Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4289 |
|---|---|
| ensemblid | ENSG00000128585.18 |
| hgncid | 7109 |
| symbol | MKLN1 |
| name | muskelin 1 |
| refseq_nuc | NM_013255.5 |
| refseq_prot | NP_037387.2 |
| ensembl_nuc | ENST00000352689.11 |
| ensembl_prot | ENSP00000323527.6 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 131327876 |
| end | 131496632 |
| strand | + |
| ver | v1.2 |
| region | chr7:131327876-131496632 |
| region5000 | chr7:131322876-131501632 |
| regionname0 | MKLN1_chr7_131327876_131496632 |
| regionname5000 | MKLN1_chr7_131322876_131501632 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 735 | 319 | 81 | 50 | 140 | 12 | 34 | 108 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0002 | 0/0 | 735 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2208 | 304 | 67 | 49 | 140 | 12 | 34 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| c0002 | 0/0 | 2208 | 8 | 7 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| c0003 | 0/0 | 2208 | 7 | 7 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| c0004 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8928 | 81 | 20 | 17 | 32 | 5 | 7 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0002 | 0/1 | 8931 | 72 | 9 | 10 | 39 | 2 | 11 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0003 | 0/0 | 8935 | 34 | 3 | 3 | 21 | 1 | 6 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0004 | 0/0 | 8915 | 11 | 0 | 0 | 11 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0005 | 0/0 | 8929 | 9 | 0 | 7 | 1 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0006 | 0/0 | 8928 | 7 | 0 | 0 | 7 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0007 | 0/0 | 8934 | 7 | 4 | 0 | 2 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0008 | 0/0 | 8935 | 6 | 6 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0009 | 0/0 | 8929 | 6 | 1 | 2 | 1 | 0 | 2 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0010 | 0/0 | 8931 | 5 | 4 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0011 | 0/0 | 8931 | 4 | 0 | 2 | 0 | 1 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0012 | 0/0 | 8932 | 3 | 1 | 0 | 1 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0013 | 0/0 | 8935 | 3 | 0 | 0 | 2 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0014 | 0/0 | 8930 | 3 | 0 | 1 | 2 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0015 | 0/0 | 8919 | 3 | 3 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0016 | 0/0 | 8928 | 3 | 1 | 0 | 1 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0017 | 0/0 | 8928 | 3 | 0 | 1 | 0 | 2 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0018 | 0/0 | 8934 | 3 | 3 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0019 | 0/0 | 8933 | 3 | 3 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0020 | 0/0 | 8933 | 2 | 0 | 0 | 2 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0021 | 0/0 | 8935 | 2 | 0 | 0 | 0 | 0 | 2 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0022 | 0/0 | 8931 | 2 | 2 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0023 | 0/0 | 8931 | 2 | 0 | 2 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0024 | 1/0 | 8929 | 2 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0025 | 0/0 | 8928 | 2 | 2 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0026 | 0/0 | 8928 | 2 | 1 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0027 | 0/0 | 8928 | 2 | 0 | 0 | 2 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0028 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0029 | 0/0 | 8928 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0030 | 0/0 | 8935 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0031 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0032 | 0/0 | 8930 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0033 | 0/0 | 8935 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0034 | 0/0 | 8932 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0035 | 0/0 | 8931 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0036 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0037 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0038 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0039 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0040 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0041 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0042 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0043 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0044 | 0/0 | 8931 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0045 | 0/0 | 8934 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0046 | 0/0 | 8934 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0047 | 0/0 | 8928 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0048 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0049 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0050 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0051 | 0/0 | 8915 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0052 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0053 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0054 | 0/0 | 8933 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0055 | 0/0 | 8936 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0056 | 0/0 | 8934 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0057 | 0/0 | 8933 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0058 | 0/0 | 8933 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0059 | 0/0 | 8928 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0060 | 0/0 | 8934 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0061 | 0/0 | 8932 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0062 | 0/0 | 8931 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0063 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0064 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| t0065 | 0/0 | 8928 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0267 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2208 | 304 | 67 | 49 | 140 | 12 | 34 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0002 | 0/0 | 2208 | 8 | 7 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0003 | 0/0 | 2208 | 7 | 7 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0002c0004 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11135 | 81 | 20 | 17 | 32 | 5 | 7 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0002 | 0/1 | 11138 | 71 | 8 | 10 | 39 | 2 | 11 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0003 | 0/0 | 11142 | 34 | 3 | 3 | 21 | 1 | 6 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0004 | 0/0 | 11122 | 11 | 0 | 0 | 11 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0005 | 0/0 | 11136 | 9 | 0 | 7 | 1 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0006 | 0/0 | 11135 | 7 | 0 | 0 | 7 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0007 | 0/0 | 11141 | 6 | 3 | 0 | 2 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0009 | 0/0 | 11136 | 6 | 1 | 2 | 1 | 0 | 2 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0010 | 0/0 | 11138 | 5 | 4 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0011 | 0/0 | 11138 | 4 | 0 | 2 | 0 | 1 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0012 | 0/0 | 11139 | 3 | 1 | 0 | 1 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0013 | 0/0 | 11142 | 3 | 0 | 0 | 2 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0014 | 0/0 | 11137 | 3 | 0 | 1 | 2 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0015 | 0/0 | 11126 | 3 | 3 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0016 | 0/0 | 11135 | 3 | 1 | 0 | 1 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0017 | 0/0 | 11135 | 3 | 0 | 1 | 0 | 2 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0018 | 0/0 | 11141 | 3 | 3 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0020 | 0/0 | 11140 | 2 | 0 | 0 | 2 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0021 | 0/0 | 11142 | 2 | 0 | 0 | 0 | 0 | 2 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0022 | 0/0 | 11138 | 2 | 2 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0023 | 0/0 | 11138 | 2 | 0 | 2 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0024 | 1/0 | 11136 | 2 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0025 | 0/0 | 11135 | 2 | 2 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0026 | 0/0 | 11135 | 2 | 1 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0027 | 0/0 | 11135 | 2 | 0 | 0 | 2 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0028 | 0/0 | 11135 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0029 | 0/0 | 11135 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0031 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0032 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0033 | 0/0 | 11142 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0034 | 0/0 | 11139 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0035 | 0/0 | 11138 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0036 | 0/0 | 11135 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0037 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0038 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0039 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0040 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0041 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0042 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0043 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0044 | 0/0 | 11138 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0046 | 0/0 | 11141 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0047 | 0/0 | 11135 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0048 | 0/0 | 11135 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0049 | 0/0 | 11135 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0050 | 0/0 | 11135 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0051 | 0/0 | 11122 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0052 | 0/0 | 11135 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0053 | 0/0 | 11135 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0055 | 0/0 | 11143 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0057 | 0/0 | 11140 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0059 | 0/0 | 11135 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0060 | 0/0 | 11141 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0061 | 0/0 | 11139 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0062 | 0/0 | 11138 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0063 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0064 | 0/0 | 11138 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0001t0065 | 0/0 | 11135 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0002t0002 | 0/0 | 11138 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0002t0019 | 0/0 | 11140 | 3 | 3 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0002t0045 | 0/0 | 11141 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0002t0054 | 0/0 | 11140 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0002t0056 | 0/0 | 11141 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0002t0058 | 0/0 | 11140 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0003t0008 | 0/0 | 11142 | 6 | 6 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0001c0003t0030 | 0/0 | 11142 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| a0002c0004t0007 | 0/0 | 11141 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | copy fasta | chr7 | 131322876 | 131501632 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0267 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0009g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0009g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0010g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0011g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0011g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0012g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0012g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0012g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0013g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0013g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0013g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0014g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0014g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0014g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0015g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0015g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0015g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0016g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0016g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0016g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0017g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0017g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0017g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0018g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0018g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0020g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0020g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0021g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0021g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0022g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0022g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0023g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0023g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0024g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0024g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0025g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0025g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0026g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0026g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0027g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0027g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0028g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0029g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0031g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0032g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0033g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0034g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0035g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0036g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0037g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0038g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0039g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0040g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0041g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0042g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0043g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0044g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0046g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0047g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0048g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0049g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0050g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0051g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0052g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0053g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0055g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0057g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0059g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0060g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0061g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0062g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0063g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0064g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0001t0065g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0002t0019g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0002t0019g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0002t0019g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0002t0045g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0002t0054g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0002t0056g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0002t0058g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0003t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0003t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0003t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0003t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0003t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0003t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0001c0003t0030g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| a0002c0004t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | GBR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00408 | hp2 | a0001 | c0001 | t0041 | g0224 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00639 | hp1 | a0001 | c0002 | t0058 | g0080 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00642 | hp1 | a0001 | c0001 | t0017 | g0018 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0102 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01069 | hp2 | a0001 | c0001 | t0014 | g0233 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0003 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01081 | hp1 | a0001 | c0001 | t0011 | g0003 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0121 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01169 | hp1 | a0001 | c0001 | t0009 | g0144 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01243 | hp1 | a0001 | c0001 | t0026 | g0073 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0101 | AMR | PUR | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0107 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0104 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01261 | hp2 | a0001 | c0001 | t0010 | g0168 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01346 | hp1 | a0001 | c0001 | t0029 | g0088 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01515 | hp1 | a0001 | c0001 | t0017 | g0020 | EUR | IBS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01515 | hp2 | a0001 | c0001 | t0011 | g0070 | EUR | IBS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0195 | EUR | IBS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01517 | hp1 | a0001 | c0001 | t0017 | g0019 | EUR | IBS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01884 | hp2 | a0001 | c0003 | t0030 | g0086 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01943 | hp2 | a0001 | c0001 | t0023 | g0223 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01978 | hp1 | a0001 | c0001 | t0044 | g0215 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01993 | hp1 | a0001 | c0001 | t0009 | g0306 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02027 | hp1 | a0001 | c0001 | t0059 | g0042 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02055 | hp2 | a0001 | c0002 | t0019 | g0310 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02071 | hp2 | a0001 | c0001 | t0063 | g0238 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02080 | hp2 | a0001 | c0001 | t0031 | g0013 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0147 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0149 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0160 | EAS | CDX | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02258 | hp1 | a0001 | c0001 | t0026 | g0159 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02258 | hp2 | a0001 | c0002 | t0054 | g0074 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02280 | hp1 | a0001 | c0001 | t0028 | g0045 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02280 | hp2 | a0001 | c0001 | t0036 | g0106 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02300 | hp1 | a0001 | c0001 | t0023 | g0222 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02523 | hp1 | a0001 | c0001 | t0038 | g0235 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02572 | hp1 | a0001 | c0001 | t0053 | g0072 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02572 | hp2 | a0001 | c0003 | t0008 | g0079 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0170 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02622 | hp1 | a0001 | c0001 | t0015 | g0241 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0167 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0313 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02630 | hp2 | a0001 | c0001 | t0032 | g0158 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02647 | hp1 | a0001 | c0003 | t0008 | g0082 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02647 | hp2 | a0002 | c0004 | t0007 | g0314 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02717 | hp1 | a0001 | c0001 | t0018 | g0212 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0178 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0228 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0171 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0211 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0273 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02895 | hp1 | a0001 | c0002 | t0019 | g0309 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02895 | hp2 | a0001 | c0003 | t0008 | g0084 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02896 | hp2 | a0001 | c0001 | t0022 | g0165 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02897 | hp1 | a0001 | c0001 | t0022 | g0166 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02897 | hp2 | a0001 | c0003 | t0008 | g0083 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02965 | hp1 | a0001 | c0003 | t0008 | g0085 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02965 | hp2 | a0001 | c0001 | t0061 | g0162 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02976 | hp1 | a0001 | c0001 | t0034 | g0169 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0316 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0145 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03041 | hp1 | a0001 | c0003 | t0008 | g0087 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0214 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03139 | hp1 | a0001 | c0002 | t0045 | g0143 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03139 | hp2 | a0001 | c0001 | t0025 | g0156 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03195 | hp1 | a0001 | c0001 | t0048 | g0058 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0164 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0148 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03491 | hp1 | a0001 | c0001 | t0016 | g0146 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03491 | hp2 | a0001 | c0001 | t0021 | g0180 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03492 | hp1 | a0001 | c0001 | t0021 | g0179 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03516 | hp1 | a0001 | c0001 | t0050 | g0064 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03516 | hp2 | a0001 | c0002 | t0019 | g0081 | AFR | ESN | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | STU | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | STU | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03831 | hp1 | a0001 | c0001 | t0013 | g0185 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0206 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03927 | hp2 | a0001 | c0001 | t0011 | g0071 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0315 | AFR | YRI | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18522 | hp2 | a0001 | c0001 | t0062 | g0161 | AFR | YRI | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18906 | hp2 | a0001 | c0001 | t0057 | g0244 | AFR | YRI | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18942 | hp1 | a0001 | c0001 | t0014 | g0251 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18944 | hp1 | a0001 | c0001 | t0047 | g0091 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18945 | hp2 | a0001 | c0001 | t0042 | g0118 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18948 | hp1 | a0001 | c0001 | t0046 | g0232 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18948 | hp2 | a0001 | c0001 | t0016 | g0110 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0240 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18960 | hp2 | a0001 | c0001 | t0013 | g0187 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18963 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18963 | hp2 | a0001 | c0001 | t0037 | g0287 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18966 | hp2 | a0001 | c0001 | t0013 | g0231 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18984 | hp2 | a0001 | c0001 | t0043 | g0037 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18987 | hp1 | a0001 | c0001 | t0027 | g0010 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18995 | hp2 | a0001 | c0001 | t0020 | g0226 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18997 | hp2 | a0001 | c0001 | t0040 | g0302 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19000 | hp1 | a0001 | c0001 | t0012 | g0278 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19010 | hp1 | a0001 | c0001 | t0020 | g0227 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19012 | hp1 | a0001 | c0001 | t0064 | g0246 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19030 | hp1 | a0001 | c0001 | t0015 | g0274 | AFR | LWK | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0052 | AFR | LWK | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19043 | hp1 | a0001 | c0001 | t0018 | g0210 | AFR | LWK | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | LWK | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19062 | hp1 | a0001 | c0001 | t0055 | g0207 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19068 | hp2 | a0001 | c0001 | t0027 | g0043 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19070 | hp2 | a0001 | c0001 | t0039 | g0236 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19075 | hp1 | a0001 | c0001 | t0007 | g0201 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19078 | hp1 | a0001 | c0001 | t0033 | g0113 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19078 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19085 | hp1 | a0001 | c0001 | t0051 | g0186 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA19240 | hp2 | a0001 | c0001 | t0060 | g0305 | AFR | YRI | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | ASW | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ASW | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA20805 | hp1 | a0001 | c0001 | t0065 | g0112 | EUR | TSI | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0269 | EUR | TSI | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | GIH | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0120 | SAS | GIH | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02109 | hp2 | a0001 | c0001 | t0035 | g0163 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | ACB | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03471 | hp1 | a0001 | c0001 | t0049 | g0044 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG03471 | hp2 | a0001 | c0002 | t0056 | g0308 | AFR | MSL | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA20300 | hp1 | a0001 | c0001 | t0024 | g0151 | AFR | USA | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | USA | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA21309 | hp1 | a0001 | c0001 | t0052 | g0034 | AFR | LWK | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| NA21309 | hp2 | a0001 | c0001 | t0025 | g0157 | AFR | LWK | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0267 | REF | REF | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0024 | g0152 | REF | REF | MKLN1_chr7_131322876_131501632 | MKLN1 | chr7 | 131322876 | 131501632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:131478633
|
T | G | 1 | a0002 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.2042T>G | p.Leu681Arg | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/18 | 2066/11136 | 2042/2208 | 681/735 | chr7 | 131478633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:131399276
|
A | G | 1 | a0001c0003 | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
synonymous_variant | LOW | c.546A>G | p.Lys182Lys | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/18 | 570/11136 | 546/2208 | 182/735 | chr7 | 131399276 | ||
| chr7:131443691
|
T | C | 2 | a0001c0002a0001c0003 | 15 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
synonymous_variant | LOW | c.1384T>C | p.Leu462Leu | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/18 | 1408/11136 | 1384/2208 | 462/735 | chr7 | 131443691 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:131487964
|
A | AAT | 4 | a0001c0001t0020a0001c0001t0031a0001c0003t0008others(1): Show | 10 | HG01884.hp2 HG02080.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*253_*254dupAT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 255 | INFO_REALIGN_3_PRIME | chr7 | 131487964 | ||||
| chr7:131487981
|
A | T | 2 | a0001c0001t0064a0001c0001t0065 | 2 | NA19012.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*253A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 253 | chr7 | 131487981 | |||||
| chr7:131487983
|
T | A | 2 | a0001c0001t0028a0001c0001t0029 | 2 | HG01346.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*255T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 255 | chr7 | 131487983 | |||||
| chr7:131488113
|
A | C | 1 | a0001c0001t0063 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 385 | chr7 | 131488113 | |||||
| chr7:131489038
|
A | C | 2 | a0001c0001t0061a0001c0001t0062 | 2 | HG02965.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1310A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 1310 | chr7 | 131489038 | |||||
| chr7:131489062
|
C | T | 1 | a0001c0001t0065 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1334C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 1334 | chr7 | 131489062 | |||||
| chr7:131489097
|
G | A | 1 | a0001c0001t0021 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1369G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 1369 | chr7 | 131489097 | |||||
| chr7:131489208
|
C | T | 1 | a0001c0001t0060 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1480C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 1480 | chr7 | 131489208 | |||||
| chr7:131489429
|
G | A | 2 | a0001c0001t0011a0001c0001t0032 | 5 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1701G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 1701 | chr7 | 131489429 | |||||
| chr7:131489502
|
A | G | 2 | a0001c0001t0011a0001c0001t0032 | 5 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1774A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 1774 | chr7 | 131489502 | |||||
| chr7:131489869
|
T | C | 2 | a0001c0003t0008a0001c0003t0030 | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2141T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 2141 | chr7 | 131489869 | |||||
| chr7:131490144
|
T | C | 1 | a0001c0001t0033 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2416T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 2416 | chr7 | 131490144 | |||||
| chr7:131490363
|
T | C | 4 | a0001c0001t0010a0001c0001t0022a0001c0001t0034others(1): Show | 9 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2635T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 2635 | chr7 | 131490363 | |||||
| chr7:131490505
|
T | C | 1 | a0001c0001t0036 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2777T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 2777 | chr7 | 131490505 | |||||
| chr7:131490646
|
G | A | 2 | a0001c0003t0008a0001c0003t0030 | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2918G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 2918 | chr7 | 131490646 | |||||
| chr7:131490735
|
T | C | 29 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(26): Show | 117 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3007T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 3007 | chr7 | 131490735 | |||||
| chr7:131490752
|
G | T | 1 | a0001c0001t0059 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3024G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 3024 | chr7 | 131490752 | |||||
| chr7:131491428
|
T | G | 1 | a0001c0001t0047 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3700T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 3700 | chr7 | 131491428 | |||||
| chr7:131492318
|
C | T | 42 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(39): Show | 177 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*4590C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 4590 | chr7 | 131492318 | |||||
| chr7:131492427
|
T | C | 1 | a0001c0002t0054 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4699T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 4699 | chr7 | 131492427 | |||||
| chr7:131492430
|
C | T | 1 | a0001c0002t0058 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4702C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 4702 | chr7 | 131492430 | |||||
| chr7:131492734
|
C | CA | 9 | a0001c0001t0007a0001c0001t0014a0001c0001t0018others(6): Show | 18 | HG01069.hp2 HG02155.hp2 HG02630.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5025dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5026 | INFO_REALIGN_3_PRIME | chr7 | 131492734 | ||||
| chr7:131492734
|
C | CAA | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(21): Show | 140 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*5024_*5025dupAA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5026 | INFO_REALIGN_3_PRIME | chr7 | 131492734 | ||||
| chr7:131492734
|
C | CAAA | 4 | a0001c0001t0012a0001c0001t0034a0001c0001t0055others(1): Show | 6 | HG02738.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5023_*5025dupAAA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5026 | INFO_REALIGN_3_PRIME | chr7 | 131492734 | ||||
| chr7:131492734
|
CA | C | 21 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(18): Show | 124 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*5025delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5025 | INFO_REALIGN_3_PRIME | chr7 | 131492734 | ||||
| chr7:131492734
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0015 | 3 | HG02622.hp1 HG02886.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5016_*5025delAAAA others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5016 | INFO_REALIGN_3_PRIME | chr7 | 131492734 | ||||
| chr7:131492757
|
T | C | 1 | a0001c0002t0056 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5029T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5029 | chr7 | 131492757 | |||||
| chr7:131492823
|
C | T | 2 | a0001c0001t0032a0001c0001t0053 | 2 | HG02572.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5095C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5095 | chr7 | 131492823 | |||||
| chr7:131492908
|
C | G | 1 | a0001c0001t0044 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5180C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5180 | chr7 | 131492908 | |||||
| chr7:131493258
|
G | A | 1 | a0001c0001t0037 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5530G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5530 | chr7 | 131493258 | |||||
| chr7:131493299
|
G | A | 1 | a0001c0001t0025 | 2 | HG03139.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5571G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5571 | chr7 | 131493299 | |||||
| chr7:131493440
|
A | G | 1 | a0001c0001t0017 | 3 | HG00642.hp1 HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5712A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5712 | chr7 | 131493440 | |||||
| chr7:131493567
|
T | C | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(43): Show | 184 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*5839T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5839 | chr7 | 131493567 | |||||
| chr7:131493650
|
A | G | 1 | a0001c0001t0043 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5922A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 5922 | chr7 | 131493650 | |||||
| chr7:131494488
|
T | TTAA | 18 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(15): Show | 68 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*6764_*6766dupTAA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 6767 | INFO_REALIGN_3_PRIME | chr7 | 131494488 | ||||
| chr7:131494758
|
C | T | 1 | a0001c0001t0052 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7030C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7030 | chr7 | 131494758 | |||||
| chr7:131494796
|
A | T | 2 | a0001c0003t0008a0001c0003t0030 | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7068A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7068 | chr7 | 131494796 | |||||
| chr7:131494934
|
CATACATT others(6): Show |
C | 2 | a0001c0001t0004a0001c0001t0051 | 12 | NA18951.hp1 NA18955.hp1 NA18970.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7209_*7221delACAT others(9): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7209 | INFO_REALIGN_3_PRIME | chr7 | 131494934 | ||||
| chr7:131494996
|
G | A | 2 | a0001c0001t0038a0001c0001t0039 | 2 | HG02523.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7268G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7268 | chr7 | 131494996 | |||||
| chr7:131495031
|
A | T | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7303A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7303 | chr7 | 131495031 | |||||
| chr7:131495032
|
G | C | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7304G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7304 | chr7 | 131495032 | |||||
| chr7:131495033
|
G | A | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7305G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7305 | chr7 | 131495033 | |||||
| chr7:131495034
|
A | C | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7306A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7306 | chr7 | 131495034 | |||||
| chr7:131495035
|
A | G | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7307A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7307 | chr7 | 131495035 | |||||
| chr7:131495036
|
A | T | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7308A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7308 | chr7 | 131495036 | |||||
| chr7:131495038
|
C | T | 19 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(16): Show | 127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*7310C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7310 | chr7 | 131495038 | |||||
| chr7:131495039
|
G | A | 1 | a0001c0001t0018 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7311G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7311 | chr7 | 131495039 | |||||
| chr7:131495041
|
A | T | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7313A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7313 | chr7 | 131495041 | |||||
| chr7:131495042
|
G | A | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7314G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7314 | chr7 | 131495042 | |||||
| chr7:131495043
|
A | T | 1 | a0001c0001t0042 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7315A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7315 | chr7 | 131495043 | |||||
| chr7:131495247
|
G | A | 1 | a0001c0001t0035 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7519G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7519 | chr7 | 131495247 | |||||
| chr7:131495324
|
C | T | 1 | a0001c0001t0051 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7596C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7596 | chr7 | 131495324 | |||||
| chr7:131495325
|
G | C | 1 | a0001c0003t0008 | 6 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7597G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7597 | chr7 | 131495325 | |||||
| chr7:131495387
|
G | A | 1 | a0001c0001t0006 | 7 | NA18963.hp1 NA18968.hp2 NA18977.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7659G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7659 | chr7 | 131495387 | |||||
| chr7:131495596
|
T | TA | 16 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(13): Show | 66 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*7878dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7879 | INFO_REALIGN_3_PRIME | chr7 | 131495596 | ||||
| chr7:131495597
|
A | T | 1 | a0001c0001t0027 | 2 | NA18987.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7869A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7869 | chr7 | 131495597 | |||||
| chr7:131495674
|
C | A | 1 | a0001c0002t0045 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7946C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7946 | chr7 | 131495674 | |||||
| chr7:131495685
|
A | G | 1 | a0001c0001t0022 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7957A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 7957 | chr7 | 131495685 | |||||
| chr7:131496075
|
T | A | 2 | a0001c0001t0028a0001c0001t0049 | 2 | HG02280.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8347T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 8347 | chr7 | 131496075 | |||||
| chr7:131496159
|
C | T | 38 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(35): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*8431C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 8431 | chr7 | 131496159 | |||||
| chr7:131496397
|
G | T | 1 | a0001c0001t0039 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8669G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 8669 | chr7 | 131496397 | |||||
| chr7:131496421
|
A | G | 2 | a0001c0001t0048a0001c0001t0050 | 2 | HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8693A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 8693 | chr7 | 131496421 | |||||
| chr7:131496457
|
A | G | 1 | a0001c0001t0041 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8729A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 8729 | chr7 | 131496457 | |||||
| chr7:131496477
|
C | G | 1 | a0001c0001t0040 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8749C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 18/18 | 8749 | chr7 | 131496477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:131328025
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.98+28G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131328025 | ||||||
| chr7:131328166
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(64): Show | 69 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.98+169G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131328166 | ||||||
| chr7:131328328
|
A | G | 1 | a0001c0001t0007g0316 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+331A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131328328 | ||||||
| chr7:131328438
|
AGT | A | 3 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071 | 4 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+444_98+445delGT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131328438 | |||||
| chr7:131328469
|
T | C | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.98+472T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131328469 | ||||||
| chr7:131328498
|
G | C | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.98+501G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131328498 | ||||||
| chr7:131328730
|
C | T | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+733C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131328730 | ||||||
| chr7:131328900
|
G | A | 1 | a0001c0002t0002g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.98+903G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131328900 | ||||||
| chr7:131329161
|
C | T | 3 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0056g0308 | 3 | HG02055.hp2 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.98+1164C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131329161 | ||||||
| chr7:131329355
|
T | C | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | NA18944.hp2 NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.98+1358T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131329355 | ||||||
| chr7:131329579
|
G | A | 1 | a0001c0003t0008g0079 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.98+1582G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131329579 | ||||||
| chr7:131329625
|
A | C | 1 | a0001c0001t0002g0307 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.98+1628A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131329625 | ||||||
| chr7:131329956
|
A | G | 1 | a0001c0001t0004g0069 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.98+1959A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131329956 | ||||||
| chr7:131329982
|
T | G | 7 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+1985T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131329982 | ||||||
| chr7:131330629
|
G | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+2632G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131330629 | ||||||
| chr7:131330745
|
A | G | 1 | a0001c0001t0009g0306 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.98+2748A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131330745 | ||||||
| chr7:131331093
|
A | G | 96 | a0001c0001t0001g0225a0001c0001t0002g0076a0001c0001t0002g0077others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.98+3096A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131331093 | ||||||
| chr7:131331105
|
G | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0054others(184): Show | 188 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.98+3108G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131331105 | ||||||
| chr7:131331332
|
C | A | 5 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+3335C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131331332 | ||||||
| chr7:131331475
|
C | G | 44 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.98+3478C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131331475 | ||||||
| chr7:131331825
|
T | C | 1 | a0001c0001t0012g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.98+3828T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131331825 | ||||||
| chr7:131332155
|
G | C | 5 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(2): Show | 5 | HG00738.hp1 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+4158G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131332155 | ||||||
| chr7:131332184
|
C | T | 1 | a0001c0001t0003g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.98+4187C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131332184 | ||||||
| chr7:131332230
|
G | GT | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.98+4236dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131332230 | |||||
| chr7:131332333
|
A | G | 9 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+4336A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131332333 | ||||||
| chr7:131332565
|
A | G | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.98+4568A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131332565 | ||||||
| chr7:131332582
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.98+4585A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131332582 | ||||||
| chr7:131332811
|
T | C | 2 | a0001c0001t0002g0307a0001c0001t0044g0215 | 2 | HG01978.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.98+4814T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131332811 | ||||||
| chr7:131333068
|
C | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+5071C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131333068 | ||||||
| chr7:131333182
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.98+5185C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131333182 | ||||||
| chr7:131333194
|
G | A | 1 | a0001c0001t0053g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98+5197G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131333194 | ||||||
| chr7:131333286
|
G | C | 2 | a0001c0001t0002g0216a0001c0001t0003g0217 | 2 | NA18999.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.98+5289G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131333286 | ||||||
| chr7:131333345
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.98+5348G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131333345 | ||||||
| chr7:131333789
|
C | T | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.98+5792C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131333789 | ||||||
| chr7:131333838
|
A | G | 1 | a0001c0001t0002g0303 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.98+5841A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131333838 | ||||||
| chr7:131334122
|
A | G | 1 | a0001c0001t0003g0209 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.98+6125A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131334122 | ||||||
| chr7:131334274
|
G | A | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.98+6277G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131334274 | ||||||
| chr7:131334320
|
A | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG01099.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.98+6323A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131334320 | ||||||
| chr7:131334372
|
G | A | 1 | a0001c0001t0004g0006 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.98+6375G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131334372 | ||||||
| chr7:131334765
|
A | G | 1 | a0001c0001t0004g0049 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.98+6768A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131334765 | ||||||
| chr7:131335170
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.98+7173T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131335170 | ||||||
| chr7:131335376
|
A | G | 179 | a0001c0001t0001g0225a0001c0001t0002g0076a0001c0001t0002g0077others(176): Show | 180 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.98+7379A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131335376 | ||||||
| chr7:131335409
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.98+7412A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131335409 | ||||||
| chr7:131335695
|
GT | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.98+7713delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131335695 | |||||
| chr7:131335832
|
A | G | 1 | a0001c0001t0003g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.98+7835A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131335832 | ||||||
| chr7:131335985
|
A | AT | 10 | a0001c0001t0001g0150a0001c0001t0001g0155a0001c0001t0040g0302others(7): Show | 10 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+8001dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131335985 | |||||
| chr7:131335985
|
AT | A | 13 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0092others(10): Show | 13 | HG01069.hp1 HG01346.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.98+8001delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131335985 | |||||
| chr7:131336049
|
A | G | 2 | a0001c0001t0002g0216a0001c0001t0003g0217 | 2 | NA18999.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.98+8052A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336049 | ||||||
| chr7:131336111
|
C | T | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG00140.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.98+8114C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336111 | ||||||
| chr7:131336112
|
T | G | 7 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+8115T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336112 | ||||||
| chr7:131336163
|
C | T | 1 | a0001c0001t0010g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.98+8166C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336163 | ||||||
| chr7:131336231
|
G | A | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.98+8234G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336231 | ||||||
| chr7:131336322
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.98+8325C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336322 | ||||||
| chr7:131336340
|
G | A | 14 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.98+8343G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336340 | ||||||
| chr7:131336465
|
ATTG | A | 7 | a0001c0001t0009g0144a0001c0001t0009g0145a0001c0001t0009g0147others(4): Show | 7 | HG01169.hp1 HG01993.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+8471_98+8473del others(3): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131336465 | |||||
| chr7:131336474
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+8477T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336474 | ||||||
| chr7:131336499
|
T | G | 1 | a0001c0001t0003g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.98+8502T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336499 | ||||||
| chr7:131336567
|
C | G | 1 | a0001c0002t0045g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.98+8570C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336567 | ||||||
| chr7:131336702
|
G | A | 1 | a0001c0001t0016g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98+8705G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336702 | ||||||
| chr7:131336775
|
A | G | 1 | a0001c0001t0055g0207 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.98+8778A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131336775 | ||||||
| chr7:131337074
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.98+9077A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337074 | ||||||
| chr7:131337142
|
T | G | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.98+9145T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337142 | ||||||
| chr7:131337197
|
A | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(50): Show | 54 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.98+9200A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337197 | ||||||
| chr7:131337209
|
G | A | 1 | a0001c0001t0016g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98+9212G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337209 | ||||||
| chr7:131337337
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.98+9340A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337337 | ||||||
| chr7:131337360
|
C | A | 1 | a0001c0001t0002g0300 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98+9363C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337360 | ||||||
| chr7:131337562
|
A | T | 1 | a0001c0003t0030g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.98+9565A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337562 | ||||||
| chr7:131337682
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.98+9685A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337682 | ||||||
| chr7:131337971
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+9974T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131337971 | ||||||
| chr7:131338002
|
T | C | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.98+10005T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131338002 | ||||||
| chr7:131338074
|
A | G | 5 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+10077A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131338074 | ||||||
| chr7:131338162
|
A | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01099.hp2 HG01891.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+10165A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131338162 | ||||||
| chr7:131338462
|
C | G | 8 | a0001c0001t0003g0206a0001c0003t0008g0079a0001c0003t0008g0082others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+10465C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131338462 | ||||||
| chr7:131338597
|
C | T | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG00140.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.98+10600C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131338597 | ||||||
| chr7:131338704
|
C | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(312): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.98+10707C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131338704 | ||||||
| chr7:131339068
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0050g0064 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.98+11071C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339068 | ||||||
| chr7:131339085
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.98+11088G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339085 | ||||||
| chr7:131339137
|
A | T | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.98+11140A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339137 | ||||||
| chr7:131339445
|
C | A | 1 | a0001c0001t0009g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.98+11448C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339445 | ||||||
| chr7:131339675
|
G | C | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.98+11678G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339675 | ||||||
| chr7:131339697
|
TC | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(301): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.98+11702delC | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131339697 | |||||
| chr7:131339698
|
CCA | C | 9 | a0001c0001t0001g0142a0001c0001t0002g0078a0001c0001t0005g0107others(6): Show | 9 | HG01257.hp2 HG01993.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.98+11702_98+11703d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339698 | ||||||
| chr7:131339699
|
C | A | 2 | a0001c0001t0005g0108a0001c0002t0054g0074 | 2 | HG02258.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.98+11702C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339699 | ||||||
| chr7:131339739
|
T | C | 44 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.98+11742T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339739 | ||||||
| chr7:131339814
|
A | T | 41 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.98+11817A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339814 | ||||||
| chr7:131339922
|
A | G | 107 | a0001c0001t0001g0225a0001c0001t0002g0048a0001c0001t0002g0076others(104): Show | 107 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.98+11925A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131339922 | ||||||
| chr7:131340001
|
A | G | 1 | a0001c0001t0002g0298 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.98+12004A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131340001 | ||||||
| chr7:131340275
|
C | CT | 175 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0039others(172): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.98+12299dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131340275 | |||||
| chr7:131340275
|
C | CTT | 58 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0154others(55): Show | 58 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.98+12298_98+12299d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131340275 | |||||
| chr7:131340360
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.98+12363C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131340360 | ||||||
| chr7:131340396
|
G | GC | 41 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.98+12406dupC | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131340396 | |||||
| chr7:131340656
|
T | C | 1 | a0001c0001t0002g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.98+12659T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131340656 | ||||||
| chr7:131341168
|
A | AT | 8 | a0001c0001t0002g0290a0001c0003t0008g0079a0001c0003t0008g0082others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+13182dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131341168 | |||||
| chr7:131341601
|
T | A | 2 | a0001c0001t0001g0154a0001c0001t0002g0109 | 2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.98+13604T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131341601 | ||||||
| chr7:131341888
|
C | T | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.98+13891C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131341888 | ||||||
| chr7:131341889
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+13892G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131341889 | ||||||
| chr7:131341895
|
C | T | 41 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.98+13898C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131341895 | ||||||
| chr7:131342156
|
A | AT | 10 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0010g0164others(7): Show | 10 | HG01261.hp1 HG01261.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+14172dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131342156 | |||||
| chr7:131342156
|
AT | A | 30 | a0001c0001t0001g0038a0001c0001t0001g0089a0001c0001t0001g0090others(27): Show | 30 | HG01069.hp1 HG01346.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.98+14172delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131342156 | |||||
| chr7:131342209
|
G | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18995.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.98+14212G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131342209 | ||||||
| chr7:131342373
|
A | G | 1 | a0001c0001t0044g0215 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.98+14376A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131342373 | ||||||
| chr7:131342455
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(51): Show | 55 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.98+14458A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131342455 | ||||||
| chr7:131342874
|
T | C | 1 | a0001c0001t0002g0221 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.98+14877T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131342874 | ||||||
| chr7:131342892
|
C | G | 49 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.98+14895C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131342892 | ||||||
| chr7:131342893
|
T | C | 1 | a0001c0001t0002g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.98+14896T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131342893 | ||||||
| chr7:131343193
|
G | A | 1 | a0001c0001t0026g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.98+15196G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131343193 | ||||||
| chr7:131343309
|
A | G | 1 | a0001c0001t0037g0287 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.98+15312A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131343309 | ||||||
| chr7:131343474
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.98+15477T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131343474 | ||||||
| chr7:131343554
|
C | G | 1 | a0001c0001t0002g0286 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.98+15557C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131343554 | ||||||
| chr7:131343718
|
T | C | 2 | a0001c0002t0002g0075a0001c0002t0019g0081 | 2 | HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.98+15721T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131343718 | ||||||
| chr7:131343742
|
A | AT | 9 | a0001c0001t0002g0048a0001c0001t0002g0281a0001c0001t0002g0282others(6): Show | 9 | HG00544.hp1 HG01934.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.98+15753dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131343742 | |||||
| chr7:131344079
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0043g0037 | 2 | HG00423.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.98+16082A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344079 | ||||||
| chr7:131344103
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.98+16106T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344103 | ||||||
| chr7:131344159
|
TGTA | T | 22 | a0001c0001t0001g0225a0001c0001t0002g0048a0001c0001t0002g0076others(19): Show | 22 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.98+16166_98+16168d others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131344159 | |||||
| chr7:131344193
|
C | T | 1 | a0001c0001t0010g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.98+16196C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344193 | ||||||
| chr7:131344210
|
G | A | 1 | a0001c0001t0065g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.98+16213G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344210 | ||||||
| chr7:131344311
|
A | G | 1 | a0001c0001t0002g0280 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.98+16314A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344311 | ||||||
| chr7:131344390
|
G | C | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.98+16393G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344390 | ||||||
| chr7:131344431
|
A | G | 7 | a0001c0001t0002g0220a0001c0002t0002g0075a0001c0002t0019g0081others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+16434A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344431 | ||||||
| chr7:131344593
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0155 | 3 | NA18995.hp1 NA19062.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.98+16596C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344593 | ||||||
| chr7:131344864
|
C | T | 1 | a0001c0001t0032g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.98+16867C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344864 | ||||||
| chr7:131344926
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+16929C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344926 | ||||||
| chr7:131344948
|
C | T | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.98+16951C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344948 | ||||||
| chr7:131344952
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.98+16955C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131344952 | ||||||
| chr7:131345237
|
C | T | 107 | a0001c0001t0001g0225a0001c0001t0002g0048a0001c0001t0002g0076others(104): Show | 107 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.98+17240C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131345237 | ||||||
| chr7:131345242
|
G | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+17245G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131345242 | ||||||
| chr7:131345298
|
T | C | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | NA18944.hp2 NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.98+17301T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131345298 | ||||||
| chr7:131345453
|
T | C | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.98+17456T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131345453 | ||||||
| chr7:131345818
|
C | T | 1 | a0001c0001t0012g0278 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.98+17821C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131345818 | ||||||
| chr7:131345908
|
A | G | 4 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0056g0308others(1): Show | 4 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+17911A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131345908 | ||||||
| chr7:131346154
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.98+18157A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131346154 | ||||||
| chr7:131346173
|
G | A | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00642.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.98+18176G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131346173 | ||||||
| chr7:131346244
|
C | T | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+18247C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131346244 | ||||||
| chr7:131346296
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.98+18299G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131346296 | ||||||
| chr7:131346409
|
C | G | 1 | a0001c0001t0035g0163 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.98+18412C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131346409 | ||||||
| chr7:131346520
|
CA | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.98+18537delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131346520 | |||||
| chr7:131346535
|
C | A | 1 | a0001c0001t0006g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.98+18538C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131346535 | ||||||
| chr7:131346762
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98+18765A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131346762 | ||||||
| chr7:131346782
|
G | T | 2 | a0001c0001t0009g0147a0001c0001t0016g0146 | 2 | HG02129.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.98+18785G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131346782 | ||||||
| chr7:131347004
|
T | C | 4 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+19007T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347004 | ||||||
| chr7:131347127
|
C | T | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.98+19130C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347127 | ||||||
| chr7:131347281
|
G | T | 2 | a0001c0001t0001g0154a0001c0001t0002g0109 | 2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.98+19284G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347281 | ||||||
| chr7:131347434
|
C | T | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+19437C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347434 | ||||||
| chr7:131347458
|
C | T | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00642.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.98+19461C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347458 | ||||||
| chr7:131347502
|
A | T | 1 | a0001c0001t0003g0204 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.98+19505A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347502 | ||||||
| chr7:131347642
|
G | C | 1 | a0001c0001t0026g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.98+19645G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347642 | ||||||
| chr7:131347673
|
C | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+19676C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347673 | ||||||
| chr7:131347717
|
A | C | 1 | a0001c0001t0048g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.98+19720A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131347717 | ||||||
| chr7:131348298
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.98+20301A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131348298 | ||||||
| chr7:131348530
|
G | GT | 44 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.98+20545dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131348530 | |||||
| chr7:131349053
|
A | G | 50 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.98+21056A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131349053 | ||||||
| chr7:131349201
|
C | CT | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.98+21216dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131349201 | |||||
| chr7:131349276
|
A | G | 9 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+21279A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131349276 | ||||||
| chr7:131349418
|
A | G | 9 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0198others(6): Show | 9 | HG02040.hp2 NA18954.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+21421A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131349418 | ||||||
| chr7:131349429
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.98+21432T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131349429 | ||||||
| chr7:131349859
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.98+21862T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131349859 | ||||||
| chr7:131349904
|
G | A | 1 | a0001c0001t0003g0196 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.98+21907G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131349904 | ||||||
| chr7:131349949
|
T | G | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.98+21952T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131349949 | ||||||
| chr7:131350001
|
CT | C | 106 | a0001c0001t0001g0225a0001c0001t0002g0048a0001c0001t0002g0076others(103): Show | 106 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.98+22006delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131350001 | |||||
| chr7:131350032
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0020g0226a0001c0001t0020g0227 | 3 | NA18945.hp1 NA18995.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.98+22035C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131350032 | ||||||
| chr7:131350257
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.98+22260C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131350257 | ||||||
| chr7:131350346
|
C | T | 7 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078others(4): Show | 7 | HG00408.hp2 HG00597.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+22349C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131350346 | ||||||
| chr7:131350375
|
T | C | 39 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.98+22378T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131350375 | ||||||
| chr7:131350493
|
A | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(65): Show | 70 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.98+22496A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131350493 | ||||||
| chr7:131350668
|
A | G | 1 | a0001c0001t0002g0276 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.98+22671A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131350668 | ||||||
| chr7:131350992
|
G | A | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.98+22995G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131350992 | ||||||
| chr7:131351022
|
T | A | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.98+23025T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131351022 | ||||||
| chr7:131351057
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.98+23060G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131351057 | ||||||
| chr7:131351105
|
A | G | 171 | a0001c0001t0001g0225a0001c0001t0002g0048a0001c0001t0002g0076others(168): Show | 171 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.98+23108A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131351105 | ||||||
| chr7:131351169
|
G | A | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.98+23172G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131351169 | ||||||
| chr7:131351239
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.98+23242C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131351239 | ||||||
| chr7:131351275
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.98+23278A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131351275 | ||||||
| chr7:131351470
|
ATTT | A | 4 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+23479_98+23481d others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131351470 | |||||
| chr7:131351599
|
C | G | 1 | a0001c0001t0002g0285 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.98+23602C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131351599 | ||||||
| chr7:131351719
|
C | A | 1 | a0001c0001t0002g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.99-23705C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131351719 | ||||||
| chr7:131352887
|
C | T | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99-22537C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131352887 | ||||||
| chr7:131352946
|
C | T | 1 | a0001c0002t0019g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.99-22478C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131352946 | ||||||
| chr7:131353033
|
G | C | 1 | a0001c0002t0002g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.99-22391G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131353033 | ||||||
| chr7:131353088
|
A | T | 1 | a0001c0001t0002g0285 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.99-22336A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131353088 | ||||||
| chr7:131353151
|
G | T | 1 | a0001c0001t0004g0035 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.99-22273G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131353151 | ||||||
| chr7:131353295
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.99-22129G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131353295 | ||||||
| chr7:131353325
|
A | AT | 41 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.99-22090dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131353325 | |||||
| chr7:131353700
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99-21724C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131353700 | ||||||
| chr7:131353903
|
T | TA | 116 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0115others(113): Show | 116 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.99-21500dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131353903 | |||||
| chr7:131353903
|
T | TAA | 9 | a0001c0001t0002g0076a0001c0001t0002g0229a0001c0001t0002g0230others(6): Show | 9 | HG01261.hp1 HG02080.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-21501_99-21500d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131353903 | |||||
| chr7:131353903
|
TA | T | 6 | a0001c0001t0003g0195a0001c0001t0006g0137a0001c0001t0025g0156others(3): Show | 6 | HG01516.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-21500delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131353903 | |||||
| chr7:131353903
|
TAAAA | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | HG00280.hp2 HG00423.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-21503_99-21500d others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131353903 | |||||
| chr7:131353903
|
TAAAAA | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(56): Show | 61 | HG00544.hp2 HG00597.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.99-21504_99-21500d others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131353903 | |||||
| chr7:131354478
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0055 | 3 | HG01496.hp2 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.99-20946C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131354478 | ||||||
| chr7:131354667
|
G | A | 1 | a0001c0003t0008g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99-20757G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131354667 | ||||||
| chr7:131354832
|
G | A | 2 | a0001c0001t0013g0231a0001c0001t0046g0232 | 2 | NA18948.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.99-20592G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131354832 | ||||||
| chr7:131355129
|
G | A | 2 | a0001c0001t0002g0216a0001c0001t0003g0217 | 2 | NA18999.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.99-20295G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131355129 | ||||||
| chr7:131355186
|
C | T | 64 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(61): Show | 64 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.99-20238C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131355186 | ||||||
| chr7:131355484
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.99-19940A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131355484 | ||||||
| chr7:131355628
|
C | CTA | 13 | a0001c0001t0001g0007a0001c0001t0001g0105a0001c0001t0001g0138others(10): Show | 13 | HG00597.hp1 HG01071.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-19776_99-19775d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATA | 9 | a0001c0001t0005g0101a0001c0001t0005g0102a0001c0001t0025g0156others(6): Show | 9 | HG00642.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-19778_99-19775d others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATATAT others(3): Show |
2 | a0001c0001t0003g0194a0001c0002t0019g0081 | 2 | HG03516.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.99-19784_99-19775d others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATATAT others(5): Show |
7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG00738.hp1 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-19786_99-19775d others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATATAT others(7): Show |
13 | a0001c0001t0003g0172a0001c0001t0003g0177a0001c0001t0003g0202others(10): Show | 13 | HG00408.hp1 HG02559.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.99-19788_99-19775d others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATATAT others(9): Show |
18 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0189others(15): Show | 18 | HG02015.hp1 HG02055.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.99-19790_99-19775d others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATATAT others(11): Show |
6 | a0001c0001t0003g0184a0001c0001t0003g0188a0001c0001t0003g0198others(3): Show | 6 | HG00639.hp1 HG02040.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-19792_99-19775d others(20): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATATAT others(13): Show |
3 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0013g0187 | 3 | HG01891.hp1 HG02559.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.99-19794_99-19775d others(22): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATATAT others(15): Show |
5 | a0001c0001t0003g0195a0001c0001t0003g0204a0001c0001t0051g0186others(2): Show | 5 | HG00438.hp1 HG01516.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-19775_99-19774i others(24): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
C | CTATATAT others(17): Show |
3 | a0001c0001t0003g0173a0001c0001t0021g0179a0001c0001t0021g0180 | 3 | HG03491.hp2 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.99-19775_99-19774i others(26): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355628
|
CTATATA | C | 106 | a0001c0001t0001g0225a0001c0001t0002g0076a0001c0001t0002g0077others(103): Show | 106 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.99-19780_99-19775d others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131355628 | |||||
| chr7:131355664
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.99-19760G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131355664 | ||||||
| chr7:131355672
|
G | T | 9 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99-19752G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131355672 | ||||||
| chr7:131355824
|
C | T | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.99-19600C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131355824 | ||||||
| chr7:131355896
|
C | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-19528C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131355896 | ||||||
| chr7:131355928
|
C | G | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.99-19496C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131355928 | ||||||
| chr7:131356015
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99-19409G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356015 | ||||||
| chr7:131356062
|
A | AT | 6 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0007g0313others(3): Show | 6 | HG00738.hp2 HG02071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-19342dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131356062 | |||||
| chr7:131356062
|
A | G | 1 | a0001c0001t0052g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99-19362A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356062 | ||||||
| chr7:131356062
|
AT | A | 6 | a0001c0001t0002g0076a0001c0001t0005g0108a0001c0001t0007g0178others(3): Show | 6 | HG01069.hp2 HG02258.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-19342delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131356062 | |||||
| chr7:131356274
|
T | C | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00642.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.99-19150T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356274 | ||||||
| chr7:131356359
|
G | A | 1 | a0001c0002t0045g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.99-19065G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356359 | ||||||
| chr7:131356431
|
G | A | 1 | a0001c0001t0009g0306 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.99-18993G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356431 | ||||||
| chr7:131356446
|
C | G | 1 | a0001c0001t0002g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.99-18978C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356446 | ||||||
| chr7:131356486
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0050g0064 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99-18938G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356486 | ||||||
| chr7:131356664
|
G | A | 1 | a0001c0001t0005g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.99-18760G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356664 | ||||||
| chr7:131356736
|
C | T | 1 | a0001c0001t0003g0194 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.99-18688C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356736 | ||||||
| chr7:131356823
|
C | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-18601C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131356823 | ||||||
| chr7:131357043
|
A | G | 41 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.99-18381A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131357043 | ||||||
| chr7:131357431
|
T | C | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99-17993T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131357431 | ||||||
| chr7:131357644
|
A | G | 1 | a0001c0001t0013g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99-17780A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131357644 | ||||||
| chr7:131357748
|
T | G | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | NA18944.hp2 NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.99-17676T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131357748 | ||||||
| chr7:131357886
|
G | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-17538G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131357886 | ||||||
| chr7:131357906
|
C | T | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.99-17518C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131357906 | ||||||
| chr7:131358057
|
C | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-17367C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131358057 | ||||||
| chr7:131358239
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0047g0091 | 2 | NA18944.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.99-17185G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131358239 | ||||||
| chr7:131358370
|
C | T | 1 | a0001c0001t0034g0169 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99-17054C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131358370 | ||||||
| chr7:131358384
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.99-17040G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131358384 | ||||||
| chr7:131358558
|
A | G | 1 | a0001c0001t0035g0163 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.99-16866A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131358558 | ||||||
| chr7:131358803
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-16621A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131358803 | ||||||
| chr7:131358946
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.99-16478T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131358946 | ||||||
| chr7:131359293
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99-16131A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131359293 | ||||||
| chr7:131359300
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99-16124A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131359300 | ||||||
| chr7:131359320
|
T | C | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99-16104T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131359320 | ||||||
| chr7:131359400
|
CAT | C | 4 | a0001c0001t0003g0134a0001c0001t0006g0135a0001c0001t0006g0136others(1): Show | 4 | NA18968.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-16019_99-16018d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131359400 | |||||
| chr7:131359586
|
T | C | 1 | a0001c0002t0045g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.99-15838T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131359586 | ||||||
| chr7:131359724
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.99-15700G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131359724 | ||||||
| chr7:131359760
|
G | A | 1 | a0001c0001t0060g0305 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99-15664G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131359760 | ||||||
| chr7:131359903
|
T | C | 9 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.99-15521T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131359903 | ||||||
| chr7:131360118
|
G | A | 1 | a0001c0001t0012g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99-15306G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131360118 | ||||||
| chr7:131360178
|
A | C | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-15246A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131360178 | ||||||
| chr7:131360494
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0028g0045others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-14930A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131360494 | ||||||
| chr7:131360571
|
G | A | 4 | a0001c0001t0010g0164a0001c0001t0022g0165a0001c0001t0022g0166others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-14853G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131360571 | ||||||
| chr7:131360657
|
A | G | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.99-14767A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131360657 | ||||||
| chr7:131360715
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.99-14709A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131360715 | ||||||
| chr7:131360988
|
T | C | 4 | a0001c0001t0002g0234a0001c0001t0002g0272a0001c0001t0002g0286others(1): Show | 4 | HG02027.hp2 HG02056.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-14436T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131360988 | ||||||
| chr7:131361100
|
A | G | 13 | a0001c0001t0002g0218a0001c0001t0002g0262a0001c0001t0002g0263others(10): Show | 13 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-14324A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131361100 | ||||||
| chr7:131361103
|
T | A | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.99-14321T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131361103 | ||||||
| chr7:131361147
|
C | G | 1 | a0001c0002t0002g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.99-14277C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131361147 | ||||||
| chr7:131361240
|
C | G | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99-14184C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131361240 | ||||||
| chr7:131361251
|
C | T | 2 | a0001c0001t0032g0158a0001c0002t0019g0310 | 2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.99-14173C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131361251 | ||||||
| chr7:131361485
|
G | A | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | NA18944.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.99-13939G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131361485 | ||||||
| chr7:131361865
|
CATTCTT | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(4): Show | 8 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-13556_99-13551d others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131361865 | |||||
| chr7:131361967
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | NA18947.hp1 NA18965.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-13457A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131361967 | ||||||
| chr7:131362040
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.99-13384G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131362040 | ||||||
| chr7:131362314
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-13110T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131362314 | ||||||
| chr7:131362533
|
G | C | 1 | a0001c0001t0010g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99-12891G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131362533 | ||||||
| chr7:131362705
|
C | A | 4 | a0001c0001t0007g0313a0001c0001t0007g0315a0001c0001t0007g0316others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-12719C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131362705 | ||||||
| chr7:131362778
|
G | C | 1 | a0001c0003t0008g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99-12646G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131362778 | ||||||
| chr7:131363128
|
T | C | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99-12296T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131363128 | ||||||
| chr7:131363358
|
G | T | 1 | a0001c0001t0032g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.99-12066G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131363358 | ||||||
| chr7:131363730
|
A | T | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.99-11694A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131363730 | ||||||
| chr7:131363760
|
A | G | 1 | a0001c0001t0028g0045 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.99-11664A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131363760 | ||||||
| chr7:131363933
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.99-11491G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131363933 | ||||||
| chr7:131364204
|
CGTTT | C | 4 | a0001c0001t0007g0313a0001c0001t0007g0315a0001c0001t0007g0316others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-11215_99-11212d others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131364204 | |||||
| chr7:131364453
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-10971T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131364453 | ||||||
| chr7:131364509
|
C | T | 2 | a0001c0001t0013g0185a0001c0001t0013g0187 | 2 | HG03831.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.99-10915C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131364509 | ||||||
| chr7:131364571
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99-10853G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131364571 | ||||||
| chr7:131364670
|
T | C | 1 | a0001c0001t0009g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99-10754T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131364670 | ||||||
| chr7:131364676
|
G | A | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.99-10748G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131364676 | ||||||
| chr7:131364725
|
C | T | 1 | a0001c0001t0003g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.99-10699C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131364725 | ||||||
| chr7:131364773
|
C | T | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.99-10651C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131364773 | ||||||
| chr7:131364972
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.99-10452G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131364972 | ||||||
| chr7:131365058
|
G | A | 1 | a0001c0001t0002g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99-10366G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131365058 | ||||||
| chr7:131365207
|
G | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-10217G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131365207 | ||||||
| chr7:131365447
|
T | A | 1 | a0001c0001t0009g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.99-9977T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131365447 | ||||||
| chr7:131365467
|
A | C | 1 | a0001c0001t0002g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.99-9957A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131365467 | ||||||
| chr7:131365613
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99-9811T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131365613 | ||||||
| chr7:131365999
|
G | A | 4 | a0001c0001t0001g0122a0001c0001t0005g0114a0001c0001t0005g0120others(1): Show | 4 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-9425G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131365999 | ||||||
| chr7:131366040
|
G | C | 1 | a0001c0001t0029g0088 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.99-9384G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131366040 | ||||||
| chr7:131366536
|
T | C | 2 | a0001c0001t0038g0235a0001c0001t0039g0236 | 2 | HG02523.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.99-8888T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131366536 | ||||||
| chr7:131366837
|
A | G | 2 | a0001c0001t0002g0279a0001c0001t0012g0228 | 2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.99-8587A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131366837 | ||||||
| chr7:131367006
|
T | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | NA18969.hp1 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.99-8418T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131367006 | ||||||
| chr7:131367158
|
T | C | 1 | a0001c0001t0027g0010 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.99-8266T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131367158 | ||||||
| chr7:131367647
|
C | G | 1 | a0001c0001t0002g0261 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.99-7777C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131367647 | ||||||
| chr7:131367943
|
A | T | 1 | a0001c0001t0002g0269 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.99-7481A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131367943 | ||||||
| chr7:131368171
|
G | A | 1 | a0001c0001t0065g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.99-7253G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131368171 | ||||||
| chr7:131368174
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.99-7250G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131368174 | ||||||
| chr7:131368494
|
T | C | 1 | a0001c0002t0002g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.99-6930T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131368494 | ||||||
| chr7:131369000
|
T | TCA | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0039others(2): Show | 5 | HG00544.hp2 HG02145.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-6401_99-6400dup others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131369000 | |||||
| chr7:131369000
|
TCA | T | 171 | a0001c0001t0001g0133a0001c0001t0002g0048a0001c0001t0002g0076others(168): Show | 171 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.99-6401_99-6400del others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131369000 | |||||
| chr7:131369015
|
C | T | 2 | a0001c0001t0038g0235a0001c0001t0039g0236 | 2 | HG02523.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.99-6409C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369015 | ||||||
| chr7:131369020
|
A | T | 39 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.99-6404A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369020 | ||||||
| chr7:131369154
|
T | A | 1 | a0001c0001t0063g0238 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.99-6270T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369154 | ||||||
| chr7:131369195
|
A | G | 3 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071 | 4 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-6229A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369195 | ||||||
| chr7:131369412
|
G | T | 3 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0213 | 3 | NA18957.hp1 NA18966.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.99-6012G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369412 | ||||||
| chr7:131369725
|
T | A | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99-5699T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369725 | ||||||
| chr7:131369784
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-5640T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369784 | ||||||
| chr7:131369905
|
C | T | 2 | a0001c0001t0020g0226a0001c0001t0020g0227 | 2 | NA18995.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.99-5519C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369905 | ||||||
| chr7:131369929
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99-5495C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131369929 | ||||||
| chr7:131370370
|
G | GT | 12 | a0001c0001t0002g0230a0001c0001t0003g0197a0001c0001t0003g0199others(9): Show | 12 | HG02630.hp1 HG02647.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.99-5040dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131370370 | |||||
| chr7:131370370
|
GT | G | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-5040delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131370370 | |||||
| chr7:131370659
|
C | A | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99-4765C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131370659 | ||||||
| chr7:131370767
|
A | G | 1 | a0001c0001t0025g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.99-4657A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131370767 | ||||||
| chr7:131371442
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99-3982A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131371442 | ||||||
| chr7:131371469
|
C | T | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.99-3955C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131371469 | ||||||
| chr7:131371601
|
C | T | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99-3823C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131371601 | ||||||
| chr7:131371765
|
C | CAT | 111 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(108): Show | 111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.99-3643_99-3642dup others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131371765 | |||||
| chr7:131371765
|
C | CATAT | 5 | a0001c0001t0002g0219a0001c0001t0002g0258a0001c0001t0002g0259others(2): Show | 5 | HG00597.hp2 HG02109.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-3645_99-3642dup others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131371765 | |||||
| chr7:131371765
|
C | CATATATA others(3): Show |
1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99-3651_99-3642dup others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131371765 | |||||
| chr7:131371781
|
T | C | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00642.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.99-3643T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131371781 | ||||||
| chr7:131371823
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.99-3601T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131371823 | ||||||
| chr7:131371829
|
A | T | 12 | a0001c0001t0003g0032a0001c0001t0004g0006a0001c0001t0004g0026others(9): Show | 12 | NA18951.hp1 NA18955.hp1 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.99-3595A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131371829 | ||||||
| chr7:131371832
|
C | T | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.99-3592C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131371832 | ||||||
| chr7:131371882
|
G | A | 178 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(175): Show | 179 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.99-3542G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131371882 | ||||||
| chr7:131372282
|
A | G | 9 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.99-3142A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131372282 | ||||||
| chr7:131372290
|
C | T | 2 | a0001c0001t0005g0104a0001c0001t0005g0107 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.99-3134C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131372290 | ||||||
| chr7:131372401
|
C | T | 1 | a0001c0001t0009g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.99-3023C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131372401 | ||||||
| chr7:131372554
|
T | G | 40 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(37): Show | 40 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.99-2870T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131372554 | ||||||
| chr7:131372721
|
GT | G | 6 | a0001c0001t0002g0239a0001c0001t0002g0262a0001c0001t0004g0026others(3): Show | 6 | HG01168.hp2 HG03041.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-2684delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131372721 | |||||
| chr7:131372745
|
A | T | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.99-2679A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131372745 | ||||||
| chr7:131372848
|
A | G | 1 | a0001c0001t0002g0257 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.99-2576A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131372848 | ||||||
| chr7:131372981
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.99-2443C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131372981 | ||||||
| chr7:131373197
|
G | A | 1 | a0001c0001t0027g0010 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.99-2227G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131373197 | ||||||
| chr7:131373315
|
C | T | 2 | a0001c0001t0002g0268a0001c0001t0002g0269 | 2 | NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.99-2109C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131373315 | ||||||
| chr7:131373478
|
T | C | 1 | a0001c0001t0026g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.99-1946T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131373478 | ||||||
| chr7:131373548
|
C | A | 155 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(152): Show | 155 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.99-1876C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131373548 | ||||||
| chr7:131373776
|
T | A | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99-1648T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131373776 | ||||||
| chr7:131374222
|
A | G | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.99-1202A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374222 | ||||||
| chr7:131374297
|
G | A | 96 | a0001c0001t0001g0105a0001c0001t0002g0048a0001c0001t0002g0076others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.99-1127G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374297 | ||||||
| chr7:131374448
|
T | C | 4 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0045g0143others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-976T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374448 | ||||||
| chr7:131374455
|
G | A | 1 | a0001c0001t0052g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99-969G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374455 | ||||||
| chr7:131374593
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.99-831C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374593 | ||||||
| chr7:131374692
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.99-732T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374692 | ||||||
| chr7:131374739
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(70): Show | 75 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.99-685A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374739 | ||||||
| chr7:131374750
|
T | C | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99-674T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374750 | ||||||
| chr7:131374932
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(299): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.99-492C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131374932 | ||||||
| chr7:131374939
|
C | CT | 50 | a0001c0001t0002g0275a0001c0001t0003g0172a0001c0001t0003g0173others(47): Show | 50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.99-470dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 131374939 | |||||
| chr7:131375055
|
C | T | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99-369C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131375055 | ||||||
| chr7:131375070
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99-354G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131375070 | ||||||
| chr7:131375293
|
C | G | 1 | a0001c0001t0002g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.99-131C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131375293 | ||||||
| chr7:131375314
|
T | C | 1 | a0001c0001t0005g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.99-110T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131375314 | ||||||
| chr7:131375358
|
T | C | 1 | a0001c0001t0060g0305 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99-66T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 1/17 | chr7 | 131375358 | ||||||
| chr7:131375518
|
G | A | 106 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(103): Show | 106 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.168+25G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131375518 | ||||||
| chr7:131375609
|
G | A | 7 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0206others(4): Show | 7 | HG02602.hp2 HG02735.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+116G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131375609 | ||||||
| chr7:131375624
|
C | T | 4 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0175others(1): Show | 4 | HG00738.hp1 HG01074.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+131C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131375624 | ||||||
| chr7:131376095
|
A | AAT | 12 | a0001c0001t0001g0132a0001c0001t0003g0190a0001c0001t0003g0208others(9): Show | 13 | HG00639.hp2 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+641_168+642dup others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376095
|
A | AATATAT | 6 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0181others(3): Show | 6 | HG01099.hp1 HG02602.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+637_168+642dup others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376095
|
A | AATATATA others(1): Show |
8 | a0001c0001t0003g0176a0001c0001t0003g0196a0001c0001t0003g0199others(5): Show | 8 | HG01074.hp1 HG01169.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+635_168+642dup others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376095
|
A | AATATATA others(3): Show |
5 | a0001c0001t0003g0172a0001c0001t0003g0175a0001c0001t0003g0189others(2): Show | 5 | HG00738.hp1 HG02559.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+633_168+642dup others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376095
|
A | AATATATA others(5): Show |
1 | a0001c0001t0003g0204 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.168+631_168+642dup others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376095
|
AAT | A | 5 | a0001c0001t0010g0171a0001c0001t0024g0151a0001c0001t0032g0158others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+641_168+642del others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376095
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.168+621_168+642del others(22): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376095
|
AATATATA others(17): Show |
A | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.168+619_168+642del others(24): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376095
|
AATATATA others(25): Show |
A | 95 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.168+611_168+642del others(32): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376095 | |||||
| chr7:131376116
|
A | G | 1 | a0001c0001t0003g0195 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.168+623A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376116 | ||||||
| chr7:131376118
|
A | G | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02056.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.168+625A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376118 | ||||||
| chr7:131376120
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0025others(7): Show | 11 | HG00280.hp2 HG01106.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+627A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376120 | ||||||
| chr7:131376121
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0003g0195 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.168+631_168+649del others(19): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376121 | |||||
| chr7:131376122
|
A | G | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0115others(6): Show | 9 | HG01099.hp2 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+629A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376122 | ||||||
| chr7:131376123
|
TATATATA others(10): Show |
T | 4 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0004g0069others(1): Show | 4 | HG02056.hp2 HG03041.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+633_168+649del others(17): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376123 | |||||
| chr7:131376124
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(59): Show | 64 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.168+631A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376124 | ||||||
| chr7:131376125
|
TATATATA others(8): Show |
T | 4 | a0001c0001t0001g0039a0001c0001t0026g0159a0001c0001t0028g0045others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+635_168+649del others(15): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376125 | |||||
| chr7:131376126
|
A | G | 16 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0056others(13): Show | 16 | HG00423.hp2 HG01099.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+633A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376126 | ||||||
| chr7:131376127
|
TATATATA others(6): Show |
T | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0018g0211others(2): Show | 5 | HG01099.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+637_168+649del others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376127 | |||||
| chr7:131376128
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(59): Show | 64 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.168+635A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376128 | ||||||
| chr7:131376129
|
TATATATG others(4): Show |
T | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(55): Show | 60 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.168+639_168+649del others(11): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376129 | |||||
| chr7:131376130
|
A | G | 13 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0056others(10): Show | 13 | HG00423.hp2 HG01496.hp1 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+637A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376130 | ||||||
| chr7:131376131
|
TATATGTA others(2): Show |
T | 11 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0056others(8): Show | 11 | HG00423.hp2 HG01496.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+641_168+649del others(9): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376131 | |||||
| chr7:131376132
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0003g0198 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.168+642_168+643ins others(22): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0130 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.168+642_168+643ins others(26): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(13): Show |
5 | a0001c0001t0001g0123a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG00438.hp2 NA18995.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+642_168+643ins others(20): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(11): Show |
6 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 6 | HG02523.hp2 NA18945.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+642_168+643ins others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0125a0001c0001t0065g0112 | 2 | HG00280.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.168+642_168+643ins others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(7): Show |
7 | a0001c0001t0001g0111a0001c0001t0001g0124a0001c0001t0005g0114others(4): Show | 7 | HG01168.hp1 HG01169.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+642_168+643ins others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(5): Show |
4 | a0001c0001t0001g0122a0001c0001t0001g0153a0001c0001t0002g0109others(1): Show | 4 | HG00140.hp1 HG01071.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+642_168+643ins others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.168+642_168+643ins others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0133a0001c0001t0006g0119a0001c0001t0036g0106 | 3 | HG02280.hp2 HG06807.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.168+642_168+643ins others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0025g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168+642_168+643ins others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | ATG | 9 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(6): Show | 9 | HG01069.hp1 HG01346.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+640_168+641ins others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376132 | |||||
| chr7:131376132
|
A | G | 14 | a0001c0001t0001g0046a0001c0001t0001g0060a0001c0001t0001g0092others(11): Show | 14 | HG00639.hp1 HG01243.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+639A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376132 | ||||||
| chr7:131376134
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0048g0058 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.168+641A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376134 | ||||||
| chr7:131376136
|
G | A | 25 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0128others(22): Show | 25 | HG00642.hp2 HG01243.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.168+643G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376136 | ||||||
| chr7:131376137
|
TATG | T | 9 | a0001c0001t0001g0129a0001c0001t0003g0311a0001c0001t0010g0164others(6): Show | 9 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+648_168+650del others(3): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376137 | |||||
| chr7:131376140
|
G | GT | 189 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0092others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.168+647_168+648ins others(1): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376140 | ||||||
| chr7:131376140
|
G | GTATGT | 18 | a0001c0001t0001g0094a0001c0001t0001g0128a0001c0001t0003g0184others(15): Show | 18 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+647_168+648ins others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376140 | ||||||
| chr7:131376140
|
G | GTATGTAT others(2): Show |
5 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0154others(2): Show | 5 | HG00642.hp2 HG01243.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+647_168+648ins others(9): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376140 | ||||||
| chr7:131376140
|
G | GTATGTAT others(6): Show |
1 | a0001c0001t0025g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.168+647_168+648ins others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376140 | ||||||
| chr7:131376140
|
G | T | 6 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+647G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376140 | ||||||
| chr7:131376171
|
C | A | 4 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0056g0308others(1): Show | 4 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+678C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376171 | ||||||
| chr7:131376342
|
T | TA | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 112 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.168+867dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376342 | |||||
| chr7:131376342
|
TA | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(52): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+867delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376342 | |||||
| chr7:131376409
|
C | T | 1 | a0001c0001t0012g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+916C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376409 | ||||||
| chr7:131376553
|
A | C | 1 | a0001c0001t0002g0257 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.168+1060A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376553 | ||||||
| chr7:131376557
|
G | A | 1 | a0001c0001t0002g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.168+1064G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376557 | ||||||
| chr7:131376640
|
C | CA | 7 | a0001c0001t0004g0069a0001c0001t0026g0073a0001c0001t0053g0072others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1162dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131376640 | |||||
| chr7:131376920
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1427A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131376920 | ||||||
| chr7:131377396
|
G | T | 1 | a0001c0001t0003g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.168+1903G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131377396 | ||||||
| chr7:131377476
|
G | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1983G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131377476 | ||||||
| chr7:131378038
|
G | A | 1 | a0001c0001t0004g0069 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.168+2545G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131378038 | ||||||
| chr7:131378125
|
T | C | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.168+2632T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131378125 | ||||||
| chr7:131378134
|
C | T | 1 | a0001c0001t0036g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.168+2641C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131378134 | ||||||
| chr7:131378171
|
G | T | 1 | a0001c0001t0002g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.168+2678G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131378171 | ||||||
| chr7:131378241
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.168+2748A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131378241 | ||||||
| chr7:131378549
|
G | A | 10 | a0001c0001t0002g0229a0001c0001t0002g0239a0001c0001t0002g0242others(7): Show | 10 | HG02622.hp1 HG02886.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+3056G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131378549 | ||||||
| chr7:131378552
|
G | A | 3 | a0001c0003t0008g0082a0001c0003t0008g0083a0001c0003t0008g0084 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.168+3059G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131378552 | ||||||
| chr7:131378882
|
C | CT | 12 | a0001c0001t0002g0036a0001c0001t0010g0164a0001c0001t0010g0167others(9): Show | 12 | HG00423.hp2 HG01261.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+3406dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131378882 | |||||
| chr7:131378961
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.168+3468C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131378961 | ||||||
| chr7:131379379
|
A | G | 1 | a0001c0001t0048g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+3886A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131379379 | ||||||
| chr7:131379776
|
G | T | 15 | a0001c0001t0002g0221a0001c0001t0002g0234a0001c0001t0002g0254others(12): Show | 15 | HG00423.hp1 HG02027.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+4283G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131379776 | ||||||
| chr7:131380066
|
GC | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(312): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.168+4574delC | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131380066 | ||||||
| chr7:131380143
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(39): Show | 43 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.168+4650G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131380143 | ||||||
| chr7:131380196
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.168+4703G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131380196 | ||||||
| chr7:131380464
|
A | G | 2 | a0001c0002t0002g0075a0001c0002t0019g0081 | 2 | HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.168+4971A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131380464 | ||||||
| chr7:131380624
|
C | A | 1 | a0001c0001t0001g0124 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.168+5131C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131380624 | ||||||
| chr7:131380813
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.168+5320A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131380813 | ||||||
| chr7:131381056
|
T | C | 1 | a0001c0001t0013g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.168+5563T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381056 | ||||||
| chr7:131381111
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+5618A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381111 | ||||||
| chr7:131381153
|
C | T | 1 | a0001c0002t0019g0309 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.168+5660C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381153 | ||||||
| chr7:131381208
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 12 | HG01496.hp2 HG02615.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+5715A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381208 | ||||||
| chr7:131381433
|
T | C | 7 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-5687T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381433 | ||||||
| chr7:131381438
|
A | G | 2 | a0001c0002t0019g0309a0001c0002t0056g0308 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-5682A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381438 | ||||||
| chr7:131381482
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.169-5638C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381482 | ||||||
| chr7:131381841
|
A | G | 2 | a0001c0001t0036g0106a0001c0002t0054g0074 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.169-5279A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381841 | ||||||
| chr7:131381878
|
C | T | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.169-5242C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131381878 | ||||||
| chr7:131382010
|
C | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-5110C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382010 | ||||||
| chr7:131382011
|
C | T | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.169-5109C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382011 | ||||||
| chr7:131382232
|
G | A | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.169-4888G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382232 | ||||||
| chr7:131382234
|
T | G | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-4886T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382234 | ||||||
| chr7:131382369
|
C | CA | 4 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0141others(1): Show | 4 | HG01891.hp1 HG01978.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4751_169-4750i others(3): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382369 | ||||||
| chr7:131382370
|
C | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(312): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.169-4750C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382370 | ||||||
| chr7:131382714
|
A | ATATTT | 155 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(152): Show | 155 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.169-4383_169-4379d others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131382714 | |||||
| chr7:131382786
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-4334C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382786 | ||||||
| chr7:131382810
|
G | A | 1 | a0001c0001t0002g0245 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.169-4310G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382810 | ||||||
| chr7:131382815
|
A | G | 41 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.169-4305A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382815 | ||||||
| chr7:131382855
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.169-4265C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382855 | ||||||
| chr7:131382916
|
G | C | 14 | a0001c0001t0002g0048a0001c0001t0002g0216a0001c0001t0002g0281others(11): Show | 14 | HG00544.hp1 HG01934.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4204G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382916 | ||||||
| chr7:131382933
|
T | C | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.169-4187T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382933 | ||||||
| chr7:131382951
|
T | C | 176 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(173): Show | 176 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.169-4169T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131382951 | ||||||
| chr7:131383302
|
A | C | 1 | a0001c0001t0005g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.169-3818A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131383302 | ||||||
| chr7:131383403
|
A | G | 170 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(167): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.169-3717A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131383403 | ||||||
| chr7:131383671
|
A | G | 1 | a0001c0001t0002g0255 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.169-3449A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131383671 | ||||||
| chr7:131383847
|
G | A | 54 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(51): Show | 55 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.169-3273G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131383847 | ||||||
| chr7:131384153
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0028g0045a0001c0001t0049g0044 | 3 | HG02145.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.169-2967A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131384153 | ||||||
| chr7:131384236
|
A | G | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.169-2884A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131384236 | ||||||
| chr7:131384274
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.169-2846G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131384274 | ||||||
| chr7:131384336
|
G | T | 1 | a0001c0001t0003g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.169-2784G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131384336 | ||||||
| chr7:131384441
|
T | C | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.169-2679T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131384441 | ||||||
| chr7:131384702
|
T | A | 170 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(167): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.169-2418T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131384702 | ||||||
| chr7:131384774
|
A | G | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.169-2346A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131384774 | ||||||
| chr7:131385103
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169-2017G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385103 | ||||||
| chr7:131385109
|
G | A | 5 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-2011G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385109 | ||||||
| chr7:131385151
|
T | C | 1 | a0001c0001t0010g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.169-1969T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385151 | ||||||
| chr7:131385217
|
T | C | 1 | a0001c0001t0063g0238 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.169-1903T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385217 | ||||||
| chr7:131385343
|
CT | C | 7 | a0001c0001t0061g0162a0001c0001t0062g0161a0001c0002t0002g0075others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-1765delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131385343 | |||||
| chr7:131385445
|
T | G | 1 | a0001c0001t0004g0284 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.169-1675T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385445 | ||||||
| chr7:131385476
|
G | T | 2 | a0001c0001t0020g0226a0001c0001t0020g0227 | 2 | NA18995.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.169-1644G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385476 | ||||||
| chr7:131385731
|
G | T | 1 | a0001c0002t0019g0309 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.169-1389G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385731 | ||||||
| chr7:131385745
|
G | A | 1 | a0001c0001t0002g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.169-1375G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385745 | ||||||
| chr7:131385882
|
ATTTAT | A | 3 | a0001c0001t0003g0197a0001c0001t0003g0200a0001c0001t0007g0201 | 3 | NA18954.hp1 NA19072.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.169-1229_169-1225d others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131385882 | |||||
| chr7:131385914
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.169-1206A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385914 | ||||||
| chr7:131385928
|
G | A | 1 | a0001c0002t0019g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.169-1192G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131385928 | ||||||
| chr7:131386014
|
C | CT | 63 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(60): Show | 64 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.169-1089dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 131386014 | |||||
| chr7:131386064
|
A | T | 2 | a0001c0001t0002g0219a0001c0001t0002g0290 | 2 | HG00597.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.169-1056A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131386064 | ||||||
| chr7:131386715
|
G | A | 1 | a0001c0001t0032g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.169-405G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131386715 | ||||||
| chr7:131386799
|
G | C | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-321G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131386799 | ||||||
| chr7:131386942
|
G | A | 48 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.169-178G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131386942 | ||||||
| chr7:131387071
|
C | T | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.169-49C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 2/17 | chr7 | 131387071 | ||||||
| chr7:131387721
|
C | T | 48 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.311+459C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131387721 | ||||||
| chr7:131388035
|
C | T | 5 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01891.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.311+773C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388035 | ||||||
| chr7:131388047
|
G | A | 39 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.311+785G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388047 | ||||||
| chr7:131388140
|
T | G | 1 | a0001c0001t0002g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.312-744T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388140 | ||||||
| chr7:131388165
|
TCAAAAAC others(5): Show |
T | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.312-703_312-692del others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 131388165 | |||||
| chr7:131388222
|
CAT | C | 48 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.312-660_312-659del others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 131388222 | |||||
| chr7:131388340
|
T | A | 1 | a0001c0001t0003g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.312-544T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388340 | ||||||
| chr7:131388492
|
G | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-392G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388492 | ||||||
| chr7:131388559
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0132 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.312-325G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388559 | ||||||
| chr7:131388571
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.312-313A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388571 | ||||||
| chr7:131388672
|
C | A | 4 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.312-212C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388672 | ||||||
| chr7:131388731
|
A | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(25): Show | 28 | HG00544.hp2 HG00597.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.312-153A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 3/17 | chr7 | 131388731 | ||||||
| chr7:131389283
|
T | C | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.400+311T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131389283 | ||||||
| chr7:131389605
|
G | A | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.400+633G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131389605 | ||||||
| chr7:131389912
|
T | A | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.400+940T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131389912 | ||||||
| chr7:131390474
|
C | T | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+1502C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131390474 | ||||||
| chr7:131390669
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.400+1697C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131390669 | ||||||
| chr7:131390816
|
G | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+1844G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131390816 | ||||||
| chr7:131391017
|
C | T | 2 | a0001c0001t0002g0230a0001c0001t0002g0253 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.400+2045C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131391017 | ||||||
| chr7:131391291
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.400+2319A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131391291 | ||||||
| chr7:131391411
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.400+2439G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131391411 | ||||||
| chr7:131392106
|
G | A | 1 | a0001c0001t0002g0293 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.400+3134G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131392106 | ||||||
| chr7:131392164
|
C | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0132 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.400+3192C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131392164 | ||||||
| chr7:131392236
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.400+3264T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131392236 | ||||||
| chr7:131392250
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.400+3278T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131392250 | ||||||
| chr7:131392472
|
A | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(52): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.400+3500A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131392472 | ||||||
| chr7:131392602
|
C | CT | 8 | a0001c0001t0001g0039a0001c0003t0008g0079a0001c0003t0008g0082others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.400+3647dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131392602 | |||||
| chr7:131392833
|
G | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(52): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.400+3861G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131392833 | ||||||
| chr7:131392842
|
C | T | 5 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(2): Show | 5 | HG00738.hp1 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+3870C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131392842 | ||||||
| chr7:131393281
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.401-3986G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131393281 | ||||||
| chr7:131393611
|
TTTTTG | T | 15 | a0001c0001t0020g0227a0001c0002t0002g0075a0001c0002t0019g0081others(12): Show | 15 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.401-3631_401-3627d others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131393611 | |||||
| chr7:131393611
|
TTTTTGTT others(3): Show |
T | 1 | a0001c0001t0002g0252 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.401-3636_401-3627d others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131393611 | |||||
| chr7:131393700
|
C | T | 1 | a0001c0001t0026g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.401-3567C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131393700 | ||||||
| chr7:131393948
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.401-3319A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131393948 | ||||||
| chr7:131393971
|
ATTTTATG others(2107): Show |
A | 1 | a0001c0001t0002g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.401-3295_401-1182d others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131393971 | ||||||
| chr7:131394152
|
TA | T | 7 | a0001c0001t0003g0134a0001c0001t0006g0117a0001c0001t0006g0119others(4): Show | 7 | NA18963.hp1 NA18968.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-3106delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131394152 | |||||
| chr7:131394326
|
T | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01099.hp2 HG01891.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-2941T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131394326 | ||||||
| chr7:131394511
|
A | T | 1 | a0001c0001t0003g0032 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.401-2756A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131394511 | ||||||
| chr7:131394711
|
A | C | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-2556A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131394711 | ||||||
| chr7:131394777
|
A | G | 169 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(166): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.401-2490A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131394777 | ||||||
| chr7:131394967
|
T | G | 1 | a0001c0002t0002g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.401-2300T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131394967 | ||||||
| chr7:131395061
|
A | G | 1 | a0001c0003t0008g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.401-2206A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131395061 | ||||||
| chr7:131395090
|
TA | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | NA18950.hp2 NA18995.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-2176delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131395090 | ||||||
| chr7:131395288
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(305): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.401-1979A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131395288 | ||||||
| chr7:131395450
|
T | TTTTTA | 25 | a0001c0001t0002g0077a0001c0001t0002g0219a0001c0001t0002g0234others(22): Show | 25 | HG00408.hp2 HG00597.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.401-1771_401-1767d others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131395450 | |||||
| chr7:131395450
|
T | TTTTTATT others(3): Show |
66 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0078others(63): Show | 66 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.401-1776_401-1767d others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131395450 | |||||
| chr7:131395450
|
T | TTTTTATT others(8): Show |
16 | a0001c0001t0002g0245a0001c0001t0002g0249a0001c0001t0002g0250others(13): Show | 16 | HG01943.hp2 HG02155.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.401-1781_401-1767d others(17): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131395450 | |||||
| chr7:131395450
|
T | TTTTTATT others(13): Show |
1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.401-1786_401-1767d others(22): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131395450 | |||||
| chr7:131395450
|
TTTTTA | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.401-1771_401-1767d others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131395450 | |||||
| chr7:131395450
|
TTTTTATT others(3): Show |
T | 7 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0099others(4): Show | 7 | HG01496.hp1 HG01978.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-1776_401-1767d others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131395450 | |||||
| chr7:131395450
|
TTTTTATT others(8): Show |
T | 9 | a0001c0001t0003g0172a0001c0001t0003g0181a0001c0001t0003g0182others(6): Show | 9 | HG02559.hp1 HG02602.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.401-1781_401-1767d others(17): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131395450 | |||||
| chr7:131395537
|
T | G | 107 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(104): Show | 107 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.401-1730T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131395537 | ||||||
| chr7:131395551
|
A | G | 7 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-1716A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131395551 | ||||||
| chr7:131395609
|
C | T | 1 | a0001c0001t0061g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.401-1658C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131395609 | ||||||
| chr7:131395683
|
A | G | 1 | a0001c0001t0012g0278 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.401-1584A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131395683 | ||||||
| chr7:131395703
|
T | G | 1 | a0001c0001t0010g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.401-1564T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131395703 | ||||||
| chr7:131395938
|
ATTTTCAG others(1): Show |
A | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-1324_401-1317d others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 131395938 | |||||
| chr7:131396078
|
A | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01099.hp2 HG01891.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-1189A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131396078 | ||||||
| chr7:131396086
|
C | A | 1 | a0001c0001t0002g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.401-1181C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131396086 | ||||||
| chr7:131396087
|
C | G | 1 | a0001c0001t0002g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.401-1180C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131396087 | ||||||
| chr7:131396089
|
C | A | 1 | a0001c0001t0002g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.401-1178C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131396089 | ||||||
| chr7:131396091
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.401-1176G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131396091 | ||||||
| chr7:131396111
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.401-1156C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131396111 | ||||||
| chr7:131397140
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.401-127T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 4/17 | chr7 | 131397140 | ||||||
| chr7:131397655
|
T | C | 50 | a0001c0001t0001g0053a0001c0001t0003g0172a0001c0001t0003g0173others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.510+279T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | chr7 | 131397655 | ||||||
| chr7:131397843
|
C | T | 48 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.510+467C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | chr7 | 131397843 | ||||||
| chr7:131398081
|
A | G | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+705A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | chr7 | 131398081 | ||||||
| chr7:131398227
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | NA18969.hp1 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.510+851T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | chr7 | 131398227 | ||||||
| chr7:131398419
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.511-822C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | chr7 | 131398419 | ||||||
| chr7:131398702
|
GA | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0154others(6): Show | 9 | HG01169.hp1 HG01993.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-528delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 131398702 | |||||
| chr7:131398712
|
A | G | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.511-529A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | chr7 | 131398712 | ||||||
| chr7:131398787
|
T | C | 7 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-454T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | chr7 | 131398787 | ||||||
| chr7:131398953
|
A | C | 13 | a0001c0001t0002g0218a0001c0001t0002g0262a0001c0001t0002g0263others(10): Show | 13 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.511-288A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 5/17 | chr7 | 131398953 | ||||||
| chr7:131399748
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.703+315A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131399748 | ||||||
| chr7:131399779
|
G | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(11): Show | 14 | HG00544.hp2 HG00597.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+346G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131399779 | ||||||
| chr7:131400057
|
C | CT | 9 | a0001c0001t0001g0150a0001c0001t0003g0134a0001c0001t0004g0069others(6): Show | 9 | HG02145.hp1 HG04184.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.703+634dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400057 | |||||
| chr7:131400509
|
T | TA | 6 | a0001c0001t0003g0182a0001c0001t0003g0189a0001c0001t0006g0183others(3): Show | 6 | HG02055.hp2 HG02965.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+1086dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400509 | |||||
| chr7:131400516
|
A | AAT | 6 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0022g0165others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+1084_703+1085i others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400516 | |||||
| chr7:131400516
|
A | AATATATA others(3): Show |
1 | a0001c0001t0011g0070 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.703+1084_703+1085i others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400516 | |||||
| chr7:131400516
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0060 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.703+1084_703+1085i others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400516 | |||||
| chr7:131400516
|
A | T | 2 | a0001c0001t0005g0104a0001c0001t0034g0169 | 2 | HG01258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.703+1083A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400516 | ||||||
| chr7:131400518
|
A | AAAAATAT others(2): Show |
9 | a0001c0001t0001g0007a0001c0001t0004g0006a0001c0001t0004g0026others(6): Show | 9 | HG00597.hp1 NA18951.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.703+1086_703+1087i others(11): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400518
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0041 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.703+1086_703+1087i others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400518
|
A | AAATATAT | 11 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(8): Show | 11 | HG01099.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.703+1086_703+1087i others(9): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400518
|
A | AAATATAT others(2): Show |
18 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 19 | HG00423.hp2 HG00544.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.703+1086_703+1087i others(11): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400518
|
A | AAATATAT others(4): Show |
9 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0047others(6): Show | 9 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+1086_703+1087i others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400518
|
A | AAT | 21 | a0001c0001t0002g0229a0001c0001t0002g0239a0001c0001t0002g0242others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.703+1106_703+1107d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400518
|
A | AATATATA others(3): Show |
7 | a0001c0001t0001g0059a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1098_703+1107d others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400518
|
A | AATATATA others(9): Show |
2 | a0001c0001t0001g0046a0001c0001t0052g0034 | 2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.703+1092_703+1107d others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400518
|
A | ATATATAT others(2): Show |
8 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0023others(5): Show | 9 | HG00280.hp2 HG01106.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.703+1085_703+1086i others(11): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400518 | ||||||
| chr7:131400518
|
A | ATATATAT others(4): Show |
4 | a0001c0001t0001g0039a0001c0001t0017g0018a0001c0001t0017g0019others(1): Show | 4 | HG00642.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+1085_703+1086i others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400518 | ||||||
| chr7:131400518
|
A | T | 21 | a0001c0001t0001g0060a0001c0001t0001g0125a0001c0001t0002g0256others(18): Show | 21 | HG00280.hp1 HG01243.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.703+1085A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400518 | ||||||
| chr7:131400518
|
AAT | A | 9 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0011g0003others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+1106_703+1107d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131400518 | |||||
| chr7:131400520
|
T | A | 43 | a0001c0001t0001g0089a0001c0001t0002g0234a0001c0001t0002g0260others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.703+1087T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400520 | ||||||
| chr7:131400520
|
T | C | 4 | a0001c0001t0002g0292a0001c0001t0002g0294a0001c0001t0002g0295others(1): Show | 4 | HG02602.hp1 HG03490.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+1087T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400520 | ||||||
| chr7:131400522
|
T | A | 7 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0199others(4): Show | 7 | NA18954.hp1 NA18966.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1089T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400522 | ||||||
| chr7:131400524
|
T | A | 4 | a0001c0001t0003g0197a0001c0001t0003g0202a0001c0001t0003g0213others(1): Show | 4 | NA18966.hp1 NA18999.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+1091T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400524 | ||||||
| chr7:131400550
|
A | G | 1 | a0001c0001t0012g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.703+1117A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400550 | ||||||
| chr7:131400689
|
A | G | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703+1256A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400689 | ||||||
| chr7:131400726
|
T | C | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703+1293T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400726 | ||||||
| chr7:131400979
|
C | T | 1 | a0001c0001t0034g0169 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703+1546C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131400979 | ||||||
| chr7:131401071
|
G | A | 7 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1638G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131401071 | ||||||
| chr7:131401079
|
G | A | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.703+1646G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131401079 | ||||||
| chr7:131401286
|
T | C | 4 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0056g0308others(1): Show | 4 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+1853T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131401286 | ||||||
| chr7:131401336
|
A | G | 4 | a0001c0001t0007g0313a0001c0001t0007g0315a0001c0001t0007g0316others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+1903A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131401336 | ||||||
| chr7:131401443
|
T | A | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+2010T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131401443 | ||||||
| chr7:131401816
|
T | C | 4 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0056g0308others(1): Show | 4 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+2383T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131401816 | ||||||
| chr7:131402467
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.703+3034T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131402467 | ||||||
| chr7:131402474
|
C | A | 1 | a0001c0001t0001g0094 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.703+3041C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131402474 | ||||||
| chr7:131402491
|
G | T | 3 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0063g0238 | 3 | HG02071.hp2 NA18975.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.703+3058G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131402491 | ||||||
| chr7:131402586
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.703+3153A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131402586 | ||||||
| chr7:131402726
|
C | T | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00642.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.703+3293C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131402726 | ||||||
| chr7:131402733
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.703+3300G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131402733 | ||||||
| chr7:131402880
|
G | A | 3 | a0001c0001t0010g0167a0001c0001t0010g0168a0001c0001t0035g0163 | 3 | HG01261.hp2 HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.703+3447G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131402880 | ||||||
| chr7:131403288
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+3855T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131403288 | ||||||
| chr7:131403406
|
G | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+3973G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131403406 | ||||||
| chr7:131403488
|
T | A | 5 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+4055T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131403488 | ||||||
| chr7:131403644
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.703+4211A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131403644 | ||||||
| chr7:131403708
|
G | A | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.703+4275G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131403708 | ||||||
| chr7:131403870
|
TGA | T | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+4446_703+4447d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131403870 | |||||
| chr7:131403908
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.703+4475A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131403908 | ||||||
| chr7:131404225
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0098 | 2 | NA18965.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.703+4792T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404225 | ||||||
| chr7:131404498
|
G | A | 4 | a0001c0001t0002g0292a0001c0001t0002g0294a0001c0001t0002g0295others(1): Show | 4 | HG02602.hp1 HG03490.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+5065G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404498 | ||||||
| chr7:131404570
|
C | T | 5 | a0001c0001t0002g0245a0001c0001t0002g0256a0001c0001t0002g0261others(2): Show | 5 | HG02155.hp1 NA18942.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+5137C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404570 | ||||||
| chr7:131404634
|
T | G | 99 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(96): Show | 99 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.703+5201T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404634 | ||||||
| chr7:131404683
|
C | T | 9 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0198others(6): Show | 9 | HG02040.hp2 NA18954.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.703+5250C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404683 | ||||||
| chr7:131404693
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.703+5260C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404693 | ||||||
| chr7:131404744
|
A | G | 51 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(48): Show | 51 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.703+5311A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404744 | ||||||
| chr7:131404875
|
T | C | 1 | a0001c0001t0004g0284 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.703+5442T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404875 | ||||||
| chr7:131404884
|
G | A | 4 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212others(1): Show | 4 | HG02717.hp1 HG02886.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+5451G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131404884 | ||||||
| chr7:131404925
|
A | AAAAC | 9 | a0001c0001t0002g0307a0001c0001t0011g0003a0001c0001t0011g0070others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+5514_703+5517d others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131404925 | |||||
| chr7:131404925
|
A | AAAACAAA others(1): Show |
151 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(148): Show | 151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.703+5510_703+5517d others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131404925 | |||||
| chr7:131404925
|
A | AAAACAAA others(5): Show |
15 | a0001c0001t0002g0234a0001c0001t0002g0263a0001c0001t0003g0173others(12): Show | 15 | HG00738.hp1 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.703+5506_703+5517d others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131404925 | |||||
| chr7:131404925
|
A | AAAACAAA others(9): Show |
4 | a0001c0001t0018g0212a0001c0003t0008g0083a0001c0003t0008g0084others(1): Show | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+5502_703+5517d others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131404925 | |||||
| chr7:131405179
|
TTGCAGGA others(121): Show |
T | 4 | a0001c0001t0002g0230a0001c0001t0002g0250a0001c0001t0002g0253others(1): Show | 4 | HG03017.hp1 HG03139.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+5877_704-5869d others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131405179 | |||||
| chr7:131405285
|
A | G | 1 | a0001c0001t0003g0311 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.703+5852A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131405285 | ||||||
| chr7:131405593
|
A | G | 1 | a0001c0001t0025g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.704-5713A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131405593 | ||||||
| chr7:131405897
|
T | C | 4 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212others(1): Show | 4 | HG02717.hp1 HG02886.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-5409T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131405897 | ||||||
| chr7:131406015
|
T | G | 1 | a0001c0003t0030g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704-5291T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131406015 | ||||||
| chr7:131406031
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.704-5275G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131406031 | ||||||
| chr7:131406122
|
T | A | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.704-5184T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131406122 | ||||||
| chr7:131406233
|
C | G | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.704-5073C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131406233 | ||||||
| chr7:131406299
|
AATTTT | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-4998_704-4994d others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 131406299 | |||||
| chr7:131406540
|
A | G | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.704-4766A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131406540 | ||||||
| chr7:131406641
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.704-4665C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131406641 | ||||||
| chr7:131406702
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.704-4604C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131406702 | ||||||
| chr7:131406973
|
A | T | 7 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-4333A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131406973 | ||||||
| chr7:131407545
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-3761A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131407545 | ||||||
| chr7:131407650
|
C | A | 2 | a0001c0001t0010g0164a0001c0001t0034g0169 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.704-3656C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131407650 | ||||||
| chr7:131407675
|
C | T | 178 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(175): Show | 179 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.704-3631C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131407675 | ||||||
| chr7:131407886
|
G | A | 178 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(175): Show | 179 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.704-3420G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131407886 | ||||||
| chr7:131408006
|
T | C | 1 | a0001c0001t0035g0163 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.704-3300T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131408006 | ||||||
| chr7:131408012
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.704-3294G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131408012 | ||||||
| chr7:131408091
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.704-3215G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131408091 | ||||||
| chr7:131408335
|
T | C | 108 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(105): Show | 108 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.704-2971T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131408335 | ||||||
| chr7:131408605
|
G | A | 2 | a0001c0001t0002g0264a0001c0001t0014g0233 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.704-2701G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131408605 | ||||||
| chr7:131408697
|
A | G | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.704-2609A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131408697 | ||||||
| chr7:131409025
|
C | G | 1 | a0001c0002t0019g0309 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.704-2281C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131409025 | ||||||
| chr7:131409171
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-2135A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131409171 | ||||||
| chr7:131409799
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.704-1507A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131409799 | ||||||
| chr7:131409817
|
G | A | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.704-1489G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131409817 | ||||||
| chr7:131409920
|
T | G | 181 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(178): Show | 182 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.704-1386T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131409920 | ||||||
| chr7:131410549
|
A | G | 109 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(106): Show | 109 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.704-757A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131410549 | ||||||
| chr7:131410660
|
T | G | 1 | a0001c0001t0002g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.704-646T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131410660 | ||||||
| chr7:131411098
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-208A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131411098 | ||||||
| chr7:131411142
|
A | G | 11 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0124others(8): Show | 11 | HG00438.hp2 HG02523.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.704-164A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131411142 | ||||||
| chr7:131411261
|
T | G | 1 | a0001c0001t0002g0286 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.704-45T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 6/17 | chr7 | 131411261 | ||||||
| chr7:131411538
|
C | T | 1 | a0001c0001t0023g0222 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.781+155C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131411538 | ||||||
| chr7:131411539
|
G | A | 1 | a0001c0001t0013g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.781+156G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131411539 | ||||||
| chr7:131411597
|
A | AC | 181 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(178): Show | 182 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.781+216dupC | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411597 | |||||
| chr7:131411626
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.781+243G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131411626 | ||||||
| chr7:131411888
|
C | G | 7 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+505C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131411888 | ||||||
| chr7:131411906
|
C | A | 1 | a0001c0002t0045g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.781+523C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131411906 | ||||||
| chr7:131411906
|
C | CAAAA | 7 | a0001c0001t0002g0259a0001c0001t0002g0264a0001c0001t0003g0312others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+551_781+554dup others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0304others(7): Show | 10 | HG01261.hp1 HG01978.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.781+547_781+554dup others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(2): Show |
10 | a0001c0001t0002g0218a0001c0001t0002g0239a0001c0001t0002g0242others(7): Show | 10 | HG01261.hp2 HG01928.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.781+546_781+554dup others(9): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0048 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.781+545_781+554dup others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0260a0002c0004t0007g0314 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.781+543_781+554dup others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0007g0315a0001c0001t0007g0316 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.781+542_781+554dup others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0076a0001c0001t0015g0241a0001c0001t0064g0246 | 3 | HG02622.hp1 NA19012.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.781+541_781+554dup others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0249a0001c0001t0002g0300a0001c0001t0043g0037 | 3 | HG00140.hp2 NA18954.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.781+540_781+554dup others(15): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0002g0279a0001c0001t0002g0301a0001c0001t0012g0228others(1): Show | 4 | HG00408.hp2 HG01257.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+539_781+554dup others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(10): Show |
6 | a0001c0001t0002g0250a0001c0001t0002g0253a0001c0001t0002g0254others(3): Show | 6 | HG00423.hp1 HG02056.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+538_781+554dup others(17): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0002g0077a0001c0001t0002g0230a0001c0001t0002g0285 | 3 | HG01934.hp2 HG04184.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.781+537_781+554dup others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0002g0078a0001c0001t0002g0282 | 2 | HG00544.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.781+536_781+554dup others(19): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0002g0303a0001c0001t0023g0222a0001c0001t0038g0235 | 3 | HG02300.hp1 HG02523.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.781+535_781+554dup others(20): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0002g0271 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.781+534_781+554dup others(21): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0002g0216a0001c0001t0002g0257 | 2 | NA18964.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.781+533_781+554dup others(22): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0002g0036a0001c0001t0023g0223 | 2 | HG00423.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.781+532_781+554dup others(23): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0002g0272a0001c0001t0020g0227 | 2 | NA18982.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.781+530_781+554dup others(25): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(19): Show |
3 | a0001c0001t0002g0283a0001c0001t0002g0298a0001c0001t0020g0226 | 3 | HG02015.hp2 NA18989.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.781+529_781+554dup others(26): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0014g0240 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.781+528_781+554dup others(27): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0002g0248 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.781+527_781+554dup others(28): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0012g0278 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.781+524_781+554dup others(31): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0002g0256a0001c0001t0013g0231 | 2 | NA18960.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.781+554_781+555ins others(32): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0002g0261 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.781+554_781+555ins others(39): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CA | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0014others(63): Show | 67 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.781+554delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAA | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(49): Show | 54 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.781+553_781+554del others(2): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAA | C | 10 | a0001c0001t0002g0290a0001c0001t0003g0172a0001c0001t0003g0181others(7): Show | 10 | HG02559.hp1 HG02602.hp2 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.781+551_781+554del others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAAA | C | 34 | a0001c0001t0002g0229a0001c0001t0003g0173a0001c0001t0003g0174others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.781+550_781+554del others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAAAA | C | 11 | a0001c0001t0002g0234a0001c0001t0002g0252a0001c0001t0002g0276others(8): Show | 11 | HG02027.hp2 HG02129.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.781+549_781+554del others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAAAAA | C | 9 | a0001c0001t0002g0220a0001c0001t0002g0247a0001c0001t0002g0258others(6): Show | 9 | HG02135.hp2 HG02602.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+548_781+554del others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0002g0299a0001c0002t0019g0309a0001c0002t0056g0308 | 3 | HG01346.hp2 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.781+545_781+554del others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAAAAA others(6): Show |
C | 10 | a0001c0001t0002g0245a0001c0001t0002g0277a0001c0001t0014g0251others(7): Show | 10 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.781+542_781+554del others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0002t0019g0310a0001c0003t0008g0087 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.781+541_781+554del others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAAAAA others(8): Show |
C | 9 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.781+540_781+554del others(15): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411906
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.781+538_781+554del others(17): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131411906 | |||||
| chr7:131411937
|
A | T | 1 | a0001c0001t0040g0302 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.781+554A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131411937 | ||||||
| chr7:131411960
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.781+577A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131411960 | ||||||
| chr7:131411979
|
T | A | 108 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(105): Show | 108 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.781+596T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131411979 | ||||||
| chr7:131412011
|
TG | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.781+631delG | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 131412011 | |||||
| chr7:131412035
|
C | T | 2 | a0001c0002t0019g0309a0001c0002t0056g0308 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.781+652C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131412035 | ||||||
| chr7:131412221
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+838G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131412221 | ||||||
| chr7:131412326
|
T | C | 3 | a0001c0001t0002g0220a0001c0001t0002g0247a0001c0001t0002g0270 | 3 | HG02135.hp2 NA18955.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.781+943T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131412326 | ||||||
| chr7:131412375
|
A | G | 50 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.781+992A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131412375 | ||||||
| chr7:131412755
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.781+1372G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131412755 | ||||||
| chr7:131412811
|
C | T | 1 | a0001c0002t0002g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.781+1428C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131412811 | ||||||
| chr7:131412856
|
C | T | 1 | a0001c0001t0015g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.781+1473C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131412856 | ||||||
| chr7:131412985
|
A | G | 3 | a0001c0001t0009g0147a0001c0001t0009g0306a0001c0001t0016g0146 | 3 | HG01993.hp1 HG02129.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.781+1602A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131412985 | ||||||
| chr7:131413252
|
T | A | 1 | a0001c0001t0049g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.782-1393T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131413252 | ||||||
| chr7:131413253
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.782-1392G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131413253 | ||||||
| chr7:131413938
|
A | G | 1 | a0001c0001t0002g0257 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.782-707A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131413938 | ||||||
| chr7:131414048
|
C | A | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.782-597C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 7/17 | chr7 | 131414048 | ||||||
| chr7:131415042
|
T | A | 3 | a0001c0001t0005g0103a0001c0001t0005g0104a0001c0001t0005g0107 | 3 | HG00639.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.847+332T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131415042 | ||||||
| chr7:131415121
|
T | G | 1 | a0001c0002t0002g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.847+411T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131415121 | ||||||
| chr7:131415560
|
A | G | 50 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.847+850A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131415560 | ||||||
| chr7:131415567
|
C | T | 1 | a0001c0001t0002g0248 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.847+857C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131415567 | ||||||
| chr7:131415752
|
C | A | 1 | a0001c0001t0002g0280 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.847+1042C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131415752 | ||||||
| chr7:131415799
|
T | G | 1 | a0001c0001t0002g0265 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.847+1089T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131415799 | ||||||
| chr7:131415964
|
A | G | 1 | a0001c0001t0002g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.847+1254A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131415964 | ||||||
| chr7:131416146
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.847+1436C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131416146 | ||||||
| chr7:131416525
|
C | CT | 106 | a0001c0001t0001g0004a0001c0001t0001g0067a0001c0001t0001g0089others(103): Show | 108 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.847+1828dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131416525 | |||||
| chr7:131416667
|
T | TACC | 3 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | NA18969.hp1 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.847+1958_847+1960d others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131416667 | |||||
| chr7:131416808
|
C | G | 2 | a0001c0002t0019g0309a0001c0002t0056g0308 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.847+2098C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131416808 | ||||||
| chr7:131416818
|
A | G | 1 | a0001c0001t0003g0312 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.847+2108A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131416818 | ||||||
| chr7:131416876
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.847+2166G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131416876 | ||||||
| chr7:131416979
|
C | CA | 29 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0040others(26): Show | 29 | HG00280.hp2 HG01346.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.847+2293dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131416979 | |||||
| chr7:131416979
|
C | CAA | 38 | a0001c0001t0002g0076a0001c0001t0002g0282a0001c0001t0003g0172others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.847+2292_847+2293d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131416979 | |||||
| chr7:131416979
|
C | CAAA | 7 | a0001c0001t0003g0175a0001c0001t0003g0182a0001c0001t0003g0184others(4): Show | 7 | HG00738.hp1 HG02056.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+2291_847+2293d others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131416979 | |||||
| chr7:131416979
|
CA | C | 14 | a0001c0001t0001g0115a0001c0001t0002g0294a0001c0001t0003g0134others(11): Show | 14 | HG01169.hp1 HG01169.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.847+2293delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131416979 | |||||
| chr7:131416979
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.847+2283_847+2293d others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131416979 | |||||
| chr7:131417103
|
C | T | 2 | a0001c0001t0003g0194a0001c0001t0051g0186 | 2 | NA19068.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.847+2393C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131417103 | ||||||
| chr7:131417190
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 19 | HG01099.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.847+2480G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131417190 | ||||||
| chr7:131417446
|
C | A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+2736C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131417446 | ||||||
| chr7:131417467
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.847+2757C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131417467 | ||||||
| chr7:131417547
|
C | T | 1 | a0001c0001t0013g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.847+2837C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131417547 | ||||||
| chr7:131417596
|
T | C | 10 | a0001c0001t0001g0125a0001c0001t0001g0150a0001c0001t0003g0134others(7): Show | 10 | HG00280.hp1 HG02145.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.847+2886T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131417596 | ||||||
| chr7:131417671
|
G | A | 1 | a0001c0001t0052g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.847+2961G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131417671 | ||||||
| chr7:131417822
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.847+3112T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131417822 | ||||||
| chr7:131418049
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.847+3339C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131418049 | ||||||
| chr7:131418134
|
C | T | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.847+3424C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131418134 | ||||||
| chr7:131418261
|
C | T | 1 | a0001c0003t0008g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.847+3551C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131418261 | ||||||
| chr7:131418300
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.847+3590C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131418300 | ||||||
| chr7:131418369
|
C | CA | 20 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0060others(17): Show | 21 | HG00438.hp1 HG01261.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.847+3682dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131418369 | |||||
| chr7:131418369
|
CA | C | 16 | a0001c0001t0001g0126a0001c0001t0002g0279a0001c0001t0002g0301others(13): Show | 16 | HG01257.hp1 HG01884.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.847+3682delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131418369 | |||||
| chr7:131418571
|
A | G | 1 | a0001c0001t0013g0231 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.847+3861A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131418571 | ||||||
| chr7:131418715
|
G | A | 5 | a0001c0001t0002g0218a0001c0001t0002g0263a0001c0001t0002g0266others(2): Show | 5 | HG00741.hp2 HG01261.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.847+4005G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131418715 | ||||||
| chr7:131418799
|
G | GGT | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.847+4090_847+4091d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131418799 | |||||
| chr7:131418961
|
C | T | 3 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071 | 4 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.847+4251C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131418961 | ||||||
| chr7:131419169
|
G | A | 1 | a0001c0001t0009g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.847+4459G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131419169 | ||||||
| chr7:131419228
|
G | GTA | 8 | a0001c0001t0001g0105a0001c0001t0003g0181a0001c0001t0003g0182others(5): Show | 8 | HG02300.hp1 HG02602.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+4536_847+4537d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131419228 | |||||
| chr7:131419228
|
G | GTATA | 3 | a0001c0001t0001g0094a0001c0001t0059g0042a0001c0002t0054g0074 | 3 | HG02027.hp1 HG02258.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.847+4534_847+4537d others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131419228 | |||||
| chr7:131419246
|
A | T | 8 | a0001c0001t0002g0280a0001c0001t0003g0311a0001c0001t0003g0312others(5): Show | 8 | HG01891.hp1 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.847+4536A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131419246 | ||||||
| chr7:131419252
|
G | GT | 50 | a0001c0001t0001g0040a0001c0001t0001g0063a0001c0001t0001g0111others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.847+4558dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131419252 | |||||
| chr7:131419252
|
G | GTT | 83 | a0001c0001t0002g0218a0001c0001t0002g0220a0001c0001t0002g0221others(80): Show | 84 | HG00140.hp2 HG00423.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.847+4557_847+4558d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131419252 | |||||
| chr7:131419252
|
G | GTTT | 24 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0216others(21): Show | 24 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.847+4556_847+4558d others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131419252 | |||||
| chr7:131419252
|
G | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0053g0072 | 3 | HG00280.hp2 HG01106.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.847+4542G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131419252 | ||||||
| chr7:131419258
|
T | G | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.847+4548T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131419258 | ||||||
| chr7:131419317
|
C | T | 3 | a0001c0001t0005g0103a0001c0001t0005g0104a0001c0001t0005g0107 | 3 | HG00639.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.847+4607C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131419317 | ||||||
| chr7:131419399
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.847+4689C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131419399 | ||||||
| chr7:131419793
|
G | A | 159 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(156): Show | 160 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.847+5083G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131419793 | ||||||
| chr7:131419819
|
G | A | 2 | a0001c0001t0021g0179a0001c0001t0021g0180 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.847+5109G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131419819 | ||||||
| chr7:131420322
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.847+5612G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131420322 | ||||||
| chr7:131420609
|
T | C | 9 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+5899T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131420609 | ||||||
| chr7:131420671
|
T | C | 1 | a0001c0001t0002g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.847+5961T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131420671 | ||||||
| chr7:131420931
|
C | T | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.847+6221C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131420931 | ||||||
| chr7:131421507
|
C | T | 1 | a0001c0001t0002g0267 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.847+6797C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131421507 | ||||||
| chr7:131421638
|
A | T | 1 | a0001c0001t0002g0272 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.847+6928A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131421638 | ||||||
| chr7:131421665
|
GATTA | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02615.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.847+6960_847+6963d others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131421665 | |||||
| chr7:131421736
|
C | G | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.847+7026C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131421736 | ||||||
| chr7:131421836
|
A | G | 1 | a0001c0001t0004g0069 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.847+7126A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131421836 | ||||||
| chr7:131421871
|
G | C | 4 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+7161G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131421871 | ||||||
| chr7:131421896
|
A | C | 1 | a0001c0001t0010g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.848-7137A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131421896 | ||||||
| chr7:131422063
|
C | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(311): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.848-6970C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131422063 | ||||||
| chr7:131422169
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.848-6864G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131422169 | ||||||
| chr7:131422345
|
C | T | 8 | a0001c0001t0002g0218a0001c0001t0002g0263a0001c0001t0002g0266others(5): Show | 9 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.848-6688C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131422345 | ||||||
| chr7:131422460
|
A | AGGAGGAT others(18): Show |
1 | a0001c0001t0002g0285 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.848-6572_848-6548d others(27): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131422460 | |||||
| chr7:131422572
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.848-6461A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131422572 | ||||||
| chr7:131422739
|
G | T | 7 | a0001c0001t0003g0134a0001c0001t0006g0117a0001c0001t0006g0119others(4): Show | 7 | NA18963.hp1 NA18968.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-6294G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131422739 | ||||||
| chr7:131422766
|
C | G | 3 | a0001c0001t0010g0167a0001c0001t0010g0168a0001c0001t0035g0163 | 3 | HG01261.hp2 HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.848-6267C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131422766 | ||||||
| chr7:131423421
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.848-5612G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131423421 | ||||||
| chr7:131423680
|
A | G | 2 | a0001c0002t0002g0075a0001c0002t0019g0081 | 2 | HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.848-5353A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131423680 | ||||||
| chr7:131424053
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.848-4980A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131424053 | ||||||
| chr7:131424188
|
TTAAAGA | T | 6 | a0001c0001t0025g0156a0001c0001t0025g0157a0001c0001t0026g0073others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-4840_848-4835d others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131424188 | |||||
| chr7:131424330
|
G | A | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.848-4703G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131424330 | ||||||
| chr7:131424587
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.848-4446A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131424587 | ||||||
| chr7:131424609
|
ACTG | A | 7 | a0001c0001t0003g0134a0001c0001t0006g0117a0001c0001t0006g0119others(4): Show | 7 | NA18963.hp1 NA18968.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-4423_848-4421d others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131424609 | ||||||
| chr7:131424652
|
A | C | 1 | a0001c0001t0004g0035 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.848-4381A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131424652 | ||||||
| chr7:131424837
|
T | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(53): Show | 57 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.848-4196T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131424837 | ||||||
| chr7:131424920
|
G | A | 1 | a0001c0001t0005g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.848-4113G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131424920 | ||||||
| chr7:131424930
|
T | C | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.848-4103T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131424930 | ||||||
| chr7:131425130
|
C | A | 2 | a0001c0001t0005g0114a0001c0001t0005g0121 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.848-3903C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131425130 | ||||||
| chr7:131425236
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.848-3797C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131425236 | ||||||
| chr7:131425292
|
C | CT | 55 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(52): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.848-3731dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131425292 | |||||
| chr7:131426198
|
C | T | 3 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0063g0238 | 3 | HG02071.hp2 NA18975.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.848-2835C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131426198 | ||||||
| chr7:131426264
|
A | G | 1 | a0001c0002t0019g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.848-2769A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131426264 | ||||||
| chr7:131426350
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(40): Show | 44 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.848-2683T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131426350 | ||||||
| chr7:131426556
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.848-2477T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131426556 | ||||||
| chr7:131426761
|
CT | C | 50 | a0001c0001t0002g0261a0001c0001t0003g0032a0001c0001t0003g0172others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.848-2260delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 131426761 | |||||
| chr7:131426891
|
A | G | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.848-2142A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131426891 | ||||||
| chr7:131426971
|
T | G | 1 | a0001c0001t0003g0198 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.848-2062T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131426971 | ||||||
| chr7:131427184
|
C | T | 8 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0199others(5): Show | 8 | NA18954.hp1 NA18957.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-1849C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131427184 | ||||||
| chr7:131427442
|
C | T | 1 | a0001c0003t0030g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.848-1591C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131427442 | ||||||
| chr7:131427700
|
C | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-1333C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131427700 | ||||||
| chr7:131427780
|
A | G | 1 | a0001c0001t0009g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.848-1253A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131427780 | ||||||
| chr7:131427861
|
C | CA | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(312): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.848-1172_848-1171i others(3): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131427861 | ||||||
| chr7:131428005
|
C | G | 6 | a0001c0001t0025g0156a0001c0001t0025g0157a0001c0001t0026g0073others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-1028C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131428005 | ||||||
| chr7:131428013
|
C | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0055 | 3 | HG01496.hp2 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.848-1020C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131428013 | ||||||
| chr7:131428014
|
A | C | 1 | a0001c0001t0064g0246 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.848-1019A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131428014 | ||||||
| chr7:131428279
|
C | G | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.848-754C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131428279 | ||||||
| chr7:131428302
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.848-731G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131428302 | ||||||
| chr7:131428304
|
G | T | 1 | a0001c0001t0002g0298 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.848-729G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131428304 | ||||||
| chr7:131428706
|
G | A | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.848-327G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131428706 | ||||||
| chr7:131428827
|
A | G | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-206A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131428827 | ||||||
| chr7:131429000
|
T | TA | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-33_848-32insA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 8/17 | chr7 | 131429000 | ||||||
| chr7:131429195
|
G | T | 6 | a0001c0001t0025g0156a0001c0001t0025g0157a0001c0001t0026g0073others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+50G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429195 | ||||||
| chr7:131429210
|
G | A | 2 | a0001c0001t0023g0222a0001c0001t0023g0223 | 2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.960+65G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429210 | ||||||
| chr7:131429429
|
G | A | 7 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+284G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429429 | ||||||
| chr7:131429615
|
A | G | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+470A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429615 | ||||||
| chr7:131429672
|
A | G | 13 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(10): Show | 13 | HG00544.hp2 HG00597.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.960+527A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429672 | ||||||
| chr7:131429727
|
C | T | 1 | a0001c0001t0009g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.960+582C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429727 | ||||||
| chr7:131429735
|
C | T | 1 | a0001c0001t0012g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.960+590C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429735 | ||||||
| chr7:131429802
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.960+657G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429802 | ||||||
| chr7:131429860
|
G | T | 3 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212 | 3 | HG02717.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.960+715G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429860 | ||||||
| chr7:131429914
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.960+769G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131429914 | ||||||
| chr7:131430233
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.960+1088G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430233 | ||||||
| chr7:131430415
|
T | C | 1 | a0001c0001t0003g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.960+1270T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430415 | ||||||
| chr7:131430471
|
A | C | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.960+1326A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430471 | ||||||
| chr7:131430471
|
A | G | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.960+1326A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430471 | ||||||
| chr7:131430620
|
C | T | 1 | a0001c0001t0007g0313 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.960+1475C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430620 | ||||||
| chr7:131430715
|
G | A | 7 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+1570G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430715 | ||||||
| chr7:131430807
|
A | T | 1 | a0001c0001t0026g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.960+1662A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430807 | ||||||
| chr7:131430867
|
G | A | 5 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(2): Show | 5 | HG00738.hp1 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+1722G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430867 | ||||||
| chr7:131430988
|
G | A | 1 | a0001c0001t0004g0069 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.960+1843G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131430988 | ||||||
| chr7:131431128
|
A | G | 1 | a0001c0001t0009g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.960+1983A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131431128 | ||||||
| chr7:131431157
|
G | A | 2 | a0001c0001t0015g0273a0001c0001t0015g0274 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.960+2012G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131431157 | ||||||
| chr7:131431231
|
C | CA | 43 | a0001c0001t0001g0009a0001c0001t0003g0134a0001c0001t0003g0172others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.960+2095dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 131431231 | |||||
| chr7:131431277
|
C | T | 1 | a0001c0001t0061g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.960+2132C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131431277 | ||||||
| chr7:131431611
|
T | C | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.960+2466T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131431611 | ||||||
| chr7:131431675
|
T | C | 103 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(100): Show | 104 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.960+2530T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131431675 | ||||||
| chr7:131432171
|
CTCTTTAG others(7): Show |
C | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.960+3027_960+3040d others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131432171 | ||||||
| chr7:131432233
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.960+3088C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131432233 | ||||||
| chr7:131432348
|
A | G | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.960+3203A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131432348 | ||||||
| chr7:131432867
|
A | G | 1 | a0001c0002t0019g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.960+3722A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131432867 | ||||||
| chr7:131433157
|
T | A | 9 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.960+4012T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433157 | ||||||
| chr7:131433158
|
T | A | 9 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.960+4013T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433158 | ||||||
| chr7:131433239
|
A | G | 1 | a0001c0001t0003g0199 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.960+4094A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433239 | ||||||
| chr7:131433292
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.960+4147A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433292 | ||||||
| chr7:131433483
|
T | TG | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.961-4302_961-4301i others(3): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433483 | ||||||
| chr7:131433484
|
T | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.961-4301T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433484 | ||||||
| chr7:131433882
|
AT | A | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(307): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.961-3885delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 131433882 | |||||
| chr7:131433947
|
G | A | 1 | a0001c0001t0009g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.961-3838G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433947 | ||||||
| chr7:131433959
|
C | T | 1 | a0001c0001t0010g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.961-3826C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433959 | ||||||
| chr7:131433985
|
G | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | NA18947.hp1 NA18965.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-3800G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131433985 | ||||||
| chr7:131434105
|
C | T | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.961-3680C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131434105 | ||||||
| chr7:131434304
|
A | G | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.961-3481A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131434304 | ||||||
| chr7:131434379
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.961-3406T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131434379 | ||||||
| chr7:131434529
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.961-3256T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131434529 | ||||||
| chr7:131434704
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0005g0114a0001c0001t0005g0120others(1): Show | 4 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-3081C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131434704 | ||||||
| chr7:131435119
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(40): Show | 44 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.961-2666T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131435119 | ||||||
| chr7:131435303
|
C | G | 2 | a0001c0001t0002g0239a0001c0001t0002g0289 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.961-2482C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131435303 | ||||||
| chr7:131435417
|
A | C | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00642.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.961-2368A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131435417 | ||||||
| chr7:131435494
|
A | G | 1 | a0001c0001t0002g0290 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.961-2291A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131435494 | ||||||
| chr7:131435543
|
A | C | 2 | a0001c0001t0002g0272a0001c0001t0002g0291 | 2 | HG02056.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.961-2242A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131435543 | ||||||
| chr7:131435634
|
T | G | 1 | a0001c0001t0025g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.961-2151T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131435634 | ||||||
| chr7:131435693
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.961-2092A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131435693 | ||||||
| chr7:131436212
|
C | T | 95 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.961-1573C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131436212 | ||||||
| chr7:131436218
|
T | C | 1 | a0001c0001t0012g0278 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.961-1567T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131436218 | ||||||
| chr7:131436362
|
A | C | 1 | a0001c0001t0027g0043 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.961-1423A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131436362 | ||||||
| chr7:131436399
|
T | C | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.961-1386T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131436399 | ||||||
| chr7:131436529
|
G | C | 1 | a0001c0001t0002g0303 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.961-1256G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131436529 | ||||||
| chr7:131436752
|
T | C | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-1033T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131436752 | ||||||
| chr7:131436830
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.961-955A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131436830 | ||||||
| chr7:131436977
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.961-808C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131436977 | ||||||
| chr7:131437008
|
T | C | 1 | a0001c0001t0041g0224 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.961-777T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131437008 | ||||||
| chr7:131437049
|
GA | G | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-732delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 131437049 | |||||
| chr7:131437064
|
T | A | 2 | a0001c0001t0001g0092a0001c0001t0047g0091 | 2 | NA18944.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.961-721T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131437064 | ||||||
| chr7:131437106
|
G | A | 1 | a0001c0001t0065g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.961-679G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131437106 | ||||||
| chr7:131437204
|
C | G | 1 | a0001c0001t0002g0250 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.961-581C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131437204 | ||||||
| chr7:131437217
|
C | G | 1 | a0001c0001t0047g0091 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.961-568C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131437217 | ||||||
| chr7:131437274
|
T | C | 1 | a0001c0001t0026g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.961-511T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131437274 | ||||||
| chr7:131437278
|
A | G | 4 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0056g0308others(1): Show | 4 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-507A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 9/17 | chr7 | 131437278 | ||||||
| chr7:131438157
|
T | C | 1 | a0001c0001t0040g0302 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1173+160T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131438157 | ||||||
| chr7:131438158
|
C | T | 1 | a0001c0001t0040g0302 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1173+161C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131438158 | ||||||
| chr7:131438570
|
A | C | 9 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+573A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131438570 | ||||||
| chr7:131439065
|
G | T | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1173+1068G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131439065 | ||||||
| chr7:131439363
|
T | C | 1 | a0001c0002t0045g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1173+1366T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131439363 | ||||||
| chr7:131439420
|
C | G | 1 | a0001c0001t0032g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1173+1423C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131439420 | ||||||
| chr7:131439710
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1173+1713G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131439710 | ||||||
| chr7:131439787
|
C | T | 1 | a0001c0001t0053g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1173+1790C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131439787 | ||||||
| chr7:131439863
|
TAAACACA others(7): Show |
T | 1 | a0001c0001t0021g0180 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1173+1868_1173+188 others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439863 | |||||
| chr7:131439863
|
TAAACACA others(10): Show |
T | 1 | a0001c0001t0006g0193 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1173+1867_1173+188 others(21): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131439863 | ||||||
| chr7:131439864
|
AAACACAC others(10): Show |
A | 2 | a0001c0001t0001g0099a0001c0001t0006g0135 | 2 | NA18947.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1173+1869_1173+188 others(21): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439864 | |||||
| chr7:131439865
|
AACACACA others(1): Show |
A | 3 | a0001c0001t0025g0156a0001c0001t0025g0157a0001c0001t0026g0159 | 3 | HG02258.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1173+1914_1173+192 others(12): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(3): Show |
A | 9 | a0001c0001t0005g0101a0001c0001t0005g0102a0001c0001t0005g0103others(6): Show | 9 | HG00639.hp2 HG00642.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+1912_1173+192 others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(5): Show |
A | 16 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0123others(13): Show | 16 | HG00280.hp1 HG01169.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1173+1910_1173+192 others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(7): Show |
A | 5 | a0001c0001t0001g0068a0001c0001t0001g0126a0001c0001t0042g0118others(2): Show | 5 | HG01891.hp2 HG01978.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+1908_1173+192 others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(9): Show |
A | 61 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0057others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1173+1906_1173+192 others(20): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(11): Show |
A | 121 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0054others(118): Show | 123 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1173+1904_1173+192 others(22): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(13): Show |
A | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(76): Show | 80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1173+1902_1173+192 others(24): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(15): Show |
A | 7 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0002t0002g0075others(4): Show | 7 | HG00639.hp1 HG02071.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+1900_1173+192 others(26): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(17): Show |
A | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+1898_1173+192 others(28): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131439865
|
AACACACA others(19): Show |
A | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1173+1896_1173+192 others(30): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131439865 | |||||
| chr7:131440173
|
T | G | 16 | a0001c0001t0001g0056a0001c0002t0002g0075a0001c0002t0019g0081others(13): Show | 16 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1173+2176T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131440173 | ||||||
| chr7:131440312
|
G | C | 1 | a0001c0001t0002g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1173+2315G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131440312 | ||||||
| chr7:131440530
|
A | G | 5 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(2): Show | 5 | HG00738.hp1 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+2533A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131440530 | ||||||
| chr7:131440659
|
G | A | 2 | a0001c0001t0003g0174a0001c0001t0003g0175 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1173+2662G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131440659 | ||||||
| chr7:131440715
|
C | CAT | 161 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(158): Show | 162 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1173+2730_1173+273 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 131440715 | |||||
| chr7:131441001
|
A | G | 1 | a0001c0001t0005g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1174-2480A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131441001 | ||||||
| chr7:131441014
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1174-2467A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131441014 | ||||||
| chr7:131441461
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1174-2020A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131441461 | ||||||
| chr7:131441477
|
A | G | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1174-2004A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131441477 | ||||||
| chr7:131441618
|
G | A | 1 | a0001c0001t0006g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1174-1863G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131441618 | ||||||
| chr7:131441685
|
G | T | 3 | a0001c0003t0008g0082a0001c0003t0008g0083a0001c0003t0008g0084 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1174-1796G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131441685 | ||||||
| chr7:131441772
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(63): Show | 68 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1174-1709G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131441772 | ||||||
| chr7:131441966
|
G | A | 1 | a0001c0001t0002g0303 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1174-1515G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131441966 | ||||||
| chr7:131442133
|
T | A | 1 | a0001c0001t0003g0200 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1174-1348T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131442133 | ||||||
| chr7:131442414
|
G | T | 1 | a0001c0001t0032g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1174-1067G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131442414 | ||||||
| chr7:131442479
|
A | G | 1 | a0001c0001t0023g0223 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1174-1002A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131442479 | ||||||
| chr7:131442524
|
G | A | 1 | a0001c0002t0019g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1174-957G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131442524 | ||||||
| chr7:131442763
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1174-718A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131442763 | ||||||
| chr7:131442906
|
A | G | 3 | a0001c0001t0005g0103a0001c0001t0005g0104a0001c0001t0005g0107 | 3 | HG00639.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1174-575A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131442906 | ||||||
| chr7:131443151
|
G | C | 9 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-330G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131443151 | ||||||
| chr7:131443187
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1174-294T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 10/17 | chr7 | 131443187 | ||||||
| chr7:131443724
|
C | T | 1 | a0001c0001t0036g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1395+22C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131443724 | ||||||
| chr7:131443873
|
C | T | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1395+171C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131443873 | ||||||
| chr7:131444108
|
C | G | 1 | a0001c0003t0008g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1395+406C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444108 | ||||||
| chr7:131444138
|
C | A | 4 | a0001c0001t0002g0292a0001c0001t0002g0294a0001c0001t0002g0295others(1): Show | 4 | HG02602.hp1 HG03490.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+436C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444138 | ||||||
| chr7:131444183
|
C | G | 7 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395+481C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444183 | ||||||
| chr7:131444378
|
C | T | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1395+676C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444378 | ||||||
| chr7:131444495
|
G | T | 1 | a0001c0001t0036g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1395+793G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444495 | ||||||
| chr7:131444546
|
A | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | NA18969.hp1 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1395+844A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444546 | ||||||
| chr7:131444600
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1395+898C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444600 | ||||||
| chr7:131444718
|
G | GAGT | 5 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0005g0114others(2): Show | 5 | HG00280.hp1 HG01106.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-1017_1396-101 others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444718 | |||||
| chr7:131444718
|
GAGT | G | 7 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0004g0027others(4): Show | 7 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-1017_1396-101 others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444718 | |||||
| chr7:131444718
|
GAGTAGT | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0067a0001c0001t0001g0068others(7): Show | 10 | HG01099.hp2 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1396-1020_1396-101 others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444718 | |||||
| chr7:131444718
|
GAGTAGTA others(2): Show |
G | 14 | a0001c0001t0002g0216a0001c0001t0002g0230a0001c0001t0002g0253others(11): Show | 14 | HG01074.hp1 HG01261.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396-1023_1396-101 others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444718 | |||||
| chr7:131444718
|
GAGTAGTA others(5): Show |
G | 67 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0220others(64): Show | 68 | HG00408.hp1 HG01074.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.1396-1026_1396-101 others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444718 | |||||
| chr7:131444718
|
GAGTAGTA others(8): Show |
G | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1396-1029_1396-101 others(19): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444718 | |||||
| chr7:131444727
|
TAGTAGTA others(29): Show |
T | 1 | a0001c0001t0044g0215 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1396-1014_1396-979 others(39): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444727 | |||||
| chr7:131444733
|
TAGTAGTA others(23): Show |
T | 5 | a0001c0001t0002g0304a0001c0001t0010g0167a0001c0001t0010g0168others(2): Show | 5 | HG00639.hp1 HG01261.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-1014_1396-985 others(33): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444733 | |||||
| chr7:131444736
|
TAGTAGTA others(20): Show |
T | 4 | a0001c0001t0002g0279a0001c0002t0019g0309a0001c0002t0019g0310others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1014_1396-988 others(30): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444736 | |||||
| chr7:131444739
|
TAGTAGTA others(17): Show |
T | 3 | a0001c0001t0002g0259a0001c0001t0002g0296a0001c0001t0015g0274 | 3 | HG02109.hp1 HG03834.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1396-1014_1396-991 others(27): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444739 | |||||
| chr7:131444742
|
TAGTAGTA others(11): Show |
T | 5 | a0001c0001t0010g0164a0001c0001t0010g0171a0001c0001t0022g0165others(2): Show | 5 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-1029_1396-101 others(22): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444742 | |||||
| chr7:131444745
|
T | A | 1 | a0001c0001t0002g0249 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1396-1029T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444745 | ||||||
| chr7:131444745
|
TAGTAGTA others(8): Show |
T | 57 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0218others(54): Show | 57 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1396-1026_1396-101 others(19): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444745 | |||||
| chr7:131444745
|
TAGTAGTA others(11): Show |
T | 12 | a0001c0001t0002g0254a0001c0001t0002g0271a0001c0001t0002g0275others(9): Show | 12 | HG00423.hp1 HG01884.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1396-1014_1396-997 others(21): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444745 | |||||
| chr7:131444748
|
T | A | 3 | a0001c0001t0002g0249a0001c0001t0007g0315a0001c0001t0007g0316 | 3 | HG02976.hp2 NA18522.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1396-1026T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444748 | ||||||
| chr7:131444751
|
T | A | 2 | a0001c0001t0007g0315a0001c0001t0007g0316 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1396-1023T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444751 | ||||||
| chr7:131444751
|
TAGTAGTA others(2): Show |
T | 4 | a0001c0001t0009g0147a0001c0001t0016g0146a0001c0001t0026g0159others(1): Show | 4 | HG02129.hp1 HG02258.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-1020_1396-101 others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444751 | |||||
| chr7:131444754
|
TAGTAGA | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(29): Show | 33 | HG00280.hp2 HG00423.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.1396-1017_1396-101 others(10): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444754 | |||||
| chr7:131444757
|
T | A | 40 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0015others(37): Show | 40 | HG00544.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1396-1017T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444757 | ||||||
| chr7:131444757
|
TAGA | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0130a0001c0001t0007g0315 | 3 | HG01943.hp1 NA18522.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1396-1011_1396-100 others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444757 | |||||
| chr7:131444760
|
A | T | 9 | a0001c0001t0001g0057a0001c0001t0001g0122a0001c0001t0001g0125others(6): Show | 9 | HG00140.hp1 HG00280.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396-1014A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444760 | ||||||
| chr7:131444760
|
AAGAAGTA others(2): Show |
A | 17 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0015others(14): Show | 17 | HG00544.hp2 HG00597.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1396-1011_1396-100 others(13): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444760 | |||||
| chr7:131444760
|
AAGAAGTA others(5): Show |
A | 3 | a0001c0001t0005g0104a0001c0001t0005g0107a0001c0001t0006g0137 | 3 | HG01257.hp2 HG01258.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1396-1011_1396-100 others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444760 | |||||
| chr7:131444760
|
AAGAAGTA others(8): Show |
A | 1 | a0001c0001t0005g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1396-1011_1396-997 others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444760 | |||||
| chr7:131444763
|
A | T | 28 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0097others(25): Show | 28 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1396-1011A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444763 | ||||||
| chr7:131444763
|
AAGT | A | 12 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0089others(9): Show | 12 | HG01433.hp1 HG02145.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-954_1396-952d others(5): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444763 | |||||
| chr7:131444763
|
AAGTAGT | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0056a0001c0001t0001g0067others(50): Show | 53 | HG00408.hp1 HG00438.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1396-957_1396-952d others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444763 | |||||
| chr7:131444763
|
AAGTAGTA others(2): Show |
A | 20 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0090others(17): Show | 21 | HG01516.hp1 HG01516.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.1396-960_1396-952d others(11): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444763 | |||||
| chr7:131444763
|
AAGTAGTA others(5): Show |
A | 1 | a0001c0001t0026g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1396-963_1396-952d others(14): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131444763 | |||||
| chr7:131444766
|
T | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1396-1008T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444766 | ||||||
| chr7:131444769
|
T | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0122a0001c0001t0001g0130others(1): Show | 4 | HG00140.hp1 HG01943.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1005T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444769 | ||||||
| chr7:131444772
|
T | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0130a0001c0001t0002g0259others(3): Show | 6 | HG01943.hp1 HG01978.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396-1002T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444772 | ||||||
| chr7:131444775
|
T | A | 12 | a0001c0001t0001g0111a0001c0001t0002g0259a0001c0001t0002g0279others(9): Show | 12 | HG01261.hp2 HG01978.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-999T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444775 | ||||||
| chr7:131444778
|
T | A | 9 | a0001c0001t0002g0279a0001c0001t0002g0304a0001c0001t0010g0167others(6): Show | 9 | HG00639.hp1 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-996T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444778 | ||||||
| chr7:131444781
|
T | A | 2 | a0001c0001t0002g0304a0001c0002t0058g0080 | 2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1396-993T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444781 | ||||||
| chr7:131444820
|
T | A | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1396-954T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444820 | ||||||
| chr7:131444903
|
C | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(53): Show | 57 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1396-871C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444903 | ||||||
| chr7:131444938
|
A | C | 6 | a0001c0002t0002g0075a0001c0002t0019g0081a0001c0002t0019g0309others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396-836A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131444938 | ||||||
| chr7:131445148
|
A | G | 1 | a0001c0001t0053g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1396-626A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131445148 | ||||||
| chr7:131445153
|
T | A | 1 | a0001c0001t0003g0195 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1396-621T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131445153 | ||||||
| chr7:131445222
|
A | AT | 8 | a0001c0001t0005g0108a0001c0003t0008g0079a0001c0003t0008g0082others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-542dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 131445222 | |||||
| chr7:131445430
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1396-344G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131445430 | ||||||
| chr7:131445559
|
C | G | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1396-215C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 11/17 | chr7 | 131445559 | ||||||
| chr7:131446154
|
C | T | 1 | a0001c0001t0002g0269 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1525+251C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131446154 | ||||||
| chr7:131446162
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1525+259G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131446162 | ||||||
| chr7:131446592
|
T | C | 1 | a0001c0001t0003g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1525+689T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131446592 | ||||||
| chr7:131446864
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1525+961G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131446864 | ||||||
| chr7:131447025
|
C | T | 2 | a0001c0001t0021g0179a0001c0001t0021g0180 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1525+1122C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131447025 | ||||||
| chr7:131447426
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0028g0045others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525+1523G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131447426 | ||||||
| chr7:131447435
|
C | T | 1 | a0001c0001t0004g0035 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1525+1532C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131447435 | ||||||
| chr7:131447581
|
A | G | 100 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(97): Show | 101 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1525+1678A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131447581 | ||||||
| chr7:131447594
|
G | T | 1 | a0001c0001t0001g0111 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1525+1691G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131447594 | ||||||
| chr7:131447690
|
T | A | 3 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0063g0238 | 3 | HG02071.hp2 NA18975.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1525+1787T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131447690 | ||||||
| chr7:131448097
|
G | A | 97 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(94): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1525+2194G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448097 | ||||||
| chr7:131448101
|
G | A | 3 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0056g0308 | 3 | HG02055.hp2 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1525+2198G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448101 | ||||||
| chr7:131448151
|
C | T | 37 | a0001c0001t0003g0032a0001c0001t0003g0172a0001c0001t0003g0173others(34): Show | 37 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1525+2248C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448151 | ||||||
| chr7:131448181
|
T | C | 101 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(98): Show | 102 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1525+2278T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448181 | ||||||
| chr7:131448325
|
C | T | 1 | a0001c0001t0035g0163 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1525+2422C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448325 | ||||||
| chr7:131448334
|
A | C | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1525+2431A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448334 | ||||||
| chr7:131448383
|
A | G | 1 | a0001c0002t0045g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1525+2480A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448383 | ||||||
| chr7:131448418
|
A | G | 1 | a0001c0001t0003g0312 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1525+2515A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448418 | ||||||
| chr7:131448493
|
A | T | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1525+2590A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448493 | ||||||
| chr7:131448520
|
T | C | 2 | a0001c0001t0002g0234a0001c0001t0002g0286 | 2 | HG02027.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1525+2617T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448520 | ||||||
| chr7:131448595
|
A | G | 1 | a0001c0001t0032g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1525+2692A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448595 | ||||||
| chr7:131448651
|
A | AT | 8 | a0001c0001t0003g0134a0001c0001t0006g0117a0001c0001t0006g0119others(5): Show | 8 | NA18963.hp1 NA18968.hp2 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525+2750dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131448651 | |||||
| chr7:131448931
|
G | C | 88 | a0001c0001t0001g0009a0001c0001t0002g0048a0001c0001t0002g0076others(85): Show | 89 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1525+3028G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131448931 | ||||||
| chr7:131449650
|
GT | G | 9 | a0001c0001t0001g0122a0001c0001t0002g0229a0001c0001t0002g0239others(6): Show | 9 | HG00140.hp1 HG02083.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1525+3756delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131449650 | |||||
| chr7:131449659
|
T | C | 1 | a0001c0001t0015g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1525+3756T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131449659 | ||||||
| chr7:131449953
|
C | G | 2 | a0001c0001t0002g0307a0001c0001t0044g0215 | 2 | HG01978.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1525+4050C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131449953 | ||||||
| chr7:131450007
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1525+4104A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131450007 | ||||||
| chr7:131450128
|
A | G | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1525+4225A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131450128 | ||||||
| chr7:131450137
|
C | T | 1 | a0001c0002t0019g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1525+4234C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131450137 | ||||||
| chr7:131450217
|
G | C | 1 | a0001c0001t0002g0218 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1525+4314G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131450217 | ||||||
| chr7:131450355
|
T | C | 1 | a0001c0001t0003g0204 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1525+4452T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131450355 | ||||||
| chr7:131450630
|
T | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(43): Show | 47 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1525+4727T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131450630 | ||||||
| chr7:131450759
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1525+4856C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131450759 | ||||||
| chr7:131450831
|
T | C | 1 | a0001c0001t0002g0076 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1525+4928T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131450831 | ||||||
| chr7:131450920
|
C | CT | 3 | a0001c0002t0045g0143a0001c0003t0008g0087a0001c0003t0030g0086 | 3 | HG01884.hp2 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1525+5019dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131450920 | |||||
| chr7:131452148
|
G | A | 1 | a0001c0001t0032g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1525+6245G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131452148 | ||||||
| chr7:131452544
|
C | CT | 142 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1525+6666dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131452544 | |||||
| chr7:131452544
|
C | CTT | 12 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0038others(9): Show | 13 | HG00741.hp1 HG01106.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525+6665_1525+666 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131452544 | |||||
| chr7:131452544
|
C | CTTT | 8 | a0001c0001t0053g0072a0001c0002t0054g0074a0001c0003t0008g0082others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525+6664_1525+666 others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131452544 | |||||
| chr7:131452544
|
CT | C | 20 | a0001c0001t0002g0229a0001c0001t0002g0239a0001c0001t0002g0242others(17): Show | 20 | HG01168.hp2 HG02559.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.1525+6666delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131452544 | |||||
| chr7:131452577
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1525+6674A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131452577 | ||||||
| chr7:131452583
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1525+6680G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131452583 | ||||||
| chr7:131452643
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1525+6740C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131452643 | ||||||
| chr7:131452838
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0065g0112 | 2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1525+6935T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131452838 | ||||||
| chr7:131453009
|
T | C | 7 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1525+7106T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131453009 | ||||||
| chr7:131453188
|
G | T | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1525+7285G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131453188 | ||||||
| chr7:131453220
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1525+7317A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131453220 | ||||||
| chr7:131453270
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1525+7367T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131453270 | ||||||
| chr7:131453302
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1525+7399A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131453302 | ||||||
| chr7:131453506
|
C | T | 3 | a0001c0001t0020g0226a0001c0001t0020g0227a0001c0002t0002g0075 | 3 | HG02723.hp1 NA18995.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1525+7603C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131453506 | ||||||
| chr7:131454060
|
C | CT | 105 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0097others(102): Show | 106 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1525+8172dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131454060 | |||||
| chr7:131454089
|
CATT | C | 7 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1525+8189_1525+819 others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131454089 | |||||
| chr7:131454279
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1525+8376G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131454279 | ||||||
| chr7:131454383
|
C | T | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1525+8480C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131454383 | ||||||
| chr7:131454418
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1525+8515G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131454418 | ||||||
| chr7:131454839
|
G | A | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1526-8378G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131454839 | ||||||
| chr7:131454937
|
T | C | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1526-8280T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131454937 | ||||||
| chr7:131455062
|
G | C | 1 | a0001c0001t0018g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1526-8155G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455062 | ||||||
| chr7:131455344
|
G | T | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00642.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1526-7873G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455344 | ||||||
| chr7:131455366
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1526-7851T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455366 | ||||||
| chr7:131455452
|
T | C | 104 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(101): Show | 105 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1526-7765T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455452 | ||||||
| chr7:131455462
|
C | G | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1526-7755C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455462 | ||||||
| chr7:131455493
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0043g0037 | 2 | HG00423.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1526-7724G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455493 | ||||||
| chr7:131455638
|
T | C | 1 | a0001c0001t0038g0235 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1526-7579T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455638 | ||||||
| chr7:131455639
|
A | C | 1 | a0001c0001t0038g0235 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1526-7578A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455639 | ||||||
| chr7:131455822
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-7395A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455822 | ||||||
| chr7:131455977
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1526-7240C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131455977 | ||||||
| chr7:131456044
|
TC | T | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(306): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1526-7171delC | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131456044 | |||||
| chr7:131456046
|
C | A | 6 | a0001c0001t0002g0254a0001c0001t0006g0135a0001c0001t0018g0210others(3): Show | 6 | HG02717.hp1 HG02886.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1526-7171C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456046 | ||||||
| chr7:131456050
|
C | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(306): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1526-7167C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456050 | ||||||
| chr7:131456050
|
CCA | C | 5 | a0001c0001t0006g0135a0001c0001t0018g0210a0001c0001t0018g0211others(2): Show | 5 | HG02717.hp1 HG02886.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-7166_1526-716 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456050 | ||||||
| chr7:131456051
|
C | A | 1 | a0001c0001t0002g0254 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1526-7166C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456051 | ||||||
| chr7:131456071
|
A | T | 5 | a0001c0001t0002g0245a0001c0001t0002g0256a0001c0001t0002g0261others(2): Show | 5 | HG02155.hp1 NA18942.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1526-7146A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456071 | ||||||
| chr7:131456536
|
G | T | 2 | a0001c0001t0001g0063a0001c0001t0048g0058 | 2 | HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1526-6681G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456536 | ||||||
| chr7:131456725
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1526-6492C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456725 | ||||||
| chr7:131456739
|
G | A | 92 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(89): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1526-6478G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456739 | ||||||
| chr7:131456845
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-6372A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456845 | ||||||
| chr7:131456920
|
G | A | 9 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1526-6297G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131456920 | ||||||
| chr7:131456934
|
C | CA | 22 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0047others(19): Show | 22 | HG00639.hp2 HG01081.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1526-6271dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131456934 | |||||
| chr7:131456934
|
CA | C | 8 | a0001c0001t0018g0212a0001c0003t0008g0079a0001c0003t0008g0082others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1526-6271delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131456934 | |||||
| chr7:131457191
|
C | T | 6 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0007g0313others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1526-6026C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131457191 | ||||||
| chr7:131457513
|
C | T | 5 | a0001c0002t0019g0081a0001c0002t0019g0309a0001c0002t0019g0310others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1526-5704C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131457513 | ||||||
| chr7:131457547
|
T | G | 1 | a0001c0001t0064g0246 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1526-5670T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131457547 | ||||||
| chr7:131457620
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-5597A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131457620 | ||||||
| chr7:131457646
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1526-5571G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131457646 | ||||||
| chr7:131457768
|
T | C | 1 | a0001c0002t0045g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1526-5449T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131457768 | ||||||
| chr7:131457782
|
G | A | 4 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0002g0303others(1): Show | 4 | HG02071.hp2 NA18975.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1526-5435G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131457782 | ||||||
| chr7:131457909
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1526-5308C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131457909 | ||||||
| chr7:131458240
|
A | G | 5 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-4977A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131458240 | ||||||
| chr7:131458309
|
C | A | 1 | a0001c0001t0039g0236 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1526-4908C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131458309 | ||||||
| chr7:131458631
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1526-4586G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131458631 | ||||||
| chr7:131458719
|
A | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0047others(6): Show | 9 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1526-4498A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131458719 | ||||||
| chr7:131458886
|
G | A | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1526-4331G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131458886 | ||||||
| chr7:131458903
|
G | C | 3 | a0001c0001t0002g0245a0001c0001t0002g0277a0001c0001t0014g0251 | 3 | NA18942.hp1 NA18984.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1526-4314G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131458903 | ||||||
| chr7:131458904
|
T | A | 3 | a0001c0001t0002g0245a0001c0001t0002g0277a0001c0001t0014g0251 | 3 | NA18942.hp1 NA18984.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1526-4313T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131458904 | ||||||
| chr7:131459009
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1526-4208G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131459009 | ||||||
| chr7:131459376
|
CTT | C | 5 | a0001c0002t0019g0081a0001c0002t0019g0309a0001c0002t0019g0310others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1526-3839_1526-383 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131459376 | |||||
| chr7:131459624
|
A | G | 1 | a0001c0001t0012g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1526-3593A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131459624 | ||||||
| chr7:131459650
|
T | G | 116 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(113): Show | 117 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1526-3567T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131459650 | ||||||
| chr7:131459741
|
A | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(52): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1526-3476A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131459741 | ||||||
| chr7:131460035
|
T | C | 1 | a0001c0001t0009g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1526-3182T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131460035 | ||||||
| chr7:131460170
|
T | G | 1 | a0001c0001t0002g0291 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1526-3047T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131460170 | ||||||
| chr7:131460531
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0048g0058 | 2 | HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1526-2686G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131460531 | ||||||
| chr7:131460711
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 9 | HG01496.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1526-2506C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131460711 | ||||||
| chr7:131460721
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1526-2496A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131460721 | ||||||
| chr7:131461256
|
G | GT | 165 | a0001c0001t0001g0039a0001c0001t0002g0036a0001c0001t0002g0048others(162): Show | 166 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1526-1949dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131461256 | |||||
| chr7:131461256
|
G | GTT | 18 | a0001c0001t0002g0265a0001c0001t0002g0280a0001c0001t0003g0203others(15): Show | 18 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1526-1950_1526-194 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 131461256 | |||||
| chr7:131461452
|
A | G | 13 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(10): Show | 13 | HG00544.hp2 HG00597.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1526-1765A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131461452 | ||||||
| chr7:131461662
|
A | G | 2 | a0001c0001t0025g0156a0001c0001t0025g0157 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1526-1555A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131461662 | ||||||
| chr7:131462008
|
A | G | 1 | a0001c0001t0003g0217 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1526-1209A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131462008 | ||||||
| chr7:131462108
|
T | C | 177 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(174): Show | 178 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.1526-1109T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131462108 | ||||||
| chr7:131462241
|
G | A | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1526-976G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131462241 | ||||||
| chr7:131462256
|
A | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-961A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131462256 | ||||||
| chr7:131462334
|
A | C | 1 | a0001c0001t0040g0302 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1526-883A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131462334 | ||||||
| chr7:131462409
|
C | T | 7 | a0001c0001t0009g0144a0001c0001t0009g0145a0001c0001t0009g0147others(4): Show | 7 | HG01169.hp1 HG01993.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-808C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131462409 | ||||||
| chr7:131462946
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1526-271A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131462946 | ||||||
| chr7:131463037
|
C | T | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1526-180C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131463037 | ||||||
| chr7:131463102
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1526-115C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131463102 | ||||||
| chr7:131463115
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-102T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 12/17 | chr7 | 131463115 | ||||||
| chr7:131463433
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1673+69A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | chr7 | 131463433 | ||||||
| chr7:131463517
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1673+153T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | chr7 | 131463517 | ||||||
| chr7:131463529
|
T | A | 1 | a0001c0001t0012g0228 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1673+165T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | chr7 | 131463529 | ||||||
| chr7:131463583
|
C | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1673+219C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | chr7 | 131463583 | ||||||
| chr7:131463747
|
C | G | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1673+383C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | chr7 | 131463747 | ||||||
| chr7:131464017
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674-277A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | chr7 | 131464017 | ||||||
| chr7:131464114
|
T | G | 1 | a0001c0001t0040g0302 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1674-180T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | chr7 | 131464114 | ||||||
| chr7:131464215
|
ATGCAGTT others(11): Show |
A | 10 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(7): Show | 10 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1674-77_1674-60del others(18): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 131464215 | |||||
| chr7:131464220
|
G | A | 1 | a0001c0001t0002g0216 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1674-74G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 13/17 | chr7 | 131464220 | ||||||
| chr7:131464490
|
A | G | 1 | a0001c0001t0007g0315 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1788+82A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131464490 | ||||||
| chr7:131464589
|
T | G | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00642.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1788+181T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131464589 | ||||||
| chr7:131464595
|
C | T | 1 | a0001c0001t0009g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1788+187C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131464595 | ||||||
| chr7:131464725
|
G | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1788+317G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131464725 | ||||||
| chr7:131464992
|
T | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1788+584T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131464992 | ||||||
| chr7:131465081
|
CCTTT | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1788+678_1788+681d others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 131465081 | |||||
| chr7:131465138
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1788+730A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131465138 | ||||||
| chr7:131465498
|
A | G | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1789-778A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131465498 | ||||||
| chr7:131465520
|
T | C | 4 | a0001c0001t0010g0164a0001c0001t0022g0165a0001c0001t0022g0166others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-756T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131465520 | ||||||
| chr7:131465746
|
C | T | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0014g0233 | 3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1789-530C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131465746 | ||||||
| chr7:131465831
|
G | T | 1 | a0001c0001t0009g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1789-445G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131465831 | ||||||
| chr7:131466191
|
G | C | 1 | a0001c0001t0060g0305 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1789-85G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 14/17 | chr7 | 131466191 | ||||||
| chr7:131466557
|
G | A | 1 | a0001c0001t0002g0237 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1928+142G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131466557 | ||||||
| chr7:131466904
|
T | TAC | 8 | a0001c0001t0002g0248a0001c0001t0009g0149a0001c0003t0008g0079others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1928+508_1928+509d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 131466904 | |||||
| chr7:131466904
|
T | TACAC | 9 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG01069.hp1 HG01346.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1928+506_1928+509d others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 131466904 | |||||
| chr7:131466904
|
T | TACACAC | 3 | a0001c0001t0025g0156a0001c0001t0025g0157a0001c0002t0058g0080 | 3 | HG00639.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1928+504_1928+509d others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 131466904 | |||||
| chr7:131466904
|
TAC | T | 3 | a0001c0001t0003g0174a0001c0001t0021g0179a0001c0001t0021g0180 | 3 | HG01099.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1928+508_1928+509d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 131466904 | |||||
| chr7:131466921
|
A | ACG | 6 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG00544.hp2 HG00597.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1928+507_1928+508i others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 131466921 | |||||
| chr7:131466921
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0105 | 2 | HG02145.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1928+506A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131466921 | ||||||
| chr7:131466923
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 73 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1928+508A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131466923 | ||||||
| chr7:131466923
|
ACG | A | 51 | a0001c0001t0002g0216a0001c0001t0003g0032a0001c0001t0003g0134others(48): Show | 51 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.1928+520_1928+521d others(4): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 131466923 | |||||
| chr7:131466925
|
G | A | 105 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(102): Show | 105 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1928+510G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131466925 | ||||||
| chr7:131466935
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1928+520G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131466935 | ||||||
| chr7:131466942
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1928+527C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131466942 | ||||||
| chr7:131467024
|
C | T | 96 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1928+609C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131467024 | ||||||
| chr7:131467602
|
G | A | 1 | a0001c0001t0026g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1928+1187G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131467602 | ||||||
| chr7:131467761
|
A | G | 2 | a0001c0001t0002g0048a0001c0001t0002g0297 | 2 | NA18993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1928+1346A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131467761 | ||||||
| chr7:131468015
|
G | A | 1 | a0001c0001t0003g0195 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1928+1600G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131468015 | ||||||
| chr7:131468321
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1928+1906G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131468321 | ||||||
| chr7:131468324
|
A | G | 4 | a0001c0001t0007g0313a0001c0001t0007g0315a0001c0001t0007g0316others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1928+1909A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131468324 | ||||||
| chr7:131468365
|
G | T | 1 | a0001c0001t0002g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1928+1950G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131468365 | ||||||
| chr7:131468403
|
A | T | 180 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(177): Show | 181 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1928+1988A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131468403 | ||||||
| chr7:131468426
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(49): Show | 53 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1928+2011C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131468426 | ||||||
| chr7:131468626
|
A | T | 1 | a0001c0001t0002g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1928+2211A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131468626 | ||||||
| chr7:131469200
|
A | AGATG | 13 | a0001c0001t0004g0006a0001c0001t0004g0026a0001c0001t0004g0027others(10): Show | 13 | NA18951.hp1 NA18955.hp1 NA18970.hp1 others(10): Show |
intron_variant | MODIFIER | c.1929-1620_1929-161 others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 131469200 | |||||
| chr7:131469200
|
A | G | 1 | a0001c0001t0059g0042 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1929-1642A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131469200 | ||||||
| chr7:131469255
|
C | G | 1 | a0001c0001t0007g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1929-1587C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131469255 | ||||||
| chr7:131469346
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1929-1496A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131469346 | ||||||
| chr7:131469607
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1929-1235C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131469607 | ||||||
| chr7:131469633
|
A | C | 1 | a0001c0001t0002g0272 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1929-1209A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131469633 | ||||||
| chr7:131469687
|
T | G | 1 | a0001c0001t0002g0262 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1929-1155T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131469687 | ||||||
| chr7:131469738
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1929-1104C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131469738 | ||||||
| chr7:131469763
|
A | C | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1929-1079A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131469763 | ||||||
| chr7:131469881
|
C | CT | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(306): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1929-949dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 131469881 | |||||
| chr7:131470098
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1929-744C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131470098 | ||||||
| chr7:131470191
|
C | T | 1 | a0001c0001t0003g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1929-651C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131470191 | ||||||
| chr7:131470259
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1929-583T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131470259 | ||||||
| chr7:131470546
|
G | A | 4 | a0001c0001t0007g0313a0001c0001t0007g0315a0001c0001t0007g0316others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929-296G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131470546 | ||||||
| chr7:131470599
|
A | C | 1 | a0001c0001t0003g0173 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1929-243A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131470599 | ||||||
| chr7:131470827
|
G | C | 52 | a0001c0001t0003g0032a0001c0001t0003g0134a0001c0001t0003g0172others(49): Show | 52 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1929-15G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131470827 | ||||||
| chr7:131470829
|
G | T | 182 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1929-13G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131470829 | ||||||
| chr7:131470833
|
A | G | 2 | a0001c0001t0002g0264a0001c0001t0014g0233 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1929-9A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 15/17 | chr7 | 131470833 | ||||||
| chr7:131471005
|
T | C | 115 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(112): Show | 116 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2031+61T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471005 | ||||||
| chr7:131471043
|
G | A | 1 | a0001c0001t0004g0035 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2031+99G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471043 | ||||||
| chr7:131471053
|
T | C | 2 | a0001c0001t0003g0174a0001c0001t0003g0175 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2031+109T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471053 | ||||||
| chr7:131471087
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2031+143C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471087 | ||||||
| chr7:131471120
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2031+176G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471120 | ||||||
| chr7:131471146
|
A | T | 5 | a0001c0002t0019g0081a0001c0002t0019g0309a0001c0002t0019g0310others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2031+202A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471146 | ||||||
| chr7:131471624
|
A | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 19 | HG01099.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.2031+680A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471624 | ||||||
| chr7:131471760
|
G | T | 3 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071 | 4 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2031+816G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471760 | ||||||
| chr7:131471870
|
C | A | 1 | a0001c0001t0003g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2031+926C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471870 | ||||||
| chr7:131471901
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG01099.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2031+957A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131471901 | ||||||
| chr7:131471966
|
AT | A | 3 | a0001c0001t0002g0237a0001c0001t0002g0293a0001c0001t0063g0238 | 3 | HG02071.hp2 NA18975.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2031+1024delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131471966 | |||||
| chr7:131472558
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2031+1614C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131472558 | ||||||
| chr7:131472594
|
ATG | A | 17 | a0001c0001t0001g0057a0001c0001t0005g0101a0001c0001t0005g0102others(14): Show | 17 | HG00639.hp2 HG00642.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.2031+1680_2031+168 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131472594 | |||||
| chr7:131472594
|
ATGTG | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(287): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.2031+1678_2031+168 others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131472594 | |||||
| chr7:131472880
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2031+1936G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131472880 | ||||||
| chr7:131472903
|
G | A | 10 | a0001c0001t0001g0046a0001c0001t0011g0003a0001c0001t0011g0070others(7): Show | 11 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.2031+1959G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131472903 | ||||||
| chr7:131472947
|
CA | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.2031+2021delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131472947 | |||||
| chr7:131472965
|
AG | A | 4 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2031+2022delG | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131472965 | ||||||
| chr7:131473600
|
A | G | 4 | a0001c0001t0018g0210a0001c0001t0018g0211a0001c0001t0018g0212others(1): Show | 4 | HG02717.hp1 HG02886.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2031+2656A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131473600 | ||||||
| chr7:131473661
|
C | G | 1 | a0001c0001t0002g0262 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2031+2717C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131473661 | ||||||
| chr7:131473770
|
A | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0070a0001c0001t0011g0071others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2031+2826A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131473770 | ||||||
| chr7:131473777
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2031+2833C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131473777 | ||||||
| chr7:131473786
|
A | T | 1 | a0001c0001t0002g0298 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2031+2842A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131473786 | ||||||
| chr7:131473866
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01106.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2031+2922G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131473866 | ||||||
| chr7:131474035
|
A | C | 1 | a0001c0002t0019g0309 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2031+3091A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474035 | ||||||
| chr7:131474056
|
A | G | 1 | a0001c0001t0002g0249 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2031+3112A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474056 | ||||||
| chr7:131474093
|
T | G | 1 | a0001c0001t0042g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2031+3149T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474093 | ||||||
| chr7:131474145
|
A | G | 2 | a0001c0002t0019g0309a0001c0002t0056g0308 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2031+3201A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474145 | ||||||
| chr7:131474419
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01099.hp2 HG01891.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2031+3475A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474419 | ||||||
| chr7:131474564
|
C | G | 5 | a0001c0002t0019g0081a0001c0002t0019g0309a0001c0002t0019g0310others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2031+3620C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474564 | ||||||
| chr7:131474592
|
T | G | 1 | a0001c0001t0001g0094 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2031+3648T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474592 | ||||||
| chr7:131474840
|
A | T | 1 | a0001c0001t0055g0207 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2032-3783A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474840 | ||||||
| chr7:131474996
|
A | T | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2032-3627A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131474996 | ||||||
| chr7:131475155
|
T | C | 1 | a0001c0001t0010g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2032-3468T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131475155 | ||||||
| chr7:131475393
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.2032-3230A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131475393 | ||||||
| chr7:131475708
|
G | C | 1 | a0001c0002t0045g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2032-2915G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131475708 | ||||||
| chr7:131475929
|
G | T | 93 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(90): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.2032-2694G>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131475929 | ||||||
| chr7:131475998
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2032-2625C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131475998 | ||||||
| chr7:131475999
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2032-2624A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131475999 | ||||||
| chr7:131476029
|
T | C | 2 | a0001c0001t0023g0222a0001c0001t0023g0223 | 2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2032-2594T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131476029 | ||||||
| chr7:131476146
|
C | G | 1 | a0001c0002t0054g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2032-2477C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131476146 | ||||||
| chr7:131476379
|
TTATG | T | 3 | a0001c0001t0001g0039a0001c0001t0028g0045a0001c0001t0049g0044 | 3 | HG02145.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2032-2241_2032-223 others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131476379 | |||||
| chr7:131476703
|
TTTG | T | 4 | a0001c0001t0003g0134a0001c0001t0003g0177a0001c0001t0007g0160others(1): Show | 4 | HG00408.hp1 HG02155.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.2032-1909_2032-190 others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131476703 | |||||
| chr7:131476720
|
T | G | 1 | a0001c0001t0002g0280 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2032-1903T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131476720 | ||||||
| chr7:131476981
|
A | T | 1 | a0001c0001t0002g0285 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2032-1642A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131476981 | ||||||
| chr7:131477344
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2032-1279T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131477344 | ||||||
| chr7:131477383
|
C | CA | 178 | a0001c0001t0001g0007a0001c0001t0002g0036a0001c0001t0002g0048others(175): Show | 179 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.2032-1226dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131477383 | |||||
| chr7:131477937
|
C | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2032-686C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131477937 | ||||||
| chr7:131477990
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2032-633A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131477990 | ||||||
| chr7:131478519
|
C | T | 2 | a0001c0001t0002g0252a0001c0001t0002g0276 | 2 | NA18977.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2032-104C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | chr7 | 131478519 | ||||||
| chr7:131478595
|
C | CT | 28 | a0001c0001t0001g0033a0001c0001t0001g0141a0001c0001t0002g0077others(25): Show | 28 | HG00639.hp1 HG01069.hp2 HG01074.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.2032-7dupT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131478595 | |||||
| chr7:131478595
|
C | CTT | 143 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(140): Show | 143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
splice_region_variant&intron_variant | LOW | c.2032-8_2032-7dupTT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131478595 | |||||
| chr7:131478595
|
C | CTTT | 19 | a0001c0001t0002g0218a0001c0001t0002g0304a0001c0001t0010g0164others(16): Show | 20 | HG01074.hp2 HG01081.hp1 HG01261.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.2032-9_2032-7dupTT others(1): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 131478595 | |||||
| chr7:131478744
|
T | G | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2086+67T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131478744 | ||||||
| chr7:131479001
|
A | G | 1 | a0001c0001t0007g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2086+324A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131479001 | ||||||
| chr7:131479218
|
C | G | 41 | a0001c0001t0003g0032a0001c0001t0003g0134a0001c0001t0003g0172others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.2086+541C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131479218 | ||||||
| chr7:131479284
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2086+607G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131479284 | ||||||
| chr7:131479385
|
C | A | 1 | a0001c0001t0041g0224 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2086+708C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131479385 | ||||||
| chr7:131479440
|
G | A | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | NA18944.hp2 NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2086+763G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131479440 | ||||||
| chr7:131479488
|
C | T | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2086+811C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131479488 | ||||||
| chr7:131479598
|
A | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(311): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.2086+921A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131479598 | ||||||
| chr7:131479830
|
A | T | 1 | a0001c0001t0002g0280 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2086+1153A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131479830 | ||||||
| chr7:131479830
|
AAAT | A | 4 | a0001c0001t0002g0220a0001c0001t0002g0247a0001c0001t0002g0258others(1): Show | 4 | HG02135.hp2 NA18953.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.2086+1168_2086+117 others(7): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131479830 | |||||
| chr7:131479850
|
TTAAA | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(296): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.2086+1195_2086+119 others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131479850 | |||||
| chr7:131480008
|
A | G | 2 | a0001c0001t0038g0235a0001c0001t0039g0236 | 2 | HG02523.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2086+1331A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480008 | ||||||
| chr7:131480020
|
C | CA | 68 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0053others(65): Show | 69 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.2086+1364dupA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131480020 | |||||
| chr7:131480020
|
CA | C | 18 | a0001c0001t0001g0124a0001c0001t0002g0229a0001c0001t0002g0239others(15): Show | 18 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.2086+1364delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131480020 | |||||
| chr7:131480042
|
T | A | 79 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(76): Show | 79 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.2086+1365T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480042 | ||||||
| chr7:131480132
|
A | G | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2086+1455A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480132 | ||||||
| chr7:131480161
|
CT | C | 8 | a0001c0001t0010g0164a0001c0001t0010g0167a0001c0001t0010g0168others(5): Show | 8 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2086+1486delT | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131480161 | |||||
| chr7:131480187
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2086+1510C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480187 | ||||||
| chr7:131480426
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2086+1749C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480426 | ||||||
| chr7:131480576
|
T | C | 1 | a0001c0001t0003g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2086+1899T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480576 | ||||||
| chr7:131480581
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0047g0091 | 2 | NA18944.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.2086+1904G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480581 | ||||||
| chr7:131480708
|
T | C | 1 | a0001c0001t0010g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2086+2031T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480708 | ||||||
| chr7:131480768
|
T | A | 4 | a0001c0002t0019g0309a0001c0002t0019g0310a0001c0002t0056g0308others(1): Show | 4 | HG00639.hp1 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2086+2091T>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480768 | ||||||
| chr7:131480768
|
T | C | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2086+2091T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480768 | ||||||
| chr7:131480875
|
A | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 19 | HG01099.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.2086+2198A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131480875 | ||||||
| chr7:131481060
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2086+2383C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131481060 | ||||||
| chr7:131481811
|
T | C | 1 | a0001c0001t0032g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2086+3134T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131481811 | ||||||
| chr7:131481812
|
GC | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(35): Show | 39 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.2086+3136delC | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131481812 | ||||||
| chr7:131481813
|
C | A | 1 | a0001c0001t0005g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2086+3136C>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131481813 | ||||||
| chr7:131481813
|
CA | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0054others(187): Show | 192 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2086+3155delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131481813 | |||||
| chr7:131481813
|
CAA | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(48): Show | 52 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2086+3154_2086+315 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131481813 | |||||
| chr7:131481842
|
A | T | 1 | a0001c0001t0023g0222 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2086+3165A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131481842 | ||||||
| chr7:131481982
|
A | C | 9 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG01069.hp1 HG01346.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2086+3305A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131481982 | ||||||
| chr7:131482184
|
C | CTATT | 3 | a0001c0001t0005g0103a0001c0001t0005g0104a0001c0001t0005g0107 | 3 | HG00639.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2086+3520_2086+352 others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131482184 | |||||
| chr7:131482184
|
CTATT | C | 3 | a0001c0001t0007g0313a0001c0001t0007g0315a0002c0004t0007g0314 | 3 | HG02630.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2086+3520_2086+352 others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131482184 | |||||
| chr7:131482234
|
A | G | 183 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0076others(180): Show | 184 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.2086+3557A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131482234 | ||||||
| chr7:131482374
|
T | C | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2086+3697T>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131482374 | ||||||
| chr7:131482384
|
T | G | 1 | a0001c0002t0058g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2086+3707T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131482384 | ||||||
| chr7:131482488
|
A | C | 1 | a0001c0001t0002g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2086+3811A>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131482488 | ||||||
| chr7:131482811
|
G | A | 180 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(177): Show | 181 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.2086+4134G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131482811 | ||||||
| chr7:131483204
|
G | A | 1 | a0001c0002t0019g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2087-4403G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131483204 | ||||||
| chr7:131483220
|
T | TCCTAGAT others(5): Show |
1 | a0001c0001t0005g0121 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2087-4384_2087-437 others(16): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131483220 | |||||
| chr7:131484030
|
CAT | C | 49 | a0001c0001t0002g0255a0001c0001t0003g0032a0001c0001t0003g0134others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2087-3574_2087-357 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131484030 | |||||
| chr7:131484119
|
G | A | 1 | a0001c0003t0030g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2087-3488G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131484119 | ||||||
| chr7:131484266
|
A | T | 2 | a0001c0001t0026g0073a0001c0001t0053g0072 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2087-3341A>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131484266 | ||||||
| chr7:131484375
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2087-3232C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131484375 | ||||||
| chr7:131484972
|
G | C | 7 | a0001c0003t0008g0079a0001c0003t0008g0082a0001c0003t0008g0083others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2087-2635G>C | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131484972 | ||||||
| chr7:131485017
|
A | G | 2 | a0001c0001t0061g0162a0001c0001t0062g0161 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2087-2590A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131485017 | ||||||
| chr7:131485213
|
C | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(66): Show | 71 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2087-2394C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131485213 | ||||||
| chr7:131485529
|
C | G | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG00140.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2087-2078C>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131485529 | ||||||
| chr7:131485740
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2087-1867A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131485740 | ||||||
| chr7:131485920
|
T | G | 1 | a0001c0001t0036g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2087-1687T>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131485920 | ||||||
| chr7:131486095
|
C | CAG | 3 | a0001c0001t0002g0303a0001c0001t0021g0179a0001c0001t0021g0180 | 3 | HG03491.hp2 HG03492.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2087-1492_2087-149 others(6): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131486095 | |||||
| chr7:131486095
|
CAGAG | C | 3 | a0001c0001t0015g0241a0001c0001t0015g0273a0001c0001t0015g0274 | 3 | HG02622.hp1 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2087-1494_2087-149 others(8): Show |
MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131486095 | |||||
| chr7:131486258
|
CA | C | 169 | a0001c0001t0002g0048a0001c0001t0002g0076a0001c0001t0002g0077others(166): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.2087-1336delA | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 131486258 | |||||
| chr7:131486552
|
A | G | 1 | a0001c0001t0002g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2087-1055A>G | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131486552 | ||||||
| chr7:131486682
|
C | T | 3 | a0001c0001t0002g0255a0001c0001t0002g0271a0001c0001t0002g0275 | 3 | HG00423.hp1 HG02083.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.2087-925C>T | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131486682 | ||||||
| chr7:131487052
|
G | A | 8 | a0001c0001t0002g0229a0001c0001t0002g0239a0001c0001t0002g0242others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2087-555G>A | MKLN1 | ENSG00000128585.18 | transcript | ENST00000352689.11 | protein_coding | 17/17 | chr7 | 131487052 |