Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79703 |
|---|---|
| ensemblid | ENSG00000173715.19 |
| hgncid | 26197 |
| symbol | C11orf80 |
| name | TOP6B like initiator of meiotic double strand breaks |
| refseq_nuc | NM_001302084.2 |
| refseq_prot | NP_001289013.1 |
| ensembl_nuc | ENST00000540737.7 |
| ensembl_prot | ENSP00000444319.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 66744769 |
| end | 66843516 |
| strand | + |
| ver | v1.2 |
| region | chr11:66744769-66843516 |
| region5000 | chr11:66739769-66848516 |
| regionname0 | C11orf80_chr11_66744769_66843516 |
| regionname5000 | C11orf80_chr11_66739769_66848516 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 511 | 237 | 56 | 30 | 119 | 10 | 20 | 92 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0002 | 0/0 | 511 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0003 | 0/0 | 511 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0004 | 0/0 | 511 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0005 | 0/0 | 511 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0006 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0007 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1536 | 188 | 43 | 20 | 101 | 7 | 16 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| c0002 | 0/1 | 1536 | 48 | 12 | 10 | 18 | 3 | 4 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| c0003 | 0/0 | 1536 | 4 | 3 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| c0004 | 0/0 | 1536 | 2 | 1 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| c0005 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| c0006 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| c0007 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| c0008 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| c0009 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 463 | 136 | 28 | 13 | 79 | 4 | 10 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0002 | 0/0 | 466 | 71 | 13 | 7 | 40 | 3 | 8 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0003 | 0/0 | 469 | 10 | 2 | 4 | 0 | 3 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0004 | 0/0 | 463 | 10 | 9 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0005 | 0/0 | 458 | 6 | 5 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0006 | 0/0 | 466 | 4 | 3 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0007 | 0/0 | 471 | 3 | 0 | 3 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0008 | 0/0 | 461 | 2 | 1 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0009 | 0/0 | 458 | 2 | 2 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0010 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0011 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0012 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| t0013 | 0/0 | 463 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1536 | 188 | 43 | 20 | 101 | 7 | 16 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0002 | 0/1 | 1536 | 48 | 12 | 10 | 18 | 3 | 4 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0007 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0002c0003 | 0/0 | 1536 | 4 | 3 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0003c0005 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0004c0004 | 0/0 | 1536 | 2 | 1 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0005c0009 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0006c0008 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0007c0006 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1998 | 92 | 17 | 5 | 61 | 2 | 6 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0002 | 0/0 | 2001 | 66 | 11 | 6 | 39 | 2 | 8 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0003 | 0/0 | 2004 | 10 | 2 | 4 | 0 | 3 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0004 | 0/0 | 1998 | 9 | 8 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0006 | 0/0 | 2001 | 4 | 3 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0007 | 0/0 | 2006 | 3 | 0 | 3 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0009 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0010 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0011 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0001t0012 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0002t0001 | 0/1 | 1998 | 43 | 11 | 8 | 17 | 2 | 4 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0002t0002 | 0/0 | 2001 | 4 | 1 | 1 | 1 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0002t0013 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0001c0007t0004 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0002c0003t0005 | 0/0 | 1993 | 4 | 3 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0003c0005t0005 | 0/0 | 1993 | 2 | 2 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0004c0004t0008 | 0/0 | 1996 | 2 | 1 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0005c0009t0001 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0006c0008t0002 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| a0007c0006t0009 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | copy fasta | chr11 | 66739769 | 66848516 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0013g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0007t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0002c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0002c0003t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0002c0003t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0002c0003t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0003c0005t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0003c0005t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0004c0004t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0004c0004t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0005c0009t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0006c0008t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0007c0006t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0150 | EUR | GBR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0073 | EUR | GBR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | FIN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0011 | EUR | FIN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | FIN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01109 | hp2 | a0004 | c0004 | t0008 | g0063 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01168 | hp1 | a0001 | c0002 | t0013 | g0071 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0226 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0228 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01243 | hp1 | a0002 | c0003 | t0005 | g0120 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0137 | EUR | IBS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01884 | hp1 | a0002 | c0003 | t0005 | g0118 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0089 | AMR | PEL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02071 | hp2 | a0001 | c0001 | t0011 | g0233 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CDX | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CDX | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02615 | hp2 | a0002 | c0003 | t0005 | g0237 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02647 | hp1 | a0003 | c0005 | t0005 | g0119 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0085 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03098 | hp1 | a0004 | c0004 | t0008 | g0062 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03195 | hp2 | a0006 | c0008 | t0002 | g0165 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03225 | hp2 | a0002 | c0003 | t0005 | g0238 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03516 | hp2 | a0001 | c0007 | t0004 | g0188 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0088 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03654 | hp1 | a0001 | c0001 | t0012 | g0144 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | CHB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18747 | hp2 | a0005 | c0009 | t0001 | g0008 | EAS | CHB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18906 | hp1 | a0003 | c0005 | t0005 | g0236 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0211 | EUR | TSI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0227 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0004 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | USA | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | USA | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA21309 | hp2 | a0007 | c0006 | t0009 | g0247 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0195 | REF | REF | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0241 | REF | REF | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:66788262
|
T | C | 1 | a0004 | 2 | HG01109.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.128T>C | p.Ile43Thr | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/15 | 308/1998 | 128/1536 | 43/511 | chr11 | 66788262 | ||
| chr11:66801077
|
T | G | 2 | a0002a0003 | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
missense_variant | MODERATE | c.322T>G | p.Leu108Val | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/15 | 502/1998 | 322/1536 | 108/511 | chr11 | 66801077 | ||
| chr11:66804173
|
A | G | 1 | a0005 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.526A>G | p.Arg176Gly | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/15 | 706/1998 | 526/1536 | 176/511 | chr11 | 66804173 | ||
| chr11:66813980
|
G | A | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.659G>A | p.Cys220Tyr | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/15 | 839/1998 | 659/1536 | 220/511 | chr11 | 66813980 | ||
| chr11:66813986
|
T | C | 1 | a0003 | 2 | HG02647.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.665T>C | p.Ile222Thr | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/15 | 845/1998 | 665/1536 | 222/511 | chr11 | 66813986 | ||
| chr11:66838419
|
A | T | 1 | a0006 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1223A>T | p.Asp408Val | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/15 | 1403/1998 | 1223/1536 | 408/511 | chr11 | 66838419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:66838438
|
C | T | 1 | a0004c0004 | 2 | HG01109.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.1242C>T | p.Leu414Leu | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/15 | 1422/1998 | 1242/1536 | 414/511 | chr11 | 66838438 | ||
| chr11:66843021
|
C | T | 1 | a0001c0007 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1422C>T | p.His474His | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 14/15 | 1602/1998 | 1422/1536 | 474/511 | chr11 | 66843021 | ||
| chr11:66843174
|
G | C | 1 | a0001c0002 | 48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
synonymous_variant | LOW | c.1476G>C | p.Val492Val | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 1656/1998 | 1476/1536 | 492/511 | chr11 | 66843174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:66744819
|
G | GGGC | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(3): Show | 80 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(77): Show |
5_prime_UTR_variant | MODIFIER | c.-106_-104dupCGG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/15 | 14226 | INFO_REALIGN_3_PRIME | chr11 | 66744819 | ||||
| chr11:66744819
|
G | GGGCGGC | 2 | a0001c0001t0003a0001c0001t0012 | 11 | HG00099.hp1 HG01074.hp1 HG01175.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-109_-104dupCGGCGG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/15 | 14226 | INFO_REALIGN_3_PRIME | chr11 | 66744819 | ||||
| chr11:66744819
|
G | GGGCGGCG others(5): Show |
1 | a0001c0001t0011 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115_-104dupCGGCGG others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/15 | 14226 | INFO_REALIGN_3_PRIME | chr11 | 66744819 | ||||
| chr11:66744819
|
G | GGGCGGCG others(8): Show |
1 | a0001c0001t0010 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118_-104dupCGGCGG others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/15 | 14226 | INFO_REALIGN_3_PRIME | chr11 | 66744819 | ||||
| chr11:66843272
|
G | T | 1 | a0001c0001t0012 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 38 | chr11 | 66843272 | |||||
| chr11:66843334
|
C | T | 1 | a0001c0002t0013 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 100 | chr11 | 66843334 | |||||
| chr11:66843352
|
G | GGGCCC | 1 | a0001c0001t0007 | 3 | HG01123.hp1 HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*121_*125dupCCCGG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 126 | INFO_REALIGN_3_PRIME | chr11 | 66843352 | ||||
| chr11:66843357
|
CGGGCG | C | 5 | a0001c0001t0009a0002c0003t0005a0003c0005t0005others(2): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*143delGGGCG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 139 | INFO_REALIGN_3_PRIME | chr11 | 66843357 | ||||
| chr11:66843423
|
G | C | 3 | a0001c0001t0009a0004c0004t0008a0007c0006t0009 | 4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*189G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 189 | chr11 | 66843423 | |||||
| chr11:66843507
|
G | C | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(1): Show | 15 | HG01243.hp2 HG01934.hp1 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*273G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 273 | chr11 | 66843507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:66744924
|
T | C | 2 | a0001c0001t0003g0001a0001c0001t0003g0002 | 2 | HG01515.hp2 HG03942.hp1 |
splice_region_variant&intron_variant | LOW | c.-30+5T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66744924 | ||||||
| chr11:66744967
|
G | GGGCTTTG others(10): Show |
1 | a0001c0001t0002g0248 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-30+50_-30+66dupGC others(15): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66744967 | |||||
| chr11:66745057
|
C | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+138C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745057 | ||||||
| chr11:66745180
|
G | A | 1 | a0001c0002t0001g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+261G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745180 | ||||||
| chr11:66745191
|
G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+272G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745191 | ||||||
| chr11:66745309
|
C | CG | 41 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0200others(38): Show | 41 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.-30+394dupG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745309 | |||||
| chr11:66745309
|
C | CGG | 10 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(7): Show | 10 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30+393_-30+394dup others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745309 | |||||
| chr11:66745311
|
G | C | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-30+392G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745311 | ||||||
| chr11:66745311
|
G | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-30+392G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745311 | ||||||
| chr11:66745312
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-30+393G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745312 | ||||||
| chr11:66745314
|
T | G | 243 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-30+395T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745314 | ||||||
| chr11:66745793
|
G | GGTTT | 42 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(39): Show | 42 | HG00323.hp1 HG00621.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.-30+903_-30+906dup others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | |||||
| chr11:66745793
|
G | GGTTTGTT others(1): Show |
3 | a0001c0001t0001g0239a0001c0001t0004g0240a0001c0002t0001g0007 | 3 | HG02109.hp1 HG02922.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-30+899_-30+906dup others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | |||||
| chr11:66745793
|
G | GGTTTGTT others(5): Show |
1 | a0001c0001t0002g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-30+895_-30+906dup others(12): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | |||||
| chr11:66745793
|
G | GGTTTGTT others(9): Show |
1 | a0001c0001t0002g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-30+891_-30+906dup others(16): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | |||||
| chr11:66745793
|
GGTTT | G | 91 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0001g0138others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-30+903_-30+906del others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | |||||
| chr11:66745793
|
GGTTTGTT others(5): Show |
G | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-30+895_-30+906del others(12): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | |||||
| chr11:66745940
|
A | G | 1 | a0001c0001t0004g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-30+1021A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745940 | ||||||
| chr11:66746263
|
C | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1344C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746263 | ||||||
| chr11:66746302
|
G | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | NA18941.hp1 NA18942.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1383G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746302 | ||||||
| chr11:66746498
|
T | G | 2 | a0001c0001t0002g0122a0001c0001t0002g0248 | 2 | NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-30+1579T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746498 | ||||||
| chr11:66746594
|
A | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-30+1675A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746594 | ||||||
| chr11:66746714
|
C | CA | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1807dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66746714 | |||||
| chr11:66746754
|
C | A | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+1835C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746754 | ||||||
| chr11:66746882
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-30+1963T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746882 | ||||||
| chr11:66747189
|
A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+2270A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747189 | ||||||
| chr11:66747196
|
G | A | 2 | a0001c0001t0002g0123a0001c0001t0002g0124 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-30+2277G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747196 | ||||||
| chr11:66747394
|
AT | A | 5 | a0001c0001t0003g0001a0002c0003t0005g0118a0002c0003t0005g0237others(2): Show | 5 | HG01515.hp2 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+2490delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66747394 | |||||
| chr11:66747427
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0002g0190 | 2 | HG02165.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-30+2508A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747427 | ||||||
| chr11:66747445
|
A | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-30+2526A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747445 | ||||||
| chr11:66747525
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-30+2606T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747525 | ||||||
| chr11:66747527
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-30+2608T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747527 | ||||||
| chr11:66747644
|
A | C | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-30+2725A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747644 | ||||||
| chr11:66747864
|
C | T | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG00280.hp2 HG01074.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30+2945C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747864 | ||||||
| chr11:66747909
|
C | T | 2 | a0001c0001t0004g0184a0001c0001t0004g0185 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-30+2990C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747909 | ||||||
| chr11:66747911
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+2992C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747911 | ||||||
| chr11:66748015
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-30+3096T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66748015 | ||||||
| chr11:66748578
|
T | C | 26 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(23): Show | 26 | HG00280.hp1 HG00609.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+3659T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66748578 | ||||||
| chr11:66748628
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-30+3709A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66748628 | ||||||
| chr11:66748681
|
A | T | 1 | a0001c0001t0001g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-30+3762A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66748681 | ||||||
| chr11:66748871
|
C | CA | 14 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 14 | HG00423.hp1 HG01109.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+3970dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66748871 | |||||
| chr11:66749048
|
TTG | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+4144_-30+4145d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66749048 | |||||
| chr11:66749078
|
T | A | 1 | a0001c0001t0002g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30+4159T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749078 | ||||||
| chr11:66749293
|
T | A | 1 | a0001c0001t0002g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-30+4374T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749293 | ||||||
| chr11:66749367
|
G | A | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-30+4448G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749367 | ||||||
| chr11:66749408
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-30+4489A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749408 | ||||||
| chr11:66749491
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-30+4572A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749491 | ||||||
| chr11:66749534
|
T | C | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-30+4615T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749534 | ||||||
| chr11:66749616
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-30+4697C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749616 | ||||||
| chr11:66749858
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+4939G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749858 | ||||||
| chr11:66750013
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+5094A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750013 | ||||||
| chr11:66750075
|
A | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0107others(4): Show | 7 | HG00438.hp2 HG02165.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+5156A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750075 | ||||||
| chr11:66750197
|
A | AT | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+5286dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66750197 | |||||
| chr11:66750215
|
T | A | 2 | a0001c0002t0001g0064a0001c0002t0002g0065 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-30+5296T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750215 | ||||||
| chr11:66750511
|
G | A | 1 | a0001c0002t0001g0009 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-30+5592G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750511 | ||||||
| chr11:66750528
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+5609A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750528 | ||||||
| chr11:66750703
|
C | CT | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG00438.hp2 HG00621.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30+5794dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66750703 | |||||
| chr11:66750789
|
G | T | 1 | a0001c0002t0001g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-30+5870G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750789 | ||||||
| chr11:66751252
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-30+6333C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751252 | ||||||
| chr11:66751418
|
C | T | 4 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(1): Show | 4 | NA18943.hp2 NA18990.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+6499C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751418 | ||||||
| chr11:66751468
|
T | C | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+6549T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751468 | ||||||
| chr11:66751498
|
A | AT | 33 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(30): Show | 33 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.-30+6598dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66751498 | |||||
| chr11:66751498
|
A | ATT | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+6597_-30+6598d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66751498 | |||||
| chr11:66751498
|
AT | A | 7 | a0001c0001t0001g0131a0001c0001t0001g0210a0001c0001t0001g0231others(4): Show | 7 | HG02738.hp1 HG02895.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+6598delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66751498 | |||||
| chr11:66751519
|
T | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-30+6600T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751519 | ||||||
| chr11:66751519
|
T | G | 1 | a0001c0001t0002g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-30+6600T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751519 | ||||||
| chr11:66751548
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-30+6629G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751548 | ||||||
| chr11:66751888
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+6969C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751888 | ||||||
| chr11:66751985
|
C | G | 1 | a0001c0002t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-7058C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751985 | ||||||
| chr11:66752019
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-29-7024A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752019 | ||||||
| chr11:66752142
|
C | CT | 8 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0091others(5): Show | 8 | HG00438.hp1 HG02735.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-6884dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66752142 | |||||
| chr11:66752142
|
CT | C | 13 | a0001c0001t0001g0092a0001c0001t0001g0199a0001c0001t0002g0129others(10): Show | 13 | HG00609.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-29-6884delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66752142 | |||||
| chr11:66752144
|
T | C | 9 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0204others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-6899T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752144 | ||||||
| chr11:66752159
|
T | A | 1 | a0001c0001t0006g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-29-6884T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752159 | ||||||
| chr11:66752544
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-6499C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752544 | ||||||
| chr11:66752749
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29-6294G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752749 | ||||||
| chr11:66752992
|
G | A | 2 | a0001c0001t0002g0127a0001c0001t0002g0135 | 2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-29-6051G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752992 | ||||||
| chr11:66753012
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29-6031C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753012 | ||||||
| chr11:66753061
|
G | A | 1 | a0001c0002t0001g0066 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-29-5982G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753061 | ||||||
| chr11:66753137
|
A | T | 132 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-29-5906A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753137 | ||||||
| chr11:66753406
|
C | CT | 5 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0002g0223others(2): Show | 5 | HG01261.hp2 HG01928.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-5619dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66753406 | |||||
| chr11:66753406
|
CT | C | 118 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(115): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-29-5619delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66753406 | |||||
| chr11:66753567
|
C | T | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.-29-5476C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753567 | ||||||
| chr11:66753607
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-29-5436C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753607 | ||||||
| chr11:66753623
|
G | T | 35 | a0001c0001t0001g0078a0001c0001t0001g0197a0001c0002t0001g0009others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29-5420G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753623 | ||||||
| chr11:66753924
|
C | T | 1 | a0001c0002t0001g0025 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-29-5119C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753924 | ||||||
| chr11:66754348
|
C | G | 2 | a0001c0001t0004g0184a0001c0001t0004g0185 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-29-4695C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754348 | ||||||
| chr11:66754432
|
C | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-29-4611C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754432 | ||||||
| chr11:66754605
|
G | A | 1 | a0001c0002t0001g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-29-4438G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754605 | ||||||
| chr11:66754797
|
C | G | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-29-4246C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754797 | ||||||
| chr11:66754846
|
A | G | 6 | a0001c0001t0002g0171a0001c0001t0006g0080a0001c0001t0006g0087others(3): Show | 6 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-4197A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754846 | ||||||
| chr11:66755120
|
G | T | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-29-3923G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755120 | ||||||
| chr11:66755121
|
A | AT | 54 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0078others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-29-3906dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66755121 | |||||
| chr11:66755121
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-3922A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755121 | ||||||
| chr11:66755121
|
AT | A | 10 | a0001c0001t0004g0081a0001c0001t0004g0082a0001c0001t0004g0121others(7): Show | 10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29-3906delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66755121 | |||||
| chr11:66755139
|
A | G | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-29-3904A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755139 | ||||||
| chr11:66755150
|
C | T | 4 | a0001c0001t0001g0078a0001c0002t0001g0031a0001c0002t0001g0076others(1): Show | 4 | HG02132.hp2 NA18960.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-3893C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755150 | ||||||
| chr11:66755160
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-29-3883C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755160 | ||||||
| chr11:66755341
|
G | C | 40 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.-29-3702G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755341 | ||||||
| chr11:66755870
|
T | C | 1 | a0001c0002t0002g0192 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-29-3173T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755870 | ||||||
| chr11:66755904
|
A | T | 9 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-3139A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755904 | ||||||
| chr11:66756331
|
T | C | 3 | a0001c0001t0002g0136a0003c0005t0005g0119a0003c0005t0005g0236 | 3 | HG02647.hp1 NA18906.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-29-2712T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756331 | ||||||
| chr11:66756338
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-29-2705T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756338 | ||||||
| chr11:66756649
|
T | G | 1 | a0001c0001t0002g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-29-2394T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756649 | ||||||
| chr11:66756780
|
C | T | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-29-2263C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756780 | ||||||
| chr11:66756795
|
T | A | 1 | a0001c0001t0002g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-29-2248T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756795 | ||||||
| chr11:66757033
|
C | T | 5 | a0001c0001t0001g0197a0001c0002t0001g0009a0001c0002t0001g0025others(2): Show | 5 | HG01169.hp2 HG01433.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-2010C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757033 | ||||||
| chr11:66757180
|
T | A | 1 | a0001c0001t0003g0137 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-29-1863T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757180 | ||||||
| chr11:66757200
|
G | A | 1 | a0001c0002t0013g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-29-1843G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757200 | ||||||
| chr11:66757291
|
T | C | 245 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-29-1752T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757291 | ||||||
| chr11:66757356
|
T | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-29-1687T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757356 | ||||||
| chr11:66757417
|
A | C | 1 | a0005c0009t0001g0008 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-29-1626A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757417 | ||||||
| chr11:66757461
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-29-1582A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757461 | ||||||
| chr11:66757754
|
T | G | 2 | a0001c0001t0002g0122a0001c0001t0002g0248 | 2 | NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-29-1289T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757754 | ||||||
| chr11:66758302
|
C | CTTTTCTT others(2): Show |
9 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 9 | HG00438.hp2 HG00621.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-737_-29-736ins others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
C | CTTTTCTT others(3): Show |
4 | a0001c0001t0001g0035a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02080.hp1 HG02165.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-737_-29-736ins others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
C | CTTTTTTT others(1): Show |
25 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0043others(22): Show | 25 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-29-721_-29-714dup others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
C | CTTTTTTT others(2): Show |
29 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.-29-722_-29-714dup others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
C | CTTTTTTT others(3): Show |
13 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01123.hp2 HG01169.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-29-723_-29-714dup others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
C | CTTTTTTT others(4): Show |
8 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0001g0232others(5): Show | 8 | HG00621.hp1 HG00738.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29-724_-29-714dup others(11): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
C | CTTTTTTT others(5): Show |
9 | a0001c0001t0001g0078a0001c0001t0001g0204a0001c0001t0001g0231others(6): Show | 9 | HG01109.hp1 HG01361.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-725_-29-714dup others(12): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0003g0243a0001c0002t0001g0079 | 2 | HG03486.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-29-726_-29-714dup others(13): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
CT | C | 33 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(30): Show | 33 | HG00408.hp1 HG00423.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-29-714delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
CTTTTT | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0163others(15): Show | 18 | HG00738.hp2 HG02109.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29-718_-29-714del others(5): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
CTTTTTT | C | 66 | a0001c0001t0001g0131a0001c0001t0001g0140a0001c0001t0001g0149others(63): Show | 66 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.-29-719_-29-714del others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758302
|
CTTTTTTT | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0002g0127others(2): Show | 5 | HG01433.hp1 HG02895.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-720_-29-714del others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | |||||
| chr11:66758304
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-29-739T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758304 | ||||||
| chr11:66758334
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0051a0001c0001t0001g0091others(4): Show | 7 | NA18946.hp2 NA18955.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-709C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758334 | ||||||
| chr11:66758420
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-623C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758420 | ||||||
| chr11:66758532
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0002g0141 | 3 | HG00609.hp1 NA18960.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-29-511T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758532 | ||||||
| chr11:66758588
|
G | A | 243 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-29-455G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758588 | ||||||
| chr11:66758593
|
C | T | 1 | a0001c0001t0002g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-29-450C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758593 | ||||||
| chr11:66758834
|
C | T | 10 | a0001c0001t0009g0004a0002c0003t0005g0118a0002c0003t0005g0120others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29-209C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758834 | ||||||
| chr11:66758861
|
T | C | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-182T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758861 | ||||||
| chr11:66759108
|
C | T | 1 | a0001c0001t0003g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.25+12C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66759108 | ||||||
| chr11:66759646
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.25+550C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66759646 | ||||||
| chr11:66759792
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.25+696A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66759792 | ||||||
| chr11:66760176
|
CCAGTGGC others(322): Show |
C | 6 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+1112_25+1440del | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760176 | |||||
| chr11:66760307
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.25+1211G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66760307 | ||||||
| chr11:66760578
|
T | G | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25+1482T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66760578 | ||||||
| chr11:66760625
|
C | CA | 81 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0057others(78): Show | 81 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.25+1558dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | |||||
| chr11:66760625
|
C | CAA | 20 | a0001c0001t0001g0094a0001c0001t0001g0189a0001c0001t0002g0122others(17): Show | 20 | HG00642.hp2 HG00738.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.25+1557_25+1558dup others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | |||||
| chr11:66760625
|
CA | C | 8 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+1558delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | |||||
| chr11:66760625
|
CAAAAAA | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02683.hp2 HG03669.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+1553_25+1558del others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | |||||
| chr11:66760625
|
CAAAAAAA | C | 20 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0046others(17): Show | 20 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.25+1552_25+1558del others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | |||||
| chr11:66760835
|
A | G | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.25+1739A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66760835 | ||||||
| chr11:66760904
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0230 | 2 | NA18939.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.25+1808C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66760904 | ||||||
| chr11:66760994
|
C | CT | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+1913dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760994 | |||||
| chr11:66760994
|
CT | C | 8 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0002g0221others(5): Show | 8 | HG01934.hp1 HG02965.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.25+1913delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760994 | |||||
| chr11:66761112
|
C | G | 2 | a0001c0001t0004g0184a0001c0001t0004g0185 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.25+2016C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761112 | ||||||
| chr11:66761147
|
G | A | 9 | a0001c0001t0001g0057a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG00408.hp1 HG02040.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+2051G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761147 | ||||||
| chr11:66761223
|
T | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.25+2127T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761223 | ||||||
| chr11:66761319
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.25+2223C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761319 | ||||||
| chr11:66761577
|
A | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0135 | 2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.25+2481A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761577 | ||||||
| chr11:66761646
|
G | T | 10 | a0001c0001t0009g0004a0002c0003t0005g0118a0002c0003t0005g0120others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+2550G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761646 | ||||||
| chr11:66761650
|
C | A | 1 | a0001c0001t0003g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25+2554C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761650 | ||||||
| chr11:66761692
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.25+2596C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761692 | ||||||
| chr11:66762246
|
A | G | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+3150A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762246 | ||||||
| chr11:66762292
|
G | A | 27 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.25+3196G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762292 | ||||||
| chr11:66762299
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0052 | 2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.25+3203C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762299 | ||||||
| chr11:66762364
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.25+3268C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762364 | ||||||
| chr11:66762368
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0234a0001c0001t0003g0002 | 3 | HG02602.hp1 HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.25+3272A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762368 | ||||||
| chr11:66762370
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+3274A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762370 | ||||||
| chr11:66762425
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.25+3329G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762425 | ||||||
| chr11:66762458
|
G | A | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.25+3362G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762458 | ||||||
| chr11:66762492
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.25+3396C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762492 | ||||||
| chr11:66762500
|
C | T | 27 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.25+3404C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762500 | ||||||
| chr11:66762637
|
T | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+3541T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762637 | ||||||
| chr11:66763002
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.25+3906A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66763002 | ||||||
| chr11:66763034
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0124 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.25+3938C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66763034 | ||||||
| chr11:66763219
|
A | G | 32 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(29): Show | 32 | HG00280.hp1 HG00609.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.25+4123A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66763219 | ||||||
| chr11:66764213
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25+5117C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764213 | ||||||
| chr11:66764254
|
T | A | 1 | a0001c0001t0002g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.25+5158T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764254 | ||||||
| chr11:66764326
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.25+5230T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764326 | ||||||
| chr11:66764456
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.25+5360G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764456 | ||||||
| chr11:66764496
|
C | CA | 20 | a0001c0001t0001g0043a0001c0001t0001g0113a0001c0001t0001g0115others(17): Show | 20 | HG00738.hp2 HG01243.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.25+5419dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66764496 | |||||
| chr11:66764496
|
C | CAA | 5 | a0001c0001t0004g0185a0002c0003t0005g0118a0002c0003t0005g0120others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+5418_25+5419dup others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66764496 | |||||
| chr11:66764568
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25+5472G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764568 | ||||||
| chr11:66764580
|
G | A | 1 | a0001c0002t0001g0193 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.25+5484G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764580 | ||||||
| chr11:66764619
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+5523C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764619 | ||||||
| chr11:66764643
|
C | T | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.25+5547C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764643 | ||||||
| chr11:66764665
|
C | CA | 47 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(44): Show | 47 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.25+5583dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66764665 | |||||
| chr11:66764680
|
TAAA | T | 26 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.25+5585_25+5587del others(3): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764680 | ||||||
| chr11:66764681
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0225 | 2 | HG00438.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.25+5585A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764681 | ||||||
| chr11:66764683
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.25+5587A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764683 | ||||||
| chr11:66764761
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0004g0240 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.25+5665C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764761 | ||||||
| chr11:66764838
|
G | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.25+5742G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764838 | ||||||
| chr11:66764968
|
CA | C | 6 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+5883delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66764968 | |||||
| chr11:66764990
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.25+5894T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764990 | ||||||
| chr11:66764994
|
G | A | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0095others(5): Show | 8 | HG00423.hp1 HG02040.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.25+5898G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764994 | ||||||
| chr11:66765109
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.25+6013A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765109 | ||||||
| chr11:66765143
|
G | A | 1 | a0001c0002t0001g0023 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.25+6047G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765143 | ||||||
| chr11:66765148
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.25+6052A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765148 | ||||||
| chr11:66765499
|
G | A | 26 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(23): Show | 26 | HG00280.hp1 HG00609.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.25+6403G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765499 | ||||||
| chr11:66765998
|
C | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+6902C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765998 | ||||||
| chr11:66766347
|
T | G | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7251T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766347 | ||||||
| chr11:66766442
|
C | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+7346C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766442 | ||||||
| chr11:66766522
|
G | C | 1 | a0001c0001t0002g0159 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.25+7426G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766522 | ||||||
| chr11:66766535
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25+7439C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766535 | ||||||
| chr11:66766766
|
A | T | 5 | a0001c0001t0006g0080a0001c0001t0006g0087a0001c0001t0006g0089others(2): Show | 5 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+7670A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766766 | ||||||
| chr11:66767045
|
T | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.25+7949T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767045 | ||||||
| chr11:66767046
|
T | C | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+7950T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767046 | ||||||
| chr11:66767084
|
C | T | 3 | a0002c0003t0005g0237a0003c0005t0005g0119a0003c0005t0005g0236 | 3 | HG02615.hp2 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.25+7988C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767084 | ||||||
| chr11:66767097
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25+8001A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767097 | ||||||
| chr11:66767178
|
A | T | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+8082A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767178 | ||||||
| chr11:66767343
|
T | G | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+8247T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767343 | ||||||
| chr11:66767852
|
A | G | 49 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.25+8756A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767852 | ||||||
| chr11:66767953
|
A | T | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+8857A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767953 | ||||||
| chr11:66768603
|
G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.25+9507G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66768603 | ||||||
| chr11:66768668
|
G | GT | 5 | a0001c0001t0001g0053a0001c0001t0001g0117a0001c0001t0002g0151others(2): Show | 5 | NA18949.hp1 NA19068.hp2 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+9587dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66768668 | |||||
| chr11:66768668
|
GT | G | 12 | a0001c0001t0001g0113a0001c0001t0006g0080a0001c0001t0006g0087others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+9587delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66768668 | |||||
| chr11:66768675
|
T | G | 3 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228 | 3 | HG01123.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.25+9579T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66768675 | ||||||
| chr11:66768983
|
G | A | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.25+9887G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66768983 | ||||||
| chr11:66769042
|
G | C | 6 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+9946G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769042 | ||||||
| chr11:66769175
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.25+10079A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769175 | ||||||
| chr11:66769318
|
A | G | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.25+10222A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769318 | ||||||
| chr11:66769343
|
A | T | 1 | a0005c0009t0001g0008 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.25+10247A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769343 | ||||||
| chr11:66769354
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+10258C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769354 | ||||||
| chr11:66769355
|
G | A | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25+10259G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769355 | ||||||
| chr11:66769435
|
G | C | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.25+10339G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769435 | ||||||
| chr11:66769448
|
T | TA | 7 | a0001c0001t0001g0028a0001c0002t0001g0064a0001c0002t0001g0067others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+10364dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66769448 | |||||
| chr11:66769639
|
T | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0210 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+10543T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769639 | ||||||
| chr11:66770155
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.25+11059G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66770155 | ||||||
| chr11:66770564
|
C | A | 24 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+11468C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66770564 | ||||||
| chr11:66770944
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+11848G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66770944 | ||||||
| chr11:66770982
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.25+11886C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66770982 | ||||||
| chr11:66771112
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0004g0240 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.25+12016A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771112 | ||||||
| chr11:66771385
|
T | C | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+12289T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771385 | ||||||
| chr11:66771581
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+12485G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771581 | ||||||
| chr11:66771687
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+12591A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771687 | ||||||
| chr11:66771718
|
T | C | 1 | a0001c0002t0001g0075 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.25+12622T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771718 | ||||||
| chr11:66772192
|
T | A | 1 | a0001c0001t0002g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.25+13096T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66772192 | ||||||
| chr11:66772370
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.25+13274C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66772370 | ||||||
| chr11:66772385
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.25+13289T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66772385 | ||||||
| chr11:66772914
|
A | G | 1 | a0001c0001t0004g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.25+13818A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66772914 | ||||||
| chr11:66773054
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.25+13958C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66773054 | ||||||
| chr11:66773483
|
C | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.25+14387C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66773483 | ||||||
| chr11:66773767
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.26-14393C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66773767 | ||||||
| chr11:66774539
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.26-13621C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774539 | ||||||
| chr11:66774589
|
G | A | 1 | a0001c0002t0001g0010 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.26-13571G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774589 | ||||||
| chr11:66774714
|
G | A | 1 | a0001c0002t0002g0011 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26-13446G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774714 | ||||||
| chr11:66774763
|
G | A | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-13397G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774763 | ||||||
| chr11:66774794
|
T | A | 1 | a0001c0001t0001g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.26-13366T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774794 | ||||||
| chr11:66775112
|
C | CA | 97 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0049others(94): Show | 97 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.26-13025dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66775112 | |||||
| chr11:66775112
|
C | CAAA | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-13027_26-13025d others(5): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66775112 | |||||
| chr11:66775113
|
A | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-13047A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775113 | ||||||
| chr11:66775242
|
C | G | 1 | a0001c0002t0001g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.26-12918C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775242 | ||||||
| chr11:66775335
|
C | T | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.26-12825C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775335 | ||||||
| chr11:66775338
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.26-12822G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775338 | ||||||
| chr11:66775459
|
A | G | 10 | a0001c0001t0001g0078a0001c0002t0001g0020a0001c0002t0001g0031others(7): Show | 10 | HG00621.hp1 HG02132.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-12701A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775459 | ||||||
| chr11:66775767
|
A | G | 227 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.26-12393A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775767 | ||||||
| chr11:66775867
|
T | C | 1 | a0001c0002t0002g0011 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26-12293T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775867 | ||||||
| chr11:66775920
|
T | C | 1 | a0001c0001t0002g0179 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.26-12240T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775920 | ||||||
| chr11:66776119
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-12041C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776119 | ||||||
| chr11:66776151
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.26-12009C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776151 | ||||||
| chr11:66776229
|
G | A | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.26-11931G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776229 | ||||||
| chr11:66776260
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.26-11900T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776260 | ||||||
| chr11:66776442
|
A | G | 3 | a0001c0001t0004g0081a0001c0001t0004g0082a0001c0001t0004g0121 | 3 | HG01243.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-11718A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776442 | ||||||
| chr11:66776501
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-11659C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776501 | ||||||
| chr11:66776504
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-11656C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776504 | ||||||
| chr11:66776588
|
G | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-11572G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776588 | ||||||
| chr11:66776603
|
C | G | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-11557C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776603 | ||||||
| chr11:66776634
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.26-11526A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776634 | ||||||
| chr11:66776836
|
C | G | 11 | a0001c0001t0001g0131a0001c0001t0001g0139a0001c0001t0001g0149others(8): Show | 11 | HG00423.hp2 HG02523.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-11324C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776836 | ||||||
| chr11:66776898
|
A | C | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-11262A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776898 | ||||||
| chr11:66777010
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.26-11150G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777010 | ||||||
| chr11:66777033
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-11127G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777033 | ||||||
| chr11:66777042
|
ACTATATC others(7): Show |
A | 1 | a0001c0002t0001g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.26-11089_26-11076d others(16): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66777042 | |||||
| chr11:66777043
|
C | CTATATCT others(31): Show |
7 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(4): Show | 7 | HG00738.hp2 HG01361.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-11077_26-11040d others(40): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66777043 | |||||
| chr11:66777057
|
CTATATCT others(17): Show |
C | 1 | a0001c0002t0013g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.26-11075_26-11052d others(26): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66777057 | |||||
| chr11:66777074
|
T | G | 3 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0238 | 3 | HG01243.hp1 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.26-11086T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777074 | ||||||
| chr11:66777081
|
ATATATCT others(7): Show |
A | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.26-11053_26-11040d others(16): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66777081 | |||||
| chr11:66777136
|
A | G | 1 | a0002c0003t0005g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.26-11024A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777136 | ||||||
| chr11:66777188
|
A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-10972A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777188 | ||||||
| chr11:66777265
|
T | G | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-10895T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777265 | ||||||
| chr11:66777367
|
C | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-10793C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777367 | ||||||
| chr11:66777832
|
A | G | 3 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0210 | 3 | HG02630.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.26-10328A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777832 | ||||||
| chr11:66778093
|
CT | C | 5 | a0001c0001t0001g0106a0001c0001t0002g0133a0001c0001t0003g0201others(2): Show | 5 | HG00099.hp2 HG01168.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-10052delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66778093 | |||||
| chr11:66778243
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26-9917G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66778243 | ||||||
| chr11:66778860
|
A | T | 1 | a0001c0001t0002g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.26-9300A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66778860 | ||||||
| chr11:66779324
|
A | G | 1 | a0002c0003t0005g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.26-8836A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779324 | ||||||
| chr11:66779343
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.26-8817G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779343 | ||||||
| chr11:66779351
|
A | G | 2 | a0001c0001t0007g0226a0001c0001t0007g0228 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.26-8809A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779351 | ||||||
| chr11:66779403
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8757G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779403 | ||||||
| chr11:66779465
|
C | T | 3 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0203 | 3 | NA19030.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.26-8695C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779465 | ||||||
| chr11:66779635
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.26-8525C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779635 | ||||||
| chr11:66779665
|
T | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-8495T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779665 | ||||||
| chr11:66779852
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.26-8308C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779852 | ||||||
| chr11:66779895
|
C | G | 1 | a0001c0001t0002g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26-8265C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779895 | ||||||
| chr11:66779911
|
C | CA | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8243dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66779911 | |||||
| chr11:66780015
|
T | TG | 19 | a0001c0001t0001g0052a0001c0001t0001g0125a0001c0001t0001g0204others(16): Show | 19 | HG00280.hp2 HG00408.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-8139dupG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66780015 | |||||
| chr11:66780016
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.26-8144G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780016 | ||||||
| chr11:66780050
|
C | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8110C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780050 | ||||||
| chr11:66780106
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.26-8054A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780106 | ||||||
| chr11:66780151
|
C | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8009C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780151 | ||||||
| chr11:66780789
|
C | G | 32 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(29): Show | 32 | HG00280.hp1 HG00609.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.26-7371C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780789 | ||||||
| chr11:66780991
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0055 | 3 | HG01928.hp1 NA18994.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.26-7169T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780991 | ||||||
| chr11:66781104
|
A | G | 26 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(23): Show | 26 | HG00280.hp1 HG00609.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.26-7056A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781104 | ||||||
| chr11:66781299
|
A | G | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.26-6861A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781299 | ||||||
| chr11:66781343
|
T | C | 2 | a0001c0002t0001g0003a0001c0002t0001g0015 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.26-6817T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781343 | ||||||
| chr11:66781425
|
G | A | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.26-6735G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781425 | ||||||
| chr11:66781435
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | NA18950.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.26-6725A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781435 | ||||||
| chr11:66781569
|
C | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.26-6591C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781569 | ||||||
| chr11:66781698
|
C | T | 3 | a0001c0002t0001g0203a0004c0004t0008g0062a0004c0004t0008g0063 | 3 | HG01109.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.26-6462C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781698 | ||||||
| chr11:66781846
|
A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-6314A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781846 | ||||||
| chr11:66781947
|
A | G | 2 | a0001c0001t0002g0191a0001c0001t0002g0221 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.26-6213A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781947 | ||||||
| chr11:66782073
|
A | G | 1 | a0001c0002t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26-6087A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782073 | ||||||
| chr11:66782269
|
C | G | 49 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.26-5891C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782269 | ||||||
| chr11:66782445
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-5715G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782445 | ||||||
| chr11:66782452
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.26-5708G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782452 | ||||||
| chr11:66782500
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0229 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.26-5660C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782500 | ||||||
| chr11:66782608
|
C | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.26-5552C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782608 | ||||||
| chr11:66782980
|
G | A | 26 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(23): Show | 26 | HG00280.hp1 HG00609.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.26-5180G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782980 | ||||||
| chr11:66783073
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.26-5087A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783073 | ||||||
| chr11:66783129
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0186a0001c0001t0001g0229 | 3 | HG00280.hp2 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.26-5031C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783129 | ||||||
| chr11:66783130
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0140 | 2 | NA18960.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.26-5030G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783130 | ||||||
| chr11:66783531
|
G | C | 48 | a0001c0001t0001g0078a0001c0001t0001g0197a0001c0002t0001g0003others(45): Show | 48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.26-4629G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783531 | ||||||
| chr11:66783611
|
G | T | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.26-4549G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783611 | ||||||
| chr11:66783612
|
C | G | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.26-4548C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783612 | ||||||
| chr11:66783645
|
T | G | 32 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(29): Show | 32 | HG00280.hp1 HG00609.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.26-4515T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783645 | ||||||
| chr11:66783672
|
C | T | 101 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0057others(98): Show | 101 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.26-4488C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783672 | ||||||
| chr11:66783796
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.26-4364A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783796 | ||||||
| chr11:66783879
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-4281G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783879 | ||||||
| chr11:66783977
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-4183C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783977 | ||||||
| chr11:66784017
|
TTTTTG | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-4123_26-4119del others(5): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66784017 | |||||
| chr11:66784049
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-4111G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784049 | ||||||
| chr11:66784099
|
C | T | 1 | a0003c0005t0005g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.26-4061C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784099 | ||||||
| chr11:66784157
|
A | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.26-4003A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784157 | ||||||
| chr11:66784537
|
C | G | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.26-3623C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784537 | ||||||
| chr11:66784669
|
G | A | 1 | a0001c0001t0002g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.26-3491G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784669 | ||||||
| chr11:66784884
|
A | G | 27 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.26-3276A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784884 | ||||||
| chr11:66784956
|
C | CT | 27 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | HG00438.hp2 HG00621.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.26-3183dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66784956 | |||||
| chr11:66784956
|
CT | C | 127 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(124): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.26-3183delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66784956 | |||||
| chr11:66784994
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-3166C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784994 | ||||||
| chr11:66785185
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-2975C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785185 | ||||||
| chr11:66785363
|
T | G | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.26-2797T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785363 | ||||||
| chr11:66785450
|
G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-2710G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785450 | ||||||
| chr11:66785529
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.26-2631T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785529 | ||||||
| chr11:66785540
|
C | A | 4 | a0001c0001t0001g0239a0001c0001t0001g0242a0001c0001t0003g0243others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-2620C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785540 | ||||||
| chr11:66785617
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.26-2543A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785617 | ||||||
| chr11:66785835
|
C | T | 3 | a0001c0001t0004g0081a0001c0001t0004g0082a0001c0001t0004g0121 | 3 | HG01243.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-2325C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785835 | ||||||
| chr11:66785981
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.26-2179C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785981 | ||||||
| chr11:66786266
|
G | C | 164 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.26-1894G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786266 | ||||||
| chr11:66786297
|
T | TA | 8 | a0001c0001t0001g0149a0001c0001t0001g0163a0001c0001t0003g0212others(5): Show | 8 | HG00423.hp2 HG01175.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-1848dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66786297 | |||||
| chr11:66786297
|
TA | T | 11 | a0001c0001t0002g0217a0001c0001t0004g0081a0001c0001t0004g0082others(8): Show | 11 | HG01243.hp2 HG01255.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-1848delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66786297 | |||||
| chr11:66786313
|
T | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0002g0224others(1): Show | 4 | HG01261.hp2 HG02080.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-1847T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786313 | ||||||
| chr11:66786318
|
G | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0157 | 2 | NA18953.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.26-1842G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786318 | ||||||
| chr11:66786937
|
G | GT | 52 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0078others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.26-1210dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66786937 | |||||
| chr11:66786937
|
G | GTT | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 7 | HG02074.hp2 HG02132.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-1211_26-1210dup others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66786937 | |||||
| chr11:66786937
|
G | T | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26-1223G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786937 | ||||||
| chr11:66786956
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.26-1204G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786956 | ||||||
| chr11:66787213
|
C | T | 1 | a0001c0002t0001g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.26-947C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787213 | ||||||
| chr11:66787431
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | NA18941.hp1 NA18942.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-729C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787431 | ||||||
| chr11:66787454
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26-706C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787454 | ||||||
| chr11:66787551
|
C | CA | 11 | a0001c0001t0001g0242a0001c0001t0002g0132a0001c0001t0002g0177others(8): Show | 11 | HG01934.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-592dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66787551 | |||||
| chr11:66787551
|
CA | C | 118 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(115): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.26-592delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66787551 | |||||
| chr11:66787568
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.26-592A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787568 | ||||||
| chr11:66787593
|
G | A | 1 | a0001c0002t0001g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.26-567G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787593 | ||||||
| chr11:66787676
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.26-484C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787676 | ||||||
| chr11:66787715
|
G | A | 1 | a0001c0002t0001g0202 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.26-445G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787715 | ||||||
| chr11:66787719
|
C | CA | 12 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0002g0132others(9): Show | 12 | HG00438.hp1 HG01175.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-426dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66787719 | |||||
| chr11:66787971
|
A | G | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-189A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787971 | ||||||
| chr11:66788001
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.26-159G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66788001 | ||||||
| chr11:66788024
|
C | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-136C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66788024 | ||||||
| chr11:66788404
|
GC | G | 6 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+137delC | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66788404 | |||||
| chr11:66788405
|
C | G | 1 | a0001c0001t0002g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.135+136C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788405 | ||||||
| chr11:66788428
|
A | G | 1 | a0001c0001t0002g0220 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.135+159A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788428 | ||||||
| chr11:66788471
|
T | C | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.135+202T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788471 | ||||||
| chr11:66788489
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0117 | 2 | NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.135+220G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788489 | ||||||
| chr11:66788596
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135+327C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788596 | ||||||
| chr11:66789084
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+815C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66789084 | ||||||
| chr11:66789297
|
A | G | 1 | a0006c0008t0002g0165 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.135+1028A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66789297 | ||||||
| chr11:66789369
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.135+1100C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66789369 | ||||||
| chr11:66789715
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+1446T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66789715 | ||||||
| chr11:66790005
|
G | A | 1 | a0001c0002t0001g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+1736G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66790005 | ||||||
| chr11:66790283
|
T | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.135+2014T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66790283 | ||||||
| chr11:66790644
|
G | A | 1 | a0001c0001t0002g0248 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.135+2375G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66790644 | ||||||
| chr11:66790962
|
G | A | 3 | a0001c0001t0004g0084a0001c0001t0004g0085a0001c0001t0004g0086 | 3 | HG02723.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.135+2693G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66790962 | ||||||
| chr11:66791271
|
T | C | 1 | a0001c0001t0012g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.135+3002T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66791271 | ||||||
| chr11:66791327
|
T | C | 10 | a0001c0001t0009g0004a0002c0003t0005g0118a0002c0003t0005g0120others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+3058T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66791327 | ||||||
| chr11:66791421
|
TTATACA | T | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.135+3157_135+3162d others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66791421 | |||||
| chr11:66791561
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+3292A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66791561 | ||||||
| chr11:66791818
|
A | AT | 8 | a0001c0001t0001g0034a0001c0001t0001g0106a0001c0001t0001g0117others(5): Show | 8 | HG01109.hp1 HG02602.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+3566dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66791818 | |||||
| chr11:66792008
|
G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.135+3739G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792008 | ||||||
| chr11:66792089
|
C | T | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.135+3820C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792089 | ||||||
| chr11:66792114
|
C | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.135+3845C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792114 | ||||||
| chr11:66792242
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.135+3973C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792242 | ||||||
| chr11:66792552
|
A | G | 48 | a0001c0001t0001g0078a0001c0001t0001g0197a0001c0002t0001g0003others(45): Show | 48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.136-3729A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792552 | ||||||
| chr11:66792792
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.136-3489G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792792 | ||||||
| chr11:66793072
|
C | T | 2 | a0001c0001t0003g0001a0001c0001t0003g0137 | 2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.136-3209C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793072 | ||||||
| chr11:66793092
|
GT | G | 49 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.136-3176delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793092 | |||||
| chr11:66793133
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-3148G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793133 | ||||||
| chr11:66793253
|
AT | A | 30 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(27): Show | 30 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.136-3019delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793253 | |||||
| chr11:66793262
|
T | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.136-3019T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793262 | ||||||
| chr11:66793409
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.136-2872T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793409 | ||||||
| chr11:66793444
|
G | GT | 55 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0047others(52): Show | 55 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.136-2817dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793444 | |||||
| chr11:66793444
|
G | GTT | 6 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0229others(3): Show | 6 | HG00099.hp1 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-2818_136-2817d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793444 | |||||
| chr11:66793444
|
G | T | 2 | a0001c0001t0002g0156a0001c0001t0002g0220 | 2 | NA18970.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.136-2837G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793444 | ||||||
| chr11:66793444
|
GT | G | 7 | a0001c0001t0009g0004a0002c0003t0005g0118a0002c0003t0005g0120others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2817delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793444 | |||||
| chr11:66793447
|
T | G | 1 | a0001c0001t0004g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.136-2834T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793447 | ||||||
| chr11:66793449
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.136-2832T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793449 | ||||||
| chr11:66793511
|
T | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.136-2770T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793511 | ||||||
| chr11:66793714
|
G | T | 1 | a0001c0001t0002g0223 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.136-2567G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793714 | ||||||
| chr11:66793908
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.136-2373C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793908 | ||||||
| chr11:66794099
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136-2182G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794099 | ||||||
| chr11:66794112
|
T | TA | 51 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0197others(48): Show | 51 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.136-2149dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66794112 | |||||
| chr11:66794112
|
TA | T | 11 | a0001c0001t0001g0083a0001c0001t0002g0044a0001c0001t0002g0130others(8): Show | 11 | HG00280.hp1 HG01109.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-2149delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66794112 | |||||
| chr11:66794440
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.136-1841C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794440 | ||||||
| chr11:66794777
|
T | C | 164 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.136-1504T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794777 | ||||||
| chr11:66794851
|
G | T | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.136-1430G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794851 | ||||||
| chr11:66794858
|
C | T | 11 | a0001c0001t0001g0131a0001c0001t0001g0139a0001c0001t0001g0149others(8): Show | 11 | HG00423.hp2 HG02523.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-1423C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794858 | ||||||
| chr11:66794960
|
C | T | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.136-1321C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794960 | ||||||
| chr11:66795134
|
C | CA | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-1138dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66795134 | |||||
| chr11:66795140
|
A | AAT | 5 | a0001c0001t0001g0057a0001c0001t0001g0093a0001c0001t0001g0097others(2): Show | 5 | HG00408.hp1 HG02074.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-1140_136-1139i others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66795140 | |||||
| chr11:66795142
|
A | T | 41 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.136-1139A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795142 | ||||||
| chr11:66795144
|
T | A | 8 | a0001c0001t0001g0047a0001c0001t0002g0145a0001c0001t0002g0148others(5): Show | 8 | HG00408.hp2 HG01109.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-1137T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795144 | ||||||
| chr11:66795205
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.136-1076T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795205 | ||||||
| chr11:66795312
|
T | G | 3 | a0001c0001t0002g0134a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | NA18941.hp2 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.136-969T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795312 | ||||||
| chr11:66795362
|
C | T | 2 | a0001c0001t0004g0184a0001c0001t0004g0185 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.136-919C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795362 | ||||||
| chr11:66795490
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-791T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795490 | ||||||
| chr11:66795494
|
G | T | 1 | a0001c0001t0002g0169 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.136-787G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795494 | ||||||
| chr11:66795591
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.136-690C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795591 | ||||||
| chr11:66795594
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136-687G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795594 | ||||||
| chr11:66795940
|
A | G | 1 | a0001c0001t0007g0227 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.136-341A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795940 | ||||||
| chr11:66795957
|
T | G | 1 | a0001c0002t0001g0193 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.136-324T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795957 | ||||||
| chr11:66795961
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.136-320A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795961 | ||||||
| chr11:66796054
|
A | G | 10 | a0001c0001t0009g0004a0002c0003t0005g0118a0002c0003t0005g0120others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-227A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66796054 | ||||||
| chr11:66796062
|
G | A | 1 | a0001c0002t0002g0011 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.136-219G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66796062 | ||||||
| chr11:66796163
|
G | C | 10 | a0001c0001t0004g0081a0001c0001t0004g0082a0001c0001t0004g0121others(7): Show | 10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-118G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66796163 | ||||||
| chr11:66796215
|
G | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-66G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66796215 | ||||||
| chr11:66796551
|
G | A | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.219+187G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796551 | ||||||
| chr11:66796699
|
C | G | 1 | a0001c0001t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.219+335C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796699 | ||||||
| chr11:66796708
|
A | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219+344A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796708 | ||||||
| chr11:66796780
|
CT | C | 5 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+419delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66796780 | |||||
| chr11:66796783
|
T | G | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.219+419T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796783 | ||||||
| chr11:66796785
|
G | A | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.219+421G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796785 | ||||||
| chr11:66796785
|
G | GA | 18 | a0001c0001t0001g0207a0001c0001t0001g0242a0001c0001t0001g0244others(15): Show | 18 | HG00438.hp1 HG01123.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.219+438dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66796785 | |||||
| chr11:66796804
|
ACAACTTT | A | 5 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG01361.hp2 HG02071.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.219+451_219+457del others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66796804 | |||||
| chr11:66796805
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.219+441C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796805 | ||||||
| chr11:66796860
|
G | GT | 24 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0083others(21): Show | 24 | HG00408.hp1 HG02040.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.219+509dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66796860 | |||||
| chr11:66796863
|
T | TG | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0100 | 3 | HG00423.hp1 HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.219+499_219+500ins others(1): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796863 | ||||||
| chr11:66797125
|
T | C | 10 | a0001c0001t0004g0081a0001c0001t0004g0082a0001c0001t0004g0121others(7): Show | 10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.219+761T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797125 | ||||||
| chr11:66797789
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0207 | 2 | NA18945.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.219+1425G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797789 | ||||||
| chr11:66797798
|
A | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | NA18941.hp1 NA18942.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+1434A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797798 | ||||||
| chr11:66797808
|
A | G | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219+1444A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797808 | ||||||
| chr11:66797824
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.219+1460A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797824 | ||||||
| chr11:66797942
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0003g0243 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.219+1578A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797942 | ||||||
| chr11:66798034
|
C | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219+1670C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798034 | ||||||
| chr11:66798105
|
A | G | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.219+1741A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798105 | ||||||
| chr11:66798263
|
C | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+1899C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798263 | ||||||
| chr11:66798304
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.219+1940A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798304 | ||||||
| chr11:66798374
|
C | T | 1 | a0002c0003t0005g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+2010C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798374 | ||||||
| chr11:66798513
|
T | G | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-2128T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798513 | ||||||
| chr11:66798597
|
C | CA | 30 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0056others(27): Show | 30 | HG00280.hp2 HG01109.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.220-2020dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66798597 | |||||
| chr11:66798597
|
CA | C | 28 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0102others(25): Show | 28 | HG00280.hp1 HG00423.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.220-2020delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66798597 | |||||
| chr11:66798797
|
G | A | 27 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.220-1844G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798797 | ||||||
| chr11:66798957
|
G | A | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-1684G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798957 | ||||||
| chr11:66799035
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0100 | 3 | HG00423.hp1 HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.220-1606C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799035 | ||||||
| chr11:66799077
|
C | A | 1 | a0001c0002t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220-1564C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799077 | ||||||
| chr11:66799094
|
C | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.220-1547C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799094 | ||||||
| chr11:66799193
|
CA | C | 10 | a0001c0001t0004g0081a0001c0001t0004g0082a0001c0001t0004g0121others(7): Show | 10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-1446delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66799193 | |||||
| chr11:66799207
|
C | CA | 17 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0094others(14): Show | 17 | HG00642.hp1 HG01433.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.220-1413dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66799207 | |||||
| chr11:66799207
|
CA | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0230a0001c0001t0002g0129others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-1413delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66799207 | |||||
| chr11:66799299
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-1342C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799299 | ||||||
| chr11:66799385
|
CA | C | 10 | a0001c0001t0001g0230a0001c0001t0001g0245a0001c0001t0007g0228others(7): Show | 10 | HG01169.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-1242delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66799385 | |||||
| chr11:66799541
|
A | G | 3 | a0001c0001t0002g0134a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | NA18941.hp2 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.220-1100A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799541 | ||||||
| chr11:66799929
|
A | T | 27 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.220-712A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799929 | ||||||
| chr11:66800004
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220-637C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66800004 | ||||||
| chr11:66800064
|
C | CA | 23 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0052others(20): Show | 23 | HG01175.hp1 HG01243.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.220-562dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66800064 | |||||
| chr11:66800344
|
A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.220-297A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66800344 | ||||||
| chr11:66801367
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.347+265A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66801367 | ||||||
| chr11:66801472
|
C | T | 175 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(172): Show | 175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.347+370C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66801472 | ||||||
| chr11:66801888
|
G | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347+786G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66801888 | ||||||
| chr11:66802014
|
T | G | 1 | a0001c0001t0002g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.347+912T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66802014 | ||||||
| chr11:66802038
|
G | T | 3 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228 | 3 | HG01123.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.347+936G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66802038 | ||||||
| chr11:66802076
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.347+974G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66802076 | ||||||
| chr11:66802925
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.348-1070C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66802925 | ||||||
| chr11:66803036
|
T | C | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.348-959T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803036 | ||||||
| chr11:66803278
|
G | A | 164 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.348-717G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803278 | ||||||
| chr11:66803369
|
G | A | 3 | a0001c0001t0004g0084a0001c0001t0004g0085a0001c0001t0004g0086 | 3 | HG02723.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.348-626G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803369 | ||||||
| chr11:66803467
|
T | C | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-528T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803467 | ||||||
| chr11:66803490
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.348-505G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803490 | ||||||
| chr11:66803515
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348-480G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803515 | ||||||
| chr11:66803867
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-128A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803867 | ||||||
| chr11:66803971
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348-24T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803971 | ||||||
| chr11:66804408
|
T | C | 1 | a0001c0001t0002g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.543+218T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66804408 | ||||||
| chr11:66804704
|
G | A | 1 | a0001c0001t0003g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.543+514G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66804704 | ||||||
| chr11:66804793
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.543+603C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66804793 | ||||||
| chr11:66805040
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.543+850C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805040 | ||||||
| chr11:66805156
|
C | T | 3 | a0001c0002t0001g0009a0001c0002t0001g0195a0001c0002t0001g0196 | 3 | HG01433.hp2 HG03492.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.543+966C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805156 | ||||||
| chr11:66805413
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0164 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.543+1223A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805413 | ||||||
| chr11:66805413
|
ATGTC | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+1229_543+1232d others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66805413 | |||||
| chr11:66805425
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.543+1235A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805425 | ||||||
| chr11:66805453
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.543+1263G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805453 | ||||||
| chr11:66805470
|
T | C | 1 | a0001c0002t0001g0211 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.543+1280T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805470 | ||||||
| chr11:66805737
|
A | G | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+1547A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805737 | ||||||
| chr11:66805931
|
C | G | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.543+1741C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805931 | ||||||
| chr11:66806346
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+2156C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66806346 | ||||||
| chr11:66806760
|
TA | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+2579delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66806760 | |||||
| chr11:66806761
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0225 | 2 | HG00438.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.543+2571A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66806761 | ||||||
| chr11:66806787
|
G | C | 1 | a0001c0002t0001g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.543+2597G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66806787 | ||||||
| chr11:66807209
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.543+3019A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807209 | ||||||
| chr11:66807363
|
G | A | 1 | a0001c0001t0003g0002 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.543+3173G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807363 | ||||||
| chr11:66807384
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+3194C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807384 | ||||||
| chr11:66807531
|
A | G | 1 | a0001c0002t0001g0030 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.543+3341A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807531 | ||||||
| chr11:66807561
|
G | A | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+3371G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807561 | ||||||
| chr11:66807925
|
T | C | 1 | a0001c0002t0001g0018 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.543+3735T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807925 | ||||||
| chr11:66808115
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.543+3925A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808115 | ||||||
| chr11:66808148
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.543+3958G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808148 | ||||||
| chr11:66808278
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.543+4088T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808278 | ||||||
| chr11:66808537
|
T | A | 3 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0150 | 3 | HG00099.hp1 HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.543+4347T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808537 | ||||||
| chr11:66808779
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+4589A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808779 | ||||||
| chr11:66808865
|
CAAAAAGA | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0232a0001c0001t0001g0234others(1): Show | 4 | HG02071.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+4676_543+4682d others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808865 | ||||||
| chr11:66808946
|
G | C | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+4756G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808946 | ||||||
| chr11:66809129
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.544-4736A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809129 | ||||||
| chr11:66809158
|
A | G | 2 | a0001c0001t0002g0191a0001c0001t0002g0221 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.544-4707A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809158 | ||||||
| chr11:66809395
|
C | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.544-4470C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809395 | ||||||
| chr11:66809792
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.544-4073C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809792 | ||||||
| chr11:66809799
|
G | C | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-4066G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809799 | ||||||
| chr11:66809886
|
A | G | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-3979A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809886 | ||||||
| chr11:66810308
|
C | G | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.544-3557C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810308 | ||||||
| chr11:66810426
|
G | A | 72 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0042others(69): Show | 72 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.544-3439G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810426 | ||||||
| chr11:66810462
|
A | G | 1 | a0001c0002t0001g0213 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.544-3403A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810462 | ||||||
| chr11:66810538
|
G | A | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-3327G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810538 | ||||||
| chr11:66810549
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-3316A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810549 | ||||||
| chr11:66810592
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-3273A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810592 | ||||||
| chr11:66810799
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.544-3066A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810799 | ||||||
| chr11:66810863
|
TC | T | 4 | a0001c0001t0003g0166a0001c0001t0003g0172a0001c0001t0003g0176others(1): Show | 4 | HG01074.hp1 HG01175.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-3001delC | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810863 | ||||||
| chr11:66810897
|
A | AG | 132 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.544-2966dupG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66810897 | |||||
| chr11:66811164
|
G | A | 132 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.544-2701G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811164 | ||||||
| chr11:66811198
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112 | 3 | HG02965.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.544-2667C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811198 | ||||||
| chr11:66811290
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.544-2575T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811290 | ||||||
| chr11:66811648
|
T | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2217T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811648 | ||||||
| chr11:66811810
|
C | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2055C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811810 | ||||||
| chr11:66811947
|
A | G | 2 | a0001c0001t0004g0184a0001c0001t0004g0185 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.544-1918A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811947 | ||||||
| chr11:66811972
|
A | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1893A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811972 | ||||||
| chr11:66812094
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.544-1771A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812094 | ||||||
| chr11:66812101
|
A | G | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.544-1764A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812101 | ||||||
| chr11:66812185
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0094a0001c0002t0013g0071a0002c0003t0005g0237others(1): Show | 4 | HG01168.hp1 HG02615.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-1671_544-1670i others(13): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66812185 | |||||
| chr11:66812185
|
C | CTTTTTTT others(5): Show |
127 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(124): Show | 127 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.544-1671_544-1670i others(14): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66812185 | |||||
| chr11:66812185
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0001g0075 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.544-1671_544-1670i others(15): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66812185 | |||||
| chr11:66812232
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-1633A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812232 | ||||||
| chr11:66812418
|
C | T | 3 | a0001c0001t0004g0084a0001c0001t0004g0085a0001c0001t0004g0086 | 3 | HG02723.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.544-1447C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812418 | ||||||
| chr11:66812466
|
G | A | 1 | a0002c0003t0005g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.544-1399G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812466 | ||||||
| chr11:66812848
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.544-1017T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812848 | ||||||
| chr11:66812940
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.544-925A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812940 | ||||||
| chr11:66813265
|
A | G | 5 | a0001c0001t0002g0136a0001c0001t0002g0143a0001c0001t0002g0146others(2): Show | 5 | NA18968.hp2 NA18977.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-600A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66813265 | ||||||
| chr11:66813597
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.544-268G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66813597 | ||||||
| chr11:66813668
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.544-197G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66813668 | ||||||
| chr11:66813711
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0002g0190 | 2 | HG02165.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.544-154C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66813711 | ||||||
| chr11:66814202
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.694+187C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814202 | ||||||
| chr11:66814206
|
C | CA | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.694+193dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 66814206 | |||||
| chr11:66814328
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.694+313G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814328 | ||||||
| chr11:66814555
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.694+540A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814555 | ||||||
| chr11:66814565
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.694+550G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814565 | ||||||
| chr11:66814739
|
A | G | 49 | a0001c0001t0001g0012a0001c0001t0001g0197a0001c0002t0001g0003others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.694+724A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814739 | ||||||
| chr11:66814971
|
C | T | 3 | a0001c0001t0004g0084a0001c0001t0004g0085a0001c0001t0004g0086 | 3 | HG02723.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.694+956C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814971 | ||||||
| chr11:66815605
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.695-448A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66815605 | ||||||
| chr11:66815624
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02080.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.695-429G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66815624 | ||||||
| chr11:66816031
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.695-22C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66816031 | ||||||
| chr11:66816288
|
A | G | 49 | a0001c0001t0001g0012a0001c0001t0001g0197a0001c0002t0001g0003others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.841+89A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66816288 | ||||||
| chr11:66816308
|
T | G | 164 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.841+109T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66816308 | ||||||
| chr11:66816480
|
T | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.841+281T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66816480 | ||||||
| chr11:66816567
|
T | TTTAAATT others(7): Show |
1 | a0001c0001t0001g0230 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.841+371_841+384dup others(14): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66816567 | |||||
| chr11:66816769
|
G | A | 1 | a0003c0005t0005g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.841+570G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66816769 | ||||||
| chr11:66817029
|
T | G | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.841+830T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66817029 | ||||||
| chr11:66817155
|
G | GAAATAAA others(3): Show |
1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.841+976_841+985dup others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66817155 | |||||
| chr11:66817155
|
G | GAAATAAA others(8): Show |
2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.841+971_841+985dup others(15): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66817155 | |||||
| chr11:66817155
|
G | GAAATAAA others(13): Show |
3 | a0002c0003t0005g0118a0002c0003t0005g0237a0002c0003t0005g0238 | 3 | HG01884.hp1 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.841+966_841+985dup others(20): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66817155 | |||||
| chr11:66817155
|
G | GAAATAAA others(18): Show |
4 | a0002c0003t0005g0120a0003c0005t0005g0119a0003c0005t0005g0236others(1): Show | 4 | HG01243.hp1 HG02647.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+961_841+985dup others(25): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66817155 | |||||
| chr11:66817267
|
G | C | 1 | a0001c0002t0001g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.841+1068G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66817267 | ||||||
| chr11:66817564
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.841+1365G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66817564 | ||||||
| chr11:66817814
|
T | G | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.841+1615T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66817814 | ||||||
| chr11:66818106
|
C | A | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.841+1907C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818106 | ||||||
| chr11:66818159
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.841+1960A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818159 | ||||||
| chr11:66818260
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.841+2061C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818260 | ||||||
| chr11:66818500
|
C | G | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.841+2301C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818500 | ||||||
| chr11:66818553
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.841+2354G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818553 | ||||||
| chr11:66819154
|
G | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-2489G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819154 | ||||||
| chr11:66819550
|
C | T | 1 | a0001c0002t0001g0023 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.842-2093C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819550 | ||||||
| chr11:66819597
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0002g0220 | 2 | NA18970.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.842-2046C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819597 | ||||||
| chr11:66819602
|
C | G | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.842-2041C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819602 | ||||||
| chr11:66819615
|
A | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.842-2028A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819615 | ||||||
| chr11:66819621
|
C | T | 1 | a0001c0001t0004g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.842-2022C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819621 | ||||||
| chr11:66819728
|
C | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-1915C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819728 | ||||||
| chr11:66819897
|
CT | C | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-1744delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66819897 | |||||
| chr11:66819904
|
TA | T | 228 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.842-1717delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66819904 | |||||
| chr11:66819906
|
A | T | 2 | a0001c0001t0001g0242a0001c0001t0003g0243 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.842-1737A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819906 | ||||||
| chr11:66820129
|
G | A | 1 | a0001c0001t0004g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.842-1514G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66820129 | ||||||
| chr11:66820148
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.842-1495A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66820148 | ||||||
| chr11:66820864
|
CTTTCTTA others(11): Show |
C | 1 | a0001c0002t0001g0020 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.842-778_842-761del others(18): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66820864 | ||||||
| chr11:66821041
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.842-602C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66821041 | ||||||
| chr11:66821286
|
AT | A | 219 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.842-338delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66821286 | |||||
| chr11:66821286
|
ATT | A | 5 | a0001c0002t0001g0009a0001c0002t0001g0025a0001c0002t0001g0195others(2): Show | 5 | HG01169.hp2 HG01433.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.842-339_842-338del others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66821286 | |||||
| chr11:66821413
|
G | A | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.842-230G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66821413 | ||||||
| chr11:66821497
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.842-146G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66821497 | ||||||
| chr11:66821907
|
G | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0210 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.963+143G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66821907 | ||||||
| chr11:66821969
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.963+205T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66821969 | ||||||
| chr11:66821988
|
T | G | 1 | a0001c0001t0002g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+224T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66821988 | ||||||
| chr11:66822396
|
C | A | 1 | a0001c0001t0002g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.964-168C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66822396 | ||||||
| chr11:66822400
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-164A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66822400 | ||||||
| chr11:66822928
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074+254C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66822928 | ||||||
| chr11:66822997
|
T | TA | 18 | a0001c0001t0001g0055a0001c0001t0001g0131a0001c0001t0001g0139others(15): Show | 18 | HG00423.hp2 HG01109.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.1074+338dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66822997 | |||||
| chr11:66822997
|
TA | T | 7 | a0001c0001t0001g0012a0002c0003t0005g0118a0002c0003t0005g0120others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074+338delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66822997 | |||||
| chr11:66823025
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1074+351T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823025 | ||||||
| chr11:66823084
|
C | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1074+410C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823084 | ||||||
| chr11:66823294
|
C | CA | 14 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0113others(11): Show | 14 | HG00621.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074+641dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66823294 | |||||
| chr11:66823384
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1074+710T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823384 | ||||||
| chr11:66823593
|
G | A | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1074+919G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823593 | ||||||
| chr11:66823790
|
C | G | 14 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0035others(11): Show | 14 | HG00438.hp2 HG00621.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074+1116C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823790 | ||||||
| chr11:66824276
|
G | A | 6 | a0001c0001t0002g0136a0001c0001t0002g0146a0001c0001t0002g0162others(3): Show | 6 | NA18968.hp2 NA18982.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+1602G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66824276 | ||||||
| chr11:66824419
|
A | T | 1 | a0001c0001t0002g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+1745A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66824419 | ||||||
| chr11:66824420
|
T | A | 1 | a0001c0001t0002g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1074+1746T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66824420 | ||||||
| chr11:66824420
|
T | TTTA | 16 | a0001c0001t0001g0046a0001c0001t0001g0098a0001c0001t0001g0197others(13): Show | 16 | HG00738.hp2 HG01928.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1074+1787_1074+178 others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | |||||
| chr11:66824420
|
T | TTTATTA | 4 | a0001c0001t0001g0100a0001c0001t0002g0132a0001c0001t0002g0187others(1): Show | 4 | HG00438.hp1 HG01433.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1784_1074+178 others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | |||||
| chr11:66824420
|
TTTA | T | 59 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0035others(56): Show | 59 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1074+1787_1074+178 others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | |||||
| chr11:66824420
|
TTTATTA | T | 16 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0055others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1074+1784_1074+178 others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | |||||
| chr11:66824420
|
TTTATTAT others(2): Show |
T | 49 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0231others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1074+1781_1074+178 others(13): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | |||||
| chr11:66824420
|
TTTATTAT others(5): Show |
T | 1 | a0001c0002t0001g0196 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1074+1778_1074+178 others(16): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | |||||
| chr11:66824420
|
TTTATTAT others(8): Show |
T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1074+1775_1074+178 others(19): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | |||||
| chr11:66824528
|
G | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1074+1854G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66824528 | ||||||
| chr11:66825036
|
G | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+2362G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825036 | ||||||
| chr11:66825110
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1074+2436C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825110 | ||||||
| chr11:66825158
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1074+2484C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825158 | ||||||
| chr11:66825187
|
G | A | 1 | a0001c0002t0001g0010 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1074+2513G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825187 | ||||||
| chr11:66825211
|
A | G | 4 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(1): Show | 4 | NA18943.hp2 NA18990.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+2537A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825211 | ||||||
| chr11:66825362
|
G | C | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1074+2688G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825362 | ||||||
| chr11:66825446
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1074+2772G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825446 | ||||||
| chr11:66825462
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1074+2788G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825462 | ||||||
| chr11:66825478
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1075-2788C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825478 | ||||||
| chr11:66825495
|
C | CA | 54 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0117others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1075-2760dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66825495 | |||||
| chr11:66825579
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-2687G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825579 | ||||||
| chr11:66825616
|
T | C | 10 | a0001c0001t0004g0081a0001c0001t0004g0082a0001c0001t0004g0121others(7): Show | 10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-2650T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825616 | ||||||
| chr11:66825841
|
C | CT | 7 | a0001c0001t0001g0182a0001c0001t0002g0221a0001c0001t0002g0223others(4): Show | 7 | HG01109.hp2 HG02738.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-2411dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66825841 | |||||
| chr11:66825982
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-2284C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825982 | ||||||
| chr11:66826045
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0101 | 3 | HG02257.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1075-2221G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826045 | ||||||
| chr11:66826078
|
C | T | 1 | a0001c0002t0013g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1075-2188C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826078 | ||||||
| chr11:66826210
|
A | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1075-2056A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826210 | ||||||
| chr11:66826255
|
T | A | 1 | a0001c0001t0011g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1075-2011T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826255 | ||||||
| chr11:66826298
|
T | C | 1 | a0001c0001t0004g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1075-1968T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826298 | ||||||
| chr11:66826323
|
T | G | 1 | a0001c0001t0004g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1075-1943T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826323 | ||||||
| chr11:66826477
|
A | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1075-1789A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826477 | ||||||
| chr11:66826691
|
AT | A | 9 | a0001c0001t0001g0055a0001c0001t0001g0131a0001c0001t0001g0139others(6): Show | 9 | HG00423.hp2 HG02523.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-1567delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66826691 | |||||
| chr11:66826709
|
T | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1075-1557T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826709 | ||||||
| chr11:66826760
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1075-1506G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826760 | ||||||
| chr11:66826981
|
C | CT | 145 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0035others(142): Show | 145 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1075-1268dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66826981 | |||||
| chr11:66826981
|
C | CTT | 7 | a0001c0001t0001g0056a0001c0001t0001g0093a0001c0001t0001g0235others(4): Show | 7 | HG00408.hp1 HG01175.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-1269_1075-126 others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66826981 | |||||
| chr11:66827042
|
C | T | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1075-1224C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66827042 | ||||||
| chr11:66827207
|
C | T | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-1059C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66827207 | ||||||
| chr11:66827955
|
ACT | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0101 | 3 | HG02257.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1075-308_1075-307d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827955 | |||||
| chr11:66827966
|
G | GA | 124 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0036others(121): Show | 124 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1075-273dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827966 | |||||
| chr11:66827966
|
G | GAA | 8 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0058others(5): Show | 8 | HG01361.hp2 HG01928.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1075-274_1075-273d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827966 | |||||
| chr11:66827966
|
GAA | G | 7 | a0001c0001t0003g0243a0002c0003t0005g0118a0002c0003t0005g0120others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-274_1075-273d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827966 | |||||
| chr11:66827966
|
GAAAAAAA others(3): Show |
G | 3 | a0001c0001t0001g0231a0001c0001t0004g0081a0001c0001t0004g0082 | 3 | HG01243.hp2 HG02630.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1075-282_1075-273d others(12): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827966 | |||||
| chr11:66827992
|
A | T | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1075-274A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66827992 | ||||||
| chr11:66828181
|
C | G | 1 | a0001c0001t0002g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1075-85C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66828181 | ||||||
| chr11:66828393
|
G | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0101 | 3 | HG02257.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1173+29G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828393 | ||||||
| chr11:66828433
|
G | T | 1 | a0002c0003t0005g0237 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+69G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828433 | ||||||
| chr11:66828508
|
A | G | 24 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.1173+144A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828508 | ||||||
| chr11:66828574
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0096 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1173+210G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828574 | ||||||
| chr11:66828611
|
C | T | 3 | a0001c0001t0002g0134a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | NA18941.hp2 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1173+247C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828611 | ||||||
| chr11:66828621
|
G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+257G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828621 | ||||||
| chr11:66828733
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1173+369G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828733 | ||||||
| chr11:66828966
|
GTGTTTTT | G | 3 | a0001c0001t0002g0134a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | NA18941.hp2 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1173+611_1173+617d others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66828966 | |||||
| chr11:66828975
|
G | GT | 44 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0078others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1173+625dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66828975 | |||||
| chr11:66828975
|
G | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0210 | 3 | HG02630.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1173+611G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828975 | ||||||
| chr11:66828975
|
GT | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+625delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66828975 | |||||
| chr11:66829041
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1173+677G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829041 | ||||||
| chr11:66829068
|
C | CA | 34 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0054others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1173+731dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66829068 | |||||
| chr11:66829068
|
CA | C | 10 | a0001c0001t0001g0043a0001c0001t0001g0208a0001c0001t0002g0220others(7): Show | 10 | HG01243.hp2 HG01515.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1173+731delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66829068 | |||||
| chr11:66829068
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0189a0001c0001t0002g0190 | 2 | HG02165.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1173+719_1173+731d others(15): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66829068 | |||||
| chr11:66829313
|
C | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+949C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829313 | ||||||
| chr11:66829341
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1173+977C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829341 | ||||||
| chr11:66829414
|
A | G | 3 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228 | 3 | HG01123.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1173+1050A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829414 | ||||||
| chr11:66829461
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1173+1097G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829461 | ||||||
| chr11:66829585
|
A | AG | 59 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0078others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1173+1221_1173+122 others(5): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829585 | ||||||
| chr11:66829732
|
T | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+1368T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829732 | ||||||
| chr11:66829763
|
C | G | 5 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+1399C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829763 | ||||||
| chr11:66829773
|
C | T | 1 | a0001c0001t0002g0143 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1173+1409C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829773 | ||||||
| chr11:66830056
|
C | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+1692C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830056 | ||||||
| chr11:66830115
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+1751A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830115 | ||||||
| chr11:66830266
|
C | T | 5 | a0001c0001t0006g0080a0001c0001t0006g0087a0001c0001t0006g0089others(2): Show | 5 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+1902C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830266 | ||||||
| chr11:66830306
|
C | T | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1173+1942C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830306 | ||||||
| chr11:66830477
|
A | C | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+2113A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830477 | ||||||
| chr11:66830559
|
T | C | 1 | a0001c0002t0001g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1173+2195T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830559 | ||||||
| chr11:66830637
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1173+2273C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830637 | ||||||
| chr11:66830982
|
G | T | 1 | a0001c0001t0002g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1173+2618G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830982 | ||||||
| chr11:66831071
|
A | C | 6 | a0001c0001t0004g0240a0001c0001t0006g0080a0001c0001t0006g0087others(3): Show | 6 | HG01934.hp1 HG02109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+2707A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831071 | ||||||
| chr11:66831180
|
C | T | 27 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.1173+2816C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831180 | ||||||
| chr11:66831351
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1173+2987C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831351 | ||||||
| chr11:66831398
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0208 | 3 | HG00408.hp1 NA18966.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1173+3034T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831398 | ||||||
| chr11:66831733
|
C | T | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1173+3369C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831733 | ||||||
| chr11:66831889
|
T | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+3525T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831889 | ||||||
| chr11:66831996
|
C | CA | 81 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0041others(78): Show | 81 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1173+3652dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66831996 | |||||
| chr11:66831996
|
CA | C | 8 | a0001c0001t0001g0096a0001c0001t0001g0235a0001c0001t0002g0146others(5): Show | 8 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+3652delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66831996 | |||||
| chr11:66832017
|
C | A | 2 | a0001c0001t0001g0204a0001c0001t0004g0081 | 2 | HG01243.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1173+3653C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832017 | ||||||
| chr11:66832259
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+3895G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832259 | ||||||
| chr11:66832276
|
A | C | 1 | a0001c0001t0002g0146 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1173+3912A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832276 | ||||||
| chr11:66832366
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1173+4002C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832366 | ||||||
| chr11:66832389
|
C | T | 6 | a0001c0001t0003g0002a0001c0001t0003g0137a0001c0001t0003g0166others(3): Show | 6 | HG01074.hp1 HG01175.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+4025C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832389 | ||||||
| chr11:66832402
|
C | A | 1 | a0001c0001t0002g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1173+4038C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832402 | ||||||
| chr11:66832851
|
G | T | 1 | a0001c0002t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1173+4487G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832851 | ||||||
| chr11:66833040
|
C | CT | 35 | a0001c0001t0001g0036a0001c0001t0001g0054a0001c0001t0001g0058others(32): Show | 35 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1173+4701dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66833040 | |||||
| chr11:66833040
|
CT | C | 15 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0091others(12): Show | 15 | HG00323.hp1 HG01243.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1173+4701delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66833040 | |||||
| chr11:66833040
|
CTTTT | C | 5 | a0001c0001t0006g0080a0001c0001t0006g0087a0001c0001t0006g0089others(2): Show | 5 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+4698_1173+470 others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66833040 | |||||
| chr11:66833101
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+4737G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833101 | ||||||
| chr11:66833488
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-4882C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833488 | ||||||
| chr11:66833567
|
C | T | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-4803C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833567 | ||||||
| chr11:66833621
|
T | C | 41 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0058others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1174-4749T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833621 | ||||||
| chr11:66833729
|
C | G | 1 | a0001c0002t0001g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1174-4641C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833729 | ||||||
| chr11:66833880
|
G | A | 1 | a0001c0002t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1174-4490G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833880 | ||||||
| chr11:66834363
|
A | G | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1174-4007A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834363 | ||||||
| chr11:66834421
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1174-3949T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834421 | ||||||
| chr11:66834437
|
C | T | 1 | a0001c0002t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1174-3933C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834437 | ||||||
| chr11:66834603
|
T | A | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1174-3767T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834603 | ||||||
| chr11:66834628
|
C | T | 164 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1174-3742C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834628 | ||||||
| chr11:66834972
|
G | A | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-3398G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834972 | ||||||
| chr11:66835022
|
C | T | 1 | a0001c0001t0012g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1174-3348C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835022 | ||||||
| chr11:66835309
|
GTTTC | G | 30 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(27): Show | 30 | HG00280.hp1 HG00609.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1174-3053_1174-305 others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66835309 | |||||
| chr11:66835483
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0225 | 2 | HG00438.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1174-2887A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835483 | ||||||
| chr11:66835658
|
G | C | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-2712G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835658 | ||||||
| chr11:66835772
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1174-2598T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835772 | ||||||
| chr11:66835809
|
G | A | 8 | a0001c0001t0002g0126a0001c0001t0002g0129a0001c0001t0002g0145others(5): Show | 8 | HG00408.hp2 NA18939.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-2561G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835809 | ||||||
| chr11:66836028
|
A | G | 2 | a0001c0001t0004g0084a0001c0001t0004g0085 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1174-2342A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836028 | ||||||
| chr11:66836240
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1174-2130G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836240 | ||||||
| chr11:66836432
|
A | G | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-1938A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836432 | ||||||
| chr11:66836545
|
T | C | 4 | a0001c0001t0009g0004a0004c0004t0008g0062a0004c0004t0008g0063others(1): Show | 4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-1825T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836545 | ||||||
| chr11:66836564
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1174-1806T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836564 | ||||||
| chr11:66836625
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1174-1745G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836625 | ||||||
| chr11:66836627
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1174-1743A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836627 | ||||||
| chr11:66836699
|
G | A | 10 | a0001c0001t0009g0004a0002c0003t0005g0118a0002c0003t0005g0120others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-1671G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836699 | ||||||
| chr11:66836700
|
A | AT | 157 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(154): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1174-1652dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66836700 | |||||
| chr11:66836700
|
A | ATT | 74 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0057others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1174-1653_1174-165 others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66836700 | |||||
| chr11:66836700
|
A | ATTT | 5 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG00423.hp1 HG01496.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-1654_1174-165 others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66836700 | |||||
| chr11:66836728
|
T | C | 4 | a0001c0001t0009g0004a0004c0004t0008g0062a0004c0004t0008g0063others(1): Show | 4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-1642T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836728 | ||||||
| chr11:66836962
|
G | A | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1174-1408G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836962 | ||||||
| chr11:66836973
|
A | G | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-1397A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836973 | ||||||
| chr11:66837252
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1174-1118G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837252 | ||||||
| chr11:66837445
|
A | AT | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(47): Show | 50 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.1174-907dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66837445 | |||||
| chr11:66837445
|
A | ATT | 5 | a0001c0001t0001g0032a0001c0001t0001g0091a0001c0001t0001g0106others(2): Show | 5 | HG01109.hp2 HG03098.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-908_1174-907d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66837445 | |||||
| chr11:66837510
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0207 | 2 | NA18945.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1174-860T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837510 | ||||||
| chr11:66837660
|
G | A | 6 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-710G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837660 | ||||||
| chr11:66837872
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1174-498C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837872 | ||||||
| chr11:66837939
|
A | C | 10 | a0001c0002t0001g0007a0001c0002t0001g0020a0001c0002t0001g0031others(7): Show | 10 | HG00621.hp1 HG02132.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-431A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837939 | ||||||
| chr11:66838212
|
G | T | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1174-158G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66838212 | ||||||
| chr11:66838321
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1174-49G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66838321 | ||||||
| chr11:66838475
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0003g0201 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1249+30G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66838475 | ||||||
| chr11:66838518
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1249+73A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66838518 | ||||||
| chr11:66839326
|
T | C | 1 | a0001c0002t0001g0074 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1249+881T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66839326 | ||||||
| chr11:66839499
|
C | A | 1 | a0001c0002t0001g0076 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1249+1054C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66839499 | ||||||
| chr11:66839583
|
G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1249+1138G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66839583 | ||||||
| chr11:66840184
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1249+1739A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840184 | ||||||
| chr11:66840282
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1249+1837C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840282 | ||||||
| chr11:66840314
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1249+1869C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840314 | ||||||
| chr11:66840391
|
C | G | 1 | a0006c0008t0002g0165 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1249+1946C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840391 | ||||||
| chr11:66840530
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1249+2085C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840530 | ||||||
| chr11:66840764
|
C | T | 2 | a0004c0004t0008g0062a0004c0004t0008g0063 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1250-2085C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840764 | ||||||
| chr11:66841050
|
G | C | 209 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(206): Show | 209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1250-1799G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841050 | ||||||
| chr11:66841104
|
C | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1250-1745C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841104 | ||||||
| chr11:66841110
|
A | AT | 78 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0053others(75): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1250-1715dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841110 | |||||
| chr11:66841110
|
A | T | 1 | a0001c0002t0001g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1250-1739A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841110 | ||||||
| chr11:66841110
|
AT | A | 14 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0002g0133others(11): Show | 14 | HG00621.hp2 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1250-1715delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841110 | |||||
| chr11:66841110
|
ATT | A | 7 | a0002c0003t0005g0118a0002c0003t0005g0120a0002c0003t0005g0237others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1250-1716_1250-171 others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841110 | |||||
| chr11:66841406
|
G | A | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1250-1443G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841406 | ||||||
| chr11:66841406
|
G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0029 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1250-1443G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841406 | ||||||
| chr11:66841417
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1250-1432A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841417 | ||||||
| chr11:66841520
|
T | C | 164 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1250-1329T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841520 | ||||||
| chr11:66841682
|
A | AGGT | 4 | a0001c0001t0009g0004a0004c0004t0008g0062a0004c0004t0008g0063others(1): Show | 4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250-1162_1250-116 others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841682 | |||||
| chr11:66841818
|
C | T | 133 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0041others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1250-1031C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841818 | ||||||
| chr11:66841850
|
T | TTTAC | 4 | a0001c0001t0009g0004a0004c0004t0008g0062a0004c0004t0008g0063others(1): Show | 4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250-997_1250-996i others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841850 | |||||
| chr11:66842281
|
A | G | 4 | a0001c0001t0001g0239a0001c0001t0001g0242a0001c0001t0003g0243others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-568A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66842281 | ||||||
| chr11:66842452
|
A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1250-397A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66842452 | ||||||
| chr11:66842500
|
G | A | 4 | a0001c0001t0006g0080a0001c0001t0006g0087a0001c0001t0006g0089others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-349G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66842500 |