr11:117259042
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.959+12094C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117259042 | ||||||
| chr11:117259148
|
G | C | 1 | a0001c0001t0001g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.959+12200G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117259148 | ||||||
| chr11:117259208
|
C | T | 1 | a0001c0001t0003g0307 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.959+12260C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117259208 | ||||||
| chr11:117260077
|
AT | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(42): Show | 49 | HG01167.hp2 HG01175.hp1 HG01975.hp1 others(46): Show |
intron_variant | MODIFIER | c.959+13142delT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260077 | |||||
| chr11:117260087
|
T | A | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+13139T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260087 | ||||||
| chr11:117260256
|
G | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(3): Show | 6 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.959+13308G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260256 | ||||||
| chr11:117260268
|
A | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0212a0001c0001t0001g0285others(1): Show | 4 | HG00609.hp1 NA18947.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+13320A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260268 | ||||||
| chr11:117260314
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.959+13366G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260314 | ||||||
| chr11:117260349
|
G | A | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+13401G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260349 | ||||||
| chr11:117260372
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+13424T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260372 | ||||||
| chr11:117260427
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.959+13479C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260427 | ||||||
| chr11:117260446
|
A | T | 1 | a0001c0001t0001g0293 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.959+13498A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260446 | ||||||
| chr11:117260472
|
T | C | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+13524T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260472 | ||||||
| chr11:117260528
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.959+13580C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260528 | ||||||
| chr11:117260533
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.959+13585C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260533 | ||||||
| chr11:117260570
|
G | A | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(170): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.959+13622G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260570 | ||||||
| chr11:117260682
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.959+13734A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260682 | ||||||
| chr11:117260692
|
C | G | 1 | a0001c0001t0006g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.959+13744C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260692 | ||||||
| chr11:117260708
|
A | G | 1 | a0001c0001t0003g0315 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.959+13760A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260708 | ||||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
1 | a0001c0001t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
1 | a0001c0001t0001g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
38 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0007others(35): Show | 41 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
1 | a0001c0001t0001g0181 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1443): Show |
1 | a0001c0001t0007g0265 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1454): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1443): Show |
4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1454): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
18 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(15): Show | 20 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(162): Show | 174 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1443): Show |
1 | a0001c0001t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1454): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
18 | a0001c0001t0001g0071a0001c0001t0001g0089a0001c0001t0001g0306others(15): Show | 18 | HG03225.hp1 HG03710.hp2 HG03834.hp2 others(15): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1443): Show |
27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(24): Show | 29 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1454): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1443): Show |
7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028others(4): Show | 7 | HG01256.hp2 HG01346.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1454): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(2): Show | 5 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1443): Show |
1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1454): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
1 | a0001c0001t0001g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
46 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(43): Show | 50 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1443): Show |
1 | a0001c0001t0001g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1454): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1443): Show |
1 | a0001c0001t0001g0038 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1454): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.959+13842_959+1384 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260777
|
C | CCCGAGTA others(1442): Show |
1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+13837_959+1383 others(1453): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117260777 | |||||
| chr11:117260803
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.959+13855C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260803 | ||||||
| chr11:117260881
|
C | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+13933C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260881 | ||||||
| chr11:117260948
|
C | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.959+14000C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117260948 | ||||||
| chr11:117261003
|
A | G | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.959+14055A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261003 | ||||||
| chr11:117261058
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.959+14110T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261058 | ||||||
| chr11:117261072
|
C | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.959+14124C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261072 | ||||||
| chr11:117261082
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+14134T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261082 | ||||||
| chr11:117261169
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.959+14221A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261169 | ||||||
| chr11:117261217
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.959+14269A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261217 | ||||||
| chr11:117261453
|
G | T | 3 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0008g0079 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.959+14505G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261453 | ||||||
| chr11:117261599
|
T | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(45): Show | 53 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.959+14651T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261599 | ||||||
| chr11:117261756
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.959+14808C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261756 | ||||||
| chr11:117261851
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.959+14903G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261851 | ||||||
| chr11:117261854
|
C | G | 1 | a0001c0001t0001g0281 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.959+14906C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261854 | ||||||
| chr11:117261938
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.959+14990A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261938 | ||||||
| chr11:117261977
|
A | G | 1 | a0001c0001t0013g0130 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.959+15029A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261977 | ||||||
| chr11:117261979
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.959+15031C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117261979 | ||||||
| chr11:117262046
|
G | GT | 8 | a0001c0001t0001g0037a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.959+15109dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262046 | |||||
| chr11:117262047
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.959+15099T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262047 | ||||||
| chr11:117262092
|
A | G | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.959+15144A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262092 | ||||||
| chr11:117262093
|
C | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.959+15145C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262093 | ||||||
| chr11:117262106
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0159a0001c0001t0001g0163others(2): Show | 7 | NA18954.hp2 NA18959.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+15158G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262106 | ||||||
| chr11:117262115
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+15167G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262115 | ||||||
| chr11:117262115
|
G | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0235 | 2 | HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.959+15167G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262115 | ||||||
| chr11:117262235
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.959+15287C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262235 | ||||||
| chr11:117262309
|
A | G | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.959+15361A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262309 | ||||||
| chr11:117262362
|
C | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(44): Show | 51 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.959+15414C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262362 | ||||||
| chr11:117262503
|
C | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(170): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.959+15555C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262503 | ||||||
| chr11:117262526
|
T | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0123a0001c0001t0001g0124others(12): Show | 16 | HG00099.hp2 HG00597.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+15578T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262526 | ||||||
| chr11:117262662
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(31): Show | 36 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.959+15714G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262662 | ||||||
| chr11:117262707
|
T | TTG | 21 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0045others(18): Show | 23 | HG00642.hp1 HG01070.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+15785_959+1578 others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262707 | |||||
| chr11:117262707
|
T | TTGTG | 25 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0169others(22): Show | 26 | HG01361.hp1 HG01433.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.959+15783_959+1578 others(8): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262707 | |||||
| chr11:117262707
|
T | TTGTGTG | 186 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(183): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.959+15781_959+1578 others(10): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262707 | |||||
| chr11:117262707
|
T | TTGTGTGT others(1): Show |
24 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0057others(21): Show | 25 | HG00099.hp1 HG00738.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.959+15779_959+1578 others(12): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262707 | |||||
| chr11:117262707
|
T | TTGTGTGT others(3): Show |
11 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0086others(8): Show | 11 | HG01243.hp1 HG01261.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.959+15777_959+1578 others(14): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262707 | |||||
| chr11:117262707
|
T | TTGTGTGT others(5): Show |
23 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0024others(20): Show | 24 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.959+15775_959+1578 others(16): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262707 | |||||
| chr11:117262707
|
T | TTGTGTGT others(7): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0034others(5): Show | 9 | HG01975.hp2 HG02027.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.959+15773_959+1578 others(18): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262707 | |||||
| chr11:117262707
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0001g0327 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.959+15771_959+1578 others(20): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262707 | |||||
| chr11:117262726
|
T | TGTGTGTG others(333): Show |
1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959+15786_959+1578 others(344): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117262726 | |||||
| chr11:117262899
|
C | T | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0004g0072 | 3 | HG02572.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.959+15951C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262899 | ||||||
| chr11:117262956
|
A | G | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.959+16008A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117262956 | ||||||
| chr11:117263026
|
T | G | 5 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | HG00673.hp2 HG02129.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+16078T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263026 | ||||||
| chr11:117263094
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.959+16146A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263094 | ||||||
| chr11:117263276
|
GA | G | 142 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(139): Show | 149 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.959+16337delA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117263276 | |||||
| chr11:117263285
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.959+16337A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263285 | ||||||
| chr11:117263286
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.959+16338C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263286 | ||||||
| chr11:117263312
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.959+16364G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263312 | ||||||
| chr11:117263318
|
T | TCTCC | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.959+16370_959+1637 others(8): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263318 | ||||||
| chr11:117263319
|
T | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.959+16371T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263319 | ||||||
| chr11:117263333
|
T | C | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+16385T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263333 | ||||||
| chr11:117263378
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(31): Show | 36 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.959+16430C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263378 | ||||||
| chr11:117263436
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 6 | HG01361.hp1 HG01433.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.960-16472C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263436 | ||||||
| chr11:117263526
|
G | C | 1 | a0001c0001t0001g0295 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.960-16382G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263526 | ||||||
| chr11:117263610
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.960-16298C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263610 | ||||||
| chr11:117263936
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.960-15972A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263936 | ||||||
| chr11:117263964
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.960-15944T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117263964 | ||||||
| chr11:117264045
|
G | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-15863G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264045 | ||||||
| chr11:117264050
|
C | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-15858C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264050 | ||||||
| chr11:117264060
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.960-15848C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264060 | ||||||
| chr11:117264106
|
C | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-15802C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264106 | ||||||
| chr11:117264107
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.960-15801G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264107 | ||||||
| chr11:117264138
|
C | T | 2 | a0001c0001t0003g0317a0001c0001t0003g0319 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.960-15770C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264138 | ||||||
| chr11:117264182
|
T | G | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-15726T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264182 | ||||||
| chr11:117264196
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.960-15712G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264196 | ||||||
| chr11:117264277
|
C | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-15631C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264277 | ||||||
| chr11:117264298
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(15): Show | 20 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.960-15610G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264298 | ||||||
| chr11:117264507
|
T | A | 3 | a0001c0001t0001g0201a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02809.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.960-15401T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264507 | ||||||
| chr11:117264559
|
G | A | 1 | a0001c0001t0012g0144 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.960-15349G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264559 | ||||||
| chr11:117264899
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.960-15009A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264899 | ||||||
| chr11:117264991
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.960-14917C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264991 | ||||||
| chr11:117264992
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.960-14916C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264992 | ||||||
| chr11:117264999
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.960-14909C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117264999 | ||||||
| chr11:117265090
|
T | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-14818T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265090 | ||||||
| chr11:117265151
|
T | G | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.960-14757T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265151 | ||||||
| chr11:117265245
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.960-14663G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265245 | ||||||
| chr11:117265354
|
T | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-14554T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265354 | ||||||
| chr11:117265413
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.960-14495G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265413 | ||||||
| chr11:117265561
|
C | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(31): Show | 36 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.960-14347C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265561 | ||||||
| chr11:117265574
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-14334C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265574 | ||||||
| chr11:117265658
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.960-14250G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265658 | ||||||
| chr11:117265662
|
G | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-14246G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265662 | ||||||
| chr11:117265704
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.960-14204C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265704 | ||||||
| chr11:117265706
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-14202C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265706 | ||||||
| chr11:117265925
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.960-13983A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117265925 | ||||||
| chr11:117266268
|
C | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-13640C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266268 | ||||||
| chr11:117266275
|
C | A | 5 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0243others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.960-13633C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266275 | ||||||
| chr11:117266286
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.960-13622T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266286 | ||||||
| chr11:117266419
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.960-13489G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266419 | ||||||
| chr11:117266424
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-13484A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266424 | ||||||
| chr11:117266462
|
C | T | 3 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0008g0079 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.960-13446C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266462 | ||||||
| chr11:117266539
|
G | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-13369G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266539 | ||||||
| chr11:117266547
|
A | G | 1 | a0001c0001t0003g0318 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.960-13361A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266547 | ||||||
| chr11:117266854
|
T | C | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-13054T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266854 | ||||||
| chr11:117266859
|
C | CT | 299 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(296): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.960-13036dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117266859 | |||||
| chr11:117266917
|
C | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-12991C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266917 | ||||||
| chr11:117266931
|
G | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-12977G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117266931 | ||||||
| chr11:117266973
|
C | CA | 110 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(107): Show | 111 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.960-12916dupA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117266973 | |||||
| chr11:117266973
|
C | CAA | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0185others(4): Show | 7 | HG00673.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.960-12917_960-1291 others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117266973 | |||||
| chr11:117267022
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.960-12886G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267022 | ||||||
| chr11:117267471
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.960-12437G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267471 | ||||||
| chr11:117267575
|
G | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-12333G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267575 | ||||||
| chr11:117267585
|
C | T | 2 | a0001c0001t0002g0304a0001c0001t0004g0060 | 2 | HG01070.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.960-12323C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267585 | ||||||
| chr11:117267687
|
C | G | 149 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 156 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.960-12221C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267687 | ||||||
| chr11:117267707
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.960-12201C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267707 | ||||||
| chr11:117267740
|
A | G | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.960-12168A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267740 | ||||||
| chr11:117267769
|
T | C | 12 | a0001c0001t0001g0015a0001c0001t0001g0264a0001c0001t0001g0268others(9): Show | 13 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.960-12139T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267769 | ||||||
| chr11:117267778
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.960-12130C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267778 | ||||||
| chr11:117267919
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-11989G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267919 | ||||||
| chr11:117267955
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.960-11953A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117267955 | ||||||
| chr11:117268120
|
T | A | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.960-11788T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268120 | ||||||
| chr11:117268160
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.960-11748G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268160 | ||||||
| chr11:117268166
|
C | A | 1 | a0001c0001t0001g0329 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.960-11742C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268166 | ||||||
| chr11:117268405
|
G | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-11503G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268405 | ||||||
| chr11:117268532
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.960-11376A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268532 | ||||||
| chr11:117268535
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.960-11373A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268535 | ||||||
| chr11:117268569
|
A | G | 1 | a0001c0001t0004g0075 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.960-11339A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268569 | ||||||
| chr11:117268772
|
T | G | 1 | a0001c0001t0001g0215 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.960-11136T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268772 | ||||||
| chr11:117268830
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.960-11078G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268830 | ||||||
| chr11:117268913
|
G | A | 1 | a0001c0001t0013g0130 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.960-10995G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117268913 | ||||||
| chr11:117269016
|
T | G | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.960-10892T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117269016 | ||||||
| chr11:117269327
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.960-10581A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117269327 | ||||||
| chr11:117269432
|
G | A | 38 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(35): Show | 40 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.960-10476G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117269432 | ||||||
| chr11:117269650
|
A | G | 1 | a0001c0001t0002g0006 | 2 | HG02027.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.960-10258A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117269650 | ||||||
| chr11:117269767
|
T | TA | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-10140dupA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117269767 | |||||
| chr11:117270183
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.960-9725T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270183 | ||||||
| chr11:117270208
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG00738.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.960-9700C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270208 | ||||||
| chr11:117270241
|
C | CT | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0043others(12): Show | 17 | HG00140.hp1 HG01261.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.960-9641dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117270241 | |||||
| chr11:117270241
|
C | CTT | 6 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0089others(3): Show | 6 | HG00642.hp1 HG02572.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.960-9642_960-9641d others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117270241 | |||||
| chr11:117270241
|
CT | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0046a0001c0001t0001g0071others(18): Show | 21 | HG00323.hp1 HG00738.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.960-9641delT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117270241 | |||||
| chr11:117270241
|
CTTTTTTT others(1): Show |
C | 21 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0050others(18): Show | 23 | HG01069.hp1 HG01070.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.960-9648_960-9641d others(10): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117270241 | |||||
| chr11:117270245
|
T | TC | 6 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01099.hp1 HG03239.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.960-9663_960-9662i others(3): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270245 | ||||||
| chr11:117270246
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(56): Show | 65 | HG00099.hp2 HG01070.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.960-9662T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270246 | ||||||
| chr11:117270247
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0071a0001c0001t0001g0167 | 3 | HG01257.hp1 HG03041.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.960-9661T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270247 | ||||||
| chr11:117270286
|
G | GT | 9 | a0001c0001t0001g0059a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG01358.hp2 HG02486.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.960-9620dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117270286 | |||||
| chr11:117270404
|
T | G | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.960-9504T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270404 | ||||||
| chr11:117270493
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.960-9415A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270493 | ||||||
| chr11:117270549
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.960-9359T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270549 | ||||||
| chr11:117270691
|
A | G | 1 | a0001c0001t0001g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.960-9217A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270691 | ||||||
| chr11:117270701
|
G | A | 1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.960-9207G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270701 | ||||||
| chr11:117270753
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(85): Show | 94 | HG00099.hp2 HG01070.hp1 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.960-9155T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270753 | ||||||
| chr11:117270928
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.960-8980G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117270928 | ||||||
| chr11:117271155
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.960-8753C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117271155 | ||||||
| chr11:117271376
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.960-8532G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117271376 | ||||||
| chr11:117271389
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.960-8519A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117271389 | ||||||
| chr11:117271698
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG00738.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-8210G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117271698 | ||||||
| chr11:117271724
|
C | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(32): Show | 37 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.960-8184C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117271724 | ||||||
| chr11:117271909
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0275 | 3 | HG01361.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.960-7999C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117271909 | ||||||
| chr11:117271964
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.960-7944C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117271964 | ||||||
| chr11:117272118
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0326others(3): Show | 8 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.960-7790T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272118 | ||||||
| chr11:117272211
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0137 | 3 | HG01361.hp1 HG01433.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.960-7697A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272211 | ||||||
| chr11:117272300
|
C | A | 1 | a0001c0001t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.960-7608C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272300 | ||||||
| chr11:117272323
|
G | A | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-7585G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272323 | ||||||
| chr11:117272436
|
G | C | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.960-7472G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272436 | ||||||
| chr11:117272469
|
G | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-7439G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272469 | ||||||
| chr11:117272470
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.960-7438G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272470 | ||||||
| chr11:117272494
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG00738.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-7414C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272494 | ||||||
| chr11:117272531
|
C | CGTTT | 38 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(35): Show | 40 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.960-7377_960-7376i others(6): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272531 | ||||||
| chr11:117272609
|
A | AT | 21 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0306others(18): Show | 23 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(20): Show |
intron_variant | MODIFIER | c.960-7283dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117272609 | |||||
| chr11:117272609
|
A | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0171 | 2 | HG03041.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.960-7299A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272609 | ||||||
| chr11:117272609
|
AT | A | 26 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0037others(23): Show | 26 | HG00323.hp2 HG01069.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.960-7283delT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117272609 | |||||
| chr11:117272610
|
T | A | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.960-7298T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272610 | ||||||
| chr11:117272624
|
T | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.960-7284T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272624 | ||||||
| chr11:117272625
|
T | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(124): Show | 133 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.960-7283T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272625 | ||||||
| chr11:117272626
|
A | T | 15 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 15 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.960-7282A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272626 | ||||||
| chr11:117272663
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-7245A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272663 | ||||||
| chr11:117272789
|
A | C | 1 | a0001c0001t0003g0307 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.960-7119A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272789 | ||||||
| chr11:117272798
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.960-7110A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272798 | ||||||
| chr11:117272865
|
T | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-7043T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272865 | ||||||
| chr11:117272889
|
G | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-7019G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117272889 | ||||||
| chr11:117273004
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.960-6904C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273004 | ||||||
| chr11:117273125
|
G | A | 1 | a0001c0001t0003g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.960-6783G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273125 | ||||||
| chr11:117273358
|
G | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(32): Show | 37 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.960-6550G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273358 | ||||||
| chr11:117273360
|
T | TTTA | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(164): Show | 176 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.960-6530_960-6528d others(5): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117273360 | |||||
| chr11:117273365
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.960-6543T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273365 | ||||||
| chr11:117273416
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.960-6492T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273416 | ||||||
| chr11:117273478
|
T | TA | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.960-6430_960-6429i others(3): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273478 | ||||||
| chr11:117273482
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.960-6426G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273482 | ||||||
| chr11:117273639
|
T | C | 38 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(35): Show | 40 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.960-6269T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273639 | ||||||
| chr11:117273782
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.960-6126C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273782 | ||||||
| chr11:117273922
|
G | T | 1 | a0001c0001t0002g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.960-5986G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117273922 | ||||||
| chr11:117274011
|
A | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-5897A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274011 | ||||||
| chr11:117274100
|
A | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(44): Show | 51 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.960-5808A>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274100 | ||||||
| chr11:117274154
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0142 | 2 | NA18964.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.960-5754A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274154 | ||||||
| chr11:117274210
|
TACATGTG others(19): Show |
T | 1 | a0001c0001t0001g0298 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.960-5696_960-5671d others(28): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274210 | |||||
| chr11:117274263
|
GAGT | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(3): Show | 6 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.960-5641_960-5639d others(5): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274263 | |||||
| chr11:117274315
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.960-5593A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274315 | ||||||
| chr11:117274337
|
C | A | 143 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.960-5571C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274337 | ||||||
| chr11:117274356
|
C | CT | 193 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(190): Show | 203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.960-5529dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274356 | |||||
| chr11:117274356
|
C | CTT | 74 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(71): Show | 78 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.960-5530_960-5529d others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274356 | |||||
| chr11:117274356
|
C | CTTT | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0031others(7): Show | 10 | HG00558.hp2 HG00621.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.960-5531_960-5529d others(5): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274356 | |||||
| chr11:117274356
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0271 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.960-5539_960-5529d others(13): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274356 | |||||
| chr11:117274364
|
T | TTC | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0326others(3): Show | 8 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.960-5543_960-5542i others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274364 | |||||
| chr11:117274536
|
T | A | 4 | a0001c0001t0001g0242a0001c0001t0001g0247a0001c0001t0001g0251others(1): Show | 4 | HG00408.hp2 NA18947.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-5372T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274536 | ||||||
| chr11:117274565
|
A | G | 2 | a0001c0001t0005g0080a0001c0001t0005g0081 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.960-5343A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274565 | ||||||
| chr11:117274583
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.960-5325A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274583 | ||||||
| chr11:117274639
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.960-5269G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274639 | ||||||
| chr11:117274675
|
C | CT | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(286): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.960-5217dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274675 | |||||
| chr11:117274675
|
C | CTT | 7 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 8 | HG01891.hp2 HG02145.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.960-5218_960-5217d others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117274675 | |||||
| chr11:117274761
|
G | A | 3 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0008g0079 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.960-5147G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274761 | ||||||
| chr11:117274848
|
T | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.960-5060T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274848 | ||||||
| chr11:117274866
|
C | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.960-5042C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274866 | ||||||
| chr11:117274867
|
G | A | 1 | a0001c0001t0003g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.960-5041G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117274867 | ||||||
| chr11:117275099
|
G | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.960-4809G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275099 | ||||||
| chr11:117275185
|
T | C | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.960-4723T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275185 | ||||||
| chr11:117275202
|
T | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.960-4706T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275202 | ||||||
| chr11:117275233
|
T | C | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.960-4675T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275233 | ||||||
| chr11:117275247
|
A | G | 1 | a0001c0001t0001g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.960-4661A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275247 | ||||||
| chr11:117275310
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.960-4598C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275310 | ||||||
| chr11:117275574
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.960-4334G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275574 | ||||||
| chr11:117275881
|
A | G | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-4027A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275881 | ||||||
| chr11:117275916
|
C | A | 1 | a0001c0001t0001g0298 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.960-3992C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275916 | ||||||
| chr11:117275917
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.960-3991A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275917 | ||||||
| chr11:117275918
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.960-3990G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117275918 | ||||||
| chr11:117276043
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.960-3865A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276043 | ||||||
| chr11:117276062
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.960-3846A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276062 | ||||||
| chr11:117276114
|
A | G | 3 | a0001c0001t0003g0308a0001c0001t0003g0311a0001c0001t0003g0316 | 3 | NA18955.hp2 NA19002.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.960-3794A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276114 | ||||||
| chr11:117276345
|
C | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG00558.hp1 NA18983.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.960-3563C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276345 | ||||||
| chr11:117276386
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.960-3522G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276386 | ||||||
| chr11:117276394
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.960-3514G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276394 | ||||||
| chr11:117276460
|
T | A | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-3448T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276460 | ||||||
| chr11:117276464
|
C | G | 3 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097 | 3 | HG00738.hp1 HG01123.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.960-3444C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276464 | ||||||
| chr11:117276494
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.960-3414A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276494 | ||||||
| chr11:117276502
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.960-3406A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276502 | ||||||
| chr11:117276564
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.960-3344C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276564 | ||||||
| chr11:117276777
|
A | G | 2 | a0001c0001t0002g0098a0001c0001t0002g0120 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.960-3131A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276777 | ||||||
| chr11:117276958
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.960-2950C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117276958 | ||||||
| chr11:117277106
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.960-2802G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117277106 | ||||||
| chr11:117277271
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.960-2637G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117277271 | ||||||
| chr11:117277330
|
T | TA | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0082others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.960-2569dupA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117277330 | |||||
| chr11:117277389
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.960-2519C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117277389 | ||||||
| chr11:117277769
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.960-2139C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117277769 | ||||||
| chr11:117277798
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.960-2110C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117277798 | ||||||
| chr11:117277867
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.960-2041G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117277867 | ||||||
| chr11:117277890
|
T | A | 3 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0002g0175 | 3 | HG03540.hp1 NA20752.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.960-2018T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117277890 | ||||||
| chr11:117277950
|
G | C | 1 | a0001c0001t0001g0219 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.960-1958G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117277950 | ||||||
| chr11:117277973
|
C | CA | 7 | a0001c0001t0001g0124a0001c0001t0001g0233a0001c0001t0001g0235others(4): Show | 8 | HG01975.hp1 HG01993.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.960-1922dupA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117277973 | |||||
| chr11:117277973
|
CA | C | 9 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0142others(6): Show | 9 | HG02258.hp2 HG02895.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.960-1922delA | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117277973 | |||||
| chr11:117278016
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.960-1892A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278016 | ||||||
| chr11:117278070
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.960-1838C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278070 | ||||||
| chr11:117278188
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG00621.hp1 NA18982.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.960-1720C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278188 | ||||||
| chr11:117278195
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.960-1713T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278195 | ||||||
| chr11:117278205
|
G | A | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.960-1703G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278205 | ||||||
| chr11:117278236
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.960-1672G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278236 | ||||||
| chr11:117278261
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.960-1647G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278261 | ||||||
| chr11:117278293
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-1615G>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278293 | ||||||
| chr11:117278296
|
T | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.960-1612T>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278296 | ||||||
| chr11:117278382
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.960-1526A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278382 | ||||||
| chr11:117278615
|
T | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 7 | HG01074.hp2 HG01243.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.960-1293T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278615 | ||||||
| chr11:117278689
|
A | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(31): Show | 36 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.960-1219A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117278689 | ||||||
| chr11:117279305
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-603A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279305 | ||||||
| chr11:117279323
|
C | CT | 49 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0051others(46): Show | 50 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.960-559dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117279323 | |||||
| chr11:117279323
|
CT | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(52): Show | 59 | HG00323.hp2 HG00558.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.960-559delT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 117279323 | |||||
| chr11:117279360
|
C | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0151others(11): Show | 16 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.960-548C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279360 | ||||||
| chr11:117279475
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.960-433G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279475 | ||||||
| chr11:117279494
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(49): Show | 56 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.960-414G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279494 | ||||||
| chr11:117279533
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0141 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.960-375C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279533 | ||||||
| chr11:117279617
|
G | A | 1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.960-291G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279617 | ||||||
| chr11:117279724
|
T | C | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02040.hp1 NA18943.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.960-184T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279724 | ||||||
| chr11:117279786
|
C | T | 3 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0009g0076 | 3 | HG01167.hp2 HG01175.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.960-122C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279786 | ||||||
| chr11:117279796
|
G | T | 3 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0008g0079 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.960-112G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279796 | ||||||
| chr11:117279844
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.960-64C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | 117279844 | ||||||
| chr11:117280058
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1056+54A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 7/14 | chr11 | 117280058 | ||||||
| chr11:117280298
|
A | AGTTT | 73 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(70): Show | 77 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1145+56_1145+59dup others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 117280298 | |||||
| chr11:117280298
|
AGTTT | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 21 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1145+56_1145+59del others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 117280298 | |||||
| chr11:117280312
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1145+53T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280312 | ||||||
| chr11:117280462
|
A | G | 3 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0008g0079 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1145+203A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280462 | ||||||
| chr11:117280476
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1145+217T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280476 | ||||||
| chr11:117280604
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1145+345C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280604 | ||||||
| chr11:117280662
|
C | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(45): Show | 52 | HG00099.hp2 HG01099.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1145+403C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280662 | ||||||
| chr11:117280696
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 87 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.1145+437G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280696 | ||||||
| chr11:117280828
|
G | T | 1 | a0001c0002t0001g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1146-486G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280828 | ||||||
| chr11:117280860
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1146-454A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280860 | ||||||
| chr11:117280891
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1146-423G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280891 | ||||||
| chr11:117280927
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1146-387G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117280927 | ||||||
| chr11:117280982
|
C | CT | 232 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(229): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1146-311dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 117280982 | |||||
| chr11:117280982
|
C | CTT | 30 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0001g0085others(27): Show | 30 | HG00597.hp2 HG02109.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.1146-312_1146-311d others(4): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 117280982 | |||||
| chr11:117280982
|
C | CTTT | 17 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0159others(14): Show | 19 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1146-313_1146-311d others(5): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 117280982 | |||||
| chr11:117281136
|
G | A | 1 | a0001c0001t0008g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1146-178G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 8/14 | chr11 | 117281136 | ||||||
| chr11:117281478
|
C | CT | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0050others(19): Show | 24 | HG01069.hp1 HG01070.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1236+78dupT | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 117281478 | |||||
| chr11:117281824
|
G | T | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.1336-70G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 10/14 | chr11 | 117281824 | ||||||
| chr11:117281847
|
T | C | 16 | a0001c0001t0001g0306a0001c0001t0003g0308a0001c0001t0003g0309others(13): Show | 16 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(13): Show |
intron_variant | MODIFIER | c.1336-47T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 10/14 | chr11 | 117281847 | ||||||
| chr11:117282704
|
T | C | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(36): Show | 41 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1846-42T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 12/14 | chr11 | 117282704 | ||||||
| chr11:117282896
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG00738.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1950+46G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 13/14 | chr11 | 117282896 | ||||||
| chr11:117282966
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1950+116G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 13/14 | chr11 | 117282966 | ||||||
| chr11:117283014
|
T | C | 3 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0321 | 3 | NA18957.hp2 NA18975.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1951-101T>C | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 13/14 | chr11 | 117283014 | ||||||
| chr11:117283099
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1951-16C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 13/14 | chr11 | 117283099 | ||||||
| chr11:117283310
|
A | G | 4 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2046+100A>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117283310 | ||||||
| chr11:117283375
|
G | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.2046+165G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117283375 | ||||||
| chr11:117283392
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2046+182G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117283392 | ||||||
| chr11:117283559
|
C | T | 1 | a0001c0001t0007g0265 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2046+349C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117283559 | ||||||
| chr11:117283601
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2046+391C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117283601 | ||||||
| chr11:117284088
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0328 | 3 | HG02486.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2046+878G>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284088 | ||||||
| chr11:117284115
|
A | T | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2046+905A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284115 | ||||||
| chr11:117284143
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2046+933C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284143 | ||||||
| chr11:117284306
|
G | T | 1 | a0001c0001t0003g0315 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2047-780G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284306 | ||||||
| chr11:117284307
|
T | G | 1 | a0001c0001t0003g0315 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2047-779T>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284307 | ||||||
| chr11:117284822
|
C | T | 2 | a0001c0001t0001g0133a0001c0002t0001g0070 | 2 | HG02451.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2047-264C>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284822 | ||||||
| chr11:117284859
|
A | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2047-227A>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284859 | ||||||
| chr11:117284861
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2047-225C>G | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284861 | ||||||
| chr11:117284965
|
C | A | 1 | a0001c0001t0002g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2047-121C>A | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284965 | ||||||
| chr11:117284980
|
G | T | 38 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0022others(35): Show | 40 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.2047-106G>T | RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 14/14 | chr11 | 117284980 |