Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2444 |
|---|---|
| ensemblid | ENSG00000111816.8 |
| hgncid | 3955 |
| symbol | FRK |
| name | fyn related Src family tyrosine kinase |
| refseq_nuc | NM_002031.3 |
| refseq_prot | NP_002022.1 |
| ensembl_nuc | ENST00000606080.2 |
| ensembl_prot | ENSP00000476145.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 115931149 |
| end | 116060891 |
| strand | - |
| ver | v1.2 |
| region | chr6:115931149-116060891 |
| region5000 | chr6:115926149-116065891 |
| regionname0 | FRK_chr6_115931149_116060891 |
| regionname5000 | FRK_chr6_115926149_116065891 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 505 | 152 | 60 | 35 | 35 | 8 | 12 | 31 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002 | 0/0 | 505 | 113 | 20 | 17 | 54 | 8 | 14 | 38 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0003 | 0/0 | 505 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0004 | 0/0 | 505 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0005 | 0/0 | 505 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0006 | 0/0 | 505 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1518 | 147 | 59 | 35 | 31 | 8 | 12 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| c0002 | 0/0 | 1518 | 111 | 18 | 17 | 54 | 8 | 14 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| c0003 | 0/0 | 1518 | 4 | 0 | 0 | 4 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| c0004 | 0/0 | 1518 | 4 | 0 | 0 | 4 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| c0005 | 0/0 | 1518 | 2 | 0 | 0 | 2 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| c0006 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| c0007 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| c0008 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| c0009 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 11842 | 56 | 21 | 11 | 12 | 5 | 7 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0002 | 0/0 | 11842 | 42 | 1 | 6 | 24 | 4 | 7 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0003 | 0/0 | 11843 | 14 | 2 | 10 | 0 | 1 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0004 | 0/0 | 11843 | 13 | 0 | 0 | 13 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0005 | 0/0 | 11845 | 12 | 0 | 2 | 10 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0006 | 0/0 | 11843 | 12 | 4 | 1 | 7 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0007 | 0/0 | 11842 | 10 | 10 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0008 | 0/0 | 11845 | 10 | 0 | 5 | 1 | 2 | 2 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0009 | 0/0 | 11843 | 5 | 0 | 0 | 5 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0010 | 0/0 | 11842 | 5 | 5 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0011 | 0/0 | 11842 | 5 | 1 | 3 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0012 | 0/0 | 11839 | 4 | 4 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0013 | 0/0 | 11843 | 4 | 0 | 2 | 0 | 0 | 2 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0014 | 0/0 | 11841 | 4 | 1 | 2 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0015 | 0/0 | 11843 | 4 | 2 | 1 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0016 | 0/0 | 11843 | 3 | 2 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0017 | 0/0 | 11845 | 3 | 3 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0018 | 0/1 | 11842 | 3 | 1 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0019 | 0/0 | 11841 | 3 | 0 | 0 | 3 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0020 | 0/0 | 11842 | 3 | 0 | 0 | 3 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0021 | 0/0 | 11843 | 3 | 0 | 1 | 0 | 2 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0022 | 0/0 | 11842 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0023 | 0/0 | 11842 | 2 | 0 | 0 | 2 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0024 | 0/0 | 11842 | 2 | 1 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0025 | 0/0 | 11843 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0026 | 0/0 | 11842 | 2 | 0 | 1 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0027 | 0/0 | 11842 | 2 | 0 | 0 | 0 | 0 | 2 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0028 | 0/0 | 11843 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0029 | 0/0 | 11843 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0030 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0031 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0032 | 1/0 | 11846 | 1 | 0 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0033 | 0/0 | 11843 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0034 | 0/0 | 11845 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0035 | 0/0 | 11841 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0036 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0037 | 0/0 | 11842 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0038 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0039 | 0/0 | 11842 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0040 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0041 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0042 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0043 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0044 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0045 | 0/0 | 11842 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0046 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0047 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0048 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0049 | 0/0 | 11842 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0050 | 0/0 | 11843 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0051 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0052 | 0/0 | 11823 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0053 | 0/0 | 11842 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0054 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0055 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0056 | 0/0 | 11842 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0057 | 0/0 | 11845 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0058 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0059 | 0/0 | 11843 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0060 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0061 | 0/0 | 11841 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0062 | 0/0 | 11841 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0063 | 0/0 | 11843 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0064 | 0/0 | 11843 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0065 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0066 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0067 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0068 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0069 | 0/0 | 11843 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0070 | 0/0 | 11843 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| t0071 | 0/0 | 11845 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1518 | 147 | 59 | 35 | 31 | 8 | 12 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0004 | 0/0 | 1518 | 4 | 0 | 0 | 4 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0009 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002 | 0/0 | 1518 | 111 | 18 | 17 | 54 | 8 | 14 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0006 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0003c0003 | 0/0 | 1518 | 4 | 0 | 0 | 4 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0004c0007 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0005c0005 | 0/0 | 1518 | 2 | 0 | 0 | 2 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0006c0008 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 13359 | 30 | 17 | 5 | 3 | 3 | 2 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0002 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0003 | 0/0 | 13360 | 14 | 2 | 10 | 0 | 1 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0004 | 0/0 | 13360 | 6 | 0 | 0 | 6 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0006 | 0/0 | 13360 | 12 | 4 | 1 | 7 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0008 | 0/0 | 13362 | 10 | 0 | 5 | 1 | 2 | 2 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0009 | 0/0 | 13360 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0010 | 0/0 | 13359 | 5 | 5 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0011 | 0/0 | 13359 | 5 | 1 | 3 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0012 | 0/0 | 13356 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0013 | 0/0 | 13360 | 4 | 0 | 2 | 0 | 0 | 2 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0014 | 0/0 | 13358 | 4 | 1 | 2 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0015 | 0/0 | 13360 | 2 | 0 | 1 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0016 | 0/0 | 13360 | 3 | 2 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0017 | 0/0 | 13362 | 3 | 3 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0018 | 0/1 | 13359 | 3 | 1 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0020 | 0/0 | 13359 | 3 | 0 | 0 | 3 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0022 | 0/0 | 13359 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0023 | 0/0 | 13359 | 2 | 0 | 0 | 2 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0024 | 0/0 | 13359 | 2 | 1 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0025 | 0/0 | 13360 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0026 | 0/0 | 13359 | 2 | 0 | 1 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0027 | 0/0 | 13359 | 2 | 0 | 0 | 0 | 0 | 2 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0028 | 0/0 | 13360 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0029 | 0/0 | 13360 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0032 | 1/0 | 13363 | 1 | 0 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0034 | 0/0 | 13362 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0035 | 0/0 | 13358 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0037 | 0/0 | 13359 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0039 | 0/0 | 13359 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0042 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0043 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0047 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0049 | 0/0 | 13359 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0050 | 0/0 | 13360 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0051 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0056 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0058 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0059 | 0/0 | 13360 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0060 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0061 | 0/0 | 13358 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0062 | 0/0 | 13358 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0063 | 0/0 | 13360 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0064 | 0/0 | 13360 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0065 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0066 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0067 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0068 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0069 | 0/0 | 13360 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0070 | 0/0 | 13360 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0001t0071 | 0/0 | 13362 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0004t0001 | 0/0 | 13359 | 3 | 0 | 0 | 3 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0004t0046 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0001c0009t0012 | 0/0 | 13356 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0001 | 0/0 | 13359 | 23 | 4 | 6 | 6 | 2 | 5 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0002 | 0/0 | 13359 | 38 | 1 | 6 | 20 | 4 | 7 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0004 | 0/0 | 13360 | 4 | 0 | 0 | 4 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0005 | 0/0 | 13362 | 12 | 0 | 2 | 10 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0007 | 0/0 | 13359 | 10 | 10 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0009 | 0/0 | 13360 | 4 | 0 | 0 | 4 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0019 | 0/0 | 13358 | 3 | 0 | 0 | 3 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0021 | 0/0 | 13360 | 3 | 0 | 1 | 0 | 2 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0030 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0031 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0033 | 0/0 | 13360 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0036 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0038 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0040 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0041 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0044 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0045 | 0/0 | 13359 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0048 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0053 | 0/0 | 13359 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0054 | 0/0 | 13359 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0055 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0002t0057 | 0/0 | 13362 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0002c0006t0012 | 0/0 | 13356 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0003c0003t0004 | 0/0 | 13360 | 3 | 0 | 0 | 3 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0003c0003t0052 | 0/0 | 13340 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0004c0007t0015 | 0/0 | 13360 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0005c0005t0002 | 0/0 | 13359 | 2 | 0 | 0 | 2 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| a0006c0008t0002 | 0/0 | 13359 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | copy fasta | chr6 | 115926149 | 116065891 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0011g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0011g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0013g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0013g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0013g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0014g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0014g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0014g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0014g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0015g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0015g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0017g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0017g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0018g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0018g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0018g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0020g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0020g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0020g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0022g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0022g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0023g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0023g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0024g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0024g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0025g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0025g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0026g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0026g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0027g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0027g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0028g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0029g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0032g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0034g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0035g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0037g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0039g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0042g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0043g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0047g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0049g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0050g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0051g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0056g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0058g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0059g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0060g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0061g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0062g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0063g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0064g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0065g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0066g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0067g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0068g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0069g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0070g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0001t0071g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0004t0046g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0001c0009t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0009g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0009g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0019g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0019g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0019g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0021g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0021g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0021g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0030g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0031g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0033g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0036g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0038g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0040g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0041g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0044g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0045g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0048g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0053g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0054g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0055g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0002t0057g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0006t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0002c0006t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0003c0003t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0003c0003t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0003c0003t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0003c0003t0052g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0004c0007t0015g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0004c0007t0015g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0005c0005t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0005c0005t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| a0006c0008t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0057 | EUR | GBR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | GBR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0167 | EUR | GBR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0024 | EUR | FIN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00280 | hp2 | a0001 | c0001 | t0011 | g0234 | EUR | FIN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00544 | hp1 | a0002 | c0002 | t0004 | g0171 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00558 | hp1 | a0002 | c0002 | t0005 | g0066 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00621 | hp1 | a0001 | c0001 | t0020 | g0138 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00621 | hp2 | a0002 | c0002 | t0019 | g0174 | EAS | CHS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00642 | hp1 | a0001 | c0001 | t0024 | g0177 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00642 | hp2 | a0001 | c0001 | t0011 | g0249 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00738 | hp1 | a0001 | c0001 | t0014 | g0261 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG00741 | hp2 | a0001 | c0001 | t0050 | g0181 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01069 | hp2 | a0001 | c0001 | t0026 | g0245 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0217 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01081 | hp2 | a0001 | c0001 | t0014 | g0262 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01099 | hp1 | a0001 | c0001 | t0037 | g0114 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01106 | hp1 | a0001 | c0001 | t0039 | g0180 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01106 | hp2 | a0001 | c0001 | t0013 | g0222 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0237 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01109 | hp2 | a0002 | c0002 | t0045 | g0085 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01169 | hp1 | a0002 | c0002 | t0021 | g0043 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01169 | hp2 | a0001 | c0001 | t0011 | g0248 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01258 | hp2 | a0001 | c0001 | t0069 | g0243 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0053 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0086 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0205 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0168 | EUR | IBS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0203 | EUR | IBS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01516 | hp1 | a0002 | c0002 | t0021 | g0008 | EUR | IBS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0204 | EUR | IBS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01517 | hp2 | a0002 | c0002 | t0021 | g0007 | EUR | IBS | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0112 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01952 | hp1 | a0002 | c0002 | t0005 | g0172 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0211 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01981 | hp2 | a0001 | c0001 | t0015 | g0231 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02004 | hp1 | a0002 | c0002 | t0005 | g0128 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02040 | hp1 | a0002 | c0002 | t0048 | g0033 | EAS | KHV | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | KHV | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02055 | hp2 | a0001 | c0001 | t0067 | g0207 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02074 | hp2 | a0002 | c0002 | t0004 | g0040 | EAS | KHV | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02080 | hp1 | a0001 | c0001 | t0026 | g0270 | EAS | KHV | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | KHV | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02132 | hp1 | a0002 | c0002 | t0004 | g0041 | EAS | KHV | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | KHV | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02145 | hp1 | a0001 | c0001 | t0060 | g0259 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | CDX | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02165 | hp2 | a0002 | c0002 | t0005 | g0035 | EAS | CDX | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02258 | hp1 | a0001 | c0001 | t0070 | g0242 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02258 | hp2 | a0001 | c0001 | t0066 | g0201 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02273 | hp2 | a0002 | c0002 | t0057 | g0126 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02280 | hp1 | a0001 | c0001 | t0029 | g0113 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0010 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0214 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PEL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02615 | hp1 | a0002 | c0002 | t0007 | g0193 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0256 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02622 | hp1 | a0001 | c0001 | t0051 | g0103 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02622 | hp2 | a0002 | c0002 | t0007 | g0157 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02630 | hp1 | a0002 | c0002 | t0007 | g0159 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02647 | hp2 | a0001 | c0001 | t0061 | g0257 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0067 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02683 | hp2 | a0001 | c0001 | t0014 | g0263 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02717 | hp1 | a0002 | c0002 | t0007 | g0158 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02809 | hp1 | a0001 | c0001 | t0035 | g0004 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02809 | hp2 | a0002 | c0002 | t0007 | g0160 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02818 | hp2 | a0001 | c0001 | t0034 | g0198 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02886 | hp1 | a0001 | c0009 | t0012 | g0120 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02886 | hp2 | a0002 | c0002 | t0007 | g0153 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02896 | hp2 | a0002 | c0002 | t0030 | g0091 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0200 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02897 | hp2 | a0002 | c0002 | t0031 | g0092 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0221 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02965 | hp2 | a0001 | c0001 | t0024 | g0006 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02976 | hp2 | a0001 | c0001 | t0017 | g0009 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03041 | hp1 | a0002 | c0006 | t0012 | g0097 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03041 | hp2 | a0001 | c0001 | t0059 | g0255 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0215 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03130 | hp1 | a0001 | c0001 | t0047 | g0186 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0271 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03139 | hp2 | a0001 | c0001 | t0022 | g0184 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03195 | hp1 | a0001 | c0001 | t0043 | g0189 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03195 | hp2 | a0002 | c0002 | t0007 | g0155 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03209 | hp2 | a0001 | c0001 | t0064 | g0219 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03225 | hp2 | a0001 | c0001 | t0058 | g0199 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03453 | hp2 | a0001 | c0001 | t0025 | g0254 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03516 | hp1 | a0001 | c0001 | t0065 | g0258 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03516 | hp2 | a0002 | c0002 | t0007 | g0154 | AFR | ESN | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | GWD | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03579 | hp1 | a0002 | c0006 | t0012 | g0096 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03669 | hp1 | a0001 | c0001 | t0049 | g0197 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03688 | hp1 | a0002 | c0002 | t0033 | g0069 | SAS | STU | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0228 | SAS | STU | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03704 | hp1 | a0001 | c0001 | t0013 | g0229 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0038 | SAS | BEB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0034 | SAS | BEB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03834 | hp1 | a0002 | c0002 | t0053 | g0068 | SAS | BEB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0213 | SAS | BEB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0071 | SAS | BEB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0212 | SAS | BEB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG04115 | hp1 | a0001 | c0001 | t0027 | g0210 | SAS | STU | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | STU | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG04199 | hp2 | a0001 | c0001 | t0027 | g0206 | SAS | STU | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18906 | hp1 | a0001 | c0001 | t0068 | g0208 | AFR | YRI | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18906 | hp2 | a0001 | c0001 | t0022 | g0185 | AFR | YRI | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18942 | hp1 | a0001 | c0001 | t0023 | g0151 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18942 | hp2 | a0002 | c0002 | t0005 | g0019 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18954 | hp2 | a0002 | c0002 | t0038 | g0073 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0266 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18962 | hp1 | a0002 | c0002 | t0005 | g0046 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18962 | hp2 | a0003 | c0003 | t0004 | g0163 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18963 | hp1 | a0002 | c0002 | t0009 | g0048 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18968 | hp2 | a0002 | c0002 | t0009 | g0098 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18970 | hp1 | a0002 | c0002 | t0005 | g0045 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18970 | hp2 | a0003 | c0003 | t0004 | g0164 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18972 | hp1 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18972 | hp2 | a0002 | c0002 | t0040 | g0011 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18973 | hp2 | a0001 | c0001 | t0016 | g0131 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18974 | hp1 | a0005 | c0005 | t0002 | g0094 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18974 | hp2 | a0001 | c0001 | t0020 | g0139 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18978 | hp1 | a0001 | c0004 | t0046 | g0166 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18981 | hp1 | a0002 | c0002 | t0044 | g0021 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18981 | hp2 | a0001 | c0001 | t0056 | g0134 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18983 | hp1 | a0001 | c0001 | t0023 | g0152 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18986 | hp1 | a0002 | c0002 | t0005 | g0018 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18986 | hp2 | a0001 | c0001 | t0071 | g0272 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18989 | hp1 | a0001 | c0001 | t0042 | g0191 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0032 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18993 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18999 | hp1 | a0002 | c0002 | t0036 | g0052 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA18999 | hp2 | a0006 | c0008 | t0002 | g0055 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19007 | hp1 | a0003 | c0003 | t0052 | g0162 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19007 | hp2 | a0002 | c0002 | t0009 | g0099 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19009 | hp1 | a0001 | c0001 | t0020 | g0137 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19010 | hp2 | a0002 | c0002 | t0009 | g0165 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19030 | hp1 | a0001 | c0001 | t0016 | g0182 | AFR | LWK | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19030 | hp2 | a0004 | c0007 | t0015 | g0267 | AFR | LWK | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0216 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19062 | hp2 | a0002 | c0002 | t0005 | g0062 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19063 | hp1 | a0001 | c0001 | t0028 | g0003 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19063 | hp2 | a0002 | c0002 | t0041 | g0089 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19064 | hp2 | a0002 | c0002 | t0005 | g0065 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19065 | hp1 | a0003 | c0003 | t0004 | g0161 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19065 | hp2 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19067 | hp1 | a0001 | c0001 | t0008 | g0233 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19067 | hp2 | a0005 | c0005 | t0002 | g0095 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19068 | hp1 | a0002 | c0002 | t0019 | g0176 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0179 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19074 | hp2 | a0001 | c0004 | t0001 | g0109 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19078 | hp1 | a0001 | c0001 | t0063 | g0223 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19083 | hp1 | a0002 | c0002 | t0055 | g0100 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19083 | hp2 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19087 | hp1 | a0002 | c0002 | t0019 | g0061 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19090 | hp1 | a0002 | c0002 | t0005 | g0016 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | YRI | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA19240 | hp2 | a0001 | c0001 | t0016 | g0117 | AFR | YRI | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | ASW | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0264 | AFR | ASW | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0244 | EUR | TSI | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0077 | EUR | TSI | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20805 | hp2 | a0001 | c0001 | t0015 | g0253 | EUR | TSI | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | GIH | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20905 | hp2 | a0001 | c0001 | t0018 | g0115 | SAS | GIH | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01123 | hp1 | a0001 | c0001 | t0013 | g0227 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02109 | hp1 | a0001 | c0001 | t0062 | g0218 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0202 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02486 | hp2 | a0001 | c0001 | t0018 | g0056 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0268 | AFR | ACB | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03471 | hp1 | a0002 | c0002 | t0054 | g0023 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG03471 | hp2 | a0001 | c0001 | t0017 | g0194 | AFR | MSL | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG06807 | hp1 | a0002 | c0002 | t0007 | g0192 | AFR | USA | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0209 | AFR | USA | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA20300 | hp2 | a0002 | c0002 | t0007 | g0156 | AFR | USA | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| NA21309 | hp2 | a0004 | c0007 | t0015 | g0230 | AFR | LWK | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0018 | g0116 | REF | REF | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0032 | g0101 | REF | REF | FRK_chr6_115926149_116065891 | FRK | chr6 | 115926149 | 116065891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:115942490
|
T | A | 1 | a0006 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.1442A>T | p.Glu481Val | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2022/13363 | 1442/1518 | 481/505 | chr6 | 115942490 | ||
| chr6:115943152
|
C | T | 1 | a0004 | 2 | NA19030.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.1174G>A | p.Glu392Lys | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 7/8 | 1754/13363 | 1174/1518 | 392/505 | chr6 | 115943152 | ||
| chr6:115968602
|
C | G | 1 | a0005 | 2 | NA18974.hp1 NA19067.hp2 |
missense_variant | MODERATE | c.604G>C | p.Val202Leu | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/8 | 1184/13363 | 604/1518 | 202/505 | chr6 | 115968602 | ||
| chr6:116003968
|
A | C | 1 | a0003 | 4 | NA18962.hp2 NA18970.hp2 NA19007.hp1 others(1): Show |
missense_variant | MODERATE | c.375T>G | p.Asp125Glu | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/8 | 955/13363 | 375/1518 | 125/505 | chr6 | 116003968 | ||
| chr6:116003979
|
C | T | 3 | a0002a0005a0006 | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
missense_variant | MODERATE | c.364G>A | p.Gly122Arg | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/8 | 944/13363 | 364/1518 | 122/505 | chr6 | 116003979 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:115944271
|
T | C | 2 | a0001c0009a0002c0006 | 3 | HG02886.hp1 HG03041.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.1113A>G | p.Ala371Ala | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/8 | 1693/13363 | 1113/1518 | 371/505 | chr6 | 115944271 | ||
| chr6:115944367
|
G | A | 1 | a0001c0004 | 4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
synonymous_variant | LOW | c.1017C>T | p.Ala339Ala | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/8 | 1597/13363 | 1017/1518 | 339/505 | chr6 | 115944367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:115931160
|
C | T | 1 | a0001c0001t0042 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11254G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 11254 | chr6 | 115931160 | |||||
| chr6:115931209
|
T | A | 5 | a0001c0001t0022a0001c0001t0060a0002c0002t0007others(2): Show | 15 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*11205A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 11205 | chr6 | 115931209 | |||||
| chr6:115931247
|
A | G | 2 | a0001c0001t0017a0001c0001t0034 | 4 | HG02280.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11167T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 11167 | chr6 | 115931247 | |||||
| chr6:115931388
|
T | A | 33 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(30): Show | 103 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*11026A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 11026 | chr6 | 115931388 | |||||
| chr6:115931499
|
A | G | 2 | a0002c0002t0038a0002c0002t0048 | 2 | HG02040.hp1 NA18954.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10915T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 10915 | chr6 | 115931499 | |||||
| chr6:115931612
|
T | C | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10802A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 10802 | chr6 | 115931612 | |||||
| chr6:115931806
|
C | T | 1 | a0001c0001t0047 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10608G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 10608 | chr6 | 115931806 | |||||
| chr6:115932035
|
C | T | 1 | a0002c0002t0036 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10379G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 10379 | chr6 | 115932035 | |||||
| chr6:115932075
|
T | G | 1 | a0001c0001t0049 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10339A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 10339 | chr6 | 115932075 | |||||
| chr6:115932095
|
T | C | 1 | a0001c0001t0067 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10319A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 10319 | chr6 | 115932095 | |||||
| chr6:115932168
|
TTATA | T | 24 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(21): Show | 71 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*10242_*10245delTA others(2): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 10242 | chr6 | 115932168 | |||||
| chr6:115932360
|
G | T | 1 | a0001c0004t0046 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10054C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 10054 | chr6 | 115932360 | |||||
| chr6:115932534
|
T | C | 1 | a0001c0001t0065 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9880A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 9880 | chr6 | 115932534 | |||||
| chr6:115932602
|
T | G | 33 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(30): Show | 103 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*9812A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 9812 | chr6 | 115932602 | |||||
| chr6:115932940
|
C | T | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*9474G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 9474 | chr6 | 115932940 | |||||
| chr6:115932978
|
A | G | 1 | a0001c0001t0014 | 4 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9436T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 9436 | chr6 | 115932978 | |||||
| chr6:115933059
|
G | T | 1 | a0002c0002t0045 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9355C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 9355 | chr6 | 115933059 | |||||
| chr6:115933212
|
A | G | 1 | a0001c0001t0065 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9202T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 9202 | chr6 | 115933212 | |||||
| chr6:115933290
|
C | T | 1 | a0002c0002t0044 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9124G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 9124 | chr6 | 115933290 | |||||
| chr6:115933315
|
A | G | 2 | a0001c0001t0066a0001c0001t0067 | 2 | HG02055.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9099T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 9099 | chr6 | 115933315 | |||||
| chr6:115933419
|
C | A | 1 | a0001c0001t0035 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8995G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8995 | chr6 | 115933419 | |||||
| chr6:115933500
|
C | T | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8914G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8914 | chr6 | 115933500 | |||||
| chr6:115933543
|
C | T | 1 | a0001c0001t0043 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8871G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8871 | chr6 | 115933543 | |||||
| chr6:115933671
|
T | C | 28 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(25): Show | 95 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*8743A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8743 | chr6 | 115933671 | |||||
| chr6:115933709
|
C | T | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8705G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8705 | chr6 | 115933709 | |||||
| chr6:115933778
|
G | T | 1 | a0001c0001t0013 | 4 | HG01106.hp2 HG01123.hp1 HG03688.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8636C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8636 | chr6 | 115933778 | |||||
| chr6:115933831
|
A | G | 5 | a0001c0001t0010a0001c0001t0027a0001c0001t0065others(2): Show | 10 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8583T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8583 | chr6 | 115933831 | |||||
| chr6:115933878
|
T | C | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8536A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8536 | chr6 | 115933878 | |||||
| chr6:115934136
|
T | A | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8278A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 8278 | chr6 | 115934136 | |||||
| chr6:115934460
|
G | A | 1 | a0001c0001t0027 | 2 | HG04115.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7954C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7954 | chr6 | 115934460 | |||||
| chr6:115934780
|
C | A | 1 | a0002c0002t0031 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7634G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7634 | chr6 | 115934780 | |||||
| chr6:115934828
|
G | A | 2 | a0001c0001t0060a0002c0002t0007 | 11 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7586C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7586 | chr6 | 115934828 | |||||
| chr6:115934890
|
A | G | 2 | a0001c0001t0020a0001c0001t0042 | 4 | HG00621.hp1 NA18974.hp2 NA18989.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7524T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7524 | chr6 | 115934890 | |||||
| chr6:115934941
|
CA | C | 66 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(63): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*7472delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7472 | chr6 | 115934941 | |||||
| chr6:115934952
|
A | AG | 9 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(6): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7461_*7462insC | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7461 | chr6 | 115934952 | |||||
| chr6:115934955
|
A | C | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7459T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7459 | chr6 | 115934955 | |||||
| chr6:115935119
|
TG | T | 1 | a0002c0002t0019 | 3 | HG00621.hp2 NA19068.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7294delC | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7294 | chr6 | 115935119 | |||||
| chr6:115935311
|
A | G | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*7103T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7103 | chr6 | 115935311 | |||||
| chr6:115935349
|
T | C | 76 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*7065A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7065 | chr6 | 115935349 | |||||
| chr6:115935350
|
G | A | 5 | a0001c0001t0012a0001c0001t0015a0001c0009t0012others(2): Show | 8 | HG01884.hp2 HG01981.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7064C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7064 | chr6 | 115935350 | |||||
| chr6:115935371
|
G | A | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7043C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7043 | chr6 | 115935371 | |||||
| chr6:115935379
|
C | T | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7035G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 7035 | chr6 | 115935379 | |||||
| chr6:115935432
|
C | A | 9 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(6): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6982G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6982 | chr6 | 115935432 | |||||
| chr6:115935566
|
C | T | 2 | a0001c0001t0060a0002c0002t0007 | 11 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6848G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6848 | chr6 | 115935566 | |||||
| chr6:115935571
|
C | T | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6843G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6843 | chr6 | 115935571 | |||||
| chr6:115935859
|
A | G | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6555T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6555 | chr6 | 115935859 | |||||
| chr6:115935939
|
C | T | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6475G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6475 | chr6 | 115935939 | |||||
| chr6:115936043
|
T | C | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6371A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6371 | chr6 | 115936043 | |||||
| chr6:115936198
|
ACAGCATC others(13): Show |
A | 1 | a0003c0003t0052 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6196_*6215delGAGG others(16): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6196 | chr6 | 115936198 | |||||
| chr6:115936265
|
G | T | 2 | a0001c0001t0017a0001c0001t0034 | 4 | HG02280.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6149C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6149 | chr6 | 115936265 | |||||
| chr6:115936374
|
A | G | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6040T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6040 | chr6 | 115936374 | |||||
| chr6:115936401
|
A | G | 2 | a0001c0001t0025a0001c0001t0059 | 3 | HG02559.hp2 HG03041.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6013T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 6013 | chr6 | 115936401 | |||||
| chr6:115936480
|
C | T | 1 | a0001c0001t0063 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5934G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5934 | chr6 | 115936480 | |||||
| chr6:115936490
|
GAA | G | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5922_*5923delTT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5922 | chr6 | 115936490 | |||||
| chr6:115936493
|
G | A | 1 | a0001c0001t0034 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5921C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5921 | chr6 | 115936493 | |||||
| chr6:115936700
|
G | A | 2 | a0001c0001t0017a0001c0001t0034 | 4 | HG02280.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5714C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5714 | chr6 | 115936700 | |||||
| chr6:115936702
|
C | T | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5712G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5712 | chr6 | 115936702 | |||||
| chr6:115936715
|
G | A | 1 | a0001c0001t0035 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5699C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5699 | chr6 | 115936715 | |||||
| chr6:115936847
|
T | G | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5567A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5567 | chr6 | 115936847 | |||||
| chr6:115936869
|
C | T | 1 | a0001c0001t0071 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5545G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5545 | chr6 | 115936869 | |||||
| chr6:115936910
|
T | G | 2 | a0001c0001t0024a0001c0001t0068 | 3 | HG00642.hp1 HG02965.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5504A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5504 | chr6 | 115936910 | |||||
| chr6:115936994
|
C | G | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5420G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5420 | chr6 | 115936994 | |||||
| chr6:115937239
|
G | A | 11 | a0001c0001t0003a0001c0001t0012a0001c0001t0014others(8): Show | 32 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5175C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 5175 | chr6 | 115937239 | |||||
| chr6:115937473
|
C | T | 1 | a0001c0001t0065 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4941G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 4941 | chr6 | 115937473 | |||||
| chr6:115937608
|
A | G | 1 | a0001c0001t0071 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4806T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 4806 | chr6 | 115937608 | |||||
| chr6:115937643
|
C | T | 2 | a0001c0001t0023a0001c0001t0069 | 3 | HG01258.hp2 NA18942.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4771G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 4771 | chr6 | 115937643 | |||||
| chr6:115937894
|
T | C | 76 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*4520A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 4520 | chr6 | 115937894 | |||||
| chr6:115938063
|
T | C | 9 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(6): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4351A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 4351 | chr6 | 115938063 | |||||
| chr6:115938116
|
TAACA | T | 3 | a0001c0001t0012a0001c0009t0012a0002c0006t0012 | 4 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4294_*4297delTGTT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 4294 | chr6 | 115938116 | |||||
| chr6:115938249
|
T | C | 76 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*4165A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 4165 | chr6 | 115938249 | |||||
| chr6:115938388
|
C | A | 1 | a0002c0002t0057 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4026G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 4026 | chr6 | 115938388 | |||||
| chr6:115938430
|
G | C | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3984C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3984 | chr6 | 115938430 | |||||
| chr6:115938566
|
G | A | 2 | a0001c0001t0017a0001c0001t0034 | 4 | HG02280.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3848C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3848 | chr6 | 115938566 | |||||
| chr6:115938687
|
T | G | 1 | a0001c0001t0051 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3727A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3727 | chr6 | 115938687 | |||||
| chr6:115938747
|
A | G | 1 | a0002c0002t0041 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3667T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3667 | chr6 | 115938747 | |||||
| chr6:115939021
|
C | CAA | 6 | a0001c0001t0006a0001c0001t0013a0001c0001t0016others(3): Show | 22 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3391_*3392dupTT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3392 | chr6 | 115939021 | |||||
| chr6:115939024
|
A | C | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3390T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3390 | chr6 | 115939024 | |||||
| chr6:115939076
|
C | CA | 7 | a0001c0001t0004a0001c0001t0009a0001c0001t0028others(4): Show | 20 | HG00544.hp1 HG00558.hp2 HG02074.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3337dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3337 | chr6 | 115939076 | |||||
| chr6:115939206
|
C | A | 1 | a0002c0002t0053 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3208G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3208 | chr6 | 115939206 | |||||
| chr6:115939373
|
A | T | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3041T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 3041 | chr6 | 115939373 | |||||
| chr6:115939415
|
C | G | 1 | a0001c0001t0039 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2999G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2999 | chr6 | 115939415 | |||||
| chr6:115939504
|
A | C | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2910T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2910 | chr6 | 115939504 | |||||
| chr6:115939534
|
G | A | 1 | a0001c0001t0070 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2880C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2880 | chr6 | 115939534 | |||||
| chr6:115939560
|
T | C | 1 | a0002c0002t0054 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2854A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2854 | chr6 | 115939560 | |||||
| chr6:115939612
|
G | A | 2 | a0001c0001t0017a0001c0001t0034 | 4 | HG02280.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2802C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2802 | chr6 | 115939612 | |||||
| chr6:115939880
|
A | T | 1 | a0001c0001t0035 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2534T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2534 | chr6 | 115939880 | |||||
| chr6:115939926
|
T | C | 1 | a0001c0001t0037 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2488A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2488 | chr6 | 115939926 | |||||
| chr6:115939932
|
C | T | 1 | a0002c0002t0033 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2482G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2482 | chr6 | 115939932 | |||||
| chr6:115939933
|
C | T | 8 | a0001c0001t0006a0001c0001t0013a0001c0001t0016others(5): Show | 24 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2481G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2481 | chr6 | 115939933 | |||||
| chr6:115939979
|
C | T | 3 | a0001c0001t0018a0001c0001t0037a0001c0001t0039 | 5 | HG01099.hp1 HG01106.hp1 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2435G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2435 | chr6 | 115939979 | |||||
| chr6:115940011
|
C | T | 1 | a0002c0002t0038 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2403 | chr6 | 115940011 | |||||
| chr6:115940028
|
T | C | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2386A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2386 | chr6 | 115940028 | |||||
| chr6:115940040
|
G | T | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2374C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2374 | chr6 | 115940040 | |||||
| chr6:115940048
|
T | C | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2366A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2366 | chr6 | 115940048 | |||||
| chr6:115940050
|
A | G | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2364T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2364 | chr6 | 115940050 | |||||
| chr6:115940051
|
T | G | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2363A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2363 | chr6 | 115940051 | |||||
| chr6:115940110
|
T | C | 1 | a0001c0001t0064 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2304A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2304 | chr6 | 115940110 | |||||
| chr6:115940196
|
C | A | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2218G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2218 | chr6 | 115940196 | |||||
| chr6:115940323
|
T | C | 1 | a0002c0002t0055 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2091A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 2091 | chr6 | 115940323 | |||||
| chr6:115940470
|
T | C | 1 | a0001c0001t0056 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1944A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1944 | chr6 | 115940470 | |||||
| chr6:115940645
|
C | T | 1 | a0001c0001t0059 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1769 | chr6 | 115940645 | |||||
| chr6:115940665
|
C | T | 2 | a0001c0001t0037a0001c0001t0061 | 2 | HG01099.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1749 | chr6 | 115940665 | |||||
| chr6:115940666
|
G | A | 1 | a0001c0001t0035 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1748C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1748 | chr6 | 115940666 | |||||
| chr6:115940682
|
C | T | 1 | a0002c0002t0036 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1732G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1732 | chr6 | 115940682 | |||||
| chr6:115940844
|
G | A | 1 | a0002c0002t0007 | 10 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1570C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1570 | chr6 | 115940844 | |||||
| chr6:115941100
|
C | T | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1314G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1314 | chr6 | 115941100 | |||||
| chr6:115941164
|
T | C | 1 | a0001c0001t0035 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1250A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1250 | chr6 | 115941164 | |||||
| chr6:115941225
|
T | C | 76 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1189A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1189 | chr6 | 115941225 | |||||
| chr6:115941306
|
A | G | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1108T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1108 | chr6 | 115941306 | |||||
| chr6:115941309
|
CAAG | C | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(45): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1102_*1104delCTT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1102 | chr6 | 115941309 | |||||
| chr6:115941317
|
G | A | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1097C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1097 | chr6 | 115941317 | |||||
| chr6:115941395
|
C | T | 2 | a0001c0001t0015a0004c0007t0015 | 4 | HG01981.hp2 NA19030.hp2 NA20805.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1019G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 1019 | chr6 | 115941395 | |||||
| chr6:115941694
|
G | A | 9 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(6): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 720 | chr6 | 115941694 | |||||
| chr6:115941813
|
G | A | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(45): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*601C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 601 | chr6 | 115941813 | |||||
| chr6:115941933
|
G | A | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*481C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 481 | chr6 | 115941933 | |||||
| chr6:115942018
|
T | C | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(45): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*396A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 396 | chr6 | 115942018 | |||||
| chr6:115942268
|
T | C | 4 | a0001c0001t0008a0001c0001t0071a0002c0002t0005others(1): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*146A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 146 | chr6 | 115942268 | |||||
| chr6:115942345
|
C | T | 3 | a0001c0001t0025a0001c0001t0029a0001c0001t0059 | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 69 | chr6 | 115942345 | |||||
| chr6:115942361
|
G | A | 4 | a0001c0001t0003a0001c0001t0069a0001c0001t0070others(1): Show | 19 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*53C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 8/8 | 53 | chr6 | 115942361 | |||||
| chr6:116060544
|
C | T | 1 | a0001c0001t0028 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-233G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/8 | 233 | chr6 | 116060544 | |||||
| chr6:116060595
|
C | A | 1 | a0001c0001t0071 | 1 | NA18986.hp2 | 5_prime_UTR_variant | MODIFIER | c.-284G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/8 | 284 | chr6 | 116060595 | |||||
| chr6:116060626
|
A | T | 1 | a0001c0001t0058 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-315T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/8 | 315 | chr6 | 116060626 | |||||
| chr6:116060831
|
T | C | 26 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(23): Show | 78 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(75): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-520A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/8 | chr6 | 116060831 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:115942656
|
C | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.1307-31G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 7/7 | chr6 | 115942656 | ||||||
| chr6:115942695
|
G | A | 1 | a0001c0001t0008g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1307-70C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 7/7 | chr6 | 115942695 | ||||||
| chr6:115942727
|
A | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.1307-102T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 7/7 | chr6 | 115942727 | ||||||
| chr6:115942752
|
T | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.1307-127A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 7/7 | chr6 | 115942752 | ||||||
| chr6:115942902
|
G | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.1306+118C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 7/7 | chr6 | 115942902 | ||||||
| chr6:115943191
|
C | A | 200 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
splice_region_variant&intron_variant | LOW | c.1141-6G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943191 | ||||||
| chr6:115943223
|
A | AT | 5 | a0001c0001t0003g0236a0001c0001t0016g0131a0001c0001t0025g0254others(2): Show | 5 | HG00735.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-39dupA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943223 | ||||||
| chr6:115943223
|
AT | A | 86 | a0001c0001t0001g0121a0001c0001t0008g0001a0001c0001t0008g0203others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1141-39delA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943223 | ||||||
| chr6:115943296
|
A | G | 4 | a0002c0002t0002g0037a0002c0002t0019g0061a0002c0002t0019g0174others(1): Show | 4 | HG00438.hp2 HG00621.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-111T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943296 | ||||||
| chr6:115943417
|
C | T | 1 | a0002c0002t0036g0052 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1141-232G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943417 | ||||||
| chr6:115943489
|
C | CA | 11 | a0001c0001t0001g0108a0001c0001t0001g0178a0001c0001t0001g0195others(8): Show | 11 | HG00621.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1141-305dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943489 | ||||||
| chr6:115943489
|
CA | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0205others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.1141-305delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943489 | ||||||
| chr6:115943521
|
T | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0149 | 2 | NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1141-336A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943521 | ||||||
| chr6:115943594
|
G | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.1141-409C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943594 | ||||||
| chr6:115943777
|
G | A | 202 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1140+467C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943777 | ||||||
| chr6:115943780
|
C | G | 1 | a0002c0002t0002g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1140+464G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115943780 | ||||||
| chr6:115944202
|
T | C | 1 | a0001c0001t0003g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1140+42A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115944202 | ||||||
| chr6:115944213
|
C | T | 1 | a0002c0002t0007g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1140+31G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 6/7 | chr6 | 115944213 | ||||||
| chr6:115944698
|
C | T | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.959-273G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115944698 | ||||||
| chr6:115944958
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.959-533G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115944958 | ||||||
| chr6:115945112
|
A | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.959-687T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115945112 | ||||||
| chr6:115945138
|
T | C | 1 | a0001c0001t0024g0177 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.959-713A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115945138 | ||||||
| chr6:115945429
|
A | G | 202 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.959-1004T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115945429 | ||||||
| chr6:115945633
|
A | G | 1 | a0001c0001t0020g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.959-1208T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115945633 | ||||||
| chr6:115946003
|
T | C | 170 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.959-1578A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946003 | ||||||
| chr6:115946070
|
G | T | 8 | a0001c0001t0012g0112a0001c0001t0015g0231a0001c0001t0015g0253others(5): Show | 8 | HG01884.hp2 HG01981.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.959-1645C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946070 | ||||||
| chr6:115946160
|
T | G | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.959-1735A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946160 | ||||||
| chr6:115946182
|
A | C | 19 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(16): Show | 19 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.959-1757T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946182 | ||||||
| chr6:115946284
|
C | CT | 4 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-1860dupA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946284 | ||||||
| chr6:115946331
|
C | T | 1 | a0001c0009t0012g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.959-1906G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946331 | ||||||
| chr6:115946757
|
G | T | 1 | a0002c0002t0002g0093 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.959-2332C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946757 | ||||||
| chr6:115946848
|
G | T | 1 | a0002c0002t0001g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.959-2423C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946848 | ||||||
| chr6:115946995
|
T | A | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.959-2570A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115946995 | ||||||
| chr6:115947159
|
C | G | 2 | a0001c0001t0010g0221a0001c0001t0065g0258 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.959-2734G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947159 | ||||||
| chr6:115947236
|
G | A | 1 | a0001c0001t0008g0214 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.959-2811C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947236 | ||||||
| chr6:115947250
|
T | C | 1 | a0002c0002t0002g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.959-2825A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947250 | ||||||
| chr6:115947317
|
A | AGTGT | 10 | a0001c0001t0060g0259a0002c0002t0007g0153a0002c0002t0007g0154others(7): Show | 10 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.959-2896_959-2893d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947317 | ||||||
| chr6:115947317
|
AGT | A | 10 | a0001c0001t0018g0056a0001c0001t0018g0115a0001c0001t0018g0116others(7): Show | 10 | HG01099.hp1 HG01106.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.959-2894_959-2893d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947317 | ||||||
| chr6:115947317
|
AGTGT | A | 140 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.959-2896_959-2893d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947317 | ||||||
| chr6:115947317
|
AGTGTGT | A | 7 | a0001c0001t0013g0228a0001c0001t0017g0009a0001c0001t0017g0010others(4): Show | 7 | HG02280.hp2 HG02602.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.959-2898_959-2893d others(8): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947317 | ||||||
| chr6:115947317
|
AGTGTGTG others(1): Show |
A | 38 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119others(35): Show | 39 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.959-2900_959-2893d others(10): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947317 | ||||||
| chr6:115947317
|
AGTGTGTG others(3): Show |
A | 35 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(32): Show | 35 | HG00735.hp2 HG00738.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.959-2902_959-2893d others(12): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947317 | ||||||
| chr6:115947317
|
AGTGTGTG others(5): Show |
A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.959-2904_959-2893d others(14): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947317 | ||||||
| chr6:115947525
|
A | T | 1 | a0002c0002t0001g0015 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.959-3100T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947525 | ||||||
| chr6:115947542
|
T | C | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.959-3117A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947542 | ||||||
| chr6:115947558
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0023g0151a0001c0001t0023g0152 | 3 | NA18942.hp1 NA18983.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.959-3133C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947558 | ||||||
| chr6:115947727
|
G | C | 1 | a0002c0002t0005g0172 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.959-3302C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947727 | ||||||
| chr6:115947734
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.959-3309T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947734 | ||||||
| chr6:115947912
|
C | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.959-3487G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115947912 | ||||||
| chr6:115948122
|
C | T | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.959-3697G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948122 | ||||||
| chr6:115948340
|
G | T | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.959-3915C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948340 | ||||||
| chr6:115948443
|
T | A | 2 | a0002c0002t0002g0037a0002c0002t0019g0174 | 2 | HG00438.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.959-4018A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948443 | ||||||
| chr6:115948455
|
G | T | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-4030C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948455 | ||||||
| chr6:115948637
|
T | C | 1 | a0002c0002t0053g0068 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.959-4212A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948637 | ||||||
| chr6:115948668
|
T | C | 4 | a0001c0001t0015g0231a0001c0001t0015g0253a0004c0007t0015g0230others(1): Show | 4 | HG01981.hp2 NA19030.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-4243A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948668 | ||||||
| chr6:115948732
|
A | G | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.959-4307T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948732 | ||||||
| chr6:115948763
|
T | C | 19 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(16): Show | 19 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.959-4338A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948763 | ||||||
| chr6:115948836
|
G | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.959-4411C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948836 | ||||||
| chr6:115948855
|
T | C | 1 | a0001c0001t0022g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.959-4430A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948855 | ||||||
| chr6:115948991
|
T | C | 19 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(16): Show | 19 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.959-4566A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115948991 | ||||||
| chr6:115949058
|
A | G | 1 | a0001c0001t0017g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.959-4633T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949058 | ||||||
| chr6:115949064
|
C | T | 1 | a0001c0001t0056g0134 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.959-4639G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949064 | ||||||
| chr6:115949170
|
T | C | 1 | a0001c0001t0011g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.959-4745A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949170 | ||||||
| chr6:115949267
|
A | AC | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.959-4843dupG | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949267 | ||||||
| chr6:115949299
|
G | A | 1 | a0001c0001t0008g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.959-4874C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949299 | ||||||
| chr6:115949422
|
T | G | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.959-4997A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949422 | ||||||
| chr6:115949651
|
C | T | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.959-5226G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949651 | ||||||
| chr6:115949694
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.959-5269T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949694 | ||||||
| chr6:115949695
|
T | C | 1 | a0001c0001t0024g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.959-5270A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949695 | ||||||
| chr6:115949758
|
A | T | 4 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-5333T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949758 | ||||||
| chr6:115949799
|
A | AAACAAAA others(15): Show |
1 | a0001c0001t0006g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.959-5396_959-5375d others(24): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949799 | ||||||
| chr6:115949820
|
G | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(3): Show | 6 | HG01243.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.959-5395C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949820 | ||||||
| chr6:115949846
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0043g0189 | 3 | HG02559.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.959-5421C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949846 | ||||||
| chr6:115949941
|
C | T | 1 | a0002c0002t0007g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.959-5516G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949941 | ||||||
| chr6:115949955
|
T | G | 61 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.959-5530A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115949955 | ||||||
| chr6:115950248
|
A | C | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.959-5823T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115950248 | ||||||
| chr6:115950259
|
GAGAAAAT others(6): Show |
G | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.959-5847_959-5835d others(15): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115950259 | ||||||
| chr6:115950376
|
G | A | 32 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(29): Show | 32 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.959-5951C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115950376 | ||||||
| chr6:115950430
|
C | T | 3 | a0002c0002t0004g0040a0002c0002t0004g0041a0002c0002t0004g0171 | 3 | HG00544.hp1 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.959-6005G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115950430 | ||||||
| chr6:115950493
|
G | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+5959C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115950493 | ||||||
| chr6:115950511
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.958+5941C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115950511 | ||||||
| chr6:115950846
|
G | A | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.958+5606C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115950846 | ||||||
| chr6:115950847
|
G | C | 1 | a0002c0002t0002g0037 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.958+5605C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115950847 | ||||||
| chr6:115951106
|
T | A | 1 | a0001c0001t0027g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.958+5346A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951106 | ||||||
| chr6:115951173
|
A | G | 1 | a0001c0001t0014g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.958+5279T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951173 | ||||||
| chr6:115951177
|
T | G | 3 | a0001c0009t0012g0120a0002c0006t0012g0096a0002c0006t0012g0097 | 3 | HG02886.hp1 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.958+5275A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951177 | ||||||
| chr6:115951189
|
A | G | 3 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0059g0255 | 3 | HG02559.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.958+5263T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951189 | ||||||
| chr6:115951251
|
A | T | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.958+5201T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951251 | ||||||
| chr6:115951420
|
G | T | 1 | a0002c0002t0002g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.958+5032C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951420 | ||||||
| chr6:115951487
|
A | T | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.958+4965T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951487 | ||||||
| chr6:115951567
|
G | GT | 5 | a0002c0002t0002g0039a0002c0002t0002g0067a0002c0002t0002g0072others(2): Show | 5 | HG01109.hp2 HG01192.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.958+4884dupA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951567 | ||||||
| chr6:115951768
|
T | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+4684A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951768 | ||||||
| chr6:115951774
|
C | T | 1 | a0002c0002t0007g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.958+4678G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951774 | ||||||
| chr6:115951880
|
T | C | 1 | a0002c0002t0005g0019 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.958+4572A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951880 | ||||||
| chr6:115951958
|
T | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+4494A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115951958 | ||||||
| chr6:115952007
|
T | C | 1 | a0002c0002t0002g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.958+4445A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952007 | ||||||
| chr6:115952124
|
T | G | 3 | a0001c0001t0001g0144a0001c0001t0002g0142a0001c0001t0004g0143 | 3 | NA18940.hp1 NA19004.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.958+4328A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952124 | ||||||
| chr6:115952136
|
T | C | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.958+4316A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952136 | ||||||
| chr6:115952324
|
C | T | 40 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.958+4128G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952324 | ||||||
| chr6:115952325
|
G | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119others(1): Show | 4 | HG00099.hp2 HG01169.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+4127C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952325 | ||||||
| chr6:115952390
|
T | C | 1 | a0001c0001t0066g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.958+4062A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952390 | ||||||
| chr6:115952493
|
C | G | 4 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+3959G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952493 | ||||||
| chr6:115952622
|
T | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+3830A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952622 | ||||||
| chr6:115952882
|
T | A | 1 | a0002c0002t0036g0052 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.958+3570A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952882 | ||||||
| chr6:115952920
|
G | T | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.958+3532C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952920 | ||||||
| chr6:115952951
|
T | C | 3 | a0001c0009t0012g0120a0002c0006t0012g0096a0002c0006t0012g0097 | 3 | HG02886.hp1 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.958+3501A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115952951 | ||||||
| chr6:115953021
|
A | C | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+3431T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953021 | ||||||
| chr6:115953039
|
T | A | 1 | a0002c0002t0001g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.958+3413A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953039 | ||||||
| chr6:115953103
|
G | GA | 27 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(24): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.958+3348dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953103 | ||||||
| chr6:115953150
|
A | G | 202 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.958+3302T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953150 | ||||||
| chr6:115953180
|
A | AC | 14 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0110others(11): Show | 14 | HG01496.hp1 HG01884.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.958+3271_958+3272i others(3): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953180 | ||||||
| chr6:115953180
|
A | ACT | 105 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0106others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.958+3271_958+3272i others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953180 | ||||||
| chr6:115953180
|
A | ACTT | 52 | a0001c0001t0001g0125a0001c0001t0001g0141a0001c0001t0001g0144others(49): Show | 52 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.958+3271_958+3272i others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953180 | ||||||
| chr6:115953180
|
A | AT | 18 | a0001c0001t0003g0235a0001c0001t0003g0244a0001c0001t0003g0252others(15): Show | 18 | HG01192.hp1 HG01261.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.958+3271dupA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953180 | ||||||
| chr6:115953180
|
A | ATT | 8 | a0001c0001t0006g0224a0001c0001t0006g0266a0001c0001t0013g0222others(5): Show | 8 | HG01106.hp2 HG01123.hp1 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.958+3270_958+3271d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953180 | ||||||
| chr6:115953180
|
AT | A | 7 | a0001c0001t0012g0112a0001c0001t0014g0262a0001c0001t0015g0231others(4): Show | 7 | HG01081.hp2 HG01884.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.958+3271delA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953180 | ||||||
| chr6:115953180
|
ATTT | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+3269_958+3271d others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953180 | ||||||
| chr6:115953181
|
T | C | 4 | a0001c0001t0025g0268a0001c0001t0029g0113a0001c0001t0059g0255others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+3271A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953181 | ||||||
| chr6:115953184
|
T | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+3268A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953184 | ||||||
| chr6:115953186
|
T | C | 2 | a0002c0002t0002g0175a0002c0002t0009g0099 | 2 | NA19007.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.958+3266A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953186 | ||||||
| chr6:115953213
|
G | A | 1 | a0002c0002t0002g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.958+3239C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953213 | ||||||
| chr6:115953228
|
C | T | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.958+3224G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953228 | ||||||
| chr6:115953282
|
T | C | 203 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.958+3170A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953282 | ||||||
| chr6:115953283
|
G | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+3169C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953283 | ||||||
| chr6:115953390
|
C | T | 1 | a0002c0002t0005g0065 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.958+3062G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953390 | ||||||
| chr6:115953432
|
G | A | 1 | a0002c0002t0002g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.958+3020C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953432 | ||||||
| chr6:115953477
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.958+2975G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953477 | ||||||
| chr6:115953558
|
T | C | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.958+2894A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953558 | ||||||
| chr6:115953567
|
C | T | 178 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.958+2885G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953567 | ||||||
| chr6:115953722
|
A | C | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.958+2730T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115953722 | ||||||
| chr6:115954115
|
G | A | 1 | a0001c0001t0026g0245 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.958+2337C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115954115 | ||||||
| chr6:115954306
|
T | C | 1 | a0001c0001t0011g0234 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.958+2146A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115954306 | ||||||
| chr6:115954435
|
C | G | 1 | a0001c0001t0008g0213 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.958+2017G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115954435 | ||||||
| chr6:115954544
|
G | A | 1 | a0002c0002t0002g0087 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.958+1908C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115954544 | ||||||
| chr6:115954681
|
T | C | 1 | a0002c0002t0002g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.958+1771A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115954681 | ||||||
| chr6:115954749
|
C | T | 2 | a0001c0001t0006g0225a0001c0001t0006g0265 | 2 | NA18953.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.958+1703G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115954749 | ||||||
| chr6:115954813
|
G | A | 1 | a0001c0001t0017g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.958+1639C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115954813 | ||||||
| chr6:115955042
|
G | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+1410C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115955042 | ||||||
| chr6:115955058
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0123 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.958+1394C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115955058 | ||||||
| chr6:115955061
|
A | G | 9 | a0001c0001t0011g0249a0002c0002t0001g0027a0002c0002t0001g0060others(6): Show | 9 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.958+1391T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115955061 | ||||||
| chr6:115955063
|
T | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0123 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.958+1389A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115955063 | ||||||
| chr6:115955420
|
C | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+1032G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115955420 | ||||||
| chr6:115955435
|
G | A | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.958+1017C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115955435 | ||||||
| chr6:115955576
|
T | G | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.958+876A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115955576 | ||||||
| chr6:115955824
|
A | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+628T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115955824 | ||||||
| chr6:115956056
|
C | A | 1 | a0003c0003t0052g0162 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.958+396G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115956056 | ||||||
| chr6:115956309
|
C | T | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.958+143G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115956309 | ||||||
| chr6:115956365
|
G | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.958+87C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115956365 | ||||||
| chr6:115956430
|
T | G | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+22A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115956430 | ||||||
| chr6:115956444
|
T | C | 1 | a0002c0002t0054g0023 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.958+8A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 5/7 | chr6 | 115956444 | ||||||
| chr6:115956629
|
G | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.800-19C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115956629 | ||||||
| chr6:115956674
|
T | C | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.800-64A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115956674 | ||||||
| chr6:115956808
|
A | G | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.800-198T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115956808 | ||||||
| chr6:115956889
|
A | G | 2 | a0002c0002t0030g0091a0002c0002t0031g0092 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.800-279T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115956889 | ||||||
| chr6:115956932
|
G | A | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.800-322C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115956932 | ||||||
| chr6:115956955
|
G | A | 7 | a0001c0001t0018g0056a0001c0001t0018g0115a0001c0001t0018g0116others(4): Show | 7 | HG01099.hp1 HG01106.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.800-345C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115956955 | ||||||
| chr6:115957084
|
T | C | 1 | a0001c0001t0027g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.800-474A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957084 | ||||||
| chr6:115957214
|
C | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.800-604G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957214 | ||||||
| chr6:115957368
|
C | T | 11 | a0001c0001t0060g0259a0002c0002t0007g0153a0002c0002t0007g0154others(8): Show | 11 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-758G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957368 | ||||||
| chr6:115957414
|
T | A | 91 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.800-804A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957414 | ||||||
| chr6:115957483
|
C | T | 1 | a0001c0001t0008g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.800-873G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957483 | ||||||
| chr6:115957562
|
G | A | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.800-952C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957562 | ||||||
| chr6:115957654
|
G | T | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.800-1044C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957654 | ||||||
| chr6:115957771
|
C | G | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-1161G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957771 | ||||||
| chr6:115957806
|
G | C | 2 | a0002c0002t0001g0028a0002c0002t0054g0023 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.800-1196C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957806 | ||||||
| chr6:115957812
|
G | C | 2 | a0002c0002t0001g0028a0002c0002t0054g0023 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.800-1202C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957812 | ||||||
| chr6:115957964
|
T | A | 1 | a0002c0002t0002g0030 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.800-1354A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957964 | ||||||
| chr6:115957988
|
C | G | 1 | a0002c0002t0045g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.800-1378G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115957988 | ||||||
| chr6:115958024
|
A | G | 224 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.800-1414T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958024 | ||||||
| chr6:115958032
|
G | C | 1 | a0002c0002t0002g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.800-1422C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958032 | ||||||
| chr6:115958133
|
G | T | 2 | a0005c0005t0002g0094a0005c0005t0002g0095 | 2 | NA18974.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.800-1523C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958133 | ||||||
| chr6:115958264
|
G | A | 1 | a0001c0001t0014g0261 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.800-1654C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958264 | ||||||
| chr6:115958275
|
C | T | 1 | a0001c0001t0004g0196 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.800-1665G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958275 | ||||||
| chr6:115958276
|
C | G | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.800-1666G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958276 | ||||||
| chr6:115958283
|
AC | A | 253 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.800-1674delG | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958283 | ||||||
| chr6:115958291
|
C | A | 2 | a0003c0003t0004g0163a0003c0003t0004g0164 | 2 | NA18962.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.800-1681G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958291 | ||||||
| chr6:115958588
|
A | G | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.800-1978T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958588 | ||||||
| chr6:115958612
|
A | C | 1 | a0001c0001t0011g0248 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.800-2002T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958612 | ||||||
| chr6:115958618
|
ACT | A | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.800-2010_800-2009d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958618 | ||||||
| chr6:115958634
|
G | GGAAAGGA others(10): Show |
1 | a0001c0001t0015g0231 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.800-2025_800-2024i others(19): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(10): Show |
G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.800-2041_800-2025d others(19): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(62): Show |
G | 1 | a0002c0002t0001g0078 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.800-2093_800-2025d others(71): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(65): Show |
G | 10 | a0001c0001t0027g0206a0002c0002t0001g0076a0002c0002t0002g0012others(7): Show | 10 | HG00544.hp1 HG00735.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.800-2096_800-2025d others(74): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(69): Show |
G | 16 | a0001c0001t0001g0188a0001c0001t0006g0225a0001c0001t0009g0140others(13): Show | 16 | HG01515.hp1 HG02074.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.800-2100_800-2025d others(78): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(73): Show |
G | 28 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0001g0147others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.800-2104_800-2025d others(82): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(77): Show |
G | 22 | a0001c0001t0001g0105a0001c0001t0001g0119a0001c0001t0006g0216others(19): Show | 22 | HG00140.hp2 HG00544.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.800-2108_800-2025d others(86): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(81): Show |
G | 6 | a0001c0001t0001g0169a0002c0002t0001g0005a0002c0002t0001g0013others(3): Show | 6 | HG00558.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.800-2112_800-2025d others(90): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(85): Show |
G | 36 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0217others(33): Show | 37 | HG00438.hp2 HG00621.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.800-2116_800-2025d others(94): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(89): Show |
G | 15 | a0001c0001t0008g0001a0001c0001t0008g0205a0001c0001t0008g0211others(12): Show | 16 | HG00741.hp1 HG00741.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.800-2120_800-2025d others(98): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958634
|
GGAAAGAA others(97): Show |
G | 1 | a0002c0002t0045g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.800-2128_800-2025d others(2): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958634 | ||||||
| chr6:115958636
|
AAAGAAAG others(61): Show |
A | 1 | a0002c0002t0002g0084 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.800-2094_800-2027d others(70): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958636 | ||||||
| chr6:115958638
|
A | G | 7 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0239others(4): Show | 7 | HG00735.hp2 HG01169.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.800-2028T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958638 | ||||||
| chr6:115958640
|
AAAGAAAA others(57): Show |
A | 1 | a0001c0001t0025g0268 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.800-2094_800-2031d others(66): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958640 | ||||||
| chr6:115958643
|
G | A | 3 | a0001c0001t0003g0241a0002c0002t0021g0007a0002c0002t0021g0008 | 3 | HG01071.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.800-2033C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958643 | ||||||
| chr6:115958643
|
GA | G | 84 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(81): Show | 84 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.800-2034delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958643 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(4): Show |
4 | a0001c0001t0003g0244a0001c0001t0003g0269a0001c0001t0012g0112others(1): Show | 4 | HG01192.hp1 HG01884.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.800-2035_800-2034i others(13): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(12): Show |
2 | a0001c0001t0003g0235a0002c0006t0012g0096 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.800-2035_800-2034i others(21): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(16): Show |
2 | a0001c0001t0003g0247a0004c0007t0015g0267 | 2 | HG01123.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.800-2035_800-2034i others(25): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(20): Show |
1 | a0004c0007t0015g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.800-2035_800-2034i others(29): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(24): Show |
2 | a0001c0001t0051g0103a0002c0002t0021g0043 | 2 | HG01169.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.800-2035_800-2034i others(33): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(32): Show |
2 | a0001c0001t0003g0238a0001c0001t0003g0240 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.800-2035_800-2034i others(41): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(36): Show |
1 | a0001c0001t0003g0246 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.800-2035_800-2034i others(45): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(40): Show |
1 | a0001c0001t0003g0260 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.800-2035_800-2034i others(49): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(44): Show |
2 | a0001c0001t0003g0239a0001c0009t0012g0120 | 2 | HG02004.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.800-2035_800-2034i others(53): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAAGAAAG others(64): Show |
1 | a0001c0001t0069g0243 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.800-2035_800-2034i others(73): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | AAGAAAGA others(7): Show |
1 | a0001c0001t0017g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.800-2035_800-2034i others(16): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
A | G | 3 | a0001c0001t0003g0241a0002c0002t0021g0007a0002c0002t0021g0008 | 3 | HG01071.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.800-2034T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
AAAAGAAA others(49): Show |
A | 1 | a0001c0001t0025g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.800-2090_800-2035d others(58): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958644
|
AAAAGAAA others(53): Show |
A | 1 | a0001c0001t0059g0255 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.800-2094_800-2035d others(62): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958644 | ||||||
| chr6:115958646
|
A | G | 1 | a0001c0001t0017g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.800-2036T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958646 | ||||||
| chr6:115958653
|
AAAGAAAG others(44): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.800-2094_800-2044d others(53): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958653 | ||||||
| chr6:115958665
|
A | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.800-2055T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958665 | ||||||
| chr6:115958673
|
AAAGAAAG others(83): Show |
A | 1 | a0001c0001t0008g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.800-2153_800-2064d others(92): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958673 | ||||||
| chr6:115958676
|
GAAAGAAA others(82): Show |
G | 1 | a0001c0001t0008g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.800-2155_800-2067d others(91): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958676 | ||||||
| chr6:115958676
|
GAAAGAAA others(83): Show |
G | 2 | a0001c0001t0014g0262a0001c0001t0014g0271 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.800-2156_800-2067d others(92): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958676 | ||||||
| chr6:115958680
|
GAAAGAAA others(78): Show |
G | 1 | a0001c0001t0043g0189 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.800-2155_800-2071d others(87): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958680 | ||||||
| chr6:115958680
|
GAAAGAAA others(79): Show |
G | 2 | a0001c0001t0011g0264a0001c0001t0014g0263 | 2 | HG02683.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.800-2156_800-2071d others(88): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958680 | ||||||
| chr6:115958684
|
GAAAGAAA others(75): Show |
G | 4 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0014g0261others(1): Show | 4 | HG00738.hp1 HG02165.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-2156_800-2075d others(84): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958684 | ||||||
| chr6:115958688
|
GAAAGAAA others(70): Show |
G | 5 | a0001c0001t0001g0130a0001c0001t0001g0190a0001c0001t0020g0137others(2): Show | 5 | HG02559.hp1 HG03516.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-2155_800-2079d others(79): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958688 | ||||||
| chr6:115958688
|
GAAAGAAA others(71): Show |
G | 15 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0121others(12): Show | 15 | HG00621.hp1 HG01258.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.800-2156_800-2079d others(80): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958688 | ||||||
| chr6:115958692
|
GAAAGAAA others(66): Show |
G | 13 | a0001c0001t0001g0122a0001c0001t0001g0187a0001c0001t0010g0202others(10): Show | 13 | HG00408.hp2 HG00642.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.800-2155_800-2083d others(75): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958692 | ||||||
| chr6:115958692
|
GAAAGAAA others(67): Show |
G | 20 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0002g0142others(17): Show | 20 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.800-2156_800-2083d others(76): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958692 | ||||||
| chr6:115958696
|
GAAAGAAA others(62): Show |
G | 1 | a0001c0001t0024g0177 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.800-2155_800-2087d others(71): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958696 | ||||||
| chr6:115958696
|
GAAAGAAA others(63): Show |
G | 9 | a0001c0001t0001g0104a0001c0001t0001g0124a0001c0001t0001g0125others(6): Show | 9 | HG01243.hp2 HG02896.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.800-2156_800-2087d others(72): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958696 | ||||||
| chr6:115958699
|
A | G | 1 | a0002c0002t0001g0079 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.800-2089T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958699 | ||||||
| chr6:115958700
|
GAAAGAAG others(58): Show |
G | 2 | a0001c0001t0001g0195a0001c0001t0011g0237 | 2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.800-2155_800-2091d others(67): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958700 | ||||||
| chr6:115958700
|
GAAAGAAG others(59): Show |
G | 4 | a0001c0001t0023g0151a0002c0002t0001g0079a0002c0002t0001g0086others(1): Show | 4 | HG01069.hp1 HG01496.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.800-2156_800-2091d others(68): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958700 | ||||||
| chr6:115958701
|
AAAG | A | 4 | a0001c0001t0003g0251a0001c0001t0017g0194a0001c0001t0029g0113others(1): Show | 4 | HG01993.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-2094_800-2092d others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958701 | ||||||
| chr6:115958702
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.800-2092T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958702 | ||||||
| chr6:115958703
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0025g0254 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.800-2093T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958703 | ||||||
| chr6:115958704
|
G | GA | 30 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(27): Show | 30 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.800-2095dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958704 | ||||||
| chr6:115958704
|
G | GAAAGAAA others(6): Show |
1 | a0001c0001t0003g0241 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.800-2095_800-2094i others(15): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958704 | ||||||
| chr6:115958704
|
G | T | 1 | a0001c0001t0025g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.800-2094C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958704 | ||||||
| chr6:115958704
|
GAAGA | G | 3 | a0001c0001t0022g0185a0002c0002t0007g0155a0002c0002t0007g0157 | 3 | HG02622.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.800-2098_800-2095d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958704 | ||||||
| chr6:115958704
|
GAAGAAAG others(55): Show |
G | 2 | a0001c0001t0001g0107a0001c0001t0001g0170 | 2 | HG03098.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.800-2156_800-2095d others(64): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958704 | ||||||
| chr6:115958707
|
G | A | 1 | a0002c0002t0007g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.800-2097C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958707 | ||||||
| chr6:115958708
|
A | G | 4 | a0002c0002t0007g0153a0002c0002t0007g0158a0002c0002t0007g0192others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-2098T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958708 | ||||||
| chr6:115958708
|
A | T | 1 | a0001c0001t0059g0255 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.800-2098T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958708 | ||||||
| chr6:115958712
|
A | G | 5 | a0002c0002t0007g0154a0002c0002t0007g0155a0002c0002t0007g0157others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-2102T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958712 | ||||||
| chr6:115958712
|
A | T | 1 | a0001c0001t0025g0268 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.800-2102T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958712 | ||||||
| chr6:115958716
|
A | G | 5 | a0002c0002t0007g0155a0002c0002t0007g0156a0002c0002t0007g0157others(2): Show | 5 | HG02622.hp2 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-2106T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958716 | ||||||
| chr6:115958724
|
A | T | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.800-2114T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958724 | ||||||
| chr6:115958763
|
GA | G | 5 | a0001c0001t0001g0188a0002c0002t0001g0076a0002c0002t0002g0030others(2): Show | 5 | HG00544.hp1 HG01261.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-2154delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958763 | ||||||
| chr6:115958764
|
A | G | 1 | a0001c0001t0050g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.800-2154T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958764 | ||||||
| chr6:115958765
|
A | G | 5 | a0001c0001t0001g0188a0001c0001t0050g0181a0002c0002t0001g0076others(2): Show | 5 | HG00544.hp1 HG00741.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-2155T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958765 | ||||||
| chr6:115958766
|
A | G | 28 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0001g0187others(25): Show | 28 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.800-2156T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958766 | ||||||
| chr6:115958767
|
GA | G | 17 | a0001c0001t0008g0001a0001c0001t0008g0205a0001c0001t0008g0211others(14): Show | 18 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.800-2158delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958767 | ||||||
| chr6:115958768
|
A | AAAGAAAG others(32): Show |
1 | a0001c0001t0034g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.800-2159_800-2158i others(41): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958768 | ||||||
| chr6:115958768
|
A | AG | 18 | a0001c0001t0003g0236a0001c0001t0003g0238a0001c0001t0003g0239others(15): Show | 18 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.800-2159dupC | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958768 | ||||||
| chr6:115958768
|
A | G | 210 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.800-2158T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958768 | ||||||
| chr6:115958769
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0035g0004 | 2 | HG01981.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.800-2159C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958769 | ||||||
| chr6:115958770
|
G | A | 1 | a0001c0001t0015g0231 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.800-2160C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958770 | ||||||
| chr6:115958774
|
G | A | 1 | a0001c0001t0070g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.800-2164C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958774 | ||||||
| chr6:115958774
|
G | C | 1 | a0002c0002t0009g0099 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.800-2164C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958774 | ||||||
| chr6:115958775
|
G | A | 1 | a0001c0001t0070g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.800-2165C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958775 | ||||||
| chr6:115958778
|
A | G | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-2168T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958778 | ||||||
| chr6:115958779
|
G | A | 1 | a0001c0001t0070g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.800-2169C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958779 | ||||||
| chr6:115958779
|
G | GGAGA | 20 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(17): Show | 21 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.800-2173_800-2170d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958779 | ||||||
| chr6:115958782
|
G | A | 1 | a0001c0001t0070g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.800-2172C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958782 | ||||||
| chr6:115958786
|
G | A | 1 | a0001c0001t0070g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.800-2176C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958786 | ||||||
| chr6:115958790
|
A | G | 3 | a0001c0001t0008g0233a0002c0002t0005g0128a0002c0002t0057g0126 | 3 | HG02004.hp1 HG02273.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.800-2180T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958790 | ||||||
| chr6:115958800
|
A | G | 3 | a0001c0001t0008g0233a0002c0002t0005g0128a0002c0002t0057g0126 | 3 | HG02004.hp1 HG02273.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.800-2190T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958800 | ||||||
| chr6:115958802
|
G | A | 3 | a0001c0001t0008g0233a0002c0002t0005g0128a0002c0002t0057g0126 | 3 | HG02004.hp1 HG02273.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.800-2192C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958802 | ||||||
| chr6:115958802
|
GAAAGAAA others(11): Show |
G | 2 | a0001c0001t0004g0132a0001c0001t0017g0194 | 2 | HG03471.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.800-2210_800-2193d others(20): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958802 | ||||||
| chr6:115958818
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0026g0245a0002c0002t0002g0026 | 3 | HG01069.hp2 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.800-2208C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958818 | ||||||
| chr6:115958820
|
A | AAAAG | 222 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.800-2214_800-2211d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958820 | ||||||
| chr6:115958820
|
A | AAGAGGGG others(31): Show |
1 | a0001c0001t0070g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.800-2211_800-2210i others(40): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958820 | ||||||
| chr6:115958820
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0026g0245a0002c0002t0002g0026 | 3 | HG01069.hp2 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.800-2210T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958820 | ||||||
| chr6:115958820
|
AAAAG | A | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-2214_800-2211d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958820 | ||||||
| chr6:115958822
|
A | G | 3 | a0001c0001t0008g0233a0002c0002t0005g0128a0002c0002t0057g0126 | 3 | HG02004.hp1 HG02273.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.800-2212T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958822 | ||||||
| chr6:115958824
|
G | A | 3 | a0001c0001t0008g0233a0002c0002t0005g0128a0002c0002t0057g0126 | 3 | HG02004.hp1 HG02273.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.800-2214C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958824 | ||||||
| chr6:115958840
|
G | A | 1 | a0001c0001t0070g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.800-2230C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958840 | ||||||
| chr6:115958903
|
G | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.800-2293C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115958903 | ||||||
| chr6:115959018
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.800-2408C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959018 | ||||||
| chr6:115959177
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.800-2567G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959177 | ||||||
| chr6:115959192
|
C | A | 5 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-2582G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959192 | ||||||
| chr6:115959193
|
C | T | 27 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(24): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.800-2583G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959193 | ||||||
| chr6:115959194
|
G | A | 1 | a0002c0002t0002g0084 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.800-2584C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959194 | ||||||
| chr6:115959404
|
G | C | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.800-2794C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959404 | ||||||
| chr6:115959437
|
G | C | 1 | a0001c0001t0017g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.800-2827C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959437 | ||||||
| chr6:115959498
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0004g0136a0001c0001t0009g0140 | 3 | HG00408.hp1 NA18968.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.800-2888T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959498 | ||||||
| chr6:115959693
|
C | G | 104 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.800-3083G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959693 | ||||||
| chr6:115959850
|
A | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.800-3240T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959850 | ||||||
| chr6:115959964
|
T | TA | 33 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(30): Show | 33 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.800-3355dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115959964 | ||||||
| chr6:115960096
|
C | G | 1 | a0002c0002t0002g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.800-3486G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960096 | ||||||
| chr6:115960182
|
G | C | 2 | a0001c0001t0017g0009a0001c0001t0017g0010 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.800-3572C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960182 | ||||||
| chr6:115960192
|
C | A | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-3582G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960192 | ||||||
| chr6:115960197
|
G | A | 104 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.800-3587C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960197 | ||||||
| chr6:115960213
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.800-3603G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960213 | ||||||
| chr6:115960266
|
G | C | 1 | a0001c0001t0012g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.800-3656C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960266 | ||||||
| chr6:115960284
|
G | A | 2 | a0001c0004t0001g0118a0001c0004t0001g0179 | 2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.800-3674C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960284 | ||||||
| chr6:115960288
|
G | A | 1 | a0002c0002t0007g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.800-3678C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960288 | ||||||
| chr6:115960302
|
G | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.800-3692C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960302 | ||||||
| chr6:115960333
|
A | T | 1 | a0001c0001t0023g0151 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.800-3723T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960333 | ||||||
| chr6:115960337
|
C | T | 1 | a0001c0001t0004g0196 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.800-3727G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960337 | ||||||
| chr6:115960352
|
C | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(3): Show | 6 | HG01243.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.800-3742G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960352 | ||||||
| chr6:115960410
|
G | A | 27 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(24): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.800-3800C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960410 | ||||||
| chr6:115960451
|
G | A | 1 | a0001c0001t0064g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.800-3841C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960451 | ||||||
| chr6:115960456
|
C | T | 25 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(22): Show | 26 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.800-3846G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960456 | ||||||
| chr6:115960459
|
G | C | 3 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263 | 3 | HG00738.hp1 HG01081.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.800-3849C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960459 | ||||||
| chr6:115960515
|
C | T | 22 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(19): Show | 23 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.800-3905G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960515 | ||||||
| chr6:115960523
|
C | T | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG00280.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.800-3913G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960523 | ||||||
| chr6:115960573
|
G | C | 10 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(7): Show | 10 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.800-3963C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960573 | ||||||
| chr6:115960637
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.800-4027C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960637 | ||||||
| chr6:115960639
|
G | A | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-4029C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960639 | ||||||
| chr6:115960648
|
T | C | 1 | a0001c0001t0003g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.800-4038A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960648 | ||||||
| chr6:115960661
|
G | A | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-4051C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960661 | ||||||
| chr6:115960678
|
C | T | 22 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(19): Show | 23 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.800-4068G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960678 | ||||||
| chr6:115960683
|
C | T | 5 | a0001c0001t0012g0112a0001c0009t0012g0120a0002c0002t0001g0031others(2): Show | 5 | HG01884.hp2 HG02602.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-4073G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960683 | ||||||
| chr6:115960709
|
G | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.800-4099C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960709 | ||||||
| chr6:115960737
|
C | T | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.800-4127G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960737 | ||||||
| chr6:115960741
|
A | G | 103 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.800-4131T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960741 | ||||||
| chr6:115960743
|
C | A | 200 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.800-4133G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960743 | ||||||
| chr6:115960744
|
A | C | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.800-4134T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960744 | ||||||
| chr6:115960804
|
G | A | 1 | a0001c0001t0051g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.800-4194C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960804 | ||||||
| chr6:115960904
|
T | C | 2 | a0001c0001t0026g0245a0002c0002t0002g0026 | 2 | HG01069.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.800-4294A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960904 | ||||||
| chr6:115960917
|
A | C | 3 | a0002c0002t0002g0063a0002c0002t0002g0064a0002c0002t0040g0011 | 3 | NA18972.hp2 NA18973.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.800-4307T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960917 | ||||||
| chr6:115960930
|
C | T | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.800-4320G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115960930 | ||||||
| chr6:115961011
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119 | 3 | HG00099.hp2 HG01516.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.800-4401C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961011 | ||||||
| chr6:115961012
|
T | C | 3 | a0002c0002t0002g0039a0002c0002t0002g0067a0002c0002t0002g0072 | 3 | HG01192.hp2 HG02300.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.800-4402A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961012 | ||||||
| chr6:115961027
|
G | A | 104 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.800-4417C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961027 | ||||||
| chr6:115961097
|
G | C | 2 | a0005c0005t0002g0094a0005c0005t0002g0095 | 2 | NA18974.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.800-4487C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961097 | ||||||
| chr6:115961108
|
G | C | 4 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-4498C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961108 | ||||||
| chr6:115961138
|
A | C | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.800-4528T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961138 | ||||||
| chr6:115961196
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.800-4586A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961196 | ||||||
| chr6:115961261
|
A | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.800-4651T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961261 | ||||||
| chr6:115961385
|
T | C | 1 | a0002c0002t0001g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.800-4775A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961385 | ||||||
| chr6:115961430
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.800-4820T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961430 | ||||||
| chr6:115961564
|
G | A | 104 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.800-4954C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961564 | ||||||
| chr6:115961653
|
G | A | 1 | a0005c0005t0002g0095 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.800-5043C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961653 | ||||||
| chr6:115961726
|
C | G | 224 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.800-5116G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961726 | ||||||
| chr6:115961732
|
G | A | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-5122C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961732 | ||||||
| chr6:115961867
|
G | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.800-5257C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961867 | ||||||
| chr6:115961868
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.800-5258G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961868 | ||||||
| chr6:115961884
|
T | G | 1 | a0001c0001t0061g0257 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.800-5274A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961884 | ||||||
| chr6:115961929
|
C | T | 27 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(24): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.800-5319G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961929 | ||||||
| chr6:115961957
|
A | T | 3 | a0002c0002t0004g0040a0002c0002t0004g0041a0002c0002t0004g0171 | 3 | HG00544.hp1 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.800-5347T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961957 | ||||||
| chr6:115961960
|
A | G | 2 | a0001c0001t0069g0243a0001c0001t0070g0242 | 2 | HG01258.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.800-5350T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961960 | ||||||
| chr6:115961962
|
C | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.800-5352G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115961962 | ||||||
| chr6:115962015
|
A | G | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.800-5405T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962015 | ||||||
| chr6:115962041
|
A | G | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-5431T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962041 | ||||||
| chr6:115962113
|
A | G | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.799+5438T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962113 | ||||||
| chr6:115962315
|
G | A | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+5236C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962315 | ||||||
| chr6:115962366
|
C | A | 1 | a0001c0001t0011g0234 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.799+5185G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962366 | ||||||
| chr6:115962381
|
C | T | 19 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(16): Show | 19 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.799+5170G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962381 | ||||||
| chr6:115962437
|
A | G | 2 | a0002c0002t0005g0062a0002c0002t0005g0066 | 2 | HG00558.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.799+5114T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962437 | ||||||
| chr6:115962541
|
C | T | 1 | a0001c0001t0025g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.799+5010G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962541 | ||||||
| chr6:115962637
|
T | C | 25 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.799+4914A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962637 | ||||||
| chr6:115962694
|
A | G | 2 | a0001c0001t0026g0245a0002c0002t0002g0026 | 2 | HG01069.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.799+4857T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962694 | ||||||
| chr6:115962947
|
A | G | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.799+4604T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962947 | ||||||
| chr6:115962988
|
T | C | 104 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.799+4563A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115962988 | ||||||
| chr6:115963081
|
A | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+4470T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963081 | ||||||
| chr6:115963112
|
G | A | 1 | a0002c0002t0002g0022 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.799+4439C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963112 | ||||||
| chr6:115963115
|
C | T | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.799+4436G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963115 | ||||||
| chr6:115963223
|
C | T | 1 | a0002c0002t0009g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.799+4328G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963223 | ||||||
| chr6:115963386
|
G | A | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+4165C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963386 | ||||||
| chr6:115963439
|
T | G | 6 | a0001c0001t0010g0221a0001c0001t0027g0206a0001c0001t0027g0210others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.799+4112A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963439 | ||||||
| chr6:115963451
|
C | T | 1 | a0002c0002t0002g0044 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.799+4100G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963451 | ||||||
| chr6:115963472
|
G | T | 21 | a0002c0002t0002g0037a0002c0002t0002g0039a0002c0002t0002g0047others(18): Show | 21 | HG00438.hp2 HG00621.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.799+4079C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963472 | ||||||
| chr6:115963478
|
A | G | 71 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.799+4073T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963478 | ||||||
| chr6:115963509
|
T | C | 5 | a0001c0001t0071g0272a0002c0002t0005g0016a0002c0002t0005g0017others(2): Show | 5 | NA18942.hp2 NA18986.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+4042A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963509 | ||||||
| chr6:115963537
|
A | G | 4 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+4014T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963537 | ||||||
| chr6:115963576
|
C | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+3975G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963576 | ||||||
| chr6:115963577
|
A | G | 221 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.799+3974T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963577 | ||||||
| chr6:115963577
|
A | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014 | 3 | HG02257.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.799+3974T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963577 | ||||||
| chr6:115963587
|
A | C | 198 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.799+3964T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963587 | ||||||
| chr6:115963666
|
G | A | 28 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(25): Show | 28 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.799+3885C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963666 | ||||||
| chr6:115963772
|
T | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+3779A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963772 | ||||||
| chr6:115963809
|
T | C | 5 | a0001c0001t0003g0241a0001c0001t0069g0243a0001c0001t0070g0242others(2): Show | 5 | HG01071.hp2 HG01258.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.799+3742A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963809 | ||||||
| chr6:115963819
|
C | G | 1 | a0002c0002t0001g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799+3732G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963819 | ||||||
| chr6:115963911
|
G | C | 1 | a0002c0002t0005g0065 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.799+3640C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963911 | ||||||
| chr6:115963970
|
A | C | 2 | a0002c0002t0002g0090a0002c0002t0041g0089 | 2 | NA18959.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.799+3581T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115963970 | ||||||
| chr6:115964058
|
C | A | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.799+3493G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964058 | ||||||
| chr6:115964061
|
G | A | 1 | a0001c0001t0018g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.799+3490C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964061 | ||||||
| chr6:115964124
|
G | A | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+3427C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964124 | ||||||
| chr6:115964133
|
G | A | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.799+3418C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964133 | ||||||
| chr6:115964208
|
T | C | 27 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(24): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.799+3343A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964208 | ||||||
| chr6:115964587
|
C | T | 1 | a0001c0001t0051g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.799+2964G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964587 | ||||||
| chr6:115964687
|
G | C | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.799+2864C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964687 | ||||||
| chr6:115964743
|
C | T | 5 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.799+2808G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964743 | ||||||
| chr6:115964852
|
A | G | 1 | a0002c0002t0001g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.799+2699T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964852 | ||||||
| chr6:115964903
|
A | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+2648T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964903 | ||||||
| chr6:115964922
|
G | A | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.799+2629C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964922 | ||||||
| chr6:115964997
|
T | A | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.799+2554A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115964997 | ||||||
| chr6:115965012
|
T | C | 255 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.799+2539A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965012 | ||||||
| chr6:115965022
|
T | A | 2 | a0001c0001t0010g0202a0002c0002t0002g0051 | 2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.799+2529A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965022 | ||||||
| chr6:115965137
|
C | T | 1 | a0001c0001t0003g0244 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.799+2414G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965137 | ||||||
| chr6:115965148
|
C | T | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+2403G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965148 | ||||||
| chr6:115965268
|
A | G | 1 | a0001c0001t0008g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.799+2283T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965268 | ||||||
| chr6:115965322
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799+2229C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965322 | ||||||
| chr6:115965345
|
A | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+2206T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965345 | ||||||
| chr6:115965411
|
A | C | 5 | a0002c0002t0002g0039a0002c0002t0002g0067a0002c0002t0002g0072others(2): Show | 5 | HG01109.hp2 HG01192.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+2140T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965411 | ||||||
| chr6:115965445
|
G | C | 130 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(127): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.799+2106C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965445 | ||||||
| chr6:115965563
|
T | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+1988A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965563 | ||||||
| chr6:115965646
|
A | G | 27 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(24): Show | 27 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.799+1905T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965646 | ||||||
| chr6:115965713
|
T | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+1838A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965713 | ||||||
| chr6:115965772
|
C | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+1779G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965772 | ||||||
| chr6:115965808
|
C | G | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+1743G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965808 | ||||||
| chr6:115965911
|
G | A | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+1640C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115965911 | ||||||
| chr6:115966033
|
T | C | 40 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.799+1518A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966033 | ||||||
| chr6:115966042
|
A | G | 1 | a0001c0001t0050g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.799+1509T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966042 | ||||||
| chr6:115966050
|
T | TA | 45 | a0001c0001t0001g0178a0001c0001t0003g0236a0001c0001t0003g0238others(42): Show | 46 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.799+1500dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966050 | ||||||
| chr6:115966050
|
TA | T | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+1500delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966050 | ||||||
| chr6:115966060
|
A | AAAT | 62 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.799+1490_799+1491i others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966060 | ||||||
| chr6:115966060
|
A | AAT | 51 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(48): Show | 51 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.799+1490_799+1491i others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966060 | ||||||
| chr6:115966061
|
T | A | 26 | a0001c0001t0003g0235a0001c0001t0008g0001a0001c0001t0008g0203others(23): Show | 27 | HG00558.hp1 HG00741.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.799+1490A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966061 | ||||||
| chr6:115966062
|
T | A | 114 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.799+1489A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966062 | ||||||
| chr6:115966062
|
T | TA | 71 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(68): Show | 71 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.799+1488dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966062 | ||||||
| chr6:115966062
|
T | TTAA | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+1488_799+1489i others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966062 | ||||||
| chr6:115966063
|
A | T | 3 | a0001c0001t0003g0235a0002c0002t0021g0043a0004c0007t0015g0230 | 3 | HG01169.hp1 HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.799+1488T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966063 | ||||||
| chr6:115966072
|
A | G | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.799+1479T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966072 | ||||||
| chr6:115966082
|
T | TA | 6 | a0001c0001t0008g0001a0001c0001t0008g0205a0001c0001t0008g0211others(3): Show | 7 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.799+1468dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966082 | ||||||
| chr6:115966082
|
T | TTAAA | 199 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.799+1468_799+1469i others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966082 | ||||||
| chr6:115966090
|
A | AAAAG | 17 | a0001c0001t0008g0203a0001c0001t0008g0204a0001c0001t0008g0212others(14): Show | 17 | HG00558.hp1 HG01515.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.799+1460_799+1461i others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966090 | ||||||
| chr6:115966090
|
A | AAAG | 32 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(29): Show | 32 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.799+1458_799+1460d others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966090 | ||||||
| chr6:115966090
|
A | G | 199 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.799+1461T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966090 | ||||||
| chr6:115966474
|
T | A | 22 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(19): Show | 23 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.799+1077A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966474 | ||||||
| chr6:115966480
|
A | G | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.799+1071T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966480 | ||||||
| chr6:115966654
|
T | C | 4 | a0001c0001t0012g0112a0001c0009t0012g0120a0002c0006t0012g0096others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+897A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966654 | ||||||
| chr6:115966814
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.799+737T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966814 | ||||||
| chr6:115966974
|
A | AG | 224 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.799+576_799+577ins others(1): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115966974 | ||||||
| chr6:115967154
|
A | T | 3 | a0001c0001t0003g0252a0001c0001t0003g0260a0001c0001t0003g0269 | 3 | HG01192.hp1 HG01261.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.799+397T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115967154 | ||||||
| chr6:115967230
|
C | G | 1 | a0002c0002t0002g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.799+321G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115967230 | ||||||
| chr6:115967434
|
A | T | 3 | a0002c0002t0002g0057a0002c0002t0007g0153a0002c0002t0007g0192 | 3 | HG00099.hp1 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.799+117T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115967434 | ||||||
| chr6:115967481
|
A | G | 4 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+70T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 4/7 | chr6 | 115967481 | ||||||
| chr6:115967749
|
T | TA | 131 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(128): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.631-31dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115967749 | ||||||
| chr6:115967749
|
T | TAA | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.631-32_631-31dupTT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115967749 | ||||||
| chr6:115967881
|
A | G | 104 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.631-162T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115967881 | ||||||
| chr6:115968002
|
C | T | 256 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.631-283G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968002 | ||||||
| chr6:115968013
|
G | A | 1 | a0002c0002t0019g0174 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.631-294C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968013 | ||||||
| chr6:115968094
|
G | C | 3 | a0001c0001t0006g0226a0002c0002t0030g0091a0002c0002t0031g0092 | 3 | HG02896.hp2 HG02897.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.631-375C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968094 | ||||||
| chr6:115968165
|
C | A | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.630+411G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968165 | ||||||
| chr6:115968170
|
T | C | 1 | a0002c0002t0002g0087 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.630+406A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968170 | ||||||
| chr6:115968302
|
C | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014 | 3 | HG02257.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.630+274G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968302 | ||||||
| chr6:115968305
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.630+271T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968305 | ||||||
| chr6:115968366
|
C | T | 1 | a0002c0002t0007g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.630+210G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968366 | ||||||
| chr6:115968367
|
A | G | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.630+209T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 3/7 | chr6 | 115968367 | ||||||
| chr6:115968995
|
C | G | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-256G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115968995 | ||||||
| chr6:115969186
|
T | C | 61 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.467-447A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115969186 | ||||||
| chr6:115969218
|
C | T | 1 | a0002c0002t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.467-479G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115969218 | ||||||
| chr6:115969257
|
A | G | 1 | a0001c0001t0047g0186 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.467-518T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115969257 | ||||||
| chr6:115969274
|
T | C | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467-535A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115969274 | ||||||
| chr6:115969519
|
C | G | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.467-780G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115969519 | ||||||
| chr6:115969552
|
G | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(3): Show | 6 | HG01243.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-813C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115969552 | ||||||
| chr6:115970131
|
AT | A | 14 | a0001c0001t0008g0205a0001c0001t0011g0248a0001c0004t0001g0179others(11): Show | 14 | HG01069.hp1 HG01169.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.467-1393delA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970131 | ||||||
| chr6:115970345
|
A | T | 6 | a0001c0001t0018g0056a0001c0001t0018g0115a0001c0001t0018g0116others(3): Show | 6 | HG01099.hp1 HG01106.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-1606T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970345 | ||||||
| chr6:115970486
|
T | C | 1 | a0001c0001t0012g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.467-1747A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970486 | ||||||
| chr6:115970653
|
T | C | 1 | a0002c0002t0055g0100 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.467-1914A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970653 | ||||||
| chr6:115970734
|
C | T | 1 | a0001c0001t0011g0249 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.467-1995G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970734 | ||||||
| chr6:115970779
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.467-2040C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970779 | ||||||
| chr6:115970828
|
A | C | 22 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(19): Show | 23 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.467-2089T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970828 | ||||||
| chr6:115970863
|
T | G | 1 | a0002c0002t0002g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.467-2124A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970863 | ||||||
| chr6:115970991
|
T | C | 37 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(34): Show | 37 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.467-2252A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970991 | ||||||
| chr6:115970992
|
A | C | 8 | a0001c0001t0018g0056a0001c0001t0018g0115a0001c0001t0018g0116others(5): Show | 8 | HG01099.hp1 HG01106.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-2253T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115970992 | ||||||
| chr6:115971127
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.467-2388A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115971127 | ||||||
| chr6:115971165
|
G | A | 1 | a0001c0001t0003g0250 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.467-2426C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115971165 | ||||||
| chr6:115971236
|
A | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-2497T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115971236 | ||||||
| chr6:115971326
|
A | G | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.467-2587T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115971326 | ||||||
| chr6:115971515
|
G | T | 22 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(19): Show | 23 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.467-2776C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115971515 | ||||||
| chr6:115971720
|
A | G | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.467-2981T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115971720 | ||||||
| chr6:115972217
|
T | G | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-3478A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115972217 | ||||||
| chr6:115972226
|
A | G | 265 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.467-3487T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115972226 | ||||||
| chr6:115972835
|
A | T | 1 | a0002c0002t0054g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.467-4096T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115972835 | ||||||
| chr6:115973325
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.467-4586C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973325 | ||||||
| chr6:115973364
|
C | T | 1 | a0002c0002t0019g0176 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.467-4625G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973364 | ||||||
| chr6:115973415
|
T | C | 266 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.467-4676A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973415 | ||||||
| chr6:115973495
|
G | A | 1 | a0001c0001t0004g0132 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.467-4756C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973495 | ||||||
| chr6:115973569
|
T | A | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.467-4830A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973569 | ||||||
| chr6:115973570
|
T | A | 266 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.467-4831A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973570 | ||||||
| chr6:115973622
|
C | T | 37 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(34): Show | 37 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.467-4883G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973622 | ||||||
| chr6:115973672
|
C | T | 2 | a0002c0002t0002g0020a0002c0002t0044g0021 | 2 | NA18981.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.467-4933G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973672 | ||||||
| chr6:115973691
|
A | G | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.467-4952T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973691 | ||||||
| chr6:115973872
|
GA | G | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.467-5134delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973872 | ||||||
| chr6:115973901
|
A | G | 5 | a0001c0001t0017g0009a0001c0001t0017g0010a0001c0001t0017g0194others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-5162T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973901 | ||||||
| chr6:115973935
|
A | C | 1 | a0002c0002t0005g0019 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.467-5196T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973935 | ||||||
| chr6:115973981
|
T | C | 4 | a0002c0002t0002g0012a0002c0002t0002g0042a0005c0005t0002g0094others(1): Show | 4 | NA18971.hp1 NA18974.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-5242A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973981 | ||||||
| chr6:115973997
|
A | G | 1 | a0001c0001t0006g0216 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.467-5258T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115973997 | ||||||
| chr6:115974047
|
A | G | 1 | a0001c0001t0064g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.467-5308T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115974047 | ||||||
| chr6:115974064
|
A | G | 8 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(5): Show | 8 | NA18953.hp2 NA18954.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-5325T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115974064 | ||||||
| chr6:115974099
|
G | A | 1 | a0001c0001t0008g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.467-5360C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115974099 | ||||||
| chr6:115974192
|
G | A | 1 | a0001c0001t0018g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.467-5453C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115974192 | ||||||
| chr6:115974489
|
T | C | 1 | a0002c0002t0007g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-5750A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115974489 | ||||||
| chr6:115974541
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.467-5802A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115974541 | ||||||
| chr6:115974616
|
C | T | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.467-5877G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115974616 | ||||||
| chr6:115975091
|
G | A | 266 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.467-6352C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975091 | ||||||
| chr6:115975230
|
A | G | 1 | a0002c0002t0033g0069 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.467-6491T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975230 | ||||||
| chr6:115975283
|
G | T | 5 | a0001c0001t0008g0001a0001c0001t0008g0205a0001c0001t0008g0211others(2): Show | 6 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-6544C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975283 | ||||||
| chr6:115975501
|
T | C | 2 | a0002c0002t0002g0074a0002c0002t0002g0075 | 2 | HG00544.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.467-6762A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975501 | ||||||
| chr6:115975603
|
A | G | 6 | a0002c0002t0007g0154a0002c0002t0007g0155a0002c0002t0007g0156others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-6864T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975603 | ||||||
| chr6:115975614
|
A | G | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467-6875T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975614 | ||||||
| chr6:115975807
|
G | T | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.467-7068C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975807 | ||||||
| chr6:115975815
|
G | A | 1 | a0001c0001t0017g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.467-7076C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975815 | ||||||
| chr6:115975982
|
G | C | 1 | a0002c0002t0007g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.467-7243C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115975982 | ||||||
| chr6:115976201
|
G | T | 1 | a0001c0004t0001g0109 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.467-7462C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976201 | ||||||
| chr6:115976202
|
G | T | 1 | a0001c0004t0001g0109 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.467-7463C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976202 | ||||||
| chr6:115976351
|
A | G | 37 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(34): Show | 37 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.467-7612T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976351 | ||||||
| chr6:115976353
|
G | T | 21 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0108others(18): Show | 21 | HG00642.hp1 HG00741.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.467-7614C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976353 | ||||||
| chr6:115976432
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.467-7693C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976432 | ||||||
| chr6:115976480
|
T | C | 1 | a0002c0002t0001g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.467-7741A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976480 | ||||||
| chr6:115976552
|
G | A | 58 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.467-7813C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976552 | ||||||
| chr6:115976555
|
C | G | 2 | a0005c0005t0002g0094a0005c0005t0002g0095 | 2 | NA18974.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.467-7816G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976555 | ||||||
| chr6:115976579
|
C | A | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-7840G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115976579 | ||||||
| chr6:115977036
|
C | G | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.467-8297G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115977036 | ||||||
| chr6:115977316
|
C | T | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.467-8577G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115977316 | ||||||
| chr6:115977629
|
C | T | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.467-8890G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115977629 | ||||||
| chr6:115977824
|
G | A | 4 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-9085C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115977824 | ||||||
| chr6:115977980
|
A | G | 1 | a0002c0002t0033g0069 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.467-9241T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115977980 | ||||||
| chr6:115978032
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.467-9293C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115978032 | ||||||
| chr6:115978220
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.467-9481A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115978220 | ||||||
| chr6:115979053
|
C | CA | 28 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(25): Show | 29 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.467-10315dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979053 | ||||||
| chr6:115979053
|
CA | C | 28 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119others(25): Show | 28 | HG00099.hp2 HG01099.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.467-10315delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979053 | ||||||
| chr6:115979064
|
A | C | 1 | a0002c0002t0002g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.467-10325T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979064 | ||||||
| chr6:115979144
|
G | T | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.467-10405C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979144 | ||||||
| chr6:115979187
|
G | A | 1 | a0001c0001t0069g0243 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.467-10448C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979187 | ||||||
| chr6:115979189
|
G | T | 266 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.467-10450C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979189 | ||||||
| chr6:115979255
|
T | C | 1 | a0001c0009t0012g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.467-10516A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979255 | ||||||
| chr6:115979289
|
A | G | 34 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.467-10550T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979289 | ||||||
| chr6:115979357
|
T | C | 201 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.467-10618A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979357 | ||||||
| chr6:115979448
|
G | C | 135 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(132): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.467-10709C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979448 | ||||||
| chr6:115979502
|
G | C | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.467-10763C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979502 | ||||||
| chr6:115979503
|
C | T | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.467-10764G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115979503 | ||||||
| chr6:115980239
|
T | C | 5 | a0001c0001t0025g0254a0001c0001t0025g0268a0001c0001t0029g0113others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-11500A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980239 | ||||||
| chr6:115980403
|
G | A | 19 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(16): Show | 19 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.467-11664C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980403 | ||||||
| chr6:115980721
|
T | C | 37 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(34): Show | 37 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.467-11982A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980721 | ||||||
| chr6:115980750
|
A | C | 266 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.467-12011T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980750 | ||||||
| chr6:115980808
|
A | G | 1 | a0001c0001t0011g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.467-12069T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980808 | ||||||
| chr6:115980873
|
C | A | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.467-12134G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980873 | ||||||
| chr6:115980886
|
T | C | 14 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(11): Show | 14 | HG01106.hp2 HG01123.hp1 HG03688.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-12147A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980886 | ||||||
| chr6:115980887
|
A | C | 7 | a0001c0001t0018g0056a0001c0001t0018g0115a0001c0001t0018g0116others(4): Show | 7 | HG01099.hp1 HG01106.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-12148T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980887 | ||||||
| chr6:115980933
|
C | G | 1 | a0002c0002t0002g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.467-12194G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980933 | ||||||
| chr6:115980960
|
T | C | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467-12221A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115980960 | ||||||
| chr6:115981040
|
A | G | 1 | a0001c0001t0016g0131 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.467-12301T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981040 | ||||||
| chr6:115981070
|
C | T | 1 | a0001c0001t0003g0250 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.467-12331G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981070 | ||||||
| chr6:115981142
|
C | A | 1 | a0001c0001t0003g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.467-12403G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981142 | ||||||
| chr6:115981248
|
A | G | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.467-12509T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981248 | ||||||
| chr6:115981254
|
G | T | 37 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(34): Show | 37 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.467-12515C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981254 | ||||||
| chr6:115981281
|
G | C | 4 | a0001c0004t0001g0109a0001c0004t0001g0118a0001c0004t0001g0179others(1): Show | 4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-12542C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981281 | ||||||
| chr6:115981438
|
T | C | 6 | a0001c0004t0001g0109a0001c0004t0001g0118a0001c0004t0001g0179others(3): Show | 6 | HG02602.hp1 HG04199.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-12699A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981438 | ||||||
| chr6:115981634
|
C | T | 1 | a0001c0001t0034g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-12895G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981634 | ||||||
| chr6:115981648
|
A | G | 1 | a0001c0001t0008g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.467-12909T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981648 | ||||||
| chr6:115981683
|
G | C | 66 | a0001c0001t0026g0245a0001c0001t0026g0270a0001c0001t0049g0197others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.467-12944C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981683 | ||||||
| chr6:115981699
|
A | T | 2 | a0004c0007t0015g0230a0004c0007t0015g0267 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.467-12960T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981699 | ||||||
| chr6:115981837
|
A | G | 4 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-13098T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981837 | ||||||
| chr6:115981904
|
A | T | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467-13165T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981904 | ||||||
| chr6:115981967
|
T | C | 1 | a0001c0001t0006g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.467-13228A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981967 | ||||||
| chr6:115981968
|
G | A | 1 | a0002c0002t0002g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.467-13229C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115981968 | ||||||
| chr6:115982208
|
G | T | 1 | a0002c0002t0002g0072 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.467-13469C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115982208 | ||||||
| chr6:115982412
|
C | T | 1 | a0001c0004t0001g0179 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.467-13673G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115982412 | ||||||
| chr6:115982748
|
C | A | 1 | a0001c0001t0042g0191 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.467-14009G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115982748 | ||||||
| chr6:115982787
|
A | T | 266 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.467-14048T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115982787 | ||||||
| chr6:115983071
|
C | CA | 67 | a0001c0001t0001g0107a0001c0001t0026g0245a0001c0001t0026g0270others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.467-14333dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983071 | ||||||
| chr6:115983071
|
CA | C | 65 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(62): Show | 66 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.467-14333delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983071 | ||||||
| chr6:115983364
|
G | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014 | 3 | HG02257.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.467-14625C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983364 | ||||||
| chr6:115983560
|
T | G | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.467-14821A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983560 | ||||||
| chr6:115983593
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.467-14854G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983593 | ||||||
| chr6:115983703
|
C | T | 39 | a0001c0001t0026g0245a0001c0001t0026g0270a0002c0002t0001g0060others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.467-14964G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983703 | ||||||
| chr6:115983704
|
G | A | 10 | a0002c0002t0007g0153a0002c0002t0007g0154a0002c0002t0007g0155others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-14965C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983704 | ||||||
| chr6:115983741
|
G | A | 1 | a0002c0002t0019g0174 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.467-15002C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983741 | ||||||
| chr6:115983901
|
T | C | 84 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(81): Show | 86 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.467-15162A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983901 | ||||||
| chr6:115983907
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.467-15168G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115983907 | ||||||
| chr6:115984020
|
G | A | 61 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(58): Show | 62 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.467-15281C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984020 | ||||||
| chr6:115984101
|
C | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014 | 3 | HG02257.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.467-15362G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984101 | ||||||
| chr6:115984109
|
G | A | 1 | a0001c0001t0012g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.467-15370C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984109 | ||||||
| chr6:115984379
|
A | G | 1 | a0002c0002t0002g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.467-15640T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984379 | ||||||
| chr6:115984474
|
T | C | 155 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(152): Show | 157 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.467-15735A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984474 | ||||||
| chr6:115984754
|
TA | T | 81 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(78): Show | 83 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.467-16016delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984754 | ||||||
| chr6:115984852
|
G | A | 2 | a0002c0002t0001g0028a0002c0002t0054g0023 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.467-16113C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984852 | ||||||
| chr6:115984859
|
C | T | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-16120G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984859 | ||||||
| chr6:115984860
|
G | A | 2 | a0001c0001t0069g0243a0001c0001t0070g0242 | 2 | HG01258.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.467-16121C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984860 | ||||||
| chr6:115984950
|
A | G | 30 | a0002c0002t0001g0015a0002c0002t0001g0173a0002c0002t0002g0037others(27): Show | 30 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.467-16211T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115984950 | ||||||
| chr6:115985005
|
G | C | 8 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(5): Show | 8 | NA18953.hp2 NA18954.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-16266C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985005 | ||||||
| chr6:115985213
|
G | A | 6 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119others(3): Show | 6 | HG00099.hp2 HG01169.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-16474C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985213 | ||||||
| chr6:115985338
|
C | G | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467-16599G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985338 | ||||||
| chr6:115985468
|
A | C | 3 | a0001c0001t0008g0233a0002c0002t0005g0128a0002c0002t0057g0126 | 3 | HG02004.hp1 HG02273.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.467-16729T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985468 | ||||||
| chr6:115985540
|
A | G | 6 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-16801T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985540 | ||||||
| chr6:115985559
|
A | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014 | 3 | HG02257.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.467-16820T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985559 | ||||||
| chr6:115985843
|
T | C | 1 | a0001c0001t0017g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.467-17104A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985843 | ||||||
| chr6:115985917
|
T | TAGAATGC others(286): Show |
1 | a0002c0002t0002g0072 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.467-17179_467-1717 others(297): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985917 | ||||||
| chr6:115985917
|
T | TAGAATGC others(285): Show |
2 | a0002c0002t0002g0038a0002c0002t0038g0073 | 2 | HG03831.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.467-17179_467-1717 others(296): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985917 | ||||||
| chr6:115985917
|
T | TAGAATGC others(286): Show |
48 | a0001c0001t0012g0112a0001c0001t0026g0245a0001c0009t0012g0120others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.467-17179_467-1717 others(297): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985917 | ||||||
| chr6:115985917
|
T | TAGAATGC others(287): Show |
31 | a0001c0001t0026g0270a0002c0002t0001g0005a0002c0002t0001g0013others(28): Show | 31 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.467-17179_467-1717 others(298): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985917 | ||||||
| chr6:115985917
|
T | TAGAATGC others(288): Show |
7 | a0002c0002t0001g0014a0002c0002t0002g0012a0002c0002t0002g0036others(4): Show | 7 | HG02074.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-17179_467-1717 others(299): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985917 | ||||||
| chr6:115985917
|
T | TAGAATGC others(289): Show |
1 | a0002c0002t0002g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.467-17179_467-1717 others(300): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115985917 | ||||||
| chr6:115986027
|
C | T | 2 | a0002c0002t0001g0060a0002c0002t0002g0059 | 2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.467-17288G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115986027 | ||||||
| chr6:115986186
|
T | C | 1 | a0002c0002t0002g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.467-17447A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115986186 | ||||||
| chr6:115986196
|
G | A | 6 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119others(3): Show | 6 | HG00099.hp2 HG01169.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-17457C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115986196 | ||||||
| chr6:115986394
|
A | C | 2 | a0001c0001t0017g0009a0001c0001t0017g0010 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.466+17483T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115986394 | ||||||
| chr6:115986455
|
C | T | 1 | a0002c0002t0001g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.466+17422G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115986455 | ||||||
| chr6:115987587
|
C | G | 1 | a0001c0001t0015g0231 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.466+16290G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115987587 | ||||||
| chr6:115987840
|
A | G | 1 | a0002c0002t0007g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.466+16037T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115987840 | ||||||
| chr6:115987881
|
T | C | 173 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(170): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.466+15996A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115987881 | ||||||
| chr6:115988158
|
A | C | 1 | a0001c0001t0014g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.466+15719T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115988158 | ||||||
| chr6:115988180
|
A | G | 1 | a0004c0007t0015g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.466+15697T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115988180 | ||||||
| chr6:115988340
|
T | C | 23 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(20): Show | 24 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.466+15537A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115988340 | ||||||
| chr6:115988486
|
T | C | 82 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(79): Show | 84 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.466+15391A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115988486 | ||||||
| chr6:115988831
|
C | A | 1 | a0001c0001t0011g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.466+15046G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115988831 | ||||||
| chr6:115988987
|
A | G | 1 | a0002c0002t0002g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.466+14890T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115988987 | ||||||
| chr6:115989080
|
A | G | 17 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.466+14797T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115989080 | ||||||
| chr6:115989124
|
T | C | 59 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(56): Show | 60 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.466+14753A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115989124 | ||||||
| chr6:115989173
|
C | T | 90 | a0001c0001t0012g0112a0001c0001t0026g0245a0001c0001t0026g0270others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.466+14704G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115989173 | ||||||
| chr6:115989274
|
A | G | 1 | a0002c0002t0002g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466+14603T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115989274 | ||||||
| chr6:115989524
|
G | A | 2 | a0002c0002t0030g0091a0002c0002t0031g0092 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466+14353C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115989524 | ||||||
| chr6:115989641
|
G | C | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.466+14236C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115989641 | ||||||
| chr6:115989697
|
A | T | 6 | a0001c0001t0003g0238a0001c0001t0003g0240a0001c0001t0003g0246others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+14180T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115989697 | ||||||
| chr6:115989916
|
C | T | 1 | a0001c0001t0008g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.466+13961G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115989916 | ||||||
| chr6:115990389
|
A | C | 269 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.466+13488T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990389 | ||||||
| chr6:115990433
|
C | A | 2 | a0001c0001t0001g0106a0001c0001t0051g0103 | 2 | HG02622.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.466+13444G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990433 | ||||||
| chr6:115990538
|
G | A | 90 | a0001c0001t0012g0112a0001c0001t0026g0245a0001c0001t0026g0270others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.466+13339C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990538 | ||||||
| chr6:115990600
|
C | G | 18 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(15): Show | 18 | HG00735.hp2 HG00738.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.466+13277G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990600 | ||||||
| chr6:115990609
|
T | A | 1 | a0001c0001t0017g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.466+13268A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990609 | ||||||
| chr6:115990630
|
G | A | 1 | a0002c0002t0048g0033 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.466+13247C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990630 | ||||||
| chr6:115990643
|
T | C | 6 | a0001c0001t0010g0221a0001c0001t0034g0198a0001c0001t0060g0259others(3): Show | 6 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+13234A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990643 | ||||||
| chr6:115990679
|
T | G | 2 | a0001c0001t0066g0201a0001c0001t0067g0207 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.466+13198A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990679 | ||||||
| chr6:115990700
|
G | C | 1 | a0002c0002t0002g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.466+13177C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990700 | ||||||
| chr6:115990837
|
C | T | 1 | a0001c0001t0006g0224 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.466+13040G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990837 | ||||||
| chr6:115990869
|
G | C | 6 | a0001c0001t0010g0221a0001c0001t0034g0198a0001c0001t0060g0259others(3): Show | 6 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+13008C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115990869 | ||||||
| chr6:115991052
|
T | C | 7 | a0001c0001t0018g0056a0001c0001t0018g0115a0001c0001t0018g0116others(4): Show | 7 | HG01099.hp1 HG01106.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.466+12825A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991052 | ||||||
| chr6:115991405
|
G | T | 1 | a0002c0002t0002g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.466+12472C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991405 | ||||||
| chr6:115991428
|
A | G | 1 | a0002c0002t0041g0089 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.466+12449T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991428 | ||||||
| chr6:115991463
|
C | G | 1 | a0002c0002t0002g0168 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.466+12414G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991463 | ||||||
| chr6:115991475
|
T | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0123 | 3 | HG01884.hp1 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.466+12402A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991475 | ||||||
| chr6:115991516
|
A | G | 2 | a0001c0001t0017g0009a0001c0001t0017g0010 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.466+12361T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991516 | ||||||
| chr6:115991535
|
T | A | 1 | a0002c0002t0002g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.466+12342A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991535 | ||||||
| chr6:115991625
|
C | T | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.466+12252G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991625 | ||||||
| chr6:115991730
|
A | T | 92 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(89): Show | 94 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.466+12147T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991730 | ||||||
| chr6:115991962
|
G | C | 6 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+11915C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115991962 | ||||||
| chr6:115992129
|
T | C | 1 | a0001c0001t0056g0134 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.466+11748A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992129 | ||||||
| chr6:115992133
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.466+11744T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992133 | ||||||
| chr6:115992230
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.466+11647C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992230 | ||||||
| chr6:115992253
|
A | G | 206 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.466+11624T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992253 | ||||||
| chr6:115992357
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.466+11520C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992357 | ||||||
| chr6:115992589
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.466+11288T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992589 | ||||||
| chr6:115992697
|
G | T | 1 | a0001c0001t0002g0142 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.466+11180C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992697 | ||||||
| chr6:115992768
|
G | C | 76 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(73): Show | 78 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.466+11109C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992768 | ||||||
| chr6:115992806
|
G | A | 3 | a0002c0002t0002g0063a0002c0002t0002g0064a0002c0002t0040g0011 | 3 | NA18972.hp2 NA18973.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.466+11071C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992806 | ||||||
| chr6:115992831
|
T | C | 1 | a0001c0001t0070g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.466+11046A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992831 | ||||||
| chr6:115992983
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.466+10894C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115992983 | ||||||
| chr6:115993091
|
A | G | 1 | a0001c0001t0016g0131 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.466+10786T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115993091 | ||||||
| chr6:115993400
|
C | G | 87 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(84): Show | 89 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.466+10477G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115993400 | ||||||
| chr6:115993442
|
C | T | 1 | a0002c0002t0007g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.466+10435G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115993442 | ||||||
| chr6:115993471
|
C | T | 87 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(84): Show | 89 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.466+10406G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115993471 | ||||||
| chr6:115993817
|
C | T | 2 | a0002c0002t0030g0091a0002c0002t0031g0092 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466+10060G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115993817 | ||||||
| chr6:115993858
|
A | G | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.466+10019T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115993858 | ||||||
| chr6:115994137
|
G | A | 2 | a0001c0001t0004g0150a0001c0001t0028g0003 | 2 | NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.466+9740C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994137 | ||||||
| chr6:115994245
|
C | T | 14 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(11): Show | 15 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.466+9632G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994245 | ||||||
| chr6:115994321
|
A | AC | 58 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0239others(55): Show | 58 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.466+9555dupG | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994321 | ||||||
| chr6:115994321
|
A | ACC | 13 | a0001c0001t0003g0238a0001c0001t0010g0200a0001c0001t0010g0202others(10): Show | 13 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(10): Show |
intron_variant | MODIFIER | c.466+9554_466+9555d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994321 | ||||||
| chr6:115994321
|
ACCTC | A | 15 | a0001c0001t0006g0002a0001c0001t0006g0216a0001c0001t0006g0217others(12): Show | 16 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.466+9552_466+9555d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994321 | ||||||
| chr6:115994322
|
CCT | C | 24 | a0001c0001t0001g0104a0001c0001t0001g0190a0001c0001t0008g0203others(21): Show | 24 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.466+9553_466+9554d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994322 | ||||||
| chr6:115994323
|
CT | C | 28 | a0001c0001t0001g0107a0001c0001t0001g0188a0001c0001t0003g0241others(25): Show | 28 | HG00280.hp1 HG01071.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.466+9553delA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994323 | ||||||
| chr6:115994324
|
T | C | 121 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(118): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.466+9553A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994324 | ||||||
| chr6:115994329
|
C | A | 1 | a0002c0002t0045g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.466+9548G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994329 | ||||||
| chr6:115994333
|
C | G | 1 | a0001c0001t0071g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.466+9544G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994333 | ||||||
| chr6:115994338
|
C | CT | 87 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(84): Show | 89 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.466+9538dupA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994338 | ||||||
| chr6:115994584
|
T | C | 1 | a0002c0002t0001g0149 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.466+9293A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994584 | ||||||
| chr6:115994632
|
A | G | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.466+9245T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994632 | ||||||
| chr6:115994731
|
A | G | 1 | a0001c0001t0013g0227 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.466+9146T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994731 | ||||||
| chr6:115994940
|
C | A | 112 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.466+8937G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115994940 | ||||||
| chr6:115995072
|
G | A | 31 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0135others(28): Show | 31 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.466+8805C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995072 | ||||||
| chr6:115995513
|
T | C | 27 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(24): Show | 28 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.466+8364A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995513 | ||||||
| chr6:115995522
|
T | C | 2 | a0001c0001t0010g0221a0001c0001t0065g0258 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.466+8355A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995522 | ||||||
| chr6:115995719
|
G | T | 112 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.466+8158C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995719 | ||||||
| chr6:115995733
|
A | G | 112 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.466+8144T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995733 | ||||||
| chr6:115995771
|
G | A | 8 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(5): Show | 8 | NA18953.hp2 NA18954.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.466+8106C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995771 | ||||||
| chr6:115995888
|
CT | C | 5 | a0001c0001t0018g0056a0001c0001t0018g0115a0001c0001t0018g0116others(2): Show | 5 | HG01099.hp1 HG01106.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+7988delA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995888 | ||||||
| chr6:115995929
|
A | C | 112 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.466+7948T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995929 | ||||||
| chr6:115995973
|
A | G | 1 | a0001c0001t0061g0257 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.466+7904T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115995973 | ||||||
| chr6:115996128
|
A | C | 1 | a0001c0001t0039g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.466+7749T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115996128 | ||||||
| chr6:115996249
|
C | T | 1 | a0003c0003t0004g0161 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.466+7628G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115996249 | ||||||
| chr6:115996281
|
T | C | 92 | a0002c0002t0001g0015a0002c0002t0001g0027a0002c0002t0001g0029others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.466+7596A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115996281 | ||||||
| chr6:115996422
|
C | T | 3 | a0002c0002t0007g0155a0002c0002t0007g0156a0002c0002t0007g0157 | 3 | HG02622.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.466+7455G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115996422 | ||||||
| chr6:115996475
|
C | T | 199 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(196): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.466+7402G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115996475 | ||||||
| chr6:115996530
|
C | T | 6 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+7347G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115996530 | ||||||
| chr6:115996979
|
C | G | 3 | a0001c0001t0047g0186a0001c0001t0058g0199a0001c0009t0012g0120 | 3 | HG02886.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.466+6898G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115996979 | ||||||
| chr6:115996987
|
T | A | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.466+6890A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115996987 | ||||||
| chr6:115997029
|
C | T | 10 | a0002c0002t0007g0153a0002c0002t0007g0154a0002c0002t0007g0155others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.466+6848G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997029 | ||||||
| chr6:115997105
|
T | TTACCCCA others(5): Show |
1 | a0002c0002t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.466+6760_466+6771d others(14): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997105 | ||||||
| chr6:115997294
|
T | C | 1 | a0002c0002t0054g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.466+6583A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997294 | ||||||
| chr6:115997382
|
G | A | 3 | a0002c0002t0001g0127a0002c0002t0005g0128a0002c0002t0057g0126 | 3 | HG02004.hp1 HG02080.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.466+6495C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997382 | ||||||
| chr6:115997391
|
A | T | 2 | a0002c0002t0001g0078a0002c0002t0001g0079 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.466+6486T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997391 | ||||||
| chr6:115997440
|
CA | C | 9 | a0001c0001t0008g0233a0001c0001t0010g0200a0001c0001t0010g0202others(6): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+6436delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997440 | ||||||
| chr6:115997498
|
T | A | 1 | a0006c0008t0002g0055 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.466+6379A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997498 | ||||||
| chr6:115997543
|
T | C | 19 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(16): Show | 20 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.466+6334A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997543 | ||||||
| chr6:115997582
|
T | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.466+6295A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997582 | ||||||
| chr6:115997913
|
G | A | 1 | a0001c0001t0012g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.466+5964C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115997913 | ||||||
| chr6:115998322
|
C | T | 1 | a0004c0007t0015g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.466+5555G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115998322 | ||||||
| chr6:115998744
|
A | T | 1 | a0001c0001t0011g0248 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.466+5133T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115998744 | ||||||
| chr6:115998918
|
G | A | 1 | a0001c0001t0014g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.466+4959C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115998918 | ||||||
| chr6:115999125
|
T | C | 6 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+4752A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999125 | ||||||
| chr6:115999269
|
G | T | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.466+4608C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999269 | ||||||
| chr6:115999404
|
C | T | 2 | a0001c0001t0008g0233a0001c0001t0071g0272 | 2 | NA18986.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.466+4473G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999404 | ||||||
| chr6:115999417
|
A | G | 1 | a0002c0002t0002g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.466+4460T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999417 | ||||||
| chr6:115999518
|
C | A | 1 | a0001c0001t0003g0250 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.466+4359G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999518 | ||||||
| chr6:115999520
|
C | T | 29 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(26): Show | 30 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.466+4357G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999520 | ||||||
| chr6:115999812
|
C | A | 2 | a0002c0002t0007g0153a0002c0002t0007g0192 | 2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.466+4065G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999812 | ||||||
| chr6:115999987
|
G | T | 1 | a0002c0002t0019g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.466+3890C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999987 | ||||||
| chr6:115999993
|
T | C | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.466+3884A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 115999993 | ||||||
| chr6:116000223
|
C | CTT | 10 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0111others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.466+3652_466+3653d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
C | CTTT | 13 | a0001c0001t0001g0110a0001c0001t0001g0124a0001c0001t0001g0130others(10): Show | 13 | HG00621.hp1 HG00642.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.466+3651_466+3653d others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
C | CTTTT | 13 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0141others(10): Show | 13 | HG01346.hp1 HG02055.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.466+3650_466+3653d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
C | CTTTTT | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0016g0131others(2): Show | 5 | HG00741.hp2 HG01106.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+3649_466+3653d others(7): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0108a0001c0001t0001g0135a0001c0001t0002g0142others(11): Show | 14 | HG00408.hp1 HG00558.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.466+3646_466+3653d others(10): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.466+3643_466+3653d others(13): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTT | C | 9 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(6): Show | 9 | HG00140.hp2 HG00438.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+3652_466+3653d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTT | C | 12 | a0002c0002t0001g0015a0002c0002t0001g0027a0002c0002t0001g0080others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(9): Show |
intron_variant | MODIFIER | c.466+3651_466+3653d others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTTT | C | 33 | a0002c0002t0001g0050a0002c0002t0001g0076a0002c0002t0001g0078others(30): Show | 33 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.466+3650_466+3653d others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0012g0112a0001c0001t0047g0186 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.466+3643_466+3653d others(13): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTTTTTT others(5): Show |
C | 2 | a0003c0003t0004g0163a0003c0003t0004g0164 | 2 | NA18962.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.466+3642_466+3653d others(14): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0022g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.466+3640_466+3653d others(16): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTTTTTT others(11): Show |
C | 6 | a0002c0002t0001g0029a0002c0002t0002g0067a0002c0002t0002g0087others(3): Show | 6 | HG02040.hp1 HG02040.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+3636_466+3653d others(20): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTTTTTT others(12): Show |
C | 47 | a0001c0001t0017g0194a0002c0002t0001g0031a0002c0002t0001g0034others(44): Show | 47 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.466+3635_466+3653d others(21): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTTTTTT others(13): Show |
C | 3 | a0002c0002t0002g0090a0002c0002t0005g0066a0002c0002t0038g0073 | 3 | HG00558.hp1 NA18954.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.466+3634_466+3653d others(22): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000223
|
CTTTTTTT others(16): Show |
C | 1 | a0002c0002t0002g0012 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.466+3631_466+3653d others(25): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000223 | ||||||
| chr6:116000227
|
T | C | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.466+3650A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000227 | ||||||
| chr6:116000232
|
T | C | 6 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+3645A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000232 | ||||||
| chr6:116000244
|
TTTTTTTT others(11): Show |
T | 3 | a0001c0001t0003g0246a0001c0001t0011g0248a0001c0001t0034g0198 | 3 | HG00738.hp2 HG01169.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.466+3615_466+3632d others(20): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000244 | ||||||
| chr6:116000245
|
TTTTTTTT others(10): Show |
T | 57 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(54): Show | 58 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.466+3615_466+3631d others(19): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000245 | ||||||
| chr6:116000246
|
TTTTTTTT others(9): Show |
T | 8 | a0001c0001t0006g0265a0001c0001t0008g0204a0001c0001t0010g0200others(5): Show | 8 | HG01517.hp1 HG02486.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.466+3615_466+3630d others(18): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000246 | ||||||
| chr6:116000247
|
TTTTTTTT others(8): Show |
T | 15 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0205others(12): Show | 16 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.466+3615_466+3629d others(17): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000247 | ||||||
| chr6:116000266
|
G | A | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.466+3611C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000266 | ||||||
| chr6:116000269
|
G | A | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.466+3608C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000269 | ||||||
| chr6:116000273
|
C | T | 57 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(54): Show | 58 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.466+3604G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000273 | ||||||
| chr6:116000274
|
G | A | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.466+3603C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000274 | ||||||
| chr6:116000390
|
G | C | 3 | a0002c0002t0002g0024a0002c0002t0002g0025a0002c0002t0002g0026 | 3 | HG00280.hp1 HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.466+3487C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000390 | ||||||
| chr6:116000430
|
A | G | 2 | a0002c0002t0030g0091a0002c0002t0031g0092 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466+3447T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000430 | ||||||
| chr6:116000904
|
A | G | 199 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(196): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.466+2973T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000904 | ||||||
| chr6:116000978
|
G | A | 1 | a0001c0001t0047g0186 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+2899C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116000978 | ||||||
| chr6:116001055
|
C | T | 2 | a0002c0002t0002g0020a0002c0002t0044g0021 | 2 | NA18981.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.466+2822G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116001055 | ||||||
| chr6:116001186
|
C | T | 98 | a0001c0001t0035g0004a0002c0002t0001g0015a0002c0002t0001g0027others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.466+2691G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116001186 | ||||||
| chr6:116001218
|
G | A | 72 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(69): Show | 73 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.466+2659C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116001218 | ||||||
| chr6:116001280
|
T | C | 2 | a0001c0001t0069g0243a0001c0001t0070g0242 | 2 | HG01258.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.466+2597A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116001280 | ||||||
| chr6:116001366
|
T | A | 1 | a0002c0002t0005g0035 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.466+2511A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116001366 | ||||||
| chr6:116001493
|
C | T | 3 | a0002c0002t0002g0024a0002c0002t0002g0025a0002c0002t0002g0026 | 3 | HG00280.hp1 HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.466+2384G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116001493 | ||||||
| chr6:116001856
|
T | TAC | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.466+2019_466+2020d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116001856 | ||||||
| chr6:116002083
|
C | A | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0130others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.466+1794G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002083 | ||||||
| chr6:116002249
|
T | C | 1 | a0002c0002t0007g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.466+1628A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002249 | ||||||
| chr6:116002256
|
G | A | 1 | a0004c0007t0015g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.466+1621C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002256 | ||||||
| chr6:116002600
|
G | A | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.466+1277C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002600 | ||||||
| chr6:116002747
|
T | A | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.466+1130A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002747 | ||||||
| chr6:116002808
|
C | A | 1 | a0002c0002t0002g0044 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.466+1069G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002808 | ||||||
| chr6:116002839
|
A | G | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+1038T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002839 | ||||||
| chr6:116002863
|
C | T | 1 | a0001c0001t0049g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.466+1014G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002863 | ||||||
| chr6:116002936
|
A | G | 1 | a0001c0001t0060g0259 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.466+941T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002936 | ||||||
| chr6:116002958
|
C | T | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.466+919G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002958 | ||||||
| chr6:116002967
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119 | 3 | HG00099.hp2 HG01516.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.466+910C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116002967 | ||||||
| chr6:116003024
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.466+853G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116003024 | ||||||
| chr6:116003297
|
A | G | 57 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(54): Show | 58 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.466+580T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116003297 | ||||||
| chr6:116003391
|
G | T | 1 | a0002c0002t0019g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.466+486C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116003391 | ||||||
| chr6:116003656
|
G | A | 2 | a0001c0001t0003g0244a0001c0001t0011g0249 | 2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.466+221C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116003656 | ||||||
| chr6:116003735
|
A | G | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.466+142T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116003735 | ||||||
| chr6:116003871
|
C | T | 1 | a0001c0001t0008g0205 | 1 | HG01496.hp2 | splice_region_variant&intron_variant | LOW | c.466+6G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 2/7 | chr6 | 116003871 | ||||||
| chr6:116004357
|
C | G | 2 | a0001c0001t0001g0133a0001c0001t0056g0134 | 2 | NA18981.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.345-359G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116004357 | ||||||
| chr6:116004357
|
CA | C | 21 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(18): Show | 22 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.345-360delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116004357 | ||||||
| chr6:116004387
|
T | C | 3 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209 | 3 | HG02486.hp1 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.345-389A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116004387 | ||||||
| chr6:116004392
|
C | T | 1 | a0001c0001t0060g0259 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.345-394G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116004392 | ||||||
| chr6:116004396
|
T | C | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-398A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116004396 | ||||||
| chr6:116004523
|
C | T | 1 | a0002c0002t0002g0047 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.345-525G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116004523 | ||||||
| chr6:116004923
|
A | G | 1 | a0004c0007t0015g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-925T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116004923 | ||||||
| chr6:116005024
|
T | G | 8 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-1026A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116005024 | ||||||
| chr6:116005189
|
T | C | 2 | a0002c0002t0009g0048a0006c0008t0002g0055 | 2 | NA18963.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.345-1191A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116005189 | ||||||
| chr6:116005418
|
C | T | 1 | a0001c0001t0027g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.345-1420G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116005418 | ||||||
| chr6:116005423
|
C | T | 1 | a0004c0007t0015g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-1425G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116005423 | ||||||
| chr6:116005790
|
A | G | 7 | a0002c0002t0001g0027a0002c0002t0001g0076a0002c0002t0001g0077others(4): Show | 7 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-1792T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116005790 | ||||||
| chr6:116005939
|
A | G | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-1941T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116005939 | ||||||
| chr6:116006170
|
A | T | 1 | a0001c0001t0017g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.345-2172T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116006170 | ||||||
| chr6:116006308
|
T | G | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-2310A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116006308 | ||||||
| chr6:116006330
|
A | G | 97 | a0002c0002t0001g0015a0002c0002t0001g0027a0002c0002t0001g0029others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.345-2332T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116006330 | ||||||
| chr6:116006416
|
C | T | 22 | a0002c0002t0001g0127a0002c0002t0002g0037a0002c0002t0002g0063others(19): Show | 22 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.345-2418G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116006416 | ||||||
| chr6:116006430
|
G | C | 1 | a0001c0001t0014g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.345-2432C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116006430 | ||||||
| chr6:116006698
|
C | T | 116 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.345-2700G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116006698 | ||||||
| chr6:116006773
|
T | C | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-2775A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116006773 | ||||||
| chr6:116006965
|
C | A | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-2967G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116006965 | ||||||
| chr6:116007089
|
G | T | 5 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-3091C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116007089 | ||||||
| chr6:116007291
|
T | C | 2 | a0001c0001t0006g0220a0001c0001t0010g0221 | 2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.345-3293A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116007291 | ||||||
| chr6:116007370
|
A | T | 22 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(19): Show | 22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.345-3372T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116007370 | ||||||
| chr6:116007840
|
A | G | 2 | a0001c0001t0008g0203a0001c0001t0008g0204 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.345-3842T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116007840 | ||||||
| chr6:116007851
|
C | CAT | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-3854_345-3853i others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116007851 | ||||||
| chr6:116008006
|
C | T | 1 | a0002c0002t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.345-4008G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116008006 | ||||||
| chr6:116008586
|
T | C | 1 | a0002c0002t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.345-4588A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116008586 | ||||||
| chr6:116008597
|
A | G | 1 | a0002c0002t0002g0168 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.345-4599T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116008597 | ||||||
| chr6:116008950
|
G | A | 2 | a0002c0006t0012g0096a0002c0006t0012g0097 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.345-4952C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116008950 | ||||||
| chr6:116009103
|
G | A | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-5105C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116009103 | ||||||
| chr6:116009122
|
G | A | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-5124C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116009122 | ||||||
| chr6:116009130
|
T | A | 2 | a0001c0001t0017g0009a0001c0001t0017g0010 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.345-5132A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116009130 | ||||||
| chr6:116009411
|
T | C | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-5413A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116009411 | ||||||
| chr6:116009779
|
C | T | 200 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(197): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.345-5781G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116009779 | ||||||
| chr6:116009970
|
G | A | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-5972C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116009970 | ||||||
| chr6:116010103
|
T | A | 8 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-6105A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116010103 | ||||||
| chr6:116010106
|
C | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014 | 3 | HG02257.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.345-6108G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116010106 | ||||||
| chr6:116010171
|
G | A | 11 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(8): Show | 12 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-6173C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116010171 | ||||||
| chr6:116010178
|
T | C | 1 | a0001c0001t0011g0234 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.345-6180A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116010178 | ||||||
| chr6:116010560
|
C | A | 1 | a0004c0007t0015g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-6562G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116010560 | ||||||
| chr6:116011058
|
G | A | 6 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-7060C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116011058 | ||||||
| chr6:116011090
|
TA | T | 86 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(83): Show | 88 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.345-7093delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116011090 | ||||||
| chr6:116011130
|
C | T | 1 | a0002c0002t0002g0047 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.345-7132G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116011130 | ||||||
| chr6:116011372
|
A | G | 2 | a0002c0002t0030g0091a0002c0002t0031g0092 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.345-7374T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116011372 | ||||||
| chr6:116011808
|
T | G | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-7810A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116011808 | ||||||
| chr6:116011864
|
T | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-7866A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116011864 | ||||||
| chr6:116011890
|
T | C | 1 | a0001c0001t0014g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.345-7892A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116011890 | ||||||
| chr6:116011996
|
C | T | 1 | a0002c0002t0057g0126 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.345-7998G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116011996 | ||||||
| chr6:116012219
|
G | C | 1 | a0002c0002t0002g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.345-8221C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116012219 | ||||||
| chr6:116012405
|
C | A | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.345-8407G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116012405 | ||||||
| chr6:116012579
|
C | G | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-8581G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116012579 | ||||||
| chr6:116012767
|
G | A | 1 | a0004c0007t0015g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345-8769C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116012767 | ||||||
| chr6:116012934
|
T | C | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.345-8936A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116012934 | ||||||
| chr6:116013020
|
G | A | 1 | a0001c0001t0014g0263 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.345-9022C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116013020 | ||||||
| chr6:116013272
|
G | T | 1 | a0001c0001t0062g0218 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.345-9274C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116013272 | ||||||
| chr6:116013588
|
A | T | 1 | a0001c0001t0042g0191 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.345-9590T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116013588 | ||||||
| chr6:116013677
|
C | A | 1 | a0002c0002t0001g0076 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.345-9679G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116013677 | ||||||
| chr6:116013740
|
A | C | 1 | a0002c0002t0002g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.345-9742T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116013740 | ||||||
| chr6:116013968
|
C | A | 84 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(81): Show | 86 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-9970G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116013968 | ||||||
| chr6:116014474
|
A | G | 28 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(25): Show | 28 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.345-10476T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116014474 | ||||||
| chr6:116014742
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.345-10744C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116014742 | ||||||
| chr6:116014902
|
G | T | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-10904C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116014902 | ||||||
| chr6:116014907
|
G | A | 6 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-10909C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116014907 | ||||||
| chr6:116014976
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.345-10978C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116014976 | ||||||
| chr6:116015425
|
A | G | 1 | a0002c0002t0009g0048 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.345-11427T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116015425 | ||||||
| chr6:116015594
|
G | C | 2 | a0001c0001t0067g0207a0001c0001t0068g0208 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.345-11596C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116015594 | ||||||
| chr6:116015757
|
T | A | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.345-11759A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116015757 | ||||||
| chr6:116015801
|
G | A | 6 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-11803C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116015801 | ||||||
| chr6:116015851
|
C | T | 1 | a0002c0002t0004g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.345-11853G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116015851 | ||||||
| chr6:116015876
|
C | T | 2 | a0002c0006t0012g0096a0002c0006t0012g0097 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.345-11878G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116015876 | ||||||
| chr6:116015984
|
G | A | 1 | a0002c0002t0002g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.345-11986C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116015984 | ||||||
| chr6:116016058
|
G | A | 3 | a0002c0002t0002g0074a0002c0002t0002g0075a0002c0002t0002g0084 | 3 | HG00544.hp2 NA18969.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.345-12060C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116016058 | ||||||
| chr6:116016340
|
G | A | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-12342C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116016340 | ||||||
| chr6:116016728
|
A | C | 1 | a0001c0001t0024g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.345-12730T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116016728 | ||||||
| chr6:116016732
|
T | A | 3 | a0001c0001t0024g0006a0002c0002t0030g0091a0002c0002t0031g0092 | 3 | HG02896.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.345-12734A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116016732 | ||||||
| chr6:116016902
|
T | C | 116 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.345-12904A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116016902 | ||||||
| chr6:116017149
|
GAAGA | G | 2 | a0001c0001t0011g0237a0001c0001t0026g0245 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.345-13155_345-1315 others(8): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116017149 | ||||||
| chr6:116017189
|
C | A | 64 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(61): Show | 65 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.345-13191G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116017189 | ||||||
| chr6:116017282
|
T | C | 5 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-13284A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116017282 | ||||||
| chr6:116017558
|
T | C | 2 | a0001c0001t0018g0056a0002c0002t0002g0057 | 2 | HG00099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.345-13560A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116017558 | ||||||
| chr6:116017829
|
T | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-13831A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116017829 | ||||||
| chr6:116018132
|
T | C | 22 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(19): Show | 22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.345-14134A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116018132 | ||||||
| chr6:116018555
|
T | C | 1 | a0002c0002t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.345-14557A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116018555 | ||||||
| chr6:116018567
|
T | C | 8 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-14569A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116018567 | ||||||
| chr6:116019224
|
C | T | 1 | a0001c0001t0006g0217 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.345-15226G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116019224 | ||||||
| chr6:116019280
|
T | C | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.345-15282A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116019280 | ||||||
| chr6:116019596
|
G | T | 1 | a0002c0002t0002g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.345-15598C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116019596 | ||||||
| chr6:116019641
|
G | A | 1 | a0001c0001t0026g0245 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.345-15643C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116019641 | ||||||
| chr6:116020031
|
A | T | 10 | a0002c0002t0007g0153a0002c0002t0007g0154a0002c0002t0007g0155others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-16033T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020031 | ||||||
| chr6:116020227
|
A | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01258.hp1 HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.345-16229T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020227 | ||||||
| chr6:116020415
|
C | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01258.hp1 HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.345-16417G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020415 | ||||||
| chr6:116020416
|
C | T | 1 | a0001c0001t0061g0257 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.345-16418G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020416 | ||||||
| chr6:116020479
|
T | A | 3 | a0001c0001t0015g0231a0001c0001t0015g0253a0004c0007t0015g0230 | 3 | HG01981.hp2 NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.345-16481A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020479 | ||||||
| chr6:116020547
|
C | T | 117 | a0001c0001t0018g0056a0002c0002t0001g0005a0002c0002t0001g0013others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.345-16549G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020547 | ||||||
| chr6:116020560
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0002g0142a0001c0001t0004g0132others(1): Show | 4 | NA18940.hp1 NA19004.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-16562C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020560 | ||||||
| chr6:116020668
|
A | G | 5 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119others(2): Show | 5 | HG00099.hp2 HG01516.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-16670T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020668 | ||||||
| chr6:116020670
|
A | G | 2 | a0002c0002t0002g0020a0002c0002t0044g0021 | 2 | NA18981.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.345-16672T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020670 | ||||||
| chr6:116020732
|
T | C | 1 | a0001c0001t0003g0246 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.345-16734A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020732 | ||||||
| chr6:116020743
|
AATTTTTC others(1): Show |
A | 8 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-16753_345-1674 others(12): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020743 | ||||||
| chr6:116020921
|
T | C | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-16923A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116020921 | ||||||
| chr6:116021024
|
G | T | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-17026C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116021024 | ||||||
| chr6:116021256
|
T | C | 1 | a0002c0002t0002g0084 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.345-17258A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116021256 | ||||||
| chr6:116021298
|
C | T | 1 | a0004c0007t0015g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345-17300G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116021298 | ||||||
| chr6:116021367
|
G | T | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.345-17369C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116021367 | ||||||
| chr6:116021431
|
T | C | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-17433A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116021431 | ||||||
| chr6:116021568
|
T | G | 1 | a0002c0002t0009g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.345-17570A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116021568 | ||||||
| chr6:116021845
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.345-17847C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116021845 | ||||||
| chr6:116022009
|
C | T | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.345-18011G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022009 | ||||||
| chr6:116022127
|
C | G | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-18129G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022127 | ||||||
| chr6:116022363
|
T | C | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-18365A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022363 | ||||||
| chr6:116022404
|
A | G | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-18406T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022404 | ||||||
| chr6:116022617
|
A | C | 3 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014 | 3 | HG02257.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.345-18619T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022617 | ||||||
| chr6:116022712
|
G | C | 2 | a0002c0002t0001g0078a0002c0002t0001g0079 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.345-18714C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022712 | ||||||
| chr6:116022789
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.345-18791G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022789 | ||||||
| chr6:116022866
|
T | C | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-18868A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022866 | ||||||
| chr6:116022950
|
C | T | 1 | a0001c0001t0071g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.345-18952G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116022950 | ||||||
| chr6:116023003
|
G | A | 2 | a0001c0001t0008g0203a0001c0001t0008g0204 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.345-19005C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023003 | ||||||
| chr6:116023009
|
C | T | 1 | a0002c0002t0001g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.345-19011G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023009 | ||||||
| chr6:116023029
|
A | G | 1 | a0001c0001t0003g0236 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.345-19031T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023029 | ||||||
| chr6:116023095
|
C | G | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.345-19097G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023095 | ||||||
| chr6:116023197
|
A | T | 19 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(16): Show | 20 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.345-19199T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023197 | ||||||
| chr6:116023220
|
A | G | 1 | a0002c0002t0001g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.345-19222T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023220 | ||||||
| chr6:116023737
|
G | A | 2 | a0002c0002t0001g0028a0002c0002t0054g0023 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.345-19739C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023737 | ||||||
| chr6:116023962
|
A | AG | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-19965dupC | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023962 | ||||||
| chr6:116023964
|
T | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-19966A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116023964 | ||||||
| chr6:116024057
|
T | TAC | 36 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(33): Show | 36 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.345-20061_345-2006 others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024057 | ||||||
| chr6:116024057
|
T | TACAC | 7 | a0001c0001t0001g0119a0001c0001t0001g0144a0001c0001t0001g0169others(4): Show | 7 | HG01516.hp2 HG02622.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-20063_345-2006 others(8): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024057 | ||||||
| chr6:116024057
|
TAC | T | 35 | a0001c0001t0001g0145a0001c0001t0001g0188a0001c0001t0001g0190others(32): Show | 35 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.345-20061_345-2006 others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024057 | ||||||
| chr6:116024057
|
TACAC | T | 134 | a0001c0001t0003g0247a0001c0001t0006g0002a0001c0001t0006g0216others(131): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.345-20063_345-2006 others(8): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024057 | ||||||
| chr6:116024057
|
TACACAC | T | 31 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(28): Show | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.345-20065_345-2006 others(10): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024057 | ||||||
| chr6:116024057
|
TACACACA others(3): Show |
T | 1 | a0002c0002t0054g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.345-20069_345-2006 others(14): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024057 | ||||||
| chr6:116024267
|
T | A | 19 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(16): Show | 20 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.345-20269A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024267 | ||||||
| chr6:116024338
|
A | G | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-20340T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024338 | ||||||
| chr6:116024372
|
G | A | 1 | a0002c0002t0001g0173 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-20374C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024372 | ||||||
| chr6:116024409
|
T | G | 1 | a0001c0001t0049g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.345-20411A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024409 | ||||||
| chr6:116024682
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(3): Show | 6 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-20684G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024682 | ||||||
| chr6:116024743
|
T | C | 1 | a0001c0001t0049g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.345-20745A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024743 | ||||||
| chr6:116024836
|
A | G | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-20838T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116024836 | ||||||
| chr6:116025010
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.345-21012A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116025010 | ||||||
| chr6:116025035
|
C | T | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-21037G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116025035 | ||||||
| chr6:116025192
|
A | C | 1 | a0001c0001t0024g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.345-21194T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116025192 | ||||||
| chr6:116025231
|
C | A | 76 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(73): Show | 78 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.345-21233G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116025231 | ||||||
| chr6:116025590
|
T | C | 1 | a0002c0002t0001g0015 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.345-21592A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116025590 | ||||||
| chr6:116025978
|
T | C | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-21980A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116025978 | ||||||
| chr6:116026136
|
C | T | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.345-22138G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026136 | ||||||
| chr6:116026138
|
G | C | 20 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(17): Show | 21 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.345-22140C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026138 | ||||||
| chr6:116026269
|
G | A | 83 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(80): Show | 85 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-22271C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026269 | ||||||
| chr6:116026270
|
C | A | 10 | a0002c0002t0007g0153a0002c0002t0007g0154a0002c0002t0007g0155others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-22272G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026270 | ||||||
| chr6:116026421
|
G | A | 3 | a0002c0002t0001g0060a0002c0002t0002g0059a0002c0002t0021g0043 | 3 | HG01169.hp1 HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.345-22423C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026421 | ||||||
| chr6:116026443
|
C | T | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-22445G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026443 | ||||||
| chr6:116026453
|
A | T | 10 | a0002c0002t0007g0153a0002c0002t0007g0154a0002c0002t0007g0155others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-22455T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026453 | ||||||
| chr6:116026489
|
CAGGA | C | 50 | a0001c0001t0001g0119a0001c0001t0018g0056a0002c0002t0001g0015others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.345-22495_345-2249 others(8): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026489 | ||||||
| chr6:116026542
|
A | AGAAG | 10 | a0001c0001t0001g0178a0001c0001t0001g0195a0001c0001t0029g0113others(7): Show | 10 | HG02055.hp1 HG02074.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-22548_345-2254 others(8): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026542 | ||||||
| chr6:116026542
|
AGAAG | A | 88 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(85): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.345-22548_345-2254 others(8): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026542 | ||||||
| chr6:116026542
|
AGAAGGAA others(13): Show |
A | 1 | a0001c0001t0017g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.345-22564_345-2254 others(24): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026542 | ||||||
| chr6:116026570
|
GGAAGGAA others(1): Show |
G | 4 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-22580_345-2257 others(12): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026570 | ||||||
| chr6:116026950
|
T | C | 1 | a0001c0001t0011g0248 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.345-22952A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116026950 | ||||||
| chr6:116027043
|
C | G | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-23045G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027043 | ||||||
| chr6:116027086
|
A | G | 269 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.345-23088T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027086 | ||||||
| chr6:116027317
|
G | T | 1 | a0004c0007t0015g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345-23319C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027317 | ||||||
| chr6:116027673
|
T | C | 1 | a0002c0002t0002g0022 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.345-23675A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027673 | ||||||
| chr6:116027678
|
G | C | 1 | a0001c0001t0027g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.345-23680C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027678 | ||||||
| chr6:116027743
|
A | G | 1 | a0001c0001t0006g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.345-23745T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027743 | ||||||
| chr6:116027768
|
A | C | 11 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(8): Show | 12 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-23770T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027768 | ||||||
| chr6:116027842
|
A | G | 1 | a0002c0002t0002g0047 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.345-23844T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027842 | ||||||
| chr6:116027878
|
C | T | 78 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(75): Show | 80 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.345-23880G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116027878 | ||||||
| chr6:116028155
|
G | C | 1 | a0001c0001t0049g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.345-24157C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116028155 | ||||||
| chr6:116028476
|
C | T | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.345-24478G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116028476 | ||||||
| chr6:116028702
|
T | C | 11 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(8): Show | 12 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-24704A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116028702 | ||||||
| chr6:116028802
|
C | G | 2 | a0002c0002t0001g0028a0002c0002t0054g0023 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.345-24804G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116028802 | ||||||
| chr6:116029053
|
C | T | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.345-25055G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116029053 | ||||||
| chr6:116029237
|
C | T | 1 | a0005c0005t0002g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.345-25239G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116029237 | ||||||
| chr6:116029467
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-25469A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116029467 | ||||||
| chr6:116029625
|
G | A | 97 | a0001c0001t0018g0056a0002c0002t0001g0015a0002c0002t0001g0027others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.345-25627C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116029625 | ||||||
| chr6:116029627
|
C | A | 5 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(2): Show | 5 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-25629G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116029627 | ||||||
| chr6:116029716
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0188others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-25718C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116029716 | ||||||
| chr6:116030164
|
T | C | 8 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-26166A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030164 | ||||||
| chr6:116030219
|
T | C | 1 | a0001c0001t0071g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.345-26221A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030219 | ||||||
| chr6:116030379
|
T | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-26381A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030379 | ||||||
| chr6:116030433
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345-26435A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030433 | ||||||
| chr6:116030552
|
A | G | 1 | a0001c0001t0015g0253 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.345-26554T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030552 | ||||||
| chr6:116030561
|
G | T | 76 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(73): Show | 78 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.345-26563C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030561 | ||||||
| chr6:116030762
|
G | A | 9 | a0002c0002t0001g0173a0002c0002t0002g0074a0002c0002t0002g0075others(6): Show | 9 | HG00544.hp2 HG02040.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-26764C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030762 | ||||||
| chr6:116030935
|
C | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119 | 3 | HG00099.hp2 HG01516.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.345-26937G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030935 | ||||||
| chr6:116030967
|
C | T | 1 | a0004c0007t0015g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345-26969G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116030967 | ||||||
| chr6:116031169
|
T | C | 22 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(19): Show | 22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.345-27171A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116031169 | ||||||
| chr6:116031307
|
G | C | 1 | a0002c0002t0001g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.345-27309C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116031307 | ||||||
| chr6:116031470
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0012g0112 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.345-27472T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116031470 | ||||||
| chr6:116031587
|
C | T | 76 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(73): Show | 78 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.345-27589G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116031587 | ||||||
| chr6:116031592
|
A | G | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.345-27594T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116031592 | ||||||
| chr6:116031931
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.345-27933T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116031931 | ||||||
| chr6:116032012
|
A | G | 1 | a0002c0002t0002g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.344+27956T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032012 | ||||||
| chr6:116032055
|
C | T | 10 | a0002c0002t0007g0153a0002c0002t0007g0154a0002c0002t0007g0155others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.344+27913G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032055 | ||||||
| chr6:116032149
|
G | A | 4 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+27819C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032149 | ||||||
| chr6:116032178
|
C | T | 1 | a0001c0001t0027g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.344+27790G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032178 | ||||||
| chr6:116032200
|
G | A | 8 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+27768C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032200 | ||||||
| chr6:116032405
|
A | T | 1 | a0004c0007t0015g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.344+27563T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032405 | ||||||
| chr6:116032510
|
T | C | 1 | a0002c0002t0002g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.344+27458A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032510 | ||||||
| chr6:116032767
|
T | C | 1 | a0001c0001t0004g0148 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.344+27201A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032767 | ||||||
| chr6:116032888
|
T | A | 6 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+27080A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116032888 | ||||||
| chr6:116033180
|
G | GA | 269 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.344+26787_344+2678 others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116033180 | ||||||
| chr6:116033216
|
A | G | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+26752T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116033216 | ||||||
| chr6:116033428
|
C | T | 76 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(73): Show | 78 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.344+26540G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116033428 | ||||||
| chr6:116033522
|
C | A | 4 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+26446G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116033522 | ||||||
| chr6:116033721
|
G | C | 1 | a0001c0001t0034g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.344+26247C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116033721 | ||||||
| chr6:116033735
|
G | A | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+26233C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116033735 | ||||||
| chr6:116033911
|
A | G | 11 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(8): Show | 12 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.344+26057T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116033911 | ||||||
| chr6:116033942
|
C | T | 2 | a0001c0001t0047g0186a0001c0009t0012g0120 | 2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.344+26026G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116033942 | ||||||
| chr6:116034025
|
C | T | 78 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(75): Show | 80 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.344+25943G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116034025 | ||||||
| chr6:116034072
|
C | A | 1 | a0001c0004t0001g0118 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.344+25896G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116034072 | ||||||
| chr6:116034474
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.344+25494C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116034474 | ||||||
| chr6:116034599
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.344+25369C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116034599 | ||||||
| chr6:116034729
|
C | T | 2 | a0002c0002t0001g0028a0002c0002t0054g0023 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.344+25239G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116034729 | ||||||
| chr6:116034878
|
G | T | 8 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(5): Show | 8 | NA18953.hp2 NA18954.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+25090C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116034878 | ||||||
| chr6:116035072
|
A | T | 22 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(19): Show | 22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.344+24896T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116035072 | ||||||
| chr6:116035421
|
AAC | A | 3 | a0002c0002t0001g0082a0002c0002t0001g0083a0002c0002t0002g0081 | 3 | HG02602.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.344+24545_344+2454 others(6): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116035421 | ||||||
| chr6:116035567
|
A | C | 27 | a0001c0001t0001g0110a0001c0001t0006g0002a0001c0001t0006g0215others(24): Show | 28 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.344+24401T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116035567 | ||||||
| chr6:116035605
|
A | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.344+24363T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116035605 | ||||||
| chr6:116035689
|
T | G | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.344+24279A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116035689 | ||||||
| chr6:116036374
|
T | A | 2 | a0002c0002t0001g0028a0002c0002t0054g0023 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.344+23594A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116036374 | ||||||
| chr6:116036489
|
C | T | 2 | a0002c0002t0005g0045a0002c0002t0005g0046 | 2 | NA18962.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.344+23479G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116036489 | ||||||
| chr6:116036575
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.344+23393C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116036575 | ||||||
| chr6:116036715
|
G | GA | 11 | a0002c0002t0002g0084a0002c0002t0007g0153a0002c0002t0007g0154others(8): Show | 11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+23252dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116036715 | ||||||
| chr6:116036789
|
A | T | 8 | a0001c0001t0010g0200a0001c0001t0010g0202a0001c0001t0010g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+23179T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116036789 | ||||||
| chr6:116037139
|
G | T | 1 | a0002c0002t0002g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.344+22829C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037139 | ||||||
| chr6:116037339
|
A | G | 2 | a0001c0001t0017g0009a0001c0001t0017g0010 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.344+22629T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037339 | ||||||
| chr6:116037388
|
A | G | 1 | a0001c0001t0034g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.344+22580T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037388 | ||||||
| chr6:116037496
|
T | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.344+22472A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037496 | ||||||
| chr6:116037657
|
T | C | 1 | a0002c0002t0045g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.344+22311A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037657 | ||||||
| chr6:116037820
|
T | TTGTC | 269 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.344+22147_344+2214 others(8): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037820 | ||||||
| chr6:116037839
|
C | T | 3 | a0002c0002t0001g0029a0002c0002t0002g0044a0002c0002t0009g0165 | 3 | NA19010.hp2 NA19060.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.344+22129G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037839 | ||||||
| chr6:116037849
|
C | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01258.hp1 HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.344+22119G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037849 | ||||||
| chr6:116037892
|
G | C | 1 | a0002c0002t0002g0037 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.344+22076C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116037892 | ||||||
| chr6:116038776
|
C | A | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+21192G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038776 | ||||||
| chr6:116038777
|
G | T | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+21191C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038777 | ||||||
| chr6:116038790
|
G | A | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+21178C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038790 | ||||||
| chr6:116038795
|
A | T | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+21173T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038795 | ||||||
| chr6:116038831
|
C | T | 3 | a0001c0001t0015g0231a0001c0001t0015g0253a0001c0001t0024g0177 | 3 | HG00642.hp1 HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.344+21137G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038831 | ||||||
| chr6:116038832
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.344+21136C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038832 | ||||||
| chr6:116038898
|
C | T | 269 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.344+21070G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038898 | ||||||
| chr6:116038919
|
G | C | 1 | a0002c0002t0001g0086 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.344+21049C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038919 | ||||||
| chr6:116038973
|
T | C | 1 | a0001c0001t0004g0148 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.344+20995A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038973 | ||||||
| chr6:116038977
|
C | T | 2 | a0001c0004t0001g0109a0001c0004t0046g0166 | 2 | NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.344+20991G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038977 | ||||||
| chr6:116038978
|
T | C | 24 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(21): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.344+20990A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116038978 | ||||||
| chr6:116039132
|
C | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0119others(1): Show | 4 | HG00099.hp2 HG01516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+20836G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039132 | ||||||
| chr6:116039232
|
G | A | 2 | a0001c0001t0023g0151a0001c0001t0023g0152 | 2 | NA18942.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.344+20736C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039232 | ||||||
| chr6:116039337
|
C | T | 1 | a0002c0002t0021g0043 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.344+20631G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039337 | ||||||
| chr6:116039399
|
C | T | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+20569G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039399 | ||||||
| chr6:116039441
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.344+20527C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039441 | ||||||
| chr6:116039447
|
T | C | 1 | a0002c0002t0002g0087 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.344+20521A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039447 | ||||||
| chr6:116039468
|
C | G | 2 | a0002c0006t0012g0096a0002c0006t0012g0097 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.344+20500G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039468 | ||||||
| chr6:116039469
|
G | A | 1 | a0002c0002t0005g0019 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.344+20499C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039469 | ||||||
| chr6:116039598
|
G | C | 1 | a0001c0001t0011g0249 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.344+20370C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039598 | ||||||
| chr6:116039603
|
C | G | 11 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(8): Show | 12 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.344+20365G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039603 | ||||||
| chr6:116039715
|
G | A | 2 | a0002c0002t0001g0173a0002c0002t0002g0088 | 2 | NA18940.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.344+20253C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039715 | ||||||
| chr6:116039816
|
C | T | 1 | a0001c0001t0061g0257 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.344+20152G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039816 | ||||||
| chr6:116039910
|
C | A | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+20058G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039910 | ||||||
| chr6:116039943
|
T | TA | 23 | a0001c0001t0001g0107a0001c0001t0001g0195a0001c0001t0008g0001others(20): Show | 24 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.344+20024dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039943 | ||||||
| chr6:116039978
|
G | T | 21 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(18): Show | 22 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.344+19990C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116039978 | ||||||
| chr6:116040164
|
G | A | 2 | a0002c0002t0001g0028a0002c0002t0054g0023 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.344+19804C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116040164 | ||||||
| chr6:116040584
|
C | T | 1 | a0002c0002t0002g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.344+19384G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116040584 | ||||||
| chr6:116040924
|
T | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+19044A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116040924 | ||||||
| chr6:116041072
|
C | T | 1 | a0001c0001t0017g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.344+18896G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116041072 | ||||||
| chr6:116041456
|
C | T | 76 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(73): Show | 78 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.344+18512G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116041456 | ||||||
| chr6:116041483
|
C | T | 1 | a0001c0001t0025g0268 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.344+18485G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116041483 | ||||||
| chr6:116041873
|
T | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+18095A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116041873 | ||||||
| chr6:116041949
|
G | T | 1 | a0002c0002t0002g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.344+18019C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116041949 | ||||||
| chr6:116041986
|
A | G | 116 | a0001c0001t0018g0056a0002c0002t0001g0005a0002c0002t0001g0013others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.344+17982T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116041986 | ||||||
| chr6:116042241
|
G | T | 1 | a0002c0002t0004g0171 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.344+17727C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116042241 | ||||||
| chr6:116042254
|
G | C | 1 | a0002c0002t0002g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.344+17714C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116042254 | ||||||
| chr6:116042329
|
G | A | 1 | a0001c0001t0061g0257 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.344+17639C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116042329 | ||||||
| chr6:116042408
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.344+17560T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116042408 | ||||||
| chr6:116042784
|
G | A | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+17184C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116042784 | ||||||
| chr6:116043360
|
A | G | 3 | a0002c0002t0004g0040a0002c0002t0004g0041a0002c0002t0004g0171 | 3 | HG00544.hp1 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.344+16608T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116043360 | ||||||
| chr6:116043568
|
T | C | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.344+16400A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116043568 | ||||||
| chr6:116043685
|
C | T | 1 | a0001c0001t0013g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.344+16283G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116043685 | ||||||
| chr6:116043738
|
C | A | 1 | a0001c0001t0014g0263 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.344+16230G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116043738 | ||||||
| chr6:116043900
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.344+16068C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116043900 | ||||||
| chr6:116044325
|
G | A | 5 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+15643C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116044325 | ||||||
| chr6:116044512
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0015g0253 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.344+15456C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116044512 | ||||||
| chr6:116044535
|
C | A | 1 | a0002c0002t0001g0027 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.344+15433G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116044535 | ||||||
| chr6:116044635
|
C | T | 1 | a0001c0001t0035g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.344+15333G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116044635 | ||||||
| chr6:116044636
|
G | A | 1 | a0002c0002t0002g0093 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.344+15332C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116044636 | ||||||
| chr6:116044667
|
T | C | 21 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(18): Show | 21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.344+15301A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116044667 | ||||||
| chr6:116044780
|
G | A | 1 | a0001c0001t0071g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.344+15188C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116044780 | ||||||
| chr6:116045145
|
TG | T | 45 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(42): Show | 46 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.344+14822delC | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116045145 | ||||||
| chr6:116045211
|
T | A | 1 | a0002c0002t0002g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.344+14757A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116045211 | ||||||
| chr6:116045263
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.344+14705G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116045263 | ||||||
| chr6:116045329
|
A | G | 1 | a0003c0003t0004g0161 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.344+14639T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116045329 | ||||||
| chr6:116045345
|
A | T | 1 | a0002c0002t0002g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.344+14623T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116045345 | ||||||
| chr6:116045607
|
G | A | 18 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111others(15): Show | 18 | HG00741.hp2 HG01099.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.344+14361C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116045607 | ||||||
| chr6:116045690
|
T | G | 1 | a0002c0002t0001g0149 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.344+14278A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116045690 | ||||||
| chr6:116045924
|
A | G | 1 | a0002c0002t0019g0176 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.344+14044T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116045924 | ||||||
| chr6:116046089
|
T | C | 4 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+13879A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046089 | ||||||
| chr6:116046103
|
A | G | 3 | a0002c0002t0005g0016a0002c0002t0005g0017a0002c0002t0005g0018 | 3 | NA18986.hp1 NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.344+13865T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046103 | ||||||
| chr6:116046106
|
T | C | 269 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.344+13862A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046106 | ||||||
| chr6:116046563
|
A | T | 78 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(75): Show | 80 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.344+13405T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046563 | ||||||
| chr6:116046568
|
G | T | 1 | a0002c0002t0002g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.344+13400C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046568 | ||||||
| chr6:116046631
|
G | C | 1 | a0002c0002t0002g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.344+13337C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046631 | ||||||
| chr6:116046783
|
TAAG | T | 5 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0043g0189others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+13182_344+1318 others(7): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046783 | ||||||
| chr6:116046786
|
G | T | 1 | a0001c0001t0065g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.344+13182C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046786 | ||||||
| chr6:116046868
|
C | G | 269 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.344+13100G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116046868 | ||||||
| chr6:116047337
|
A | G | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+12631T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047337 | ||||||
| chr6:116047604
|
T | TACAAGCA others(542): Show |
1 | a0002c0002t0019g0174 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.344+12363_344+1236 others(553): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047604 | ||||||
| chr6:116047604
|
T | TACAAGCA others(542): Show |
21 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(18): Show | 21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.344+12363_344+1236 others(553): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047604 | ||||||
| chr6:116047604
|
T | TACAAGCA others(542): Show |
237 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.344+12363_344+1236 others(553): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047604 | ||||||
| chr6:116047604
|
T | TACAAGCA others(542): Show |
11 | a0002c0002t0001g0034a0002c0002t0002g0030a0002c0002t0002g0036others(8): Show | 11 | HG00438.hp2 HG02040.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+12363_344+1236 others(553): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047604 | ||||||
| chr6:116047604
|
T | TACAAGCA others(542): Show |
1 | a0002c0002t0001g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.344+12363_344+1236 others(553): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047604 | ||||||
| chr6:116047650
|
G | A | 78 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(75): Show | 80 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.344+12318C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047650 | ||||||
| chr6:116047736
|
T | C | 3 | a0002c0002t0002g0012a0005c0005t0002g0094a0005c0005t0002g0095 | 3 | NA18974.hp1 NA19067.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.344+12232A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047736 | ||||||
| chr6:116047751
|
A | T | 1 | a0002c0002t0002g0030 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.344+12217T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047751 | ||||||
| chr6:116047889
|
C | A | 78 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(75): Show | 80 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.344+12079G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047889 | ||||||
| chr6:116047915
|
G | A | 1 | a0001c0001t0003g0250 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.344+12053C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047915 | ||||||
| chr6:116047947
|
G | A | 19 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(16): Show | 20 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.344+12021C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116047947 | ||||||
| chr6:116048002
|
C | T | 1 | a0002c0002t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.344+11966G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048002 | ||||||
| chr6:116048007
|
A | T | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+11961T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048007 | ||||||
| chr6:116048248
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344+11720A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048248 | ||||||
| chr6:116048262
|
C | T | 1 | a0001c0001t0003g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.344+11706G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048262 | ||||||
| chr6:116048673
|
A | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.344+11295T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048673 | ||||||
| chr6:116048679
|
C | T | 1 | a0001c0001t0025g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.344+11289G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048679 | ||||||
| chr6:116048686
|
C | T | 1 | a0002c0002t0001g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.344+11282G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048686 | ||||||
| chr6:116048751
|
T | C | 1 | a0001c0001t0024g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.344+11217A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048751 | ||||||
| chr6:116048857
|
T | C | 1 | a0001c0001t0003g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.344+11111A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048857 | ||||||
| chr6:116048883
|
C | T | 1 | a0001c0001t0011g0234 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.344+11085G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048883 | ||||||
| chr6:116048975
|
CTTT | C | 56 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(53): Show | 57 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.344+10990_344+1099 others(7): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116048975 | ||||||
| chr6:116049058
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.344+10910A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116049058 | ||||||
| chr6:116049117
|
T | C | 12 | a0002c0002t0007g0153a0002c0002t0007g0154a0002c0002t0007g0155others(9): Show | 12 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.344+10851A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116049117 | ||||||
| chr6:116049180
|
A | G | 1 | a0001c0001t0034g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.344+10788T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116049180 | ||||||
| chr6:116049285
|
C | T | 1 | a0002c0002t0009g0098 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.344+10683G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116049285 | ||||||
| chr6:116049286
|
G | A | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.344+10682C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116049286 | ||||||
| chr6:116049566
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.344+10402T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116049566 | ||||||
| chr6:116050003
|
T | G | 5 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0043g0189others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+9965A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116050003 | ||||||
| chr6:116050199
|
C | A | 26 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(23): Show | 27 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.344+9769G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116050199 | ||||||
| chr6:116050283
|
T | C | 1 | a0004c0007t0015g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+9685A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116050283 | ||||||
| chr6:116050439
|
T | C | 4 | a0001c0001t0004g0150a0001c0001t0023g0151a0001c0001t0023g0152others(1): Show | 4 | NA18942.hp1 NA18983.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+9529A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116050439 | ||||||
| chr6:116050467
|
C | T | 4 | a0002c0002t0001g0027a0002c0002t0002g0024a0002c0002t0002g0025others(1): Show | 4 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+9501G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116050467 | ||||||
| chr6:116050504
|
T | C | 2 | a0002c0002t0002g0020a0002c0002t0044g0021 | 2 | NA18981.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.344+9464A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116050504 | ||||||
| chr6:116050830
|
T | C | 1 | a0002c0002t0054g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.344+9138A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116050830 | ||||||
| chr6:116051079
|
G | A | 4 | a0002c0002t0002g0175a0002c0002t0009g0098a0002c0002t0009g0099others(1): Show | 4 | NA18968.hp2 NA19007.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+8889C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116051079 | ||||||
| chr6:116051162
|
T | G | 1 | a0002c0002t0019g0176 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.344+8806A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116051162 | ||||||
| chr6:116051255
|
C | T | 20 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(17): Show | 21 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.344+8713G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116051255 | ||||||
| chr6:116051294
|
T | C | 1 | a0001c0001t0006g0232 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.344+8674A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116051294 | ||||||
| chr6:116051375
|
C | T | 4 | a0002c0002t0005g0016a0002c0002t0005g0017a0002c0002t0005g0018others(1): Show | 4 | NA18942.hp2 NA18986.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+8593G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116051375 | ||||||
| chr6:116051402
|
T | C | 1 | a0001c0001t0071g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.344+8566A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116051402 | ||||||
| chr6:116051542
|
T | C | 3 | a0001c0001t0003g0252a0001c0001t0003g0260a0001c0001t0003g0269 | 3 | HG01192.hp1 HG01261.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.344+8426A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116051542 | ||||||
| chr6:116052115
|
C | T | 1 | a0004c0007t0015g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+7853G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116052115 | ||||||
| chr6:116052173
|
C | T | 1 | a0002c0002t0054g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.344+7795G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116052173 | ||||||
| chr6:116052207
|
A | G | 1 | a0002c0002t0002g0022 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.344+7761T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116052207 | ||||||
| chr6:116052213
|
A | C | 1 | a0001c0001t0006g0216 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.344+7755T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116052213 | ||||||
| chr6:116052368
|
A | G | 203 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(200): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.344+7600T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116052368 | ||||||
| chr6:116052386
|
C | T | 1 | a0001c0001t0024g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.344+7582G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116052386 | ||||||
| chr6:116052453
|
C | T | 57 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(54): Show | 58 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.344+7515G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116052453 | ||||||
| chr6:116052503
|
C | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.344+7465G>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116052503 | ||||||
| chr6:116053044
|
C | T | 19 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(16): Show | 20 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.344+6924G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116053044 | ||||||
| chr6:116053121
|
C | T | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+6847G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116053121 | ||||||
| chr6:116054015
|
G | A | 3 | a0002c0002t0001g0127a0002c0002t0005g0128a0002c0002t0057g0126 | 3 | HG02004.hp1 HG02080.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.344+5953C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054015 | ||||||
| chr6:116054139
|
A | G | 76 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(73): Show | 78 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.344+5829T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054139 | ||||||
| chr6:116054259
|
A | T | 2 | a0002c0002t0002g0020a0002c0002t0044g0021 | 2 | NA18981.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.344+5709T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054259 | ||||||
| chr6:116054434
|
T | C | 1 | a0002c0002t0002g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.344+5534A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054434 | ||||||
| chr6:116054451
|
T | A | 19 | a0001c0001t0008g0001a0001c0001t0008g0203a0001c0001t0008g0204others(16): Show | 20 | HG00741.hp1 HG01361.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.344+5517A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054451 | ||||||
| chr6:116054457
|
A | T | 4 | a0002c0002t0005g0016a0002c0002t0005g0017a0002c0002t0005g0018others(1): Show | 4 | NA18942.hp2 NA18986.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+5511T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054457 | ||||||
| chr6:116054484
|
A | G | 1 | a0002c0002t0001g0015 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.344+5484T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054484 | ||||||
| chr6:116054495
|
A | T | 1 | a0001c0001t0008g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.344+5473T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054495 | ||||||
| chr6:116054500
|
AT | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0043g0189 | 3 | HG02559.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.344+5467delA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054500 | ||||||
| chr6:116054504
|
TA | T | 5 | a0001c0001t0014g0261a0001c0001t0014g0262a0001c0001t0014g0263others(2): Show | 5 | HG00738.hp1 HG01081.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+5463delT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116054504 | ||||||
| chr6:116055091
|
T | C | 32 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0135others(29): Show | 32 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.344+4877A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116055091 | ||||||
| chr6:116055098
|
G | A | 10 | a0002c0002t0007g0153a0002c0002t0007g0154a0002c0002t0007g0155others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.344+4870C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116055098 | ||||||
| chr6:116055307
|
C | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0014 | 3 | HG02257.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.344+4661G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116055307 | ||||||
| chr6:116055755
|
A | C | 30 | a0001c0001t0006g0002a0001c0001t0006g0215a0001c0001t0006g0216others(27): Show | 31 | HG00738.hp1 HG01074.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.344+4213T>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116055755 | ||||||
| chr6:116055758
|
C | G | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+4210G>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116055758 | ||||||
| chr6:116055759
|
A | G | 1 | a0001c0001t0008g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.344+4209T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116055759 | ||||||
| chr6:116056058
|
T | G | 4 | a0003c0003t0004g0161a0003c0003t0004g0163a0003c0003t0004g0164others(1): Show | 4 | NA18962.hp2 NA18970.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+3910A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116056058 | ||||||
| chr6:116056148
|
T | TAA | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+3819_344+3820i others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116056148 | ||||||
| chr6:116056163
|
G | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+3805C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116056163 | ||||||
| chr6:116056200
|
G | GT | 11 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0003g0260others(8): Show | 11 | HG01515.hp1 HG02080.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+3767dupA | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116056200 | ||||||
| chr6:116056512
|
A | T | 1 | a0001c0001t0065g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.344+3456T>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116056512 | ||||||
| chr6:116056756
|
G | A | 1 | a0001c0001t0015g0253 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.344+3212C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116056756 | ||||||
| chr6:116057471
|
T | G | 1 | a0002c0002t0009g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.344+2497A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116057471 | ||||||
| chr6:116057498
|
C | T | 2 | a0001c0001t0017g0009a0001c0001t0017g0010 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.344+2470G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116057498 | ||||||
| chr6:116057660
|
A | G | 2 | a0002c0002t0021g0007a0002c0002t0021g0008 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.344+2308T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116057660 | ||||||
| chr6:116057867
|
C | T | 1 | a0001c0001t0024g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.344+2101G>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116057867 | ||||||
| chr6:116058105
|
T | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+1863A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058105 | ||||||
| chr6:116058250
|
T | C | 5 | a0001c0001t0010g0256a0001c0001t0025g0254a0001c0001t0025g0268others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+1718A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058250 | ||||||
| chr6:116058545
|
A | G | 2 | a0001c0001t0008g0203a0001c0001t0008g0204 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.344+1423T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058545 | ||||||
| chr6:116058600
|
G | A | 1 | a0001c0004t0046g0166 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.344+1368C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058600 | ||||||
| chr6:116058772
|
G | T | 1 | a0001c0001t0058g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+1196C>A | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058772 | ||||||
| chr6:116058788
|
G | A | 1 | a0001c0001t0017g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.344+1180C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058788 | ||||||
| chr6:116058828
|
G | A | 1 | a0002c0002t0002g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.344+1140C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058828 | ||||||
| chr6:116058889
|
G | C | 2 | a0001c0001t0034g0198a0001c0001t0035g0004 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.344+1079C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058889 | ||||||
| chr6:116058910
|
C | CA | 43 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0178others(40): Show | 44 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.344+1057dupT | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058910 | ||||||
| chr6:116058910
|
C | CAA | 47 | a0001c0001t0001g0195a0001c0001t0003g0235a0001c0001t0003g0236others(44): Show | 48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.344+1056_344+1057d others(4): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058910 | ||||||
| chr6:116058910
|
C | CAAA | 12 | a0001c0001t0003g0260a0001c0001t0006g0265a0001c0001t0006g0266others(9): Show | 12 | HG00738.hp1 HG01081.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.344+1055_344+1057d others(5): Show |
FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116058910 | ||||||
| chr6:116059010
|
G | A | 1 | a0001c0001t0003g0269 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.344+958C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059010 | ||||||
| chr6:116059384
|
G | C | 1 | a0001c0001t0004g0196 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.344+584C>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059384 | ||||||
| chr6:116059400
|
G | A | 1 | a0001c0001t0014g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.344+568C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059400 | ||||||
| chr6:116059632
|
A | G | 1 | a0002c0002t0001g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.344+336T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059632 | ||||||
| chr6:116059746
|
A | G | 78 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0238others(75): Show | 80 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.344+222T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059746 | ||||||
| chr6:116059752
|
A | G | 1 | a0001c0001t0049g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.344+216T>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059752 | ||||||
| chr6:116059753
|
T | A | 1 | a0001c0001t0026g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.344+215A>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059753 | ||||||
| chr6:116059810
|
G | A | 1 | a0001c0001t0014g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.344+158C>T | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059810 | ||||||
| chr6:116059856
|
T | C | 1 | a0001c0001t0049g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.344+112A>G | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059856 | ||||||
| chr6:116059927
|
T | G | 1 | a0001c0001t0034g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.344+41A>C | FRK | ENSG00000111816.8 | transcript | ENST00000606080.2 | protein_coding | 1/7 | chr6 | 116059927 |