Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9053 |
| ensemblid | ENSG00000135525.19 |
| hgncid | 6869 |
| symbol | MAP7 |
| name | microtubule associated protein 7 |
| refseq_nuc | NM_003980.6 |
| refseq_prot | NP_003971.1 |
| ensembl_nuc | ENST00000354570.8 |
| ensembl_prot | ENSP00000346581.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 136342734 |
| end | 136550422 |
| strand | - |
| ver | v1.2 |
| region | chr6:136342734-136550422 |
| region5000 | chr6:136337734-136555422 |
| regionname0 | MAP7_chr6_136342734_136550422 |
| regionname5000 | MAP7_chr6_136337734_136555422 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 749 | 111 | 23 | 23 | 58 | 1 | 5 | 44 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002 | 1/0 | 749 | 103 | 21 | 13 | 60 | 1 | 7 | 50 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0003 | 0/0 | 749 | 16 | 2 | 5 | 9 | 0 | 0 | 8 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0004 | 0/0 | 748 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0005 | 0/0 | 743 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0006 | 0/0 | 749 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0007 | 0/0 | 749 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0008 | 0/0 | 749 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0009 | 0/0 | 749 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0010 | 0/0 | 749 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2250 | 109 | 23 | 22 | 57 | 1 | 5 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0002 | 1/0 | 2250 | 102 | 21 | 13 | 60 | 1 | 6 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0003 | 0/0 | 2250 | 15 | 2 | 5 | 8 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0004 | 0/0 | 2247 | 6 | 6 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0005 | 0/0 | 2232 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0006 | 0/0 | 2250 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0007 | 0/0 | 2250 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0008 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0009 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0010 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0011 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0012 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0013 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| c0014 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1509 | 92 | 22 | 17 | 46 | 1 | 5 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0002 | 1/0 | 1509 | 64 | 13 | 7 | 35 | 1 | 7 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0003 | 0/0 | 1510 | 43 | 4 | 9 | 30 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0004 | 0/0 | 1511 | 24 | 4 | 6 | 14 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0005 | 0/0 | 1511 | 6 | 0 | 0 | 6 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0006 | 0/0 | 1510 | 5 | 5 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0007 | 0/0 | 1509 | 4 | 4 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0008 | 0/0 | 1509 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0009 | 0/0 | 1509 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0010 | 0/0 | 1509 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0011 | 0/0 | 1509 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0012 | 0/0 | 1509 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0013 | 0/0 | 1509 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| t0014 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2250 | 109 | 23 | 22 | 57 | 1 | 5 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0010 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0012 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0002 | 1/0 | 2250 | 102 | 21 | 13 | 60 | 1 | 6 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0014 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0003c0003 | 0/0 | 2250 | 15 | 2 | 5 | 8 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0003c0009 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0004c0004 | 0/0 | 2247 | 6 | 6 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0005c0005 | 0/0 | 2232 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0006c0006 | 0/0 | 2250 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0007c0007 | 0/0 | 2250 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0008c0008 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0009c0013 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0010c0011 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3758 | 79 | 15 | 15 | 42 | 1 | 5 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0001t0004 | 0/0 | 3760 | 24 | 4 | 6 | 14 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0001t0008 | 0/0 | 3758 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0001t0012 | 0/0 | 3758 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0001t0013 | 0/0 | 3758 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0001t0014 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0010t0001 | 0/0 | 3758 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0001c0012t0001 | 0/0 | 3758 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0002t0002 | 1/0 | 3758 | 61 | 13 | 7 | 33 | 1 | 6 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0002t0003 | 0/0 | 3759 | 27 | 2 | 4 | 21 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0002t0005 | 0/0 | 3760 | 6 | 0 | 0 | 6 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0002t0007 | 0/0 | 3758 | 4 | 4 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0002t0009 | 0/0 | 3758 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0002t0010 | 0/0 | 3758 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0002t0011 | 0/0 | 3758 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0002c0014t0002 | 0/0 | 3758 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0003c0003t0003 | 0/0 | 3759 | 15 | 2 | 5 | 8 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0003c0009t0003 | 0/0 | 3759 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0004c0004t0001 | 0/0 | 3755 | 6 | 6 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0005c0005t0001 | 0/0 | 3740 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0006c0006t0006 | 0/0 | 3759 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0007c0007t0002 | 0/0 | 3758 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0008c0008t0006 | 0/0 | 3759 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0009c0013t0001 | 0/0 | 3758 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| a0010c0011t0001 | 0/0 | 3758 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | copy fasta | chr6 | 136337734 | 136555422 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0012g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0001t0014g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0010t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0001c0012t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0009g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0009g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0002t0011g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0002c0014t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0003c0009t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0004c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0004c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0004c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0004c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0004c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0004c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0005c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0005c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0005c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0006c0006t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0006c0006t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0006c0006t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0007c0007t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0007c0007t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0008c0008t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0008c0008t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0009c0013t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| a0010c0011t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0220 | EUR | FIN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00408 | hp1 | a0002 | c0002 | t0005 | g0020 | EAS | CHS | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | CHS | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00423 | hp1 | a0005 | c0005 | t0001 | g0104 | EAS | CHS | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | CHS | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | CHS | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | CHS | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0019 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0216 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00733 | hp2 | a0002 | c0002 | t0009 | g0223 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0218 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01074 | hp1 | a0009 | c0013 | t0001 | g0083 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0234 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01106 | hp1 | a0003 | c0003 | t0003 | g0010 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01192 | hp2 | a0002 | c0002 | t0009 | g0224 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0217 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01257 | hp2 | a0003 | c0003 | t0003 | g0025 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01258 | hp2 | a0003 | c0003 | t0003 | g0011 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01346 | hp2 | a0003 | c0003 | t0003 | g0015 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0085 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01934 | hp1 | a0001 | c0001 | t0012 | g0132 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01943 | hp1 | a0001 | c0010 | t0001 | g0151 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0201 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01993 | hp2 | a0003 | c0003 | t0003 | g0013 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02015 | hp1 | a0002 | c0002 | t0005 | g0008 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0248 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02080 | hp1 | a0005 | c0005 | t0001 | g0105 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | CDX | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02155 | hp2 | a0003 | c0003 | t0003 | g0189 | EAS | CDX | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02165 | hp1 | a0005 | c0005 | t0001 | g0169 | EAS | CDX | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | CDX | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02280 | hp1 | a0006 | c0006 | t0006 | g0180 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02280 | hp2 | a0003 | c0003 | t0003 | g0031 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02300 | hp2 | a0002 | c0002 | t0003 | g0021 | AMR | PEL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02451 | hp1 | a0002 | c0002 | t0010 | g0042 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02451 | hp2 | a0004 | c0004 | t0001 | g0080 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02622 | hp2 | a0006 | c0006 | t0006 | g0182 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02723 | hp1 | a0002 | c0002 | t0007 | g0206 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02723 | hp2 | a0004 | c0004 | t0001 | g0118 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0227 | SAS | PJL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02809 | hp1 | a0004 | c0004 | t0001 | g0121 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02897 | hp2 | a0004 | c0004 | t0001 | g0119 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0112 | AFR | ESN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | ESN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | ESN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02965 | hp2 | a0008 | c0008 | t0006 | g0026 | AFR | ESN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03041 | hp1 | a0006 | c0006 | t0006 | g0181 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03130 | hp2 | a0002 | c0002 | t0007 | g0205 | AFR | ESN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03139 | hp1 | a0004 | c0004 | t0001 | g0096 | AFR | ESN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03139 | hp2 | a0002 | c0002 | t0007 | g0207 | AFR | ESN | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0094 | AFR | MSL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | MSL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0003 | AFR | MSL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | MSL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0235 | SAS | PJL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0204 | SAS | PJL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03540 | hp1 | a0004 | c0004 | t0001 | g0120 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03540 | hp2 | a0002 | c0002 | t0011 | g0245 | AFR | GWD | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0111 | AFR | MSL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03654 | hp1 | a0002 | c0014 | t0002 | g0146 | SAS | PJL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0233 | SAS | PJL | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0221 | SAS | STU | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | STU | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | YRI | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0177 | AFR | YRI | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | CHB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0179 | AFR | YRI | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18939 | hp2 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18942 | hp1 | a0003 | c0003 | t0003 | g0125 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18946 | hp2 | a0003 | c0003 | t0003 | g0186 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18947 | hp2 | a0003 | c0009 | t0003 | g0190 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18956 | hp2 | a0003 | c0003 | t0003 | g0191 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18961 | hp2 | a0007 | c0007 | t0002 | g0229 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0018 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18970 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18974 | hp1 | a0003 | c0003 | t0003 | g0192 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18978 | hp2 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18980 | hp1 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18982 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18995 | hp1 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19000 | hp2 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19001 | hp2 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19002 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19007 | hp1 | a0002 | c0002 | t0005 | g0007 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19009 | hp1 | a0001 | c0001 | t0014 | g0060 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19010 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19030 | hp2 | a0002 | c0002 | t0007 | g0246 | AFR | LWK | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19060 | hp2 | a0003 | c0003 | t0003 | g0187 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19062 | hp1 | a0003 | c0003 | t0003 | g0185 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19063 | hp1 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19066 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0047 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19074 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19079 | hp1 | a0002 | c0002 | t0005 | g0014 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19084 | hp1 | a0007 | c0007 | t0002 | g0228 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19084 | hp2 | a0001 | c0012 | t0001 | g0174 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19086 | hp1 | a0003 | c0003 | t0003 | g0188 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19240 | hp1 | a0003 | c0003 | t0003 | g0059 | AFR | YRI | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0089 | AMR | CLM | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02109 | hp1 | a0010 | c0011 | t0001 | g0028 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA21309 | hp1 | a0008 | c0008 | t0006 | g0027 | AFR | LWK | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | LWK | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0172 | REF | REF | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0127 | REF | REF | MAP7_chr6_136337734_136555422 | MAP7 | chr6 | 136337734 | 136555422 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:136356761 | G | A | 1 | a0006 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.1946C>T | p.Pro649Leu | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/18 | 1960/3758 | 1946/2250 | 649/749 | chr6 | 136356761 | ||
| chr6:136356770 | G | C | 2 | a0006a0008 | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
missense_variant | MODERATE | c.1937C>G | p.Thr646Arg | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/18 | 1951/3758 | 1937/2250 | 646/749 | chr6 | 136356770 | ||
| chr6:136360785 | GCTT | G | 1 | a0004 | 6 | HG02451.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
disruptive_inframe_deletion | MODERATE | c.1712_1714delAAG | p.Glu571del | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/18 | 1728/3758 | 1712/2250 | 571/749 | chr6 | 136360785 | ||
| chr6:136361034 | G | A | 5 | a0001a0004a0005others(2): Show | 122 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
missense_variant | MODERATE | c.1672C>T | p.Arg558Trp | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 12/18 | 1686/3758 | 1672/2250 | 558/749 | chr6 | 136361034 | ||
| chr6:136362637 | GGGCTGGA others(11): Show |
G | 1 | a0005 | 3 | HG00423.hp1 HG02080.hp1 HG02165.hp1 |
conservative_inframe_deletion | MODERATE | c.1321_1338delTCGGCC others(12): Show |
p.Ser441_Ala446del | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/18 | 1352/3758 | 1321/2250 | 441/749 | chr6 | 136362637 | ||
| chr6:136362672 | G | A | 1 | a0003 | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
missense_variant | MODERATE | c.1304C>T | p.Ser435Leu | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/18 | 1318/3758 | 1304/2250 | 435/749 | chr6 | 136362672 | ||
| chr6:136362690 | A | G | 1 | a0003 | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
missense_variant | MODERATE | c.1286T>C | p.Met429Thr | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/18 | 1300/3758 | 1286/2250 | 429/749 | chr6 | 136362690 | ||
| chr6:136366333 | C | T | 1 | a0003 | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
missense_variant | MODERATE | c.983G>A | p.Arg328Gln | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 9/18 | 997/3758 | 983/2250 | 328/749 | chr6 | 136366333 | ||
| chr6:136366354 | G | A | 1 | a0009 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.962C>T | p.Ala321Val | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 9/18 | 976/3758 | 962/2250 | 321/749 | chr6 | 136366354 | ||
| chr6:136372542 | G | T | 1 | a0010 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.835C>A | p.Pro279Thr | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/18 | 849/3758 | 835/2250 | 279/749 | chr6 | 136372542 | ||
| chr6:136388506 | C | T | 1 | a0007 | 2 | NA18961.hp2 NA19084.hp1 |
missense_variant | MODERATE | c.413G>A | p.Arg138His | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/18 | 427/3758 | 413/2250 | 138/749 | chr6 | 136388506 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:136346040 | T | C | 1 | a0001c0012 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.2055A>G | p.Val685Val | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/18 | 2069/3758 | 2055/2250 | 685/749 | chr6 | 136346040 | ||
| chr6:136360718 | T | C | 2 | a0003c0003a0003c0009 | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
synonymous_variant | LOW | c.1782A>G | p.Gln594Gln | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/18 | 1796/3758 | 1782/2250 | 594/749 | chr6 | 136360718 | ||
| chr6:136389444 | C | T | 1 | a0001c0010 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.318G>A | p.Arg106Arg | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/18 | 332/3758 | 318/2250 | 106/749 | chr6 | 136389444 | ||
| chr6:136411681 | T | C | 1 | a0002c0014 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.183A>G | p.Leu61Leu | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/18 | 197/3758 | 183/2250 | 61/749 | chr6 | 136411681 | ||
| chr6:136421750 | A | C | 1 | a0003c0009 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.117T>G | p.Pro39Pro | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/18 | 131/3758 | 117/2250 | 39/749 | chr6 | 136421750 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:136342810 | A | C | 10 | a0001c0001t0001a0001c0001t0008a0001c0001t0012others(7): Show | 97 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1418T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 1418 | chr6 | 136342810 | |||||
| chr6:136342923 | T | TA | 6 | a0002c0002t0003a0002c0002t0005a0003c0003t0003others(3): Show | 54 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1304dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 1304 | chr6 | 136342923 | |||||
| chr6:136342923 | T | TAA | 2 | a0001c0001t0004a0001c0001t0014 | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304dupTT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 1304 | chr6 | 136342923 | |||||
| chr6:136343001 | C | A | 1 | a0001c0001t0012 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1227G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 1227 | chr6 | 136343001 | |||||
| chr6:136343200 | T | A | 1 | a0002c0002t0011 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1028A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 1028 | chr6 | 136343200 | |||||
| chr6:136343450 | G | A | 1 | a0001c0001t0013 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 778 | chr6 | 136343450 | |||||
| chr6:136343556 | T | C | 2 | a0006c0006t0006a0008c0008t0006 | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*672A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 672 | chr6 | 136343556 | |||||
| chr6:136343583 | G | T | 1 | a0002c0002t0011 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*645C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 645 | chr6 | 136343583 | |||||
| chr6:136343765 | A | T | 1 | a0002c0002t0007 | 4 | HG02723.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*463T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 463 | chr6 | 136343765 | |||||
| chr6:136343846 | T | TA | 1 | a0002c0002t0005 | 6 | HG00408.hp1 HG02015.hp1 NA18978.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*381dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 381 | chr6 | 136343846 | |||||
| chr6:136343853 | T | A | 1 | a0001c0001t0014 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*375A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 375 | chr6 | 136343853 | |||||
| chr6:136343859 | T | A | 2 | a0001c0001t0004a0001c0001t0014 | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*369A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 369 | chr6 | 136343859 | |||||
| chr6:136343861 | G | C | 1 | a0001c0001t0008 | 3 | HG02922.hp1 HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*367C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 367 | chr6 | 136343861 | |||||
| chr6:136343889 | C | G | 1 | a0002c0002t0009 | 2 | HG00733.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*339G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 339 | chr6 | 136343889 | |||||
| chr6:136344174 | A | C | 1 | a0002c0002t0010 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 18/18 | 54 | chr6 | 136344174 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:136344624 | G | A | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2240-386C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136344624 | ||||||
| chr6:136344633 | TAACATGA others(6): Show |
T | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2240-408_2240-396d others(15): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136344633 | ||||||
| chr6:136344686 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2240-448C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136344686 | ||||||
| chr6:136344724 | A | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.2240-486T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136344724 | ||||||
| chr6:136344866 | C | T | 8 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0069others(5): Show | 8 | NA18953.hp2 NA18961.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.2240-628G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136344866 | ||||||
| chr6:136344975 | A | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.2240-737T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136344975 | ||||||
| chr6:136345028 | T | A | 1 | a0005c0005t0001g0169 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2240-790A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136345028 | ||||||
| chr6:136345211 | G | A | 1 | a0002c0002t0003g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2239+645C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136345211 | ||||||
| chr6:136345503 | G | A | 1 | a0002c0002t0002g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2239+353C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136345503 | ||||||
| chr6:136345640 | G | C | 1 | a0001c0001t0004g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2239+216C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136345640 | ||||||
| chr6:136345778 | G | A | 1 | a0001c0001t0004g0088 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2239+78C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 17/17 | chr6 | 136345778 | ||||||
| chr6:136346158 | T | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2016-79A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136346158 | ||||||
| chr6:136346205 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2016-126C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136346205 | ||||||
| chr6:136346400 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2016-321G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136346400 | ||||||
| chr6:136346668 | T | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG00735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2016-589A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136346668 | ||||||
| chr6:136346727 | T | TAA | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.2016-649_2016-648i others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136346727 | ||||||
| chr6:136346959 | G | A | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.2016-880C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136346959 | ||||||
| chr6:136347107 | C | CTCCAACT others(17): Show |
16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2016-1029_2016-102 others(28): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136347107 | ||||||
| chr6:136347265 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2016-1186C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136347265 | ||||||
| chr6:136347330 | A | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.2016-1251T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136347330 | ||||||
| chr6:136347375 | C | CT | 15 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(12): Show | 15 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2016-1297dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136347375 | ||||||
| chr6:136347640 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2016-1561C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136347640 | ||||||
| chr6:136347667 | A | G | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2016-1588T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136347667 | ||||||
| chr6:136347798 | T | G | 1 | a0002c0002t0003g0009 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2016-1719A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136347798 | ||||||
| chr6:136347981 | A | G | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.2016-1902T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136347981 | ||||||
| chr6:136348011 | GC | G | 55 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0102others(52): Show | 55 | HG00408.hp2 HG01106.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.2016-1933delG | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136348011 | ||||||
| chr6:136348140 | T | G | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2016-2061A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136348140 | ||||||
| chr6:136348214 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2016-2135G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136348214 | ||||||
| chr6:136348413 | G | A | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.2016-2334C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136348413 | ||||||
| chr6:136348426 | A | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2016-2347T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136348426 | ||||||
| chr6:136348661 | T | C | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2016-2582A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136348661 | ||||||
| chr6:136348877 | C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0117 | 3 | HG02572.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2016-2798G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136348877 | ||||||
| chr6:136349534 | C | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2016-3455G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136349534 | ||||||
| chr6:136349789 | A | T | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2016-3710T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136349789 | ||||||
| chr6:136349799 | T | C | 1 | a0002c0002t0002g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2016-3720A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136349799 | ||||||
| chr6:136349818 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2016-3739C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136349818 | ||||||
| chr6:136349857 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2016-3778T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136349857 | ||||||
| chr6:136349924 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2016-3845C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136349924 | ||||||
| chr6:136349946 | G | A | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2016-3867C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136349946 | ||||||
| chr6:136350208 | G | A | 15 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(12): Show | 15 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2016-4129C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136350208 | ||||||
| chr6:136350400 | C | G | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2016-4321G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136350400 | ||||||
| chr6:136350583 | C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0143 | 3 | NA18957.hp2 NA19062.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2016-4504G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136350583 | ||||||
| chr6:136350956 | T | G | 24 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(21): Show | 24 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2016-4877A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136350956 | ||||||
| chr6:136350973 | C | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2016-4894G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136350973 | ||||||
| chr6:136351011 | T | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2016-4932A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351011 | ||||||
| chr6:136351124 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2016-5045G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351124 | ||||||
| chr6:136351236 | T | TA | 40 | a0001c0001t0004g0069a0001c0001t0004g0248a0002c0002t0002g0034others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.2016-5158dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351236 | ||||||
| chr6:136351236 | TA | T | 10 | a0001c0001t0004g0068a0002c0002t0003g0003a0002c0002t0003g0177others(7): Show | 10 | HG01346.hp2 HG02155.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2016-5158delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351236 | ||||||
| chr6:136351236 | TAA | T | 12 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(9): Show | 12 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2016-5159_2016-515 others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351236 | ||||||
| chr6:136351249 | A | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(90): Show | 93 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2016-5170T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351249 | ||||||
| chr6:136351372 | T | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2016-5293A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351372 | ||||||
| chr6:136351824 | G | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2015+4868C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351824 | ||||||
| chr6:136351965 | G | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.2015+4727C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136351965 | ||||||
| chr6:136352156 | G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2015+4536C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136352156 | ||||||
| chr6:136352190 | A | AT | 124 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(121): Show | 124 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2015+4501dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136352190 | ||||||
| chr6:136352190 | A | ATT | 29 | a0001c0001t0004g0071a0002c0002t0003g0006a0002c0002t0003g0009others(26): Show | 29 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.2015+4500_2015+450 others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136352190 | ||||||
| chr6:136352190 | AT | A | 6 | a0002c0002t0002g0225a0002c0002t0002g0227a0002c0002t0003g0003others(3): Show | 6 | HG01358.hp1 HG02451.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2015+4501delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136352190 | ||||||
| chr6:136352214 | G | A | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2015+4478C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136352214 | ||||||
| chr6:136352571 | A | C | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2015+4121T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136352571 | ||||||
| chr6:136352612 | T | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2015+4080A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136352612 | ||||||
| chr6:136352996 | T | A | 1 | a0002c0002t0002g0199 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2015+3696A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136352996 | ||||||
| chr6:136353173 | A | C | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2015+3519T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136353173 | ||||||
| chr6:136353245 | T | A | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2015+3447A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136353245 | ||||||
| chr6:136353249 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2015+3443T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136353249 | ||||||
| chr6:136353517 | T | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2015+3175A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136353517 | ||||||
| chr6:136353520 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2015+3172A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136353520 | ||||||
| chr6:136353658 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2015+3034T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136353658 | ||||||
| chr6:136353710 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2015+2982A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136353710 | ||||||
| chr6:136354122 | A | T | 48 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(45): Show | 48 | HG00408.hp2 HG01106.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.2015+2570T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354122 | ||||||
| chr6:136354123 | T | A | 48 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(45): Show | 48 | HG00408.hp2 HG01106.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.2015+2569A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354123 | ||||||
| chr6:136354123 | T | TTA | 147 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(144): Show | 147 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2015+2567_2015+256 others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354123 | ||||||
| chr6:136354143 | CATCTACT others(16): Show |
C | 6 | a0004c0004t0001g0080a0004c0004t0001g0096a0004c0004t0001g0118others(3): Show | 6 | HG02451.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2015+2526_2015+254 others(27): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354143 | ||||||
| chr6:136354150 | T | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2015+2542A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354150 | ||||||
| chr6:136354200 | T | C | 1 | a0001c0001t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2015+2492A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354200 | ||||||
| chr6:136354204 | TAA | T | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.2015+2486_2015+248 others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354204 | ||||||
| chr6:136354351 | AATATATA others(35): Show |
A | 1 | a0002c0002t0002g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2015+2299_2015+234 others(46): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354351 | ||||||
| chr6:136354386 | T | C | 1 | a0009c0013t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2015+2306A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354386 | ||||||
| chr6:136354391 | GAT | G | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2015+2299_2015+230 others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354391 | ||||||
| chr6:136354442 | ATATAG | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.2015+2245_2015+224 others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354442 | ||||||
| chr6:136354448 | T | A | 15 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(12): Show | 15 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2015+2244A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354448 | ||||||
| chr6:136354464 | T | C | 1 | a0001c0001t0004g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2015+2228A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354464 | ||||||
| chr6:136354520 | G | A | 1 | a0002c0002t0011g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2015+2172C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354520 | ||||||
| chr6:136354625 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2015+2067G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354625 | ||||||
| chr6:136354753 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2015+1939A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136354753 | ||||||
| chr6:136355231 | G | A | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2015+1461C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355231 | ||||||
| chr6:136355268 | A | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(91): Show | 94 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2015+1424T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355268 | ||||||
| chr6:136355269 | A | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0175 | 2 | NA19006.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2015+1423T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355269 | ||||||
| chr6:136355279 | C | T | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.2015+1413G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355279 | ||||||
| chr6:136355325 | TA | T | 3 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2015+1366delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355325 | ||||||
| chr6:136355398 | T | G | 1 | a0004c0004t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2015+1294A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355398 | ||||||
| chr6:136355477 | T | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2015+1215A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355477 | ||||||
| chr6:136355492 | C | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2015+1200G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355492 | ||||||
| chr6:136355562 | CATTACAT others(6): Show |
C | 17 | a0001c0001t0014g0060a0003c0003t0003g0010a0003c0003t0003g0011others(14): Show | 17 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2015+1117_2015+112 others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355562 | ||||||
| chr6:136355583 | T | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2015+1109A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355583 | ||||||
| chr6:136355649 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2015+1043G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355649 | ||||||
| chr6:136355840 | C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2015+852G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355840 | ||||||
| chr6:136355864 | C | T | 2 | a0001c0001t0004g0061a0003c0003t0003g0188 | 2 | NA18522.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2015+828G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355864 | ||||||
| chr6:136355865 | G | C | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2015+827C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355865 | ||||||
| chr6:136355866 | T | G | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2015+826A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355866 | ||||||
| chr6:136355907 | G | T | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2015+785C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136355907 | ||||||
| chr6:136356141 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2015+551T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136356141 | ||||||
| chr6:136356163 | C | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2015+529G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136356163 | ||||||
| chr6:136356337 | A | AT | 59 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0001g0173others(56): Show | 59 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.2015+354dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136356337 | ||||||
| chr6:136356524 | G | GA | 31 | a0001c0001t0001g0063a0001c0001t0001g0101a0001c0001t0001g0108others(28): Show | 31 | HG00323.hp1 HG00621.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.2015+167dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136356524 | ||||||
| chr6:136356586 | GC | G | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.2015+105delG | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136356586 | ||||||
| chr6:136356638 | C | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2015+54G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136356638 | ||||||
| chr6:136356675 | T | C | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2015+17A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 16/17 | chr6 | 136356675 | ||||||
| chr6:136356996 | GTATTAA | G | 3 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177 | 3 | HG01358.hp1 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1913-208_1913-203d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136356996 | ||||||
| chr6:136357122 | A | G | 1 | a0002c0002t0002g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1913-328T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136357122 | ||||||
| chr6:136357405 | T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(173): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1913-611A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136357405 | ||||||
| chr6:136357411 | A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(173): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1913-617T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136357411 | ||||||
| chr6:136357420 | G | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1913-626C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136357420 | ||||||
| chr6:136357425 | A | G | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1913-631T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136357425 | ||||||
| chr6:136357866 | C | T | 3 | a0002c0002t0007g0205a0002c0002t0007g0206a0002c0002t0007g0207 | 3 | HG02723.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1913-1072G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136357866 | ||||||
| chr6:136357966 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1913-1172T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136357966 | ||||||
| chr6:136358131 | G | T | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1913-1337C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136358131 | ||||||
| chr6:136358238 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1913-1444G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136358238 | ||||||
| chr6:136358338 | T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(173): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1912+1482A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136358338 | ||||||
| chr6:136358420 | G | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1912+1400C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136358420 | ||||||
| chr6:136358678 | A | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.1912+1142T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136358678 | ||||||
| chr6:136359086 | CTTAATA | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1912+728_1912+733d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136359086 | ||||||
| chr6:136359108 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1912+712A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136359108 | ||||||
| chr6:136359158 | CA | C | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.1912+661delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136359158 | ||||||
| chr6:136359590 | A | C | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1912+230T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136359590 | ||||||
| chr6:136359760 | C | A | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1912+60G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 15/17 | chr6 | 136359760 | ||||||
| chr6:136360153 | C | CT | 27 | a0001c0001t0001g0043a0001c0001t0004g0016a0001c0001t0004g0061others(24): Show | 27 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1804-123dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/17 | chr6 | 136360153 | ||||||
| chr6:136360153 | CT | C | 30 | a0001c0001t0001g0063a0001c0001t0001g0101a0001c0001t0001g0108others(27): Show | 30 | HG00323.hp1 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.1804-123delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/17 | chr6 | 136360153 | ||||||
| chr6:136360266 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1804-235G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/17 | chr6 | 136360266 | ||||||
| chr6:136360351 | G | A | 3 | a0002c0002t0007g0205a0002c0002t0007g0206a0002c0002t0007g0207 | 3 | HG02723.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1804-320C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/17 | chr6 | 136360351 | ||||||
| chr6:136360368 | A | G | 1 | a0003c0003t0003g0010 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1803+329T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/17 | chr6 | 136360368 | ||||||
| chr6:136360535 | A | G | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1803+162T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/17 | chr6 | 136360535 | ||||||
| chr6:136360579 | G | C | 8 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0036others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1803+118C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 13/17 | chr6 | 136360579 | ||||||
| chr6:136360880 | G | A | 2 | a0002c0002t0007g0246a0002c0002t0011g0245 | 2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1702-82C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 12/17 | chr6 | 136360880 | ||||||
| chr6:136361258 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1527-79A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136361258 | ||||||
| chr6:136361311 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1527-132T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136361311 | ||||||
| chr6:136361418 | T | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.1527-239A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136361418 | ||||||
| chr6:136361617 | A | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(173): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1527-438T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136361617 | ||||||
| chr6:136361930 | A | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.1526+520T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136361930 | ||||||
| chr6:136362003 | C | T | 1 | a0002c0002t0002g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1526+447G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136362003 | ||||||
| chr6:136362065 | T | A | 1 | a0001c0001t0004g0084 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1526+385A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136362065 | ||||||
| chr6:136362074 | AT | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1526+375delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136362074 | ||||||
| chr6:136362302 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1526+148A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136362302 | ||||||
| chr6:136362395 | G | A | 1 | a0002c0002t0002g0235 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1526+55C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 11/17 | chr6 | 136362395 | ||||||
| chr6:136362878 | T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0163a0001c0012t0001g0174 | 3 | HG02273.hp1 NA18969.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1274-176A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136362878 | ||||||
| chr6:136362900 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1274-198C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136362900 | ||||||
| chr6:136363126 | C | A | 1 | a0002c0002t0002g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1274-424G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136363126 | ||||||
| chr6:136363220 | C | T | 1 | a0002c0002t0002g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1274-518G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136363220 | ||||||
| chr6:136363399 | C | T | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1274-697G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136363399 | ||||||
| chr6:136363407 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1274-705T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136363407 | ||||||
| chr6:136363662 | C | T | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1274-960G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136363662 | ||||||
| chr6:136363713 | G | A | 19 | a0001c0001t0004g0016a0001c0001t0004g0065a0001c0001t0004g0066others(16): Show | 19 | HG00408.hp2 HG01433.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.1274-1011C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136363713 | ||||||
| chr6:136363944 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1274-1242G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136363944 | ||||||
| chr6:136363987 | A | G | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1274-1285T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136363987 | ||||||
| chr6:136364332 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1273+1403G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136364332 | ||||||
| chr6:136364337 | A | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0072others(76): Show | 79 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1273+1398T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136364337 | ||||||
| chr6:136364372 | A | G | 2 | a0002c0002t0002g0235a0002c0002t0003g0003 | 2 | HG03453.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1273+1363T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136364372 | ||||||
| chr6:136364536 | T | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(173): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1273+1199A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136364536 | ||||||
| chr6:136364804 | T | G | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+931A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136364804 | ||||||
| chr6:136364995 | T | C | 3 | a0003c0003t0003g0185a0003c0003t0003g0187a0003c0003t0003g0188 | 3 | NA19060.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1273+740A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136364995 | ||||||
| chr6:136365064 | T | C | 1 | a0001c0001t0014g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1273+671A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136365064 | ||||||
| chr6:136365228 | C | T | 1 | a0001c0001t0012g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1273+507G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136365228 | ||||||
| chr6:136365242 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1273+493A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136365242 | ||||||
| chr6:136365573 | C | T | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.1273+162G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136365573 | ||||||
| chr6:136365611 | T | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1273+124A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136365611 | ||||||
| chr6:136365688 | G | A | 1 | a0001c0001t0004g0084 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1273+47C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 10/17 | chr6 | 136365688 | ||||||
| chr6:136366848 | C | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(172): Show | 175 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.877-409G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136366848 | ||||||
| chr6:136366850 | AC | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.877-412delG | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136366850 | ||||||
| chr6:136367298 | A | AT | 7 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(4): Show | 7 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.877-860dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136367298 | ||||||
| chr6:136367818 | C | A | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.877-1379G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136367818 | ||||||
| chr6:136367881 | C | CT | 112 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(109): Show | 112 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.877-1443dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136367881 | ||||||
| chr6:136368014 | G | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.877-1575C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368014 | ||||||
| chr6:136368222 | A | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(109): Show | 112 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.877-1783T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368222 | ||||||
| chr6:136368255 | C | A | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.877-1816G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368255 | ||||||
| chr6:136368275 | C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0175 | 2 | NA19006.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.877-1836G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368275 | ||||||
| chr6:136368292 | A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(109): Show | 112 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.877-1853T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368292 | ||||||
| chr6:136368416 | A | C | 1 | a0001c0001t0004g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.877-1977T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368416 | ||||||
| chr6:136368712 | G | A | 1 | a0006c0006t0006g0180 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.877-2273C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368712 | ||||||
| chr6:136368755 | AAC | A | 55 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(52): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.877-2318_877-2317d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368755 | ||||||
| chr6:136368759 | CAAAT | C | 3 | a0004c0004t0001g0118a0004c0004t0001g0119a0004c0004t0001g0120 | 3 | HG02723.hp2 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.877-2324_877-2321d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368759 | ||||||
| chr6:136368785 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.877-2346C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136368785 | ||||||
| chr6:136369089 | C | T | 1 | a0002c0002t0011g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.877-2650G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136369089 | ||||||
| chr6:136369101 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.877-2662C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136369101 | ||||||
| chr6:136369178 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.877-2739T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136369178 | ||||||
| chr6:136369262 | A | T | 1 | a0001c0001t0001g0173 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.877-2823T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136369262 | ||||||
| chr6:136369325 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.877-2886C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136369325 | ||||||
| chr6:136369570 | C | CA | 111 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(108): Show | 111 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.876+2930dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136369570 | ||||||
| chr6:136369873 | A | G | 1 | a0003c0003t0003g0191 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.876+2628T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136369873 | ||||||
| chr6:136370034 | T | TA | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+2466dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370034 | ||||||
| chr6:136370200 | T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.876+2301A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370200 | ||||||
| chr6:136370362 | T | G | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.876+2139A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370362 | ||||||
| chr6:136370445 | A | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.876+2056T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370445 | ||||||
| chr6:136370490 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.876+2011G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370490 | ||||||
| chr6:136370824 | A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.876+1677T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370824 | ||||||
| chr6:136370905 | CT | C | 57 | a0001c0001t0001g0043a0001c0001t0004g0061a0001c0001t0004g0248others(54): Show | 57 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.876+1595delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370905 | ||||||
| chr6:136370905 | CTT | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(94): Show | 97 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.876+1594_876+1595d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370905 | ||||||
| chr6:136370905 | CTTT | C | 23 | a0001c0001t0004g0016a0001c0001t0004g0064a0001c0001t0004g0065others(20): Show | 23 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.876+1593_876+1595d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370905 | ||||||
| chr6:136370913 | T | A | 1 | a0002c0002t0003g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.876+1588A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370913 | ||||||
| chr6:136370973 | G | A | 1 | a0002c0002t0002g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.876+1528C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136370973 | ||||||
| chr6:136371252 | C | A | 12 | a0002c0002t0002g0032a0002c0002t0002g0033a0002c0002t0002g0034others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.876+1249G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136371252 | ||||||
| chr6:136371323 | C | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(172): Show | 175 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.876+1178G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136371323 | ||||||
| chr6:136372221 | C | T | 55 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(52): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.876+280G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136372221 | ||||||
| chr6:136372368 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.876+133T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 8/17 | chr6 | 136372368 | ||||||
| chr6:136373251 | T | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.752-626A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136373251 | ||||||
| chr6:136373459 | A | C | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.752-834T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136373459 | ||||||
| chr6:136373471 | T | C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-846A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136373471 | ||||||
| chr6:136373743 | C | G | 1 | a0010c0011t0001g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.752-1118G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136373743 | ||||||
| chr6:136374074 | G | A | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.752-1449C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136374074 | ||||||
| chr6:136374136 | T | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.752-1511A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136374136 | ||||||
| chr6:136374173 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.752-1548C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136374173 | ||||||
| chr6:136374530 | A | G | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.752-1905T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136374530 | ||||||
| chr6:136374714 | A | G | 1 | a0001c0001t0004g0077 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.752-2089T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136374714 | ||||||
| chr6:136375146 | T | C | 1 | a0001c0001t0004g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.752-2521A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375146 | ||||||
| chr6:136375165 | A | G | 3 | a0001c0001t0008g0094a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | HG02922.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.752-2540T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375165 | ||||||
| chr6:136375188 | C | T | 2 | a0002c0002t0002g0242a0002c0002t0002g0243 | 2 | NA18971.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.752-2563G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375188 | ||||||
| chr6:136375286 | C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0123 | 2 | NA18948.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.751+2469G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375286 | ||||||
| chr6:136375287 | G | A | 1 | a0002c0002t0002g0210 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.751+2468C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375287 | ||||||
| chr6:136375291 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.751+2464T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375291 | ||||||
| chr6:136375406 | T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(173): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.751+2349A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375406 | ||||||
| chr6:136375453 | A | G | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.751+2302T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375453 | ||||||
| chr6:136375456 | G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00544.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.751+2299C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375456 | ||||||
| chr6:136375668 | T | C | 1 | a0002c0002t0002g0236 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.751+2087A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375668 | ||||||
| chr6:136375691 | T | C | 1 | a0002c0002t0005g0020 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.751+2064A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375691 | ||||||
| chr6:136375734 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.751+2021C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375734 | ||||||
| chr6:136375927 | A | AT | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.751+1827dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375927 | ||||||
| chr6:136375948 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.751+1807T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136375948 | ||||||
| chr6:136376104 | G | GT | 10 | a0001c0001t0001g0092a0001c0001t0001g0142a0001c0001t0001g0158others(7): Show | 10 | HG01106.hp2 HG01258.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.751+1650dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376104 | ||||||
| chr6:136376121 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.751+1634G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376121 | ||||||
| chr6:136376122 | G | C | 3 | a0001c0001t0008g0094a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | HG02922.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.751+1633C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376122 | ||||||
| chr6:136376230 | C | A | 1 | a0003c0003t0003g0125 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.751+1525G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376230 | ||||||
| chr6:136376260 | G | T | 10 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0099others(7): Show | 10 | HG02135.hp2 NA18939.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.751+1495C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376260 | ||||||
| chr6:136376320 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.751+1435C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376320 | ||||||
| chr6:136376333 | CA | C | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.751+1421delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376333 | ||||||
| chr6:136376350 | C | T | 13 | a0002c0002t0002g0062a0002c0002t0002g0199a0002c0002t0002g0208others(10): Show | 13 | HG00423.hp2 HG00544.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.751+1405G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376350 | ||||||
| chr6:136376390 | C | T | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.751+1365G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376390 | ||||||
| chr6:136376550 | C | G | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.751+1205G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376550 | ||||||
| chr6:136376635 | T | C | 7 | a0001c0001t0004g0016a0001c0001t0004g0071a0001c0001t0004g0077others(4): Show | 7 | HG00408.hp2 HG01433.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.751+1120A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376635 | ||||||
| chr6:136376812 | C | T | 1 | a0002c0002t0005g0020 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.751+943G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376812 | ||||||
| chr6:136376966 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.751+789A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136376966 | ||||||
| chr6:136377043 | GGATGTAG others(12): Show |
G | 2 | a0001c0001t0001g0113a0001c0001t0004g0075 | 2 | HG01123.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.751+693_751+711del others(19): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136377043 | ||||||
| chr6:136377077 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.751+678C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136377077 | ||||||
| chr6:136377133 | T | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.751+622A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136377133 | ||||||
| chr6:136377181 | G | A | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.751+574C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136377181 | ||||||
| chr6:136377350 | T | C | 15 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(12): Show | 15 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.751+405A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136377350 | ||||||
| chr6:136377369 | C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.751+386G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136377369 | ||||||
| chr6:136377531 | C | A | 14 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(11): Show | 14 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.751+224G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136377531 | ||||||
| chr6:136377559 | C | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.751+196G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 7/17 | chr6 | 136377559 | ||||||
| chr6:136378349 | G | A | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-481C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136378349 | ||||||
| chr6:136378444 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.638-576C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136378444 | ||||||
| chr6:136378685 | T | C | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-817A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136378685 | ||||||
| chr6:136379214 | A | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.638-1346T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379214 | ||||||
| chr6:136379215 | A | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.638-1347T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379215 | ||||||
| chr6:136379224 | T | G | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.638-1356A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379224 | ||||||
| chr6:136379225 | A | G | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.638-1357T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379225 | ||||||
| chr6:136379228 | A | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.638-1360T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379228 | ||||||
| chr6:136379229 | A | G | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.638-1361T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379229 | ||||||
| chr6:136379230 | T | A | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.638-1362A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379230 | ||||||
| chr6:136379260 | T | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.638-1392A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379260 | ||||||
| chr6:136379821 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.638-1953T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379821 | ||||||
| chr6:136379835 | G | T | 1 | a0002c0002t0002g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.638-1967C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136379835 | ||||||
| chr6:136380069 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.638-2201G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136380069 | ||||||
| chr6:136380231 | C | T | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-2363G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136380231 | ||||||
| chr6:136380335 | A | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.638-2467T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136380335 | ||||||
| chr6:136380494 | G | T | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-2626C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136380494 | ||||||
| chr6:136380545 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.638-2677C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136380545 | ||||||
| chr6:136380755 | T | C | 1 | a0002c0002t0002g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.638-2887A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136380755 | ||||||
| chr6:136380852 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+2819G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136380852 | ||||||
| chr6:136381100 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.637+2571T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381100 | ||||||
| chr6:136381347 | T | A | 1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637+2324A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381347 | ||||||
| chr6:136381610 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+2061C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381610 | ||||||
| chr6:136381873 | A | C | 2 | a0002c0002t0009g0223a0002c0002t0009g0224 | 2 | HG00733.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.637+1798T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381873 | ||||||
| chr6:136381877 | T | TACAC | 3 | a0001c0001t0013g0179a0002c0002t0002g0233a0002c0014t0002g0146 | 3 | HG03654.hp1 HG03654.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+1790_637+1793d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0043a0001c0001t0004g0064a0001c0001t0004g0075others(1): Show | 4 | HG02040.hp2 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1784_637+1793d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | T | TACACACA others(5): Show |
1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637+1782_637+1793d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | T | TACACACA others(7): Show |
1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.637+1780_637+1793d others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | T | TACACACA others(9): Show |
8 | a0001c0001t0004g0066a0001c0001t0004g0069a0001c0001t0004g0070others(5): Show | 8 | HG02300.hp1 HG03041.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+1778_637+1793d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | T | TACACACA others(11): Show |
10 | a0001c0001t0004g0016a0001c0001t0004g0068a0001c0001t0004g0071others(7): Show | 10 | HG00408.hp2 HG01433.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+1776_637+1793d others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | T | TACACACA others(13): Show |
2 | a0001c0001t0004g0065a0006c0006t0006g0182 | 2 | HG02622.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.637+1774_637+1793d others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | T | TACACACA others(15): Show |
2 | a0001c0001t0004g0067a0001c0001t0004g0089 | 2 | HG01123.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.637+1772_637+1793d others(24): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | T | TACACACA others(17): Show |
1 | a0001c0001t0004g0077 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.637+1770_637+1793d others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | TAC | T | 60 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.637+1792_637+1793d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | TACAC | T | 16 | a0002c0002t0002g0045a0002c0002t0005g0007a0003c0003t0003g0010others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+1790_637+1793d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381877 | TACACAC | T | 7 | a0001c0001t0001g0162a0002c0002t0002g0208a0002c0002t0002g0212others(4): Show | 7 | HG01074.hp1 HG02074.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+1788_637+1793d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381877 | ||||||
| chr6:136381915 | CACACAGA others(3): Show |
C | 1 | a0002c0002t0003g0009 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.637+1746_637+1755d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381915 | ||||||
| chr6:136381919 | C | CACACACA others(15): Show |
1 | a0001c0001t0001g0175 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.637+1751_637+1752i others(24): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(11): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0170 | 2 | NA18949.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.637+1751_637+1752i others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(9): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0172others(1): Show | 4 | HG00733.hp1 HG02080.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1751_637+1752i others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(7): Show |
11 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0107others(8): Show | 11 | HG00642.hp2 HG02015.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.637+1751_637+1752i others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(9): Show |
1 | a0004c0004t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.637+1751_637+1752i others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(13): Show |
1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.637+1751_637+1752i others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(5): Show |
10 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0001g0147others(7): Show | 10 | HG00423.hp1 HG00639.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+1751_637+1752i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(7): Show |
1 | a0001c0001t0001g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.637+1751_637+1752i others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(3): Show |
11 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0116others(8): Show | 11 | HG00544.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.637+1751_637+1752i others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(5): Show |
1 | a0004c0004t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.637+1751_637+1752i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACACA others(1): Show |
16 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(13): Show | 16 | HG01258.hp1 HG01433.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.637+1751_637+1752i others(10): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACACAG | 8 | a0001c0001t0001g0093a0001c0001t0001g0131a0001c0001t0001g0158others(5): Show | 8 | HG01978.hp2 HG02055.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+1751_637+1752i others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CACAG | 4 | a0001c0001t0001g0063a0001c0001t0001g0126a0001c0001t0001g0153others(1): Show | 4 | HG00621.hp1 HG01346.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1751_637+1752i others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | CAG | 22 | a0001c0001t0001g0079a0001c0001t0001g0101a0001c0001t0001g0108others(19): Show | 22 | HG00323.hp1 HG01123.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.637+1750_637+1751d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381919 | C | G | 50 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0183others(47): Show | 50 | HG00408.hp1 HG00639.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.637+1752G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381919 | ||||||
| chr6:136381921 | G | C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+1750C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381921 | ||||||
| chr6:136381923 | G | C | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.637+1748C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381923 | ||||||
| chr6:136381982 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+1689C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136381982 | ||||||
| chr6:136382005 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637+1666C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382005 | ||||||
| chr6:136382044 | C | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.637+1627G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382044 | ||||||
| chr6:136382129 | T | C | 17 | a0001c0001t0013g0179a0003c0003t0003g0010a0003c0003t0003g0011others(14): Show | 17 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.637+1542A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382129 | ||||||
| chr6:136382166 | C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(77): Show | 80 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.637+1505G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382166 | ||||||
| chr6:136382170 | CAG | C | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+1499_637+1500d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382170 | ||||||
| chr6:136382210 | T | C | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.637+1461A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382210 | ||||||
| chr6:136382427 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.637+1244G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382427 | ||||||
| chr6:136382579 | T | C | 1 | a0002c0002t0002g0244 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.637+1092A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382579 | ||||||
| chr6:136382750 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.637+921G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382750 | ||||||
| chr6:136382989 | T | C | 1 | a0002c0002t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.637+682A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 6/17 | chr6 | 136382989 | ||||||
| chr6:136384087 | C | T | 1 | a0002c0002t0002g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.527-306G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384087 | ||||||
| chr6:136384115 | G | A | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-334C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384115 | ||||||
| chr6:136384396 | C | T | 1 | a0002c0002t0003g0012 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.527-615G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384396 | ||||||
| chr6:136384425 | T | C | 2 | a0001c0001t0001g0150a0001c0010t0001g0151 | 2 | HG01358.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.527-644A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384425 | ||||||
| chr6:136384494 | C | CT | 17 | a0001c0001t0001g0183a0003c0003t0003g0010a0003c0003t0003g0011others(14): Show | 17 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.527-714dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384494 | ||||||
| chr6:136384508 | T | G | 4 | a0001c0001t0001g0159a0002c0002t0002g0201a0002c0002t0005g0004others(1): Show | 4 | HG01943.hp2 NA18978.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-727A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384508 | ||||||
| chr6:136384641 | G | A | 3 | a0003c0003t0003g0125a0003c0003t0003g0189a0003c0003t0003g0191 | 3 | HG02155.hp2 NA18942.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.527-860C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384641 | ||||||
| chr6:136384744 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.527-963G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384744 | ||||||
| chr6:136384902 | G | A | 1 | a0002c0002t0002g0235 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.527-1121C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136384902 | ||||||
| chr6:136385008 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.527-1227C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385008 | ||||||
| chr6:136385108 | G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0123 | 2 | NA18948.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.527-1327C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385108 | ||||||
| chr6:136385172 | T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(173): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.527-1391A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385172 | ||||||
| chr6:136385270 | TA | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.527-1490delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385270 | ||||||
| chr6:136385291 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.527-1510C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385291 | ||||||
| chr6:136385374 | A | G | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.527-1593T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385374 | ||||||
| chr6:136385391 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.527-1610A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385391 | ||||||
| chr6:136385468 | T | C | 1 | a0002c0002t0002g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.527-1687A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385468 | ||||||
| chr6:136385931 | C | A | 1 | a0001c0001t0004g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.527-2150G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385931 | ||||||
| chr6:136385932 | G | A | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.527-2151C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385932 | ||||||
| chr6:136385941 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.527-2160A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385941 | ||||||
| chr6:136385961 | T | G | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.527-2180A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385961 | ||||||
| chr6:136385968 | T | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.527-2187A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385968 | ||||||
| chr6:136385974 | T | C | 3 | a0004c0004t0001g0118a0004c0004t0001g0119a0004c0004t0001g0120 | 3 | HG02723.hp2 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.527-2193A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136385974 | ||||||
| chr6:136386665 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.526+1728C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136386665 | ||||||
| chr6:136386674 | A | G | 55 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(52): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.526+1719T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136386674 | ||||||
| chr6:136386699 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.526+1694C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136386699 | ||||||
| chr6:136387069 | C | T | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.526+1324G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136387069 | ||||||
| chr6:136387250 | CG | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0136a0001c0001t0001g0141 | 3 | NA18939.hp1 NA18944.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.526+1142delC | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136387250 | ||||||
| chr6:136387475 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.526+918T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136387475 | ||||||
| chr6:136387525 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.526+868A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136387525 | ||||||
| chr6:136387536 | T | C | 14 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(11): Show | 14 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.526+857A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136387536 | ||||||
| chr6:136387833 | T | C | 1 | a0002c0002t0002g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.526+560A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136387833 | ||||||
| chr6:136387910 | T | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.526+483A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136387910 | ||||||
| chr6:136387951 | A | T | 1 | a0002c0002t0002g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.526+442T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136387951 | ||||||
| chr6:136388031 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526+362A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136388031 | ||||||
| chr6:136388120 | T | A | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.526+273A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 5/17 | chr6 | 136388120 | ||||||
| chr6:136388708 | A | G | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.409-198T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/17 | chr6 | 136388708 | ||||||
| chr6:136388761 | G | A | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.409-251C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/17 | chr6 | 136388761 | ||||||
| chr6:136388787 | T | G | 14 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(11): Show | 14 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-277A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/17 | chr6 | 136388787 | ||||||
| chr6:136388817 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.409-307G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/17 | chr6 | 136388817 | ||||||
| chr6:136388829 | C | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.409-319G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/17 | chr6 | 136388829 | ||||||
| chr6:136389148 | T | C | 1 | a0001c0001t0004g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.408+206A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/17 | chr6 | 136389148 | ||||||
| chr6:136389261 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.408+93A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/17 | chr6 | 136389261 | ||||||
| chr6:136389340 | G | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.408+14C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 4/17 | chr6 | 136389340 | ||||||
| chr6:136389522 | G | A | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | splice_region_variant&intron_variant | LOW | c.245-5C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136389522 | ||||||
| chr6:136389530 | TTA | T | 15 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(12): Show | 15 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.245-15_245-14delTA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136389530 | ||||||
| chr6:136389531 | TA | T | 17 | a0001c0001t0001g0063a0001c0001t0001g0147a0001c0001t0001g0160others(14): Show | 17 | HG00423.hp2 HG01358.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.245-15delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136389531 | ||||||
| chr6:136389531 | TAAA | T | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-17_245-15delTT others(1): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136389531 | ||||||
| chr6:136389840 | T | C | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245-323A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136389840 | ||||||
| chr6:136390066 | TTTAG | T | 8 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0069others(5): Show | 8 | NA18953.hp2 NA18961.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-553_245-550del others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136390066 | ||||||
| chr6:136390329 | A | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.245-812T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136390329 | ||||||
| chr6:136390576 | T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.245-1059A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136390576 | ||||||
| chr6:136390655 | AAAACAAA others(5): Show |
A | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.245-1150_245-1139d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136390655 | ||||||
| chr6:136391123 | C | A | 1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.245-1606G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391123 | ||||||
| chr6:136391151 | G | A | 5 | a0001c0001t0004g0016a0001c0001t0004g0077a0001c0001t0004g0078others(2): Show | 5 | HG01433.hp2 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-1634C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391151 | ||||||
| chr6:136391188 | T | C | 1 | a0003c0003t0003g0015 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.245-1671A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391188 | ||||||
| chr6:136391266 | C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.245-1749G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391266 | ||||||
| chr6:136391407 | C | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.245-1890G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391407 | ||||||
| chr6:136391415 | G | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.245-1898C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391415 | ||||||
| chr6:136391449 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.245-1932G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391449 | ||||||
| chr6:136391488 | A | G | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.245-1971T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391488 | ||||||
| chr6:136391511 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.245-1994G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391511 | ||||||
| chr6:136391543 | G | C | 1 | a0002c0002t0002g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.245-2026C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391543 | ||||||
| chr6:136391555 | A | AAAACAAC others(3): Show |
1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.245-2039_245-2038i others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391555 | ||||||
| chr6:136391555 | A | AAAC | 94 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(91): Show | 94 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.245-2041_245-2039d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391555 | ||||||
| chr6:136391555 | A | AAACAAC | 23 | a0001c0001t0001g0072a0001c0001t0001g0128a0002c0002t0003g0003others(20): Show | 23 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.245-2044_245-2039d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391555 | ||||||
| chr6:136391555 | AAAC | A | 27 | a0001c0001t0001g0043a0001c0001t0004g0016a0001c0001t0004g0061others(24): Show | 27 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.245-2041_245-2039d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391555 | ||||||
| chr6:136391555 | AAACAAC | A | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.245-2044_245-2039d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391555 | ||||||
| chr6:136391645 | C | CAAAAAAT | 63 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(60): Show | 63 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.245-2135_245-2129d others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391645 | ||||||
| chr6:136391673 | C | CA | 114 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0072others(111): Show | 114 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.245-2157dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391673 | ||||||
| chr6:136391709 | T | C | 1 | a0002c0002t0002g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.245-2192A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136391709 | ||||||
| chr6:136392223 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.245-2706C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392223 | ||||||
| chr6:136392283 | T | C | 1 | a0002c0002t0002g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.245-2766A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392283 | ||||||
| chr6:136392325 | T | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.245-2808A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392325 | ||||||
| chr6:136392368 | C | T | 1 | a0001c0001t0004g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.245-2851G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392368 | ||||||
| chr6:136392388 | C | CTTT | 15 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(12): Show | 15 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.245-2874_245-2872d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392388 | ||||||
| chr6:136392388 | CT | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(133): Show | 136 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.245-2872delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392388 | ||||||
| chr6:136392388 | CTT | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0141a0001c0001t0013g0179others(3): Show | 6 | HG01358.hp1 NA18906.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-2873_245-2872d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392388 | ||||||
| chr6:136392611 | G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-3094C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392611 | ||||||
| chr6:136392779 | G | A | 1 | a0002c0002t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-3262C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136392779 | ||||||
| chr6:136393343 | T | C | 1 | a0002c0002t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-3826A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393343 | ||||||
| chr6:136393394 | T | C | 1 | a0002c0002t0002g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.245-3877A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393394 | ||||||
| chr6:136393679 | C | T | 1 | a0002c0002t0002g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.245-4162G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393679 | ||||||
| chr6:136393798 | A | AT | 6 | a0002c0002t0002g0001a0002c0002t0002g0034a0002c0002t0002g0193others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-4282dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393798 | ||||||
| chr6:136393798 | AT | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(128): Show | 131 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.245-4282delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393798 | ||||||
| chr6:136393798 | ATT | A | 33 | a0001c0001t0001g0102a0001c0001t0001g0128a0001c0001t0001g0139others(30): Show | 33 | HG00323.hp1 HG00408.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.245-4283_245-4282d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393798 | ||||||
| chr6:136393977 | T | TA | 100 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0073others(97): Show | 100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.245-4461dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393977 | ||||||
| chr6:136393978 | A | AAT | 6 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0165others(3): Show | 6 | HG01106.hp1 HG03453.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-4462_245-4461i others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393978 | ||||||
| chr6:136393978 | A | AT | 6 | a0002c0002t0002g0032a0002c0002t0002g0193a0002c0002t0002g0230others(3): Show | 6 | HG02572.hp2 NA18940.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-4462dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393978 | ||||||
| chr6:136393978 | AT | A | 61 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(58): Show | 61 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.245-4462delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393978 | ||||||
| chr6:136393979 | T | A | 9 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0123others(6): Show | 9 | HG01257.hp2 HG03579.hp1 HG04204.hp2 others(6): Show |
intron_variant | MODIFIER | c.245-4462A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393979 | ||||||
| chr6:136393980 | T | A | 59 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(56): Show | 59 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.245-4463A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393980 | ||||||
| chr6:136393981 | T | A | 2 | a0002c0002t0003g0018a0002c0002t0003g0085 | 2 | HG01358.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.245-4464A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136393981 | ||||||
| chr6:136394129 | G | A | 2 | a0004c0004t0001g0118a0004c0004t0001g0120 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.245-4612C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394129 | ||||||
| chr6:136394227 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.245-4710G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394227 | ||||||
| chr6:136394273 | G | A | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.245-4756C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394273 | ||||||
| chr6:136394279 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.245-4762C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394279 | ||||||
| chr6:136394426 | AT | A | 40 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(37): Show | 40 | HG00408.hp2 HG01106.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.245-4910delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394426 | ||||||
| chr6:136394759 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.245-5242G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394759 | ||||||
| chr6:136394808 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.245-5291A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394808 | ||||||
| chr6:136394858 | T | C | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.245-5341A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394858 | ||||||
| chr6:136394930 | T | TCATATAT others(13): Show |
1 | a0002c0002t0002g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.245-5433_245-5414d others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394930 | ||||||
| chr6:136394931 | C | CAT | 12 | a0001c0001t0001g0134a0001c0001t0001g0137a0002c0002t0002g0220others(9): Show | 12 | HG00323.hp2 HG01106.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.245-5416_245-5415d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATAT | 27 | a0001c0001t0001g0029a0001c0001t0001g0074a0001c0001t0001g0100others(24): Show | 27 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.245-5418_245-5415d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATAT | 56 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0072others(53): Show | 56 | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.245-5420_245-5415d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(1): Show |
18 | a0001c0001t0001g0101a0001c0001t0001g0107a0001c0001t0001g0113others(15): Show | 18 | HG00642.hp2 HG01123.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.245-5422_245-5415d others(10): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(3): Show |
12 | a0001c0001t0001g0108a0001c0001t0001g0147a0001c0001t0001g0157others(9): Show | 12 | HG01074.hp1 HG01943.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.245-5424_245-5415d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(5): Show |
17 | a0001c0001t0001g0063a0001c0001t0001g0117a0001c0001t0001g0143others(14): Show | 17 | HG00621.hp2 HG01358.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.245-5426_245-5415d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(7): Show |
20 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0001t0001g0135others(17): Show | 20 | HG00423.hp2 HG00639.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.245-5428_245-5415d others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(9): Show |
19 | a0001c0001t0001g0079a0001c0001t0001g0123a0001c0001t0001g0155others(16): Show | 19 | HG00423.hp1 HG00735.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.245-5430_245-5415d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(11): Show |
7 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0001g0166others(4): Show | 7 | HG00408.hp1 HG00642.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-5432_245-5415d others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(17): Show |
1 | a0002c0002t0002g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.245-5415_245-5414i others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(19): Show |
7 | a0002c0002t0002g0034a0002c0002t0002g0036a0002c0002t0002g0037others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-5415_245-5414i others(28): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(27): Show |
1 | a0002c0002t0002g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.245-5415_245-5414i others(36): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(55): Show |
1 | a0002c0002t0002g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.245-5415_245-5414i others(64): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | C | CATATATA others(15): Show |
1 | a0002c0002t0002g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.245-5436_245-5415d others(24): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | CAT | C | 4 | a0001c0001t0001g0140a0002c0002t0002g0045a0002c0002t0002g0235others(1): Show | 4 | HG03490.hp2 HG04204.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-5416_245-5415d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | CATATATA others(1): Show |
C | 4 | a0001c0001t0001g0162a0001c0001t0008g0094a0001c0001t0008g0111others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-5422_245-5415d others(10): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | CATATATA others(3): Show |
C | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.245-5424_245-5415d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | CATATATA others(5): Show |
C | 1 | a0006c0006t0006g0180 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-5426_245-5415d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | CATATATA others(7): Show |
C | 19 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0065others(16): Show | 19 | HG00408.hp2 HG01433.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.245-5428_245-5415d others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | CATATATA others(9): Show |
C | 7 | a0001c0001t0004g0064a0001c0001t0004g0075a0001c0001t0004g0089others(4): Show | 7 | HG01123.hp2 HG02040.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-5430_245-5415d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394931 | CATATATA others(11): Show |
C | 1 | a0001c0001t0001g0159 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.245-5432_245-5415d others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394931 | ||||||
| chr6:136394968 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.245-5452_245-5451i others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394968 | ||||||
| chr6:136394972 | C | A | 1 | a0002c0002t0002g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.245-5455G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136394972 | ||||||
| chr6:136395408 | A | AT | 6 | a0001c0001t0001g0100a0001c0001t0001g0157a0002c0002t0002g0212others(3): Show | 6 | HG00544.hp2 HG02074.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-5892dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136395408 | ||||||
| chr6:136395408 | AT | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0072others(107): Show | 110 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.245-5892delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136395408 | ||||||
| chr6:136395408 | ATT | A | 46 | a0001c0001t0001g0137a0002c0002t0003g0006a0002c0002t0003g0009others(43): Show | 46 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.245-5893_245-5892d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136395408 | ||||||
| chr6:136395408 | ATTT | A | 6 | a0002c0002t0003g0003a0002c0002t0003g0177a0003c0003t0003g0031others(3): Show | 6 | HG02280.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-5894_245-5892d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136395408 | ||||||
| chr6:136395418 | T | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.245-5901A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136395418 | ||||||
| chr6:136395642 | C | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245-6125G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136395642 | ||||||
| chr6:136395720 | T | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.245-6203A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136395720 | ||||||
| chr6:136396157 | A | AT | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-6641dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136396157 | ||||||
| chr6:136396179 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.245-6662G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136396179 | ||||||
| chr6:136396618 | A | C | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.245-7101T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136396618 | ||||||
| chr6:136396884 | A | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.245-7367T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136396884 | ||||||
| chr6:136396909 | AT | A | 14 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(11): Show | 14 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.245-7393delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136396909 | ||||||
| chr6:136396915 | G | A | 14 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(11): Show | 14 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.245-7398C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136396915 | ||||||
| chr6:136396962 | T | C | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.245-7445A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136396962 | ||||||
| chr6:136397153 | G | A | 7 | a0001c0001t0004g0016a0001c0001t0004g0071a0001c0001t0004g0077others(4): Show | 7 | HG00408.hp2 HG01433.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-7636C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136397153 | ||||||
| chr6:136397454 | C | T | 7 | a0002c0002t0003g0085a0002c0002t0003g0177a0006c0006t0006g0180others(4): Show | 7 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.245-7937G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136397454 | ||||||
| chr6:136397493 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.245-7976G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136397493 | ||||||
| chr6:136397712 | G | C | 5 | a0002c0002t0002g0227a0002c0002t0002g0233a0002c0002t0009g0223others(2): Show | 5 | HG00733.hp2 HG01192.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-8195C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136397712 | ||||||
| chr6:136397724 | C | T | 15 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(12): Show | 15 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.245-8207G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136397724 | ||||||
| chr6:136397824 | T | G | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.245-8307A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136397824 | ||||||
| chr6:136397866 | C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(190): Show | 193 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.245-8349G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136397866 | ||||||
| chr6:136398316 | C | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.245-8799G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136398316 | ||||||
| chr6:136398674 | G | T | 1 | a0002c0002t0011g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.245-9157C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136398674 | ||||||
| chr6:136398682 | C | T | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.245-9165G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136398682 | ||||||
| chr6:136398697 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.245-9180G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136398697 | ||||||
| chr6:136399209 | C | T | 24 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(21): Show | 24 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.245-9692G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399209 | ||||||
| chr6:136399248 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.245-9731G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399248 | ||||||
| chr6:136399330 | A | G | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.245-9813T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399330 | ||||||
| chr6:136399388 | A | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.245-9871T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399388 | ||||||
| chr6:136399510 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.245-9993C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399510 | ||||||
| chr6:136399590 | G | C | 1 | a0002c0002t0002g0230 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.245-10073C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399590 | ||||||
| chr6:136399591 | C | A | 1 | a0002c0002t0002g0230 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.245-10074G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399591 | ||||||
| chr6:136399592 | A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(192): Show | 195 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.245-10075T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399592 | ||||||
| chr6:136399705 | T | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.245-10188A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136399705 | ||||||
| chr6:136400071 | C | T | 1 | a0004c0004t0001g0121 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-10554G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136400071 | ||||||
| chr6:136400101 | GT | G | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-10585delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136400101 | ||||||
| chr6:136400164 | C | T | 1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.245-10647G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136400164 | ||||||
| chr6:136400262 | A | G | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.245-10745T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136400262 | ||||||
| chr6:136400369 | T | C | 2 | a0002c0002t0002g0244a0002c0002t0003g0085 | 2 | HG01358.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.245-10852A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136400369 | ||||||
| chr6:136400388 | C | G | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-10871G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136400388 | ||||||
| chr6:136400714 | G | T | 24 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(21): Show | 24 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.244+10906C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136400714 | ||||||
| chr6:136401154 | G | C | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+10466C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136401154 | ||||||
| chr6:136401722 | T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0145a0004c0004t0001g0118others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+9898A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136401722 | ||||||
| chr6:136401916 | T | C | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.244+9704A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136401916 | ||||||
| chr6:136401991 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.244+9629C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136401991 | ||||||
| chr6:136402206 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.244+9414A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402206 | ||||||
| chr6:136402224 | C | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244+9396G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402224 | ||||||
| chr6:136402250 | T | C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+9370A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402250 | ||||||
| chr6:136402561 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244+9059C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402561 | ||||||
| chr6:136402669 | G | A | 55 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(52): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.244+8951C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402669 | ||||||
| chr6:136402733 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.244+8887G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402733 | ||||||
| chr6:136402866 | A | G | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.244+8754T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402866 | ||||||
| chr6:136402901 | G | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.244+8719C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402901 | ||||||
| chr6:136402905 | C | CA | 21 | a0001c0001t0001g0160a0002c0002t0002g0062a0002c0002t0002g0199others(18): Show | 21 | HG00544.hp2 HG00735.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.244+8714dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | C | CAA | 17 | a0002c0002t0002g0194a0002c0002t0002g0195a0002c0002t0002g0196others(14): Show | 17 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.244+8713_244+8714d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CA | C | 12 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(9): Show | 12 | HG00733.hp2 HG01243.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+8714delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAA | C | 14 | a0001c0001t0004g0016a0001c0001t0004g0065a0001c0001t0004g0069others(11): Show | 14 | HG00408.hp1 HG00408.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+8710_244+8714d others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAA | C | 11 | a0001c0001t0004g0061a0001c0001t0004g0064a0001c0001t0004g0075others(8): Show | 11 | HG01123.hp2 HG02015.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.244+8709_244+8714d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA | C | 26 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0178others(23): Show | 26 | HG00639.hp1 HG01978.hp1 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.244+8708_244+8714d others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(3): Show |
C | 13 | a0001c0001t0001g0097a0003c0003t0003g0010a0003c0003t0003g0011others(10): Show | 13 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+8705_244+8714d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(4): Show |
C | 11 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0100others(8): Show | 11 | HG00544.hp1 HG02074.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.244+8704_244+8714d others(13): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(5): Show |
C | 79 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(76): Show | 79 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.244+8703_244+8714d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0001g0145others(2): Show | 5 | HG00621.hp1 HG01074.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+8702_244+8714d others(15): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244+8699_244+8714d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(10): Show |
C | 1 | a0002c0002t0002g0210 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.244+8698_244+8714d others(19): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.244+8696_244+8714d others(21): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(17): Show |
C | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.244+8691_244+8714d others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402905 | CAAAAAAA others(18): Show |
C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+8690_244+8714d others(27): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402905 | ||||||
| chr6:136402938 | A | G | 18 | a0002c0002t0003g0003a0002c0002t0003g0177a0003c0003t0003g0010others(15): Show | 18 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.244+8682T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402938 | ||||||
| chr6:136402946 | G | A | 18 | a0002c0002t0003g0003a0002c0002t0003g0177a0003c0003t0003g0010others(15): Show | 18 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.244+8674C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136402946 | ||||||
| chr6:136403016 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244+8604A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136403016 | ||||||
| chr6:136403117 | A | G | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.244+8503T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136403117 | ||||||
| chr6:136403189 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.244+8431G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136403189 | ||||||
| chr6:136403409 | G | A | 6 | a0002c0002t0003g0085a0006c0006t0006g0180a0006c0006t0006g0181others(3): Show | 6 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+8211C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136403409 | ||||||
| chr6:136404161 | A | G | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+7459T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136404161 | ||||||
| chr6:136404582 | G | A | 1 | a0004c0004t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+7038C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136404582 | ||||||
| chr6:136404888 | G | C | 1 | a0003c0003t0003g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.244+6732C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136404888 | ||||||
| chr6:136405139 | A | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+6481T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136405139 | ||||||
| chr6:136405389 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.244+6231G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136405389 | ||||||
| chr6:136405550 | C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(94): Show | 97 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.244+6070G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136405550 | ||||||
| chr6:136405676 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.244+5944C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136405676 | ||||||
| chr6:136405686 | A | T | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.244+5934T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136405686 | ||||||
| chr6:136405812 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.244+5808C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136405812 | ||||||
| chr6:136406011 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.244+5609C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406011 | ||||||
| chr6:136406149 | GA | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(1): Show | 4 | NA18940.hp1 NA18949.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+5470delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406149 | ||||||
| chr6:136406172 | C | G | 1 | a0001c0001t0004g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.244+5448G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406172 | ||||||
| chr6:136406345 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.244+5275C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406345 | ||||||
| chr6:136406465 | T | C | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.244+5155A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406465 | ||||||
| chr6:136406467 | C | T | 2 | a0001c0001t0008g0111a0001c0001t0008g0112 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.244+5153G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406467 | ||||||
| chr6:136406485 | CA | C | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.244+5134delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406485 | ||||||
| chr6:136406696 | C | T | 3 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177 | 3 | HG01358.hp1 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.244+4924G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406696 | ||||||
| chr6:136406747 | G | A | 1 | a0005c0005t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.244+4873C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406747 | ||||||
| chr6:136406861 | G | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.244+4759C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406861 | ||||||
| chr6:136406892 | T | A | 2 | a0006c0006t0006g0180a0006c0006t0006g0181 | 2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.244+4728A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406892 | ||||||
| chr6:136406950 | T | C | 55 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(52): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.244+4670A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136406950 | ||||||
| chr6:136407011 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244+4609G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407011 | ||||||
| chr6:136407046 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244+4574A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407046 | ||||||
| chr6:136407078 | T | C | 1 | a0002c0002t0002g0197 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.244+4542A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407078 | ||||||
| chr6:136407176 | CAAAT | C | 15 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(12): Show | 15 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.244+4440_244+4443d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407176 | ||||||
| chr6:136407333 | A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.244+4287T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407333 | ||||||
| chr6:136407359 | C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.244+4261G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407359 | ||||||
| chr6:136407386 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.244+4234A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407386 | ||||||
| chr6:136407437 | A | G | 1 | a0001c0001t0004g0076 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.244+4183T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407437 | ||||||
| chr6:136407469 | G | A | 1 | a0007c0007t0002g0229 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.244+4151C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407469 | ||||||
| chr6:136407552 | G | A | 1 | a0001c0001t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.244+4068C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407552 | ||||||
| chr6:136407608 | G | C | 1 | a0002c0002t0002g0034 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244+4012C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407608 | ||||||
| chr6:136407740 | A | C | 1 | a0004c0004t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+3880T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407740 | ||||||
| chr6:136407878 | T | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+3742A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136407878 | ||||||
| chr6:136408122 | G | A | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.244+3498C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136408122 | ||||||
| chr6:136408150 | C | T | 2 | a0001c0001t0001g0145a0010c0011t0001g0028 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.244+3470G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136408150 | ||||||
| chr6:136408409 | T | G | 18 | a0002c0002t0003g0003a0002c0002t0003g0177a0003c0003t0003g0010others(15): Show | 18 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.244+3211A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136408409 | ||||||
| chr6:136408456 | A | C | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.244+3164T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136408456 | ||||||
| chr6:136408552 | A | G | 1 | a0001c0001t0004g0077 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.244+3068T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136408552 | ||||||
| chr6:136408641 | G | C | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.244+2979C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136408641 | ||||||
| chr6:136408702 | AT | A | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.244+2917delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136408702 | ||||||
| chr6:136409029 | T | C | 3 | a0003c0003t0003g0125a0003c0003t0003g0189a0003c0003t0003g0191 | 3 | HG02155.hp2 NA18942.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.244+2591A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136409029 | ||||||
| chr6:136409046 | T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0145a0010c0011t0001g0028 | 3 | HG02109.hp1 HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.244+2574A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136409046 | ||||||
| chr6:136409240 | C | T | 1 | a0002c0002t0007g0207 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.244+2380G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136409240 | ||||||
| chr6:136409324 | C | T | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+2296G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136409324 | ||||||
| chr6:136409395 | G | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.244+2225C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136409395 | ||||||
| chr6:136409551 | T | C | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.244+2069A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136409551 | ||||||
| chr6:136409643 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.244+1977C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136409643 | ||||||
| chr6:136409733 | T | C | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG01074.hp1 HG02615.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+1887A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136409733 | ||||||
| chr6:136410064 | T | C | 8 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0036others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+1556A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136410064 | ||||||
| chr6:136410179 | C | T | 4 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0236others(1): Show | 4 | NA18952.hp2 NA18979.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+1441G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136410179 | ||||||
| chr6:136410264 | A | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(190): Show | 193 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.244+1356T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136410264 | ||||||
| chr6:136410377 | C | A | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+1243G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136410377 | ||||||
| chr6:136410949 | A | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.244+671T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136410949 | ||||||
| chr6:136411043 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.244+577C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136411043 | ||||||
| chr6:136411231 | C | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.244+389G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136411231 | ||||||
| chr6:136411268 | T | G | 18 | a0002c0002t0003g0003a0002c0002t0003g0177a0003c0003t0003g0010others(15): Show | 18 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.244+352A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136411268 | ||||||
| chr6:136411439 | C | T | 1 | a0002c0002t0011g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.244+181G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136411439 | ||||||
| chr6:136411526 | G | A | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.244+94C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 3/17 | chr6 | 136411526 | ||||||
| chr6:136411747 | A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0145a0010c0011t0001g0028 | 3 | HG02109.hp1 HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.167-50T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136411747 | ||||||
| chr6:136412150 | G | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.167-453C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136412150 | ||||||
| chr6:136412689 | T | C | 8 | a0002c0002t0003g0003a0002c0002t0003g0085a0002c0002t0003g0177others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.167-992A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136412689 | ||||||
| chr6:136412790 | A | T | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.167-1093T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136412790 | ||||||
| chr6:136413053 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.167-1356A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136413053 | ||||||
| chr6:136413143 | C | G | 1 | a0002c0002t0011g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.167-1446G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136413143 | ||||||
| chr6:136413201 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.167-1504G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136413201 | ||||||
| chr6:136413525 | G | GA | 7 | a0002c0002t0003g0085a0002c0002t0003g0177a0006c0006t0006g0180others(4): Show | 7 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-1829dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136413525 | ||||||
| chr6:136413525 | GA | G | 18 | a0002c0002t0002g0235a0003c0003t0003g0010a0003c0003t0003g0011others(15): Show | 18 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.167-1829delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136413525 | ||||||
| chr6:136413585 | A | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.167-1888T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136413585 | ||||||
| chr6:136413777 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.167-2080T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136413777 | ||||||
| chr6:136413888 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.167-2191C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136413888 | ||||||
| chr6:136414020 | C | T | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.167-2323G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414020 | ||||||
| chr6:136414109 | C | T | 1 | a0002c0002t0002g0199 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.167-2412G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414109 | ||||||
| chr6:136414110 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.167-2413C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414110 | ||||||
| chr6:136414147 | G | C | 1 | a0002c0002t0003g0058 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.167-2450C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414147 | ||||||
| chr6:136414196 | T | C | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.167-2499A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414196 | ||||||
| chr6:136414252 | C | CA | 20 | a0001c0001t0001g0163a0002c0002t0002g0033a0002c0002t0002g0062others(17): Show | 20 | HG00423.hp2 HG00733.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.167-2556dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAA | 25 | a0001c0001t0001g0138a0002c0002t0002g0032a0002c0002t0002g0036others(22): Show | 25 | HG00423.hp1 HG00544.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.167-2557_167-2556d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAA | 15 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0039others(12): Show | 15 | HG00323.hp2 HG00621.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.167-2558_167-2556d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAA | 8 | a0002c0002t0002g0194a0002c0002t0002g0195a0002c0002t0002g0213others(5): Show | 8 | HG01106.hp2 HG02451.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.167-2559_167-2556d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0145a0003c0003t0003g0013a0003c0003t0003g0015others(1): Show | 4 | HG01346.hp2 HG01993.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.167-2565_167-2556d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0176a0003c0003t0003g0010 | 3 | HG01106.hp1 HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.167-2566_167-2556d others(13): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0063a0001c0001t0012g0132 | 2 | HG01934.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.167-2567_167-2556d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0101a0001c0001t0001g0109a0001c0001t0001g0128others(5): Show | 8 | HG01192.hp1 HG02109.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.167-2568_167-2556d others(15): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(7): Show |
15 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0095others(12): Show | 15 | HG00323.hp1 HG02135.hp2 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.167-2569_167-2556d others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(8): Show |
13 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0134others(10): Show | 13 | HG01943.hp1 HG02015.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.167-2570_167-2556d others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(9): Show |
12 | a0001c0001t0001g0043a0001c0001t0001g0113a0001c0001t0001g0114others(9): Show | 12 | HG00735.hp1 HG01123.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.167-2571_167-2556d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0100a0001c0001t0001g0142others(1): Show | 4 | HG01993.hp1 HG02257.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.167-2572_167-2556d others(19): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(11): Show |
10 | a0001c0001t0001g0099a0001c0001t0001g0126a0001c0001t0001g0137others(7): Show | 10 | HG00544.hp1 HG01346.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.167-2573_167-2556d others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0175 | 3 | HG01243.hp2 HG02055.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.167-2574_167-2556d others(21): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0103a0001c0001t0001g0153others(1): Show | 4 | HG00621.hp1 HG01978.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.167-2575_167-2556d others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(14): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0150a0003c0003t0003g0192 | 3 | HG01358.hp2 NA18974.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.167-2576_167-2556d others(23): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0136 | 2 | HG01258.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.167-2577_167-2556d others(24): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.167-2578_167-2556d others(25): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.167-2581_167-2556d others(28): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | C | CAAAAAAA others(20): Show |
1 | a0004c0004t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.167-2582_167-2556d others(29): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | CA | C | 14 | a0001c0001t0001g0074a0001c0001t0001g0144a0001c0001t0004g0016others(11): Show | 14 | HG01433.hp2 HG01928.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.167-2556delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | CAA | C | 23 | a0001c0001t0004g0061a0001c0001t0004g0064a0001c0001t0004g0065others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.167-2557_167-2556d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | CAAA | C | 22 | a0001c0001t0004g0078a0002c0002t0003g0009a0002c0002t0003g0012others(19): Show | 22 | HG00639.hp1 HG02015.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.167-2558_167-2556d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | CAAAA | C | 5 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0001g0129others(2): Show | 5 | HG00733.hp1 HG02074.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.167-2559_167-2556d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | CAAAAAAA others(3): Show |
C | 1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.167-2565_167-2556d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.167-2566_167-2556d others(13): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414252 | CAAAAAAA others(5): Show |
C | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.167-2567_167-2556d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414252 | ||||||
| chr6:136414284 | A | T | 1 | a0001c0001t0004g0087 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.167-2587T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414284 | ||||||
| chr6:136414551 | G | C | 1 | a0004c0004t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.167-2854C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414551 | ||||||
| chr6:136414608 | ATACTCCT others(16): Show |
A | 8 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0069others(5): Show | 8 | NA18953.hp2 NA18961.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.167-2934_167-2912d others(25): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414608 | ||||||
| chr6:136414614 | C | T | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.167-2917G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414614 | ||||||
| chr6:136414649 | CT | C | 9 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0069others(6): Show | 9 | NA18953.hp2 NA18961.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.167-2953delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414649 | ||||||
| chr6:136414758 | C | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.167-3061G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414758 | ||||||
| chr6:136414803 | A | C | 1 | a0002c0002t0002g0244 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.167-3106T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414803 | ||||||
| chr6:136414808 | A | AT | 40 | a0001c0001t0001g0137a0001c0001t0001g0165a0001c0001t0004g0016others(37): Show | 40 | HG00408.hp2 HG00621.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.167-3112dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136414808 | ||||||
| chr6:136415055 | T | C | 18 | a0002c0002t0003g0003a0002c0002t0003g0177a0003c0003t0003g0010others(15): Show | 18 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.167-3358A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415055 | ||||||
| chr6:136415075 | C | G | 78 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(75): Show | 78 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.167-3378G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415075 | ||||||
| chr6:136415238 | C | T | 1 | a0001c0001t0012g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.167-3541G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415238 | ||||||
| chr6:136415303 | T | C | 18 | a0002c0002t0003g0003a0002c0002t0003g0177a0003c0003t0003g0010others(15): Show | 18 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.167-3606A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415303 | ||||||
| chr6:136415379 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.167-3682G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415379 | ||||||
| chr6:136415422 | G | C | 2 | a0007c0007t0002g0228a0007c0007t0002g0229 | 2 | NA18961.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.167-3725C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415422 | ||||||
| chr6:136415576 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.167-3879G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415576 | ||||||
| chr6:136415710 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.167-4013G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415710 | ||||||
| chr6:136415724 | A | G | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.167-4027T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136415724 | ||||||
| chr6:136416207 | C | A | 2 | a0001c0001t0001g0145a0010c0011t0001g0028 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.167-4510G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416207 | ||||||
| chr6:136416227 | C | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.167-4530G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416227 | ||||||
| chr6:136416484 | A | C | 2 | a0001c0001t0001g0163a0001c0012t0001g0174 | 2 | NA18969.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.167-4787T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416484 | ||||||
| chr6:136416663 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.167-4966T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416663 | ||||||
| chr6:136416678 | C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.167-4981G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416678 | ||||||
| chr6:136416738 | G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.166+4963C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416738 | ||||||
| chr6:136416742 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.166+4959C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416742 | ||||||
| chr6:136416792 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.166+4909G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416792 | ||||||
| chr6:136416805 | C | CA | 13 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0133others(10): Show | 13 | HG00423.hp1 HG02451.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.166+4895dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416805 | ||||||
| chr6:136416805 | CA | C | 7 | a0002c0002t0002g0034a0002c0002t0002g0036a0002c0002t0002g0037others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.166+4895delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416805 | ||||||
| chr6:136416902 | A | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(158): Show | 161 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.166+4799T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416902 | ||||||
| chr6:136416977 | A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.166+4724T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136416977 | ||||||
| chr6:136417153 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.166+4548A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136417153 | ||||||
| chr6:136417237 | G | A | 4 | a0002c0002t0002g0227a0002c0002t0009g0223a0002c0002t0009g0224others(1): Show | 4 | HG00733.hp2 HG01192.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.166+4464C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136417237 | ||||||
| chr6:136417466 | C | G | 1 | a0002c0002t0002g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.166+4235G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136417466 | ||||||
| chr6:136418072 | G | T | 1 | a0002c0002t0002g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.166+3629C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418072 | ||||||
| chr6:136418139 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.166+3562C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418139 | ||||||
| chr6:136418187 | C | T | 1 | a0002c0002t0011g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.166+3514G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418187 | ||||||
| chr6:136418276 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.166+3425G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418276 | ||||||
| chr6:136418277 | G | A | 2 | a0002c0002t0002g0196a0002c0002t0002g0210 | 2 | NA18956.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.166+3424C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418277 | ||||||
| chr6:136418283 | C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(95): Show | 98 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.166+3418G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418283 | ||||||
| chr6:136418337 | C | T | 1 | a0002c0002t0002g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.166+3364G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418337 | ||||||
| chr6:136418622 | G | A | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.166+3079C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418622 | ||||||
| chr6:136418778 | C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(95): Show | 98 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.166+2923G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418778 | ||||||
| chr6:136418867 | T | C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.166+2834A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418867 | ||||||
| chr6:136418892 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.166+2809C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418892 | ||||||
| chr6:136418973 | A | AG | 161 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(158): Show | 161 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.166+2727dupC | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136418973 | ||||||
| chr6:136419347 | G | A | 1 | a0002c0002t0003g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.166+2354C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136419347 | ||||||
| chr6:136419364 | C | A | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.166+2337G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136419364 | ||||||
| chr6:136419434 | T | G | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166+2267A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136419434 | ||||||
| chr6:136419500 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.166+2201C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136419500 | ||||||
| chr6:136419568 | AG | A | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.166+2132delC | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136419568 | ||||||
| chr6:136419605 | A | C | 1 | a0002c0002t0007g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.166+2096T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136419605 | ||||||
| chr6:136420055 | G | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(150): Show | 153 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.166+1646C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420055 | ||||||
| chr6:136420229 | T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.166+1472A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420229 | ||||||
| chr6:136420275 | G | A | 1 | a0001c0001t0014g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.166+1426C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420275 | ||||||
| chr6:136420552 | C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.166+1149G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420552 | ||||||
| chr6:136420611 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.166+1090A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420611 | ||||||
| chr6:136420816 | GA | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(107): Show | 110 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.166+884delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420816 | ||||||
| chr6:136420816 | GAA | G | 55 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(52): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.166+883_166+884del others(2): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420816 | ||||||
| chr6:136420816 | GAAA | G | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.166+882_166+884del others(3): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420816 | ||||||
| chr6:136420954 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.166+747T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420954 | ||||||
| chr6:136420993 | C | T | 17 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(14): Show | 17 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.166+708G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 2/17 | chr6 | 136420993 | ||||||
| chr6:136421832 | T | C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-33A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136421832 | ||||||
| chr6:136421911 | G | C | 1 | a0003c0009t0003g0190 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.68-112C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136421911 | ||||||
| chr6:136421997 | G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(90): Show | 93 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.68-198C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136421997 | ||||||
| chr6:136422095 | G | A | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-296C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422095 | ||||||
| chr6:136422180 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.68-381G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422180 | ||||||
| chr6:136422274 | A | G | 1 | a0002c0002t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.68-475T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422274 | ||||||
| chr6:136422303 | G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(90): Show | 93 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.68-504C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422303 | ||||||
| chr6:136422423 | T | TA | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-625dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422423 | ||||||
| chr6:136422738 | T | G | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68-939A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422738 | ||||||
| chr6:136422822 | C | A | 3 | a0004c0004t0001g0118a0004c0004t0001g0119a0004c0004t0001g0120 | 3 | HG02723.hp2 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.68-1023G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422822 | ||||||
| chr6:136422832 | G | A | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-1033C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422832 | ||||||
| chr6:136422878 | T | C | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-1079A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136422878 | ||||||
| chr6:136423334 | C | T | 1 | a0002c0002t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-1535G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423334 | ||||||
| chr6:136423372 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.68-1573T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423372 | ||||||
| chr6:136423510 | C | T | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68-1711G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423510 | ||||||
| chr6:136423543 | G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0091 | 2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.68-1744C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423543 | ||||||
| chr6:136423725 | T | TA | 43 | a0001c0001t0001g0175a0001c0001t0004g0016a0001c0001t0004g0061others(40): Show | 43 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-1927dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423725 | ||||||
| chr6:136423735 | A | AC | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1937_68-1936ins others(1): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423735 | ||||||
| chr6:136423782 | G | GT | 166 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(163): Show | 166 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.68-1984dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423782 | ||||||
| chr6:136423787 | T | TG | 13 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(10): Show | 13 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-1989_68-1988ins others(1): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423787 | ||||||
| chr6:136423790 | T | TG | 38 | a0002c0002t0003g0003a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-1992_68-1991ins others(1): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423790 | ||||||
| chr6:136423791 | T | TTG | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-1993_68-1992ins others(2): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423791 | ||||||
| chr6:136423882 | C | T | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-2083G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136423882 | ||||||
| chr6:136424241 | C | T | 1 | a0002c0014t0002g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.68-2442G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424241 | ||||||
| chr6:136424282 | A | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-2483T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424282 | ||||||
| chr6:136424327 | TA | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(172): Show | 175 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.68-2529delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424327 | ||||||
| chr6:136424329 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.68-2530T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424329 | ||||||
| chr6:136424519 | A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.68-2720T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424519 | ||||||
| chr6:136424652 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.68-2853G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424652 | ||||||
| chr6:136424735 | T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(158): Show | 161 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.68-2936A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424735 | ||||||
| chr6:136424946 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.68-3147G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424946 | ||||||
| chr6:136424970 | A | T | 1 | a0002c0002t0002g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68-3171T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136424970 | ||||||
| chr6:136425029 | T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(94): Show | 97 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.68-3230A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136425029 | ||||||
| chr6:136425037 | C | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(158): Show | 161 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.68-3238G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136425037 | ||||||
| chr6:136425165 | A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(190): Show | 193 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.68-3366T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136425165 | ||||||
| chr6:136425237 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-3438A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136425237 | ||||||
| chr6:136425641 | A | G | 1 | a0001c0001t0004g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.68-3842T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136425641 | ||||||
| chr6:136425644 | G | A | 1 | a0002c0002t0007g0207 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.68-3845C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136425644 | ||||||
| chr6:136426155 | G | A | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-4356C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136426155 | ||||||
| chr6:136426474 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.68-4675T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136426474 | ||||||
| chr6:136426504 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.68-4705G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136426504 | ||||||
| chr6:136426956 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.68-5157G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136426956 | ||||||
| chr6:136427023 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.68-5224C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136427023 | ||||||
| chr6:136427076 | T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.68-5277A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136427076 | ||||||
| chr6:136427179 | C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(150): Show | 153 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.68-5380G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136427179 | ||||||
| chr6:136427268 | G | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-5469C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136427268 | ||||||
| chr6:136427613 | C | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(158): Show | 161 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.68-5814G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136427613 | ||||||
| chr6:136427928 | T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(158): Show | 161 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.68-6129A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136427928 | ||||||
| chr6:136428119 | A | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(158): Show | 161 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.68-6320T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428119 | ||||||
| chr6:136428195 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-6396A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428195 | ||||||
| chr6:136428295 | C | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-6496G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428295 | ||||||
| chr6:136428434 | C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(150): Show | 153 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.68-6635G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428434 | ||||||
| chr6:136428523 | G | GAATAAAT others(5): Show |
14 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(11): Show | 14 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-6736_68-6725dup others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428523 | ||||||
| chr6:136428523 | G | GAATAAAT others(9): Show |
1 | a0003c0003t0003g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.68-6740_68-6725dup others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428523 | ||||||
| chr6:136428559 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.68-6760G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428559 | ||||||
| chr6:136428609 | T | C | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-6810A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428609 | ||||||
| chr6:136428906 | G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0175 | 2 | NA19006.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.68-7107C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428906 | ||||||
| chr6:136428999 | A | G | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-7200T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136428999 | ||||||
| chr6:136429074 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.68-7275G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136429074 | ||||||
| chr6:136429478 | T | C | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-7679A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136429478 | ||||||
| chr6:136429654 | C | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-7855G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136429654 | ||||||
| chr6:136429853 | T | C | 17 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(14): Show | 17 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-8054A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136429853 | ||||||
| chr6:136429856 | C | T | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-8057G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136429856 | ||||||
| chr6:136429980 | G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(95): Show | 98 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-8181C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136429980 | ||||||
| chr6:136430111 | C | T | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-8312G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136430111 | ||||||
| chr6:136430298 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.68-8499T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136430298 | ||||||
| chr6:136430425 | C | T | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-8626G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136430425 | ||||||
| chr6:136430685 | G | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-8886C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136430685 | ||||||
| chr6:136430827 | T | C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-9028A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136430827 | ||||||
| chr6:136430912 | C | T | 16 | a0003c0003t0003g0010a0003c0003t0003g0011a0003c0003t0003g0013others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-9113G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136430912 | ||||||
| chr6:136430954 | G | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.68-9155C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136430954 | ||||||
| chr6:136431259 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.68-9460G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431259 | ||||||
| chr6:136431260 | T | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-9461A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431260 | ||||||
| chr6:136431378 | A | G | 79 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.68-9579T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431378 | ||||||
| chr6:136431384 | T | C | 18 | a0002c0002t0003g0003a0002c0002t0003g0177a0003c0003t0003g0010others(15): Show | 18 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-9585A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431384 | ||||||
| chr6:136431414 | T | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0175 | 2 | NA19006.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.68-9615A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431414 | ||||||
| chr6:136431478 | T | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(94): Show | 97 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.68-9679A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431478 | ||||||
| chr6:136431492 | C | CTTTA | 67 | a0001c0001t0001g0029a0001c0001t0001g0099a0001c0001t0001g0100others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.68-9697_68-9694dup others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431492 | ||||||
| chr6:136431492 | C | CTTTATTT others(1): Show |
77 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0072others(74): Show | 77 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.68-9701_68-9694dup others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431492 | ||||||
| chr6:136431492 | C | CTTTATTT others(5): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0107others(1): Show | 4 | HG00642.hp2 HG01258.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-9705_68-9694dup others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431492 | ||||||
| chr6:136431492 | CTTTA | C | 72 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0034others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.68-9697_68-9694del others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431492 | ||||||
| chr6:136431519 | TATTTATT others(2): Show |
T | 16 | a0002c0002t0003g0177a0003c0003t0003g0010a0003c0003t0003g0011others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-9729_68-9721del others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431519 | ||||||
| chr6:136431598 | A | T | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-9799T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431598 | ||||||
| chr6:136431642 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.68-9843G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431642 | ||||||
| chr6:136431798 | G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG00735.hp1 HG01074.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-9999C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136431798 | ||||||
| chr6:136432080 | T | C | 29 | a0001c0001t0001g0063a0001c0001t0001g0101a0001c0001t0001g0108others(26): Show | 29 | HG00323.hp1 HG00621.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.68-10281A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136432080 | ||||||
| chr6:136432256 | T | C | 2 | a0002c0002t0007g0246a0002c0002t0011g0245 | 2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.68-10457A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136432256 | ||||||
| chr6:136432415 | G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.68-10616C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136432415 | ||||||
| chr6:136432643 | G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0175 | 2 | NA19006.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.68-10844C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136432643 | ||||||
| chr6:136432700 | A | G | 1 | a0004c0004t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-10901T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136432700 | ||||||
| chr6:136432756 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68-10957T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136432756 | ||||||
| chr6:136432810 | C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(190): Show | 193 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.68-11011G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136432810 | ||||||
| chr6:136432903 | T | C | 3 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195 | 3 | NA18940.hp2 NA18945.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.68-11104A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136432903 | ||||||
| chr6:136433037 | G | A | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68-11238C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136433037 | ||||||
| chr6:136433159 | G | A | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-11360C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136433159 | ||||||
| chr6:136433359 | A | G | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-11560T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136433359 | ||||||
| chr6:136433612 | T | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-11813A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136433612 | ||||||
| chr6:136433961 | T | A | 4 | a0002c0002t0002g0227a0002c0002t0009g0223a0002c0002t0009g0224others(1): Show | 4 | HG00733.hp2 HG01192.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-12162A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136433961 | ||||||
| chr6:136434035 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.68-12236C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434035 | ||||||
| chr6:136434086 | C | T | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-12287G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434086 | ||||||
| chr6:136434116 | G | A | 1 | a0004c0004t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-12317C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434116 | ||||||
| chr6:136434135 | G | A | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-12336C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434135 | ||||||
| chr6:136434190 | C | T | 1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-12391G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434190 | ||||||
| chr6:136434192 | A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0063others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.68-12393T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434192 | ||||||
| chr6:136434221 | C | T | 1 | a0001c0001t0012g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.68-12422G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434221 | ||||||
| chr6:136434306 | CA | C | 45 | a0001c0001t0001g0043a0001c0001t0001g0135a0001c0001t0004g0016others(42): Show | 45 | HG00408.hp2 HG01106.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.68-12508delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434306 | ||||||
| chr6:136434443 | T | C | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-12644A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434443 | ||||||
| chr6:136434598 | A | AT | 60 | a0001c0001t0001g0029a0001c0001t0001g0103a0001c0001t0001g0106others(57): Show | 60 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.68-12800dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434598 | ||||||
| chr6:136434598 | AT | A | 20 | a0001c0001t0001g0145a0001c0001t0013g0179a0002c0002t0002g0226others(17): Show | 20 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.68-12800delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434598 | ||||||
| chr6:136434894 | C | G | 1 | a0002c0002t0002g0235 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.68-13095G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136434894 | ||||||
| chr6:136435287 | G | A | 25 | a0001c0001t0004g0016a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-13488C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136435287 | ||||||
| chr6:136435296 | G | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-13497C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136435296 | ||||||
| chr6:136435301 | A | T | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-13502T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136435301 | ||||||
| chr6:136435453 | A | G | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.68-13654T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136435453 | ||||||
| chr6:136435806 | T | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-14007A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136435806 | ||||||
| chr6:136436144 | C | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-14345G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136436144 | ||||||
| chr6:136436284 | C | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-14485G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136436284 | ||||||
| chr6:136436378 | A | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-14579T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136436378 | ||||||
| chr6:136436381 | AT | A | 66 | a0001c0001t0001g0166a0001c0001t0004g0016a0001c0001t0004g0061others(63): Show | 66 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.68-14583delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136436381 | ||||||
| chr6:136436515 | GACTACAG others(3): Show |
G | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-14726_68-14717d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136436515 | ||||||
| chr6:136436657 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.68-14858C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136436657 | ||||||
| chr6:136437736 | C | G | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-15937G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136437736 | ||||||
| chr6:136437898 | A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.68-16099T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136437898 | ||||||
| chr6:136438014 | T | C | 1 | a0002c0002t0002g0037 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.68-16215A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438014 | ||||||
| chr6:136438022 | A | G | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-16223T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438022 | ||||||
| chr6:136438212 | T | C | 30 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-16413A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438212 | ||||||
| chr6:136438229 | G | A | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-16430C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438229 | ||||||
| chr6:136438369 | A | C | 1 | a0001c0001t0004g0087 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.68-16570T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438369 | ||||||
| chr6:136438391 | T | C | 6 | a0004c0004t0001g0080a0004c0004t0001g0096a0004c0004t0001g0118others(3): Show | 6 | HG02451.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-16592A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438391 | ||||||
| chr6:136438463 | G | A | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-16664C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438463 | ||||||
| chr6:136438586 | G | C | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-16787C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438586 | ||||||
| chr6:136438747 | A | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-16948T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438747 | ||||||
| chr6:136438748 | G | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-16949C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438748 | ||||||
| chr6:136438797 | G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(86): Show | 89 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.68-16998C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438797 | ||||||
| chr6:136438861 | T | A | 1 | a0006c0006t0006g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.68-17062A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438861 | ||||||
| chr6:136438912 | A | C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-17113T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136438912 | ||||||
| chr6:136439443 | T | C | 28 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(25): Show | 28 | HG00408.hp2 HG00621.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.68-17644A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136439443 | ||||||
| chr6:136439494 | T | G | 2 | a0002c0002t0002g0204a0002c0002t0002g0221 | 2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.68-17695A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136439494 | ||||||
| chr6:136439520 | T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.68-17721A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136439520 | ||||||
| chr6:136439767 | G | C | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-17968C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136439767 | ||||||
| chr6:136439813 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-18014C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136439813 | ||||||
| chr6:136440042 | G | A | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-18243C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136440042 | ||||||
| chr6:136440256 | G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(137): Show | 140 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.68-18457C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136440256 | ||||||
| chr6:136440662 | T | C | 1 | a0005c0005t0001g0169 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68-18863A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136440662 | ||||||
| chr6:136440768 | C | T | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68-18969G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136440768 | ||||||
| chr6:136440817 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-19018A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136440817 | ||||||
| chr6:136440872 | T | C | 9 | a0003c0003t0003g0125a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-19073A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136440872 | ||||||
| chr6:136440943 | C | T | 39 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-19144G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136440943 | ||||||
| chr6:136441117 | T | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-19318A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441117 | ||||||
| chr6:136441192 | T | C | 2 | a0006c0006t0006g0180a0006c0006t0006g0181 | 2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.68-19393A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441192 | ||||||
| chr6:136441197 | G | T | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-19398C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441197 | ||||||
| chr6:136441300 | T | C | 1 | a0002c0002t0002g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68-19501A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441300 | ||||||
| chr6:136441327 | C | CTCCATTT others(36): Show |
1 | a0010c0011t0001g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-19571_68-19529d others(45): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441327 | ||||||
| chr6:136441516 | A | C | 1 | a0002c0002t0003g0012 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.68-19717T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441516 | ||||||
| chr6:136441540 | G | A | 1 | a0004c0004t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.68-19741C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441540 | ||||||
| chr6:136441543 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-19744C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441543 | ||||||
| chr6:136441544 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.68-19745G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441544 | ||||||
| chr6:136441832 | C | T | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-20033G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136441832 | ||||||
| chr6:136442112 | G | T | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-20313C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442112 | ||||||
| chr6:136442149 | T | C | 1 | a0002c0002t0002g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.68-20350A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442149 | ||||||
| chr6:136442297 | G | A | 1 | a0002c0002t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-20498C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442297 | ||||||
| chr6:136442405 | C | CA | 50 | a0001c0001t0014g0060a0002c0002t0002g0033a0002c0002t0002g0212others(47): Show | 50 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.68-20607dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442405 | ||||||
| chr6:136442405 | CA | C | 7 | a0001c0001t0001g0100a0001c0001t0001g0130a0001c0001t0001g0165others(4): Show | 7 | HG02897.hp1 HG03453.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-20607delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442405 | ||||||
| chr6:136442405 | CAA | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(89): Show | 92 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.68-20608_68-20607d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442405 | ||||||
| chr6:136442587 | C | G | 1 | a0002c0002t0002g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.68-20788G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442587 | ||||||
| chr6:136442785 | C | A | 27 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(24): Show | 27 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.68-20986G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442785 | ||||||
| chr6:136442878 | C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.68-21079G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136442878 | ||||||
| chr6:136443330 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.68-21531G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136443330 | ||||||
| chr6:136443406 | T | TAAAACCT others(224): Show |
1 | a0001c0001t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-21608_68-21607i others(233): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136443406 | ||||||
| chr6:136443449 | C | CT | 31 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(28): Show | 31 | HG00408.hp2 HG00423.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.68-21651dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136443449 | ||||||
| chr6:136443449 | CT | C | 50 | a0001c0001t0001g0043a0001c0001t0001g0147a0002c0002t0002g0034others(47): Show | 50 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.68-21651delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136443449 | ||||||
| chr6:136443449 | CTT | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.68-21652_68-21651d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136443449 | ||||||
| chr6:136443728 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.68-21929C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136443728 | ||||||
| chr6:136443741 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-21942G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136443741 | ||||||
| chr6:136443763 | G | A | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-21964C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136443763 | ||||||
| chr6:136444064 | T | C | 17 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(14): Show | 17 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-22265A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444064 | ||||||
| chr6:136444190 | G | A | 10 | a0003c0003t0003g0059a0003c0003t0003g0125a0003c0003t0003g0185others(7): Show | 10 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-22391C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444190 | ||||||
| chr6:136444215 | A | G | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-22416T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444215 | ||||||
| chr6:136444223 | G | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-22424C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444223 | ||||||
| chr6:136444321 | C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.68-22522G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444321 | ||||||
| chr6:136444351 | A | G | 2 | a0002c0002t0009g0223a0002c0002t0009g0224 | 2 | HG00733.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.68-22552T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444351 | ||||||
| chr6:136444406 | T | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0117 | 3 | HG02572.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.68-22607A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444406 | ||||||
| chr6:136444585 | T | C | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-22786A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444585 | ||||||
| chr6:136444651 | G | A | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-22852C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444651 | ||||||
| chr6:136444704 | C | T | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-22905G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444704 | ||||||
| chr6:136444973 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.68-23174G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136444973 | ||||||
| chr6:136445080 | C | T | 3 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.68-23281G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136445080 | ||||||
| chr6:136445288 | T | C | 42 | a0002c0002t0003g0003a0002c0002t0003g0006a0002c0002t0003g0009others(39): Show | 42 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.68-23489A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136445288 | ||||||
| chr6:136446173 | C | A | 10 | a0003c0003t0003g0059a0003c0003t0003g0125a0003c0003t0003g0185others(7): Show | 10 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-24374G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136446173 | ||||||
| chr6:136446261 | G | A | 26 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0064others(23): Show | 26 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.68-24462C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136446261 | ||||||
| chr6:136446392 | G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.68-24593C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136446392 | ||||||
| chr6:136446787 | A | G | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-24988T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136446787 | ||||||
| chr6:136446795 | C | T | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-24996G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136446795 | ||||||
| chr6:136446831 | G | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-25032C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136446831 | ||||||
| chr6:136446864 | A | G | 3 | a0002c0002t0003g0003a0002c0002t0003g0177a0002c0002t0010g0042 | 3 | HG02451.hp1 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-25065T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136446864 | ||||||
| chr6:136447072 | T | C | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-25273A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136447072 | ||||||
| chr6:136447164 | C | T | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-25365G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136447164 | ||||||
| chr6:136447265 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-25466A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136447265 | ||||||
| chr6:136447312 | A | C | 23 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0064others(20): Show | 23 | HG00408.hp2 HG01123.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.68-25513T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136447312 | ||||||
| chr6:136447324 | G | C | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-25525C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136447324 | ||||||
| chr6:136447491 | CT | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(94): Show | 97 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.68-25693delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136447491 | ||||||
| chr6:136447930 | G | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-26131C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136447930 | ||||||
| chr6:136448051 | G | A | 1 | a0002c0002t0011g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.68-26252C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448051 | ||||||
| chr6:136448075 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.68-26276G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448075 | ||||||
| chr6:136448120 | A | C | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-26321T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448120 | ||||||
| chr6:136448141 | G | A | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-26342C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448141 | ||||||
| chr6:136448178 | C | A | 42 | a0002c0002t0003g0003a0002c0002t0003g0006a0002c0002t0003g0009others(39): Show | 42 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.68-26379G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448178 | ||||||
| chr6:136448415 | A | AT | 9 | a0001c0001t0001g0166a0002c0002t0002g0211a0002c0002t0002g0212others(6): Show | 9 | HG00423.hp2 HG02074.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-26617dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448415 | ||||||
| chr6:136448430 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-26631A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448430 | ||||||
| chr6:136448729 | T | C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-26930A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448729 | ||||||
| chr6:136448952 | A | G | 28 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(25): Show | 28 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.68-27153T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136448952 | ||||||
| chr6:136449002 | T | TA | 9 | a0003c0003t0003g0125a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-27204dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449002 | ||||||
| chr6:136449002 | TA | T | 67 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(64): Show | 67 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.68-27204delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449002 | ||||||
| chr6:136449018 | A | AAAAG | 8 | a0001c0001t0001g0170a0001c0001t0013g0179a0002c0002t0003g0022others(5): Show | 8 | HG02280.hp1 HG02622.hp2 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-27220_68-27219i others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449018 | ||||||
| chr6:136449018 | A | AAAG | 152 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(149): Show | 152 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.68-27222_68-27220d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449018 | ||||||
| chr6:136449018 | A | AAG | 6 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0143others(3): Show | 6 | HG01074.hp1 NA18957.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-27220_68-27219i others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449018 | ||||||
| chr6:136449022 | A | AAGC | 2 | a0006c0006t0006g0181a0008c0008t0006g0026 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.68-27226_68-27224d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449022 | ||||||
| chr6:136449022 | A | C | 3 | a0006c0006t0006g0180a0006c0006t0006g0182a0008c0008t0006g0027 | 3 | HG02280.hp1 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.68-27223T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449022 | ||||||
| chr6:136449151 | C | T | 1 | a0002c0002t0002g0199 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.68-27352G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449151 | ||||||
| chr6:136449204 | A | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-27405T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449204 | ||||||
| chr6:136449258 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-27459T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449258 | ||||||
| chr6:136449291 | T | TCAAA | 71 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-27496_68-27493d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449291 | ||||||
| chr6:136449291 | TCAAACAA others(1): Show |
T | 11 | a0003c0003t0003g0031a0003c0003t0003g0059a0003c0003t0003g0125others(8): Show | 11 | HG02155.hp2 HG02280.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-27500_68-27493d others(10): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449291 | ||||||
| chr6:136449355 | T | C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-27556A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449355 | ||||||
| chr6:136449382 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.68-27583G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449382 | ||||||
| chr6:136449439 | G | A | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG01074.hp1 HG02615.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-27640C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449439 | ||||||
| chr6:136449520 | G | C | 28 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(25): Show | 28 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.68-27721C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449520 | ||||||
| chr6:136449763 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.68-27964G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449763 | ||||||
| chr6:136449788 | T | G | 3 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195 | 3 | NA18940.hp2 NA18945.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.68-27989A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449788 | ||||||
| chr6:136449864 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.68-28065T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136449864 | ||||||
| chr6:136450000 | A | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-28201T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450000 | ||||||
| chr6:136450126 | G | T | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-28327C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450126 | ||||||
| chr6:136450171 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68-28372G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450171 | ||||||
| chr6:136450227 | T | C | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.68-28428A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450227 | ||||||
| chr6:136450232 | C | T | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-28433G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450232 | ||||||
| chr6:136450367 | T | A | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-28568A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450367 | ||||||
| chr6:136450368 | T | A | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-28569A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450368 | ||||||
| chr6:136450369 | A | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.68-28570T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450369 | ||||||
| chr6:136450445 | A | T | 3 | a0002c0002t0002g0227a0002c0002t0009g0223a0002c0002t0009g0224 | 3 | HG00733.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.68-28646T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450445 | ||||||
| chr6:136450516 | A | T | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-28717T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450516 | ||||||
| chr6:136450669 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.68-28870T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450669 | ||||||
| chr6:136450695 | A | T | 11 | a0003c0003t0003g0031a0003c0003t0003g0059a0003c0003t0003g0125others(8): Show | 11 | HG02155.hp2 HG02280.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-28896T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450695 | ||||||
| chr6:136450709 | G | A | 39 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(36): Show | 39 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-28910C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450709 | ||||||
| chr6:136450784 | C | CA | 41 | a0001c0001t0001g0093a0002c0002t0003g0006a0002c0002t0003g0009others(38): Show | 41 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.68-28986dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450784 | ||||||
| chr6:136450872 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.68-29073T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136450872 | ||||||
| chr6:136451080 | T | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-29281A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136451080 | ||||||
| chr6:136451157 | C | T | 2 | a0002c0002t0002g0233a0008c0008t0006g0027 | 2 | HG03654.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.68-29358G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136451157 | ||||||
| chr6:136451254 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.68-29455G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136451254 | ||||||
| chr6:136451452 | T | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-29653A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136451452 | ||||||
| chr6:136451945 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.68-30146G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136451945 | ||||||
| chr6:136451968 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.68-30169C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136451968 | ||||||
| chr6:136452193 | C | CAAACA | 76 | a0001c0001t0001g0043a0001c0001t0001g0093a0001c0001t0001g0095others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.68-30399_68-30395d others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452193 | ||||||
| chr6:136452193 | C | CAAACAAA others(3): Show |
29 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(26): Show | 29 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.68-30404_68-30395d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452193 | ||||||
| chr6:136452193 | C | CAAACAAA others(8): Show |
4 | a0001c0001t0001g0106a0001c0001t0001g0147a0001c0001t0001g0163others(1): Show | 4 | HG02273.hp1 HG02735.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-30409_68-30395d others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452193 | ||||||
| chr6:136452193 | CAAACA | C | 12 | a0001c0001t0001g0149a0001c0001t0004g0087a0002c0002t0002g0034others(9): Show | 12 | HG00408.hp2 HG02083.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-30399_68-30395d others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452193 | ||||||
| chr6:136452193 | CAAACAAA others(3): Show |
C | 27 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(24): Show | 27 | HG01123.hp2 HG01358.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.68-30404_68-30395d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452193 | ||||||
| chr6:136452342 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.68-30543C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452342 | ||||||
| chr6:136452557 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.68-30758A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452557 | ||||||
| chr6:136452615 | C | T | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-30816G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452615 | ||||||
| chr6:136452716 | C | T | 2 | a0002c0002t0003g0017a0002c0002t0003g0023 | 2 | NA18942.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.68-30917G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452716 | ||||||
| chr6:136452913 | A | C | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-31114T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136452913 | ||||||
| chr6:136453027 | A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(176): Show | 179 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-31228T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136453027 | ||||||
| chr6:136453088 | G | T | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-31289C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136453088 | ||||||
| chr6:136453598 | C | T | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-31799G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136453598 | ||||||
| chr6:136453806 | T | A | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-32007A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136453806 | ||||||
| chr6:136453863 | C | T | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-32064G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136453863 | ||||||
| chr6:136454043 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-32244T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454043 | ||||||
| chr6:136454194 | C | T | 11 | a0003c0003t0003g0031a0003c0003t0003g0059a0003c0003t0003g0125others(8): Show | 11 | HG02155.hp2 HG02280.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-32395G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454194 | ||||||
| chr6:136454272 | G | GATCT | 69 | a0001c0001t0001g0043a0001c0001t0001g0092a0001c0001t0001g0095others(66): Show | 69 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.68-32477_68-32474d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454272 | ||||||
| chr6:136454272 | G | GATCTATC others(1): Show |
53 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(50): Show | 53 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.68-32481_68-32474d others(10): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454272 | ||||||
| chr6:136454272 | G | GATCTATC others(5): Show |
14 | a0001c0001t0001g0079a0001c0001t0001g0098a0001c0001t0001g0136others(11): Show | 14 | HG00544.hp1 HG01243.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-32485_68-32474d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454272 | ||||||
| chr6:136454272 | G | GATCTATC others(9): Show |
4 | a0002c0002t0007g0246a0002c0002t0009g0223a0002c0002t0009g0224others(1): Show | 4 | HG00733.hp2 HG01192.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-32489_68-32474d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454272 | ||||||
| chr6:136454272 | GATCT | G | 8 | a0001c0001t0001g0063a0001c0001t0001g0161a0001c0001t0004g0067others(5): Show | 8 | HG00639.hp2 HG02132.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-32477_68-32474d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454272 | ||||||
| chr6:136454272 | GATCTATC others(1): Show |
G | 16 | a0001c0001t0001g0153a0001c0001t0004g0016a0001c0001t0004g0065others(13): Show | 16 | HG00408.hp2 HG00621.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-32481_68-32474d others(10): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454272 | ||||||
| chr6:136454272 | GATCTATC others(5): Show |
G | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.68-32485_68-32474d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454272 | ||||||
| chr6:136454536 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-32737C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454536 | ||||||
| chr6:136454586 | C | A | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-32787G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454586 | ||||||
| chr6:136454643 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.68-32844C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454643 | ||||||
| chr6:136454988 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-33189C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136454988 | ||||||
| chr6:136455194 | T | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-33395A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136455194 | ||||||
| chr6:136455504 | A | G | 2 | a0001c0001t0008g0111a0001c0001t0008g0112 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.68-33705T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136455504 | ||||||
| chr6:136455636 | T | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-33837A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136455636 | ||||||
| chr6:136455707 | T | A | 1 | a0001c0001t0008g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.68-33908A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136455707 | ||||||
| chr6:136455777 | A | C | 3 | a0002c0002t0007g0205a0002c0002t0007g0206a0002c0002t0007g0207 | 3 | HG02723.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.68-33978T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136455777 | ||||||
| chr6:136455932 | A | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-34133T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136455932 | ||||||
| chr6:136455960 | T | C | 1 | a0002c0002t0002g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.68-34161A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136455960 | ||||||
| chr6:136456117 | T | G | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-34318A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456117 | ||||||
| chr6:136456366 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68-34567C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456366 | ||||||
| chr6:136456392 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-34593G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456392 | ||||||
| chr6:136456407 | C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.68-34608G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456407 | ||||||
| chr6:136456645 | C | A | 3 | a0001c0001t0008g0094a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | HG02922.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.68-34846G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456645 | ||||||
| chr6:136456673 | AAAAGAAG | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(107): Show | 110 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.68-34881_68-34875d others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456673 | ||||||
| chr6:136456691 | GAAGA | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-34896_68-34893d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456691 | ||||||
| chr6:136456692 | A | T | 28 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(25): Show | 28 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.68-34893T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456692 | ||||||
| chr6:136456701 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-34902C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456701 | ||||||
| chr6:136456744 | A | AAGG | 3 | a0001c0001t0004g0065a0001c0001t0008g0111a0003c0003t0003g0059 | 3 | HG03579.hp2 NA18982.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.68-34948_68-34946d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456744 | ||||||
| chr6:136456744 | A | AAGGAGG | 2 | a0001c0001t0004g0064a0004c0004t0001g0080 | 2 | HG02040.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.68-34951_68-34946d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456744 | ||||||
| chr6:136456764 | G | GGAA | 3 | a0002c0002t0002g0033a0002c0002t0007g0205a0002c0002t0007g0206 | 3 | HG02723.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.68-34966_68-34965i others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456764 | ||||||
| chr6:136456764 | G | GGAAGAAG others(5): Show |
8 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0035others(5): Show | 8 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-34966_68-34965i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456764 | ||||||
| chr6:136456767 | G | A | 52 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(49): Show | 52 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.68-34968C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAA | 5 | a0002c0002t0002g0199a0002c0002t0002g0214a0002c0002t0002g0233others(2): Show | 5 | HG02080.hp2 HG02165.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-34971_68-34969d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAAGAA | 7 | a0002c0002t0002g0197a0002c0002t0002g0202a0002c0002t0002g0210others(4): Show | 7 | NA18949.hp1 NA18953.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-34974_68-34969d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAAGAAG others(2): Show |
10 | a0002c0002t0002g0198a0002c0002t0002g0200a0002c0002t0002g0211others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-34977_68-34969d others(11): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAAGAAG others(5): Show |
12 | a0002c0002t0002g0201a0002c0002t0002g0203a0002c0002t0002g0209others(9): Show | 12 | HG01106.hp2 HG01192.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-34980_68-34969d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAAGAAG others(8): Show |
4 | a0002c0002t0002g0195a0002c0002t0002g0208a0002c0002t0002g0227others(1): Show | 4 | HG02735.hp2 NA18944.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-34983_68-34969d others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAAGAAG others(11): Show |
5 | a0002c0002t0002g0196a0002c0002t0002g0204a0002c0002t0002g0215others(2): Show | 5 | HG03491.hp2 NA18964.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-34986_68-34969d others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAAGAAG others(14): Show |
2 | a0002c0002t0002g0194a0002c0002t0002g0247 | 2 | NA18957.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.68-34989_68-34969d others(23): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGAAGA others(7): Show |
1 | a0002c0002t0009g0223 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.68-34969_68-34968i others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGAAGA others(19): Show |
1 | a0002c0002t0002g0193 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.68-34969_68-34968i others(28): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAAG others(2): Show |
8 | a0001c0001t0001g0063a0001c0001t0004g0066a0001c0001t0004g0069others(5): Show | 8 | HG02055.hp1 HG02622.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-34969_68-34968i others(11): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAAG others(5): Show |
9 | a0001c0001t0004g0061a0001c0001t0004g0070a0001c0001t0004g0071others(6): Show | 9 | HG01934.hp2 HG02135.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-34969_68-34968i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAAG others(8): Show |
3 | a0001c0001t0001g0093a0001c0001t0004g0088a0001c0001t0004g0089 | 3 | HG01123.hp2 HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.68-34969_68-34968i others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAAG others(11): Show |
3 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0014g0060 | 3 | HG02132.hp2 HG02155.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.68-34969_68-34968i others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAAG others(14): Show |
2 | a0001c0001t0004g0016a0001c0001t0004g0087 | 2 | HG00408.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.68-34969_68-34968i others(23): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAGG others(5): Show |
1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-34969_68-34968i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAGG others(8): Show |
1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-34969_68-34968i others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAGG others(17): Show |
1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-34969_68-34968i others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456767 | G | GGAGGAGG others(32): Show |
1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-34969_68-34968i others(41): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456767 | ||||||
| chr6:136456770 | A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(99): Show | 102 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.68-34971T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456770 | ||||||
| chr6:136456773 | A | G | 13 | a0001c0001t0001g0176a0001c0001t0008g0094a0001c0001t0008g0112others(10): Show | 13 | HG02155.hp2 HG02922.hp1 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-34974T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456773 | ||||||
| chr6:136456776 | A | G | 4 | a0002c0002t0003g0085a0003c0003t0003g0125a0003c0003t0003g0189others(1): Show | 4 | HG01358.hp1 HG02155.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-34977T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456776 | ||||||
| chr6:136456797 | AGAAGAAG others(18): Show |
A | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.68-35023_68-34999d others(27): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456797 | ||||||
| chr6:136456800 | A | AGAAGAAG others(6): Show |
2 | a0006c0006t0006g0180a0006c0006t0006g0182 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.68-35014_68-35002d others(15): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456800 | ||||||
| chr6:136456800 | A | AGAAGAAG others(9): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG00735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.68-35017_68-35002d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456800 | ||||||
| chr6:136456800 | A | AGAAGAAG others(12): Show |
1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.68-35020_68-35002d others(21): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456800 | ||||||
| chr6:136456803 | A | AGAAGAAG others(3): Show |
1 | a0006c0006t0006g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.68-35014_68-35005d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456803 | ||||||
| chr6:136456803 | A | AGAAGAAG others(6): Show |
2 | a0001c0001t0001g0099a0004c0004t0001g0118 | 2 | HG02723.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.68-35017_68-35005d others(15): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456803 | ||||||
| chr6:136456803 | A | AGAAGAAG others(9): Show |
2 | a0001c0001t0001g0136a0008c0008t0006g0027 | 2 | NA19002.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.68-35020_68-35005d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456803 | ||||||
| chr6:136456806 | A | AGAAGAAG others(3): Show |
1 | a0001c0001t0001g0137 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.68-35017_68-35008d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456806 | ||||||
| chr6:136456806 | AGAAGAAG others(36): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.68-35050_68-35008d others(45): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456806 | ||||||
| chr6:136456809 | A | AGAAGAAG others(3): Show |
1 | a0004c0004t0001g0121 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.68-35020_68-35011d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456809 | ||||||
| chr6:136456809 | AGAAGAAG others(33): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.68-35050_68-35011d others(42): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456809 | ||||||
| chr6:136456812 | AGAAGAAG others(30): Show |
A | 2 | a0001c0001t0001g0133a0001c0001t0001g0183 | 2 | HG02132.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.68-35050_68-35014d others(39): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456812 | ||||||
| chr6:136456813 | GAAGAA | G | 6 | a0003c0003t0003g0125a0003c0003t0003g0186a0003c0003t0003g0189others(3): Show | 6 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-35019_68-35015d others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456813 | ||||||
| chr6:136456815 | AGAAGAAG others(27): Show |
A | 4 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0129others(1): Show | 4 | HG01346.hp1 HG01993.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-35050_68-35017d others(36): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456815 | ||||||
| chr6:136456818 | AGAAGGAA others(24): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.68-35050_68-35020d others(33): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456818 | ||||||
| chr6:136456821 | AG | A | 9 | a0003c0003t0003g0125a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-35023delC | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456821 | ||||||
| chr6:136456822 | G | GAA | 15 | a0001c0001t0001g0002a0001c0001t0001g0099a0001c0001t0001g0136others(12): Show | 15 | HG00735.hp1 HG02280.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(7): Show |
1 | a0002c0002t0002g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(10): Show |
1 | a0001c0001t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(19): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(22): Show |
1 | a0002c0002t0003g0054 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(31): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(25): Show |
3 | a0001c0001t0001g0117a0002c0002t0003g0006a0002c0002t0005g0014 | 3 | HG01978.hp1 HG02572.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(34): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(31): Show |
1 | a0002c0002t0003g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(40): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(37): Show |
1 | a0002c0002t0003g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(46): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(41): Show |
1 | a0002c0014t0002g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(50): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(14): Show |
1 | a0002c0002t0002g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(23): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(23): Show |
1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(32): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(29): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0144a0002c0002t0005g0007 | 3 | HG01928.hp2 NA18940.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(38): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(32): Show |
3 | a0001c0001t0001g0170a0002c0002t0003g0009a0010c0011t0001g0028 | 3 | HG02109.hp1 NA18949.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(41): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(35): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0164 | 2 | NA18952.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(44): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(38): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0156 | 2 | HG03130.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(47): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(11): Show |
2 | a0001c0001t0001g0148a0002c0002t0002g0217 | 2 | HG00733.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(26): Show |
3 | a0001c0001t0001g0072a0002c0002t0005g0008a0002c0002t0005g0020 | 3 | HG00408.hp1 HG02015.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(35): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(32): Show |
1 | a0001c0001t0001g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(41): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(35): Show |
3 | a0001c0001t0001g0123a0001c0001t0001g0165a0001c0001t0001g0173 | 3 | NA18978.hp1 NA19012.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(44): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(17): Show |
1 | a0001c0001t0001g0162 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(23): Show |
4 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0008g0094others(1): Show | 4 | HG01346.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(32): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(26): Show |
6 | a0001c0001t0001g0029a0001c0001t0001g0158a0001c0001t0013g0179others(3): Show | 6 | HG02896.hp2 NA18906.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(35): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(29): Show |
4 | a0001c0001t0001g0150a0001c0001t0001g0168a0002c0002t0003g0047others(1): Show | 4 | HG00544.hp1 HG01358.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(38): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(38): Show |
1 | a0001c0001t0001g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(47): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(20): Show |
2 | a0001c0001t0001g0139a0002c0002t0003g0019 | 2 | HG00323.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(29): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(23): Show |
2 | a0003c0003t0003g0010a0003c0003t0003g0013 | 2 | HG01106.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(32): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(26): Show |
5 | a0001c0001t0001g0097a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | NA18982.hp2 NA19030.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(35): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(29): Show |
3 | a0001c0001t0008g0112a0001c0012t0001g0174a0002c0002t0003g0056 | 3 | HG02922.hp1 NA19009.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(38): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGA others(35): Show |
2 | a0003c0003t0003g0011a0003c0003t0003g0025 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(44): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(5): Show |
1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(8): Show |
1 | a0001c0001t0001g0092 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(11): Show |
1 | a0001c0010t0001g0151 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(14): Show |
1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(23): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(17): Show |
5 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0001g0135others(2): Show | 5 | HG02257.hp1 HG02273.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(20): Show |
8 | a0001c0001t0001g0079a0001c0001t0001g0159a0002c0002t0003g0018others(5): Show | 8 | HG02615.hp2 NA18939.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(29): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(26): Show |
2 | a0002c0002t0003g0022a0002c0002t0003g0051 | 2 | NA18980.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(35): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(29): Show |
3 | a0001c0001t0001g0140a0002c0002t0003g0048a0009c0013t0001g0083 | 3 | HG01074.hp1 HG04204.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.68-35024_68-35023i others(38): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGAAGG others(32): Show |
1 | a0002c0002t0003g0030 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.68-35024_68-35023i others(41): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGGAAG others(5): Show |
1 | a0001c0001t0001g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGGAAG others(11): Show |
1 | a0001c0001t0001g0167 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGGAAG others(14): Show |
4 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0155others(1): Show | 4 | HG00642.hp2 HG02300.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(23): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGGAAG others(17): Show |
6 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0130others(3): Show | 6 | HG02083.hp1 NA18947.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGGAAG others(20): Show |
1 | a0001c0001t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-35024_68-35023i others(29): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GAAGGAAG others(23): Show |
4 | a0001c0001t0001g0115a0001c0001t0001g0143a0005c0005t0001g0104others(1): Show | 4 | HG00423.hp1 HG02015.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-35024_68-35023i others(32): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GGAAGAAG others(5): Show |
1 | a0004c0004t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-35035_68-35024d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GGAAGAAG others(8): Show |
1 | a0002c0002t0005g0005 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.68-35038_68-35024d others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GGAAGAAG others(11): Show |
3 | a0001c0001t0001g0141a0001c0001t0001g0153a0004c0004t0001g0120 | 3 | HG00621.hp1 HG03540.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.68-35041_68-35024d others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GGAAGAAG others(14): Show |
5 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0161others(2): Show | 5 | HG00639.hp2 HG01934.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-35044_68-35024d others(23): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456822 | G | GGAAGAAG others(17): Show |
5 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0138others(2): Show | 5 | HG02080.hp1 HG02135.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-35047_68-35024d others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456822 | ||||||
| chr6:136456823 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.68-35024C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456823 | ||||||
| chr6:136456825 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.68-35026T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456825 | ||||||
| chr6:136456840 | A | G | 9 | a0003c0003t0003g0125a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-35041T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456840 | ||||||
| chr6:136456849 | G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(139): Show | 142 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.68-35050C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456849 | ||||||
| chr6:136456870 | A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172others(1): Show | 4 | HG00735.hp1 HG02040.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-35071T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456870 | ||||||
| chr6:136456872 | A | AAGAAGAA others(19): Show |
1 | a0001c0001t0008g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.68-35074_68-35073i others(28): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136456872 | ||||||
| chr6:136457024 | G | GT | 95 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0072others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.68-35226dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136457024 | ||||||
| chr6:136457025 | T | C | 3 | a0002c0002t0002g0039a0002c0002t0002g0041a0002c0002t0002g0044 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.68-35226A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136457025 | ||||||
| chr6:136457045 | T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0136a0001c0001t0001g0141 | 3 | NA18939.hp1 NA18944.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.68-35246A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136457045 | ||||||
| chr6:136457122 | A | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0110 | 3 | HG01243.hp2 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.68-35323T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136457122 | ||||||
| chr6:136457308 | T | TA | 15 | a0001c0001t0001g0103a0001c0001t0001g0162a0001c0001t0001g0170others(12): Show | 15 | HG02155.hp2 HG02280.hp2 NA18942.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-35510dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136457308 | ||||||
| chr6:136458071 | G | A | 6 | a0002c0002t0002g0200a0002c0002t0002g0204a0002c0002t0002g0217others(3): Show | 6 | HG00323.hp2 HG01243.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-36272C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136458071 | ||||||
| chr6:136458125 | T | G | 1 | a0003c0003t0003g0191 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.68-36326A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136458125 | ||||||
| chr6:136458159 | A | G | 10 | a0003c0003t0003g0059a0003c0003t0003g0125a0003c0003t0003g0185others(7): Show | 10 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-36360T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136458159 | ||||||
| chr6:136458595 | G | C | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-36796C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136458595 | ||||||
| chr6:136458840 | TC | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0117 | 3 | HG02572.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.68-37042delG | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136458840 | ||||||
| chr6:136459115 | C | A | 21 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(18): Show | 21 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.68-37316G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136459115 | ||||||
| chr6:136459274 | T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(95): Show | 98 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-37475A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136459274 | ||||||
| chr6:136459895 | C | T | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-38096G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136459895 | ||||||
| chr6:136460030 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-38231A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136460030 | ||||||
| chr6:136460142 | G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.68-38343C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136460142 | ||||||
| chr6:136460303 | C | T | 1 | a0002c0002t0002g0225 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.68-38504G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136460303 | ||||||
| chr6:136460379 | G | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-38580C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136460379 | ||||||
| chr6:136460593 | A | G | 1 | a0005c0005t0001g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.68-38794T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136460593 | ||||||
| chr6:136460798 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.68-38999T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136460798 | ||||||
| chr6:136460801 | A | AT | 5 | a0002c0002t0003g0046a0002c0002t0003g0050a0002c0002t0003g0054others(2): Show | 5 | NA18939.hp2 NA18995.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-39003dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136460801 | ||||||
| chr6:136460885 | A | G | 6 | a0002c0002t0005g0004a0002c0002t0005g0005a0002c0002t0005g0007others(3): Show | 6 | HG00408.hp1 HG02015.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-39086T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136460885 | ||||||
| chr6:136461056 | C | T | 2 | a0002c0002t0002g0211a0006c0006t0006g0182 | 2 | HG00423.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.68-39257G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136461056 | ||||||
| chr6:136461160 | T | C | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-39361A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136461160 | ||||||
| chr6:136461166 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.68-39367T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136461166 | ||||||
| chr6:136461195 | T | C | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-39396A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136461195 | ||||||
| chr6:136461295 | G | A | 28 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(25): Show | 28 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.68-39496C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136461295 | ||||||
| chr6:136461324 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-39525G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136461324 | ||||||
| chr6:136461398 | G | T | 1 | a0002c0002t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-39599C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136461398 | ||||||
| chr6:136461904 | T | C | 17 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(14): Show | 17 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-40105A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136461904 | ||||||
| chr6:136462080 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.68-40281G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136462080 | ||||||
| chr6:136462169 | T | TA | 91 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(88): Show | 91 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.68-40371dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136462169 | ||||||
| chr6:136462169 | TA | T | 42 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(39): Show | 42 | HG00408.hp1 HG00408.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.68-40371delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136462169 | ||||||
| chr6:136462291 | A | G | 1 | a0002c0002t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.68-40492T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136462291 | ||||||
| chr6:136462395 | A | C | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-40596T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136462395 | ||||||
| chr6:136462954 | C | CA | 103 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(100): Show | 103 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.68-41156dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136462954 | ||||||
| chr6:136463016 | C | T | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-41217G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136463016 | ||||||
| chr6:136463065 | T | G | 1 | a0001c0001t0004g0068 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.68-41266A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136463065 | ||||||
| chr6:136463117 | G | A | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-41318C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136463117 | ||||||
| chr6:136463322 | G | C | 1 | a0001c0001t0004g0016 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.68-41523C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136463322 | ||||||
| chr6:136463377 | A | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-41578T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136463377 | ||||||
| chr6:136463513 | T | C | 1 | a0002c0002t0002g0197 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.68-41714A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136463513 | ||||||
| chr6:136463593 | A | G | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-41794T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136463593 | ||||||
| chr6:136463997 | G | A | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-42198C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136463997 | ||||||
| chr6:136464021 | G | A | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-42222C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464021 | ||||||
| chr6:136464039 | G | A | 10 | a0003c0003t0003g0059a0003c0003t0003g0125a0003c0003t0003g0185others(7): Show | 10 | HG02155.hp2 NA18942.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-42240C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464039 | ||||||
| chr6:136464371 | C | T | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-42572G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464371 | ||||||
| chr6:136464407 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.68-42608T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464407 | ||||||
| chr6:136464574 | T | G | 1 | a0001c0001t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-42775A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464574 | ||||||
| chr6:136464731 | T | C | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-42932A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464731 | ||||||
| chr6:136464794 | C | G | 1 | a0002c0002t0002g0213 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.68-42995G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464794 | ||||||
| chr6:136464817 | G | A | 7 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(4): Show | 7 | NA18940.hp2 NA18945.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-43018C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464817 | ||||||
| chr6:136464966 | G | T | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-43167C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136464966 | ||||||
| chr6:136465255 | C | G | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-43456G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136465255 | ||||||
| chr6:136465400 | A | C | 1 | a0001c0001t0004g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.68-43601T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136465400 | ||||||
| chr6:136465423 | A | G | 1 | a0001c0001t0004g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.68-43624T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136465423 | ||||||
| chr6:136465505 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68-43706A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136465505 | ||||||
| chr6:136465601 | T | G | 3 | a0002c0002t0002g0227a0002c0002t0009g0223a0002c0002t0009g0224 | 3 | HG00733.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.68-43802A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136465601 | ||||||
| chr6:136465707 | C | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-43908G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136465707 | ||||||
| chr6:136465799 | T | A | 1 | a0003c0003t0003g0015 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.68-44000A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136465799 | ||||||
| chr6:136466039 | C | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-44240G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136466039 | ||||||
| chr6:136466283 | C | T | 39 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(36): Show | 39 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-44484G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136466283 | ||||||
| chr6:136466300 | T | C | 4 | a0002c0002t0007g0205a0002c0002t0007g0206a0002c0002t0007g0207others(1): Show | 4 | HG02723.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-44501A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136466300 | ||||||
| chr6:136466342 | T | C | 2 | a0002c0002t0002g0230a0002c0002t0002g0232 | 2 | NA18985.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.68-44543A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136466342 | ||||||
| chr6:136466448 | A | G | 3 | a0003c0003t0003g0185a0003c0003t0003g0187a0003c0003t0003g0188 | 3 | NA19060.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.68-44649T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136466448 | ||||||
| chr6:136466564 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.68-44765T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136466564 | ||||||
| chr6:136467022 | G | A | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-45223C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136467022 | ||||||
| chr6:136467123 | C | T | 2 | a0001c0001t0001g0145a0010c0011t0001g0028 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-45324G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136467123 | ||||||
| chr6:136467236 | G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0145a0010c0011t0001g0028 | 3 | HG02109.hp1 HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.68-45437C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136467236 | ||||||
| chr6:136467509 | A | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-45710T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136467509 | ||||||
| chr6:136467513 | G | C | 4 | a0003c0003t0003g0185a0003c0003t0003g0187a0003c0003t0003g0188others(1): Show | 4 | NA18974.hp1 NA19060.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-45714C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136467513 | ||||||
| chr6:136467674 | C | A | 1 | a0002c0002t0002g0202 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.68-45875G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136467674 | ||||||
| chr6:136467945 | T | C | 3 | a0002c0002t0002g0227a0002c0002t0009g0223a0002c0002t0009g0224 | 3 | HG00733.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.68-46146A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136467945 | ||||||
| chr6:136468228 | C | T | 1 | a0002c0002t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.68-46429G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468228 | ||||||
| chr6:136468344 | T | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-46545A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468344 | ||||||
| chr6:136468365 | G | A | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-46566C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468365 | ||||||
| chr6:136468412 | A | G | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-46613T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468412 | ||||||
| chr6:136468458 | C | T | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-46659G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468458 | ||||||
| chr6:136468470 | T | C | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-46671A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468470 | ||||||
| chr6:136468728 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68-46929A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468728 | ||||||
| chr6:136468992 | G | GT | 6 | a0001c0001t0001g0043a0001c0001t0001g0165a0001c0001t0013g0179others(3): Show | 6 | HG02280.hp2 HG03139.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-47194dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468992 | ||||||
| chr6:136468992 | G | T | 1 | a0002c0002t0007g0207 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.68-47193C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468992 | ||||||
| chr6:136468995 | T | G | 1 | a0002c0002t0002g0196 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.68-47196A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136468995 | ||||||
| chr6:136469039 | T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.68-47240A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136469039 | ||||||
| chr6:136469252 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-47453G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136469252 | ||||||
| chr6:136469673 | A | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-47874T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136469673 | ||||||
| chr6:136469915 | G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG00735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.68-48116C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136469915 | ||||||
| chr6:136470134 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68-48335C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470134 | ||||||
| chr6:136470150 | C | G | 35 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-48351G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470150 | ||||||
| chr6:136470266 | C | G | 5 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-48467G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470266 | ||||||
| chr6:136470425 | C | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-48626G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470425 | ||||||
| chr6:136470748 | G | A | 1 | a0002c0002t0002g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.68-48949C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470748 | ||||||
| chr6:136470750 | G | A | 11 | a0003c0003t0003g0031a0003c0003t0003g0059a0003c0003t0003g0125others(8): Show | 11 | HG02155.hp2 HG02280.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-48951C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470750 | ||||||
| chr6:136470844 | G | GAA | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-49047_68-49046d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470844 | ||||||
| chr6:136470891 | T | A | 1 | a0002c0002t0002g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.68-49092A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470891 | ||||||
| chr6:136470997 | T | C | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-49198A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136470997 | ||||||
| chr6:136471021 | A | G | 1 | a0001c0001t0004g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.68-49222T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471021 | ||||||
| chr6:136471026 | T | A | 1 | a0002c0002t0002g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.68-49227A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471026 | ||||||
| chr6:136471047 | T | C | 14 | a0002c0002t0003g0030a0002c0002t0003g0046a0002c0002t0003g0047others(11): Show | 14 | NA18939.hp2 NA18948.hp1 NA18970.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-49248A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471047 | ||||||
| chr6:136471227 | T | C | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-49428A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471227 | ||||||
| chr6:136471307 | G | A | 1 | a0002c0002t0002g0197 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.68-49508C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471307 | ||||||
| chr6:136471335 | A | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(175): Show | 178 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.68-49536T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471335 | ||||||
| chr6:136471472 | A | T | 3 | a0003c0003t0003g0185a0003c0003t0003g0187a0003c0003t0003g0188 | 3 | NA19060.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.68-49673T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471472 | ||||||
| chr6:136471557 | G | GT | 42 | a0002c0002t0003g0003a0002c0002t0003g0006a0002c0002t0003g0009others(39): Show | 42 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.68-49759dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471557 | ||||||
| chr6:136471679 | C | T | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-49880G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471679 | ||||||
| chr6:136471826 | C | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(95): Show | 98 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-50027G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471826 | ||||||
| chr6:136471960 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.68-50161G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136471960 | ||||||
| chr6:136472002 | G | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-50203C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136472002 | ||||||
| chr6:136472281 | T | G | 11 | a0003c0003t0003g0031a0003c0003t0003g0059a0003c0003t0003g0125others(8): Show | 11 | HG02155.hp2 HG02280.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-50482A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136472281 | ||||||
| chr6:136472321 | A | G | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-50522T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136472321 | ||||||
| chr6:136472711 | C | G | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-50912G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136472711 | ||||||
| chr6:136472833 | TA | T | 27 | a0001c0001t0001g0063a0001c0001t0004g0016a0001c0001t0004g0061others(24): Show | 27 | HG00408.hp2 HG01358.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.68-51035delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136472833 | ||||||
| chr6:136472930 | C | A | 40 | a0002c0002t0003g0006a0002c0002t0003g0009a0002c0002t0003g0012others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.68-51131G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136472930 | ||||||
| chr6:136473210 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.68-51411A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136473210 | ||||||
| chr6:136473381 | T | C | 3 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.68-51582A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136473381 | ||||||
| chr6:136473600 | A | G | 45 | a0001c0001t0001g0099a0001c0001t0001g0136a0001c0001t0001g0137others(42): Show | 45 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.68-51801T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136473600 | ||||||
| chr6:136473619 | T | C | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-51820A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136473619 | ||||||
| chr6:136473890 | C | T | 26 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0109others(23): Show | 26 | HG00323.hp1 HG01106.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.68-52091G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136473890 | ||||||
| chr6:136474092 | G | C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-52293C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474092 | ||||||
| chr6:136474150 | A | G | 27 | a0001c0001t0001g0099a0001c0001t0001g0163a0001c0001t0001g0164others(24): Show | 27 | HG02080.hp2 HG02155.hp2 NA18939.hp2 others(24): Show |
intron_variant | MODIFIER | c.68-52351T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474150 | ||||||
| chr6:136474282 | C | A | 1 | a0002c0002t0002g0062 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.68-52483G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474282 | ||||||
| chr6:136474300 | G | A | 39 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-52501C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474300 | ||||||
| chr6:136474492 | G | A | 4 | a0002c0002t0003g0003a0006c0006t0006g0180a0006c0006t0006g0181others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-52693C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474492 | ||||||
| chr6:136474539 | A | G | 34 | a0001c0001t0001g0135a0001c0001t0004g0016a0002c0002t0003g0006others(31): Show | 34 | HG00408.hp1 HG00639.hp1 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.68-52740T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474539 | ||||||
| chr6:136474557 | C | T | 32 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(29): Show | 32 | HG00408.hp1 HG00639.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.68-52758G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474557 | ||||||
| chr6:136474618 | T | A | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-52819A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474618 | ||||||
| chr6:136474627 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.68-52828T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474627 | ||||||
| chr6:136474671 | T | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-52872A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474671 | ||||||
| chr6:136474721 | C | CT | 7 | a0001c0001t0001g0029a0001c0001t0001g0145a0002c0002t0003g0003others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-52923dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474721 | ||||||
| chr6:136474721 | CT | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0091a0001c0001t0001g0092others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.68-52923delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474721 | ||||||
| chr6:136474857 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68-53058C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474857 | ||||||
| chr6:136474906 | G | A | 3 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195 | 3 | NA18940.hp2 NA18945.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.68-53107C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474906 | ||||||
| chr6:136474956 | T | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-53157A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474956 | ||||||
| chr6:136474994 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.68-53195C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136474994 | ||||||
| chr6:136475010 | A | G | 25 | a0001c0001t0001g0063a0001c0001t0004g0061a0001c0001t0004g0064others(22): Show | 25 | HG00408.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-53211T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475010 | ||||||
| chr6:136475087 | T | C | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-53288A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475087 | ||||||
| chr6:136475226 | G | A | 192 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(189): Show | 192 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.68-53427C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475226 | ||||||
| chr6:136475303 | T | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-53504A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475303 | ||||||
| chr6:136475378 | C | T | 1 | a0002c0002t0003g0021 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.68-53579G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475378 | ||||||
| chr6:136475485 | T | C | 33 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.68-53686A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475485 | ||||||
| chr6:136475512 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.68-53713A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475512 | ||||||
| chr6:136475702 | G | A | 1 | a0002c0002t0003g0018 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.68-53903C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475702 | ||||||
| chr6:136475716 | T | G | 1 | a0001c0001t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68-53917A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475716 | ||||||
| chr6:136475718 | A | AT | 37 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(34): Show | 37 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.68-53920dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475718 | ||||||
| chr6:136475918 | G | A | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-54119C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475918 | ||||||
| chr6:136475959 | A | G | 1 | a0002c0002t0002g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.68-54160T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136475959 | ||||||
| chr6:136476073 | G | A | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.68-54274C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476073 | ||||||
| chr6:136476157 | C | T | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-54358G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476157 | ||||||
| chr6:136476201 | T | C | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-54402A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476201 | ||||||
| chr6:136476211 | C | T | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-54412G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476211 | ||||||
| chr6:136476214 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.68-54415A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476214 | ||||||
| chr6:136476247 | G | T | 5 | a0004c0004t0001g0096a0004c0004t0001g0118a0004c0004t0001g0119others(2): Show | 5 | HG02723.hp2 HG02809.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-54448C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476247 | ||||||
| chr6:136476248 | G | A | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-54449C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476248 | ||||||
| chr6:136476315 | C | T | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-54516G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476315 | ||||||
| chr6:136476396 | T | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-54597A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476396 | ||||||
| chr6:136476484 | T | A | 81 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.68-54685A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476484 | ||||||
| chr6:136476507 | G | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0117 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.68-54708C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476507 | ||||||
| chr6:136476561 | T | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-54762A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476561 | ||||||
| chr6:136476619 | G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0091a0001c0001t0001g0092others(72): Show | 75 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.68-54820C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476619 | ||||||
| chr6:136476694 | G | C | 1 | a0004c0004t0001g0118 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.68-54895C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476694 | ||||||
| chr6:136476770 | CAT | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.68-54973_68-54972d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476770 | ||||||
| chr6:136476862 | A | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-55063T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476862 | ||||||
| chr6:136476894 | T | G | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-55095A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136476894 | ||||||
| chr6:136477061 | T | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-55262A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136477061 | ||||||
| chr6:136477151 | C | T | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-55352G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136477151 | ||||||
| chr6:136477154 | G | A | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-55355C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136477154 | ||||||
| chr6:136477242 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.68-55443C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136477242 | ||||||
| chr6:136477521 | G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0091others(89): Show | 92 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.68-55722C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136477521 | ||||||
| chr6:136477806 | G | C | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-56007C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136477806 | ||||||
| chr6:136477840 | T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0043others(191): Show | 194 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.68-56041A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136477840 | ||||||
| chr6:136477881 | T | C | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.68-56082A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136477881 | ||||||
| chr6:136478015 | C | T | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-56216G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478015 | ||||||
| chr6:136478087 | G | A | 1 | a0004c0004t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.68-56288C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478087 | ||||||
| chr6:136478318 | C | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-56519G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478318 | ||||||
| chr6:136478399 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.68-56600T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478399 | ||||||
| chr6:136478442 | A | AAACAAAC | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-56644_68-56643i others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478442 | ||||||
| chr6:136478443 | C | A | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-56644G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478443 | ||||||
| chr6:136478466 | G | C | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-56667C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478466 | ||||||
| chr6:136478633 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.68-56834C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478633 | ||||||
| chr6:136478727 | TACCAAAG others(4): Show |
T | 2 | a0006c0006t0006g0180a0006c0006t0006g0181 | 2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.68-56939_68-56929d others(13): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478727 | ||||||
| chr6:136478842 | T | C | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-57043A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478842 | ||||||
| chr6:136478889 | T | C | 3 | a0002c0002t0002g0216a0002c0002t0002g0218a0002c0002t0002g0234 | 3 | HG00642.hp1 HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.68-57090A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478889 | ||||||
| chr6:136478896 | AT | A | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-57098delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478896 | ||||||
| chr6:136478959 | C | T | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-57160G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478959 | ||||||
| chr6:136478979 | C | CA | 20 | a0001c0001t0001g0100a0001c0001t0001g0115a0001c0001t0001g0130others(17): Show | 20 | HG00733.hp2 HG01192.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.68-57181dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478979 | ||||||
| chr6:136478979 | CA | C | 35 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(32): Show | 35 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.68-57181delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478979 | ||||||
| chr6:136478992 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.68-57193T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478992 | ||||||
| chr6:136478996 | G | A | 35 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-57197C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136478996 | ||||||
| chr6:136479000 | G | GA | 4 | a0002c0002t0003g0003a0002c0002t0003g0058a0008c0008t0006g0026others(1): Show | 4 | HG02965.hp2 HG03453.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-57202dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479000 | ||||||
| chr6:136479000 | G | GAAAGAAA others(2): Show |
35 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-57202_68-57201i others(11): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479000 | ||||||
| chr6:136479404 | T | C | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-57605A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479404 | ||||||
| chr6:136479629 | C | T | 1 | a0002c0002t0002g0062 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.68-57830G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479629 | ||||||
| chr6:136479700 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.68-57901A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479700 | ||||||
| chr6:136479701 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.68-57902A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479701 | ||||||
| chr6:136479702 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.68-57903G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479702 | ||||||
| chr6:136479742 | C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0142 | 2 | HG01346.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.68-57943G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479742 | ||||||
| chr6:136479760 | A | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.68-57961T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479760 | ||||||
| chr6:136479835 | C | A | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-58036G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479835 | ||||||
| chr6:136479847 | G | A | 1 | a0002c0002t0002g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.68-58048C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479847 | ||||||
| chr6:136479965 | T | A | 1 | a0002c0002t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.68-58166A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479965 | ||||||
| chr6:136479970 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.68-58171A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479970 | ||||||
| chr6:136479991 | C | A | 8 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0036others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-58192G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479991 | ||||||
| chr6:136479995 | C | T | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-58196G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136479995 | ||||||
| chr6:136480103 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.68-58304C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480103 | ||||||
| chr6:136480221 | T | G | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-58422A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480221 | ||||||
| chr6:136480360 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.68-58561G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480360 | ||||||
| chr6:136480383 | T | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.68-58584A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480383 | ||||||
| chr6:136480413 | T | C | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-58614A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480413 | ||||||
| chr6:136480503 | A | C | 1 | a0002c0014t0002g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.68-58704T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480503 | ||||||
| chr6:136480513 | G | A | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.68-58714C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480513 | ||||||
| chr6:136480595 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.68-58796A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480595 | ||||||
| chr6:136480641 | C | CA | 65 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(62): Show | 65 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.68-58843dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480641 | ||||||
| chr6:136480641 | C | CAA | 14 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0153others(11): Show | 14 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-58844_68-58843d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480641 | ||||||
| chr6:136480641 | C | CAAA | 6 | a0002c0002t0002g0216a0002c0002t0002g0218a0002c0002t0007g0205others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-58845_68-58843d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480641 | ||||||
| chr6:136480641 | CA | C | 17 | a0001c0001t0001g0183a0001c0001t0013g0179a0002c0002t0002g0247others(14): Show | 17 | HG00408.hp1 HG01074.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-58843delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480641 | ||||||
| chr6:136480641 | CAA | C | 26 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(23): Show | 26 | HG00639.hp1 HG01106.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-58844_68-58843d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480641 | ||||||
| chr6:136480662 | A | AG | 4 | a0003c0003t0003g0185a0003c0003t0003g0187a0003c0003t0003g0188others(1): Show | 4 | NA19060.hp2 NA19062.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-58864_68-58863i others(3): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480662 | ||||||
| chr6:136480662 | A | G | 6 | a0003c0003t0003g0059a0003c0003t0003g0186a0003c0003t0003g0189others(3): Show | 6 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-58863T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480662 | ||||||
| chr6:136480738 | G | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-58939C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480738 | ||||||
| chr6:136480868 | C | G | 1 | a0001c0001t0004g0016 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.68-59069G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480868 | ||||||
| chr6:136480869 | T | G | 1 | a0001c0001t0004g0016 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.68-59070A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480869 | ||||||
| chr6:136480870 | A | G | 1 | a0001c0001t0004g0016 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.68-59071T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480870 | ||||||
| chr6:136480896 | T | C | 52 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.68-59097A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136480896 | ||||||
| chr6:136481105 | A | G | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-59306T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136481105 | ||||||
| chr6:136481139 | A | G | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-59340T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136481139 | ||||||
| chr6:136481224 | T | A | 39 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-59425A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136481224 | ||||||
| chr6:136481436 | T | TA | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.68-59638dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136481436 | ||||||
| chr6:136481759 | T | C | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-59960A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136481759 | ||||||
| chr6:136481916 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.68-60117A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136481916 | ||||||
| chr6:136482159 | G | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-60360C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482159 | ||||||
| chr6:136482574 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.68-60775G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482574 | ||||||
| chr6:136482600 | C | CA | 6 | a0001c0001t0001g0099a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | NA18747.hp1 NA18939.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-60802dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482600 | ||||||
| chr6:136482600 | CA | C | 101 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0004g0061others(98): Show | 101 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.68-60802delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482600 | ||||||
| chr6:136482614 | A | AAAAAC | 5 | a0002c0002t0003g0003a0002c0002t0003g0052a0002c0002t0003g0056others(2): Show | 5 | HG02965.hp2 HG03453.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-60816_68-60815i others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482614 | ||||||
| chr6:136482614 | A | AAAAC | 34 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(31): Show | 34 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.68-60816_68-60815i others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482614 | ||||||
| chr6:136482619 | C | T | 1 | a0002c0002t0002g0236 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.68-60820G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482619 | ||||||
| chr6:136482729 | C | A | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-60930G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482729 | ||||||
| chr6:136482770 | G | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-60971C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482770 | ||||||
| chr6:136482847 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.68-61048A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482847 | ||||||
| chr6:136482933 | C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0116 | 2 | NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.68-61134G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482933 | ||||||
| chr6:136482962 | A | G | 42 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(39): Show | 42 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.68-61163T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136482962 | ||||||
| chr6:136483010 | C | A | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.68-61211G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483010 | ||||||
| chr6:136483121 | G | A | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-61322C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483121 | ||||||
| chr6:136483129 | C | CAAA | 35 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-61333_68-61331d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483129 | ||||||
| chr6:136483129 | CA | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0098others(16): Show | 19 | HG01433.hp1 HG02109.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-61331delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483129 | ||||||
| chr6:136483129 | CAAAAAAA | C | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-61337_68-61331d others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483129 | ||||||
| chr6:136483167 | T | C | 8 | a0003c0003t0003g0185a0003c0003t0003g0186a0003c0003t0003g0187others(5): Show | 8 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-61368A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483167 | ||||||
| chr6:136483275 | G | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.68-61476C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483275 | ||||||
| chr6:136483348 | G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG00735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.68-61549C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483348 | ||||||
| chr6:136483403 | T | A | 99 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(96): Show | 99 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.68-61604A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483403 | ||||||
| chr6:136483777 | A | G | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.68-61978T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483777 | ||||||
| chr6:136483817 | A | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-62018T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483817 | ||||||
| chr6:136483871 | C | T | 1 | a0002c0014t0002g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.68-62072G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483871 | ||||||
| chr6:136483971 | T | C | 1 | a0001c0001t0004g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.68-62172A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136483971 | ||||||
| chr6:136484020 | C | T | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.68-62221G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484020 | ||||||
| chr6:136484081 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.68-62282C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484081 | ||||||
| chr6:136484395 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-62596G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484395 | ||||||
| chr6:136484489 | T | G | 1 | a0002c0002t0002g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.68-62690A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484489 | ||||||
| chr6:136484610 | T | C | 8 | a0003c0003t0003g0185a0003c0003t0003g0186a0003c0003t0003g0187others(5): Show | 8 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-62811A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484610 | ||||||
| chr6:136484644 | C | T | 171 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(168): Show | 171 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.68-62845G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484644 | ||||||
| chr6:136484857 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-63058A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484857 | ||||||
| chr6:136484879 | G | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.68-63080C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484879 | ||||||
| chr6:136484891 | T | C | 45 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.68-63092A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484891 | ||||||
| chr6:136484933 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.68-63134C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136484933 | ||||||
| chr6:136485326 | T | A | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-63527A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485326 | ||||||
| chr6:136485327 | T | G | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-63528A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485327 | ||||||
| chr6:136485348 | T | C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-63549A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485348 | ||||||
| chr6:136485552 | C | A | 1 | a0005c0005t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.68-63753G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485552 | ||||||
| chr6:136485555 | A | AT | 24 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0117others(21): Show | 24 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.68-63757dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485555 | A | ATT | 50 | a0001c0001t0001g0043a0001c0001t0001g0140a0002c0002t0002g0193others(47): Show | 50 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-63758_68-63757d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485555 | A | ATTT | 11 | a0002c0002t0002g0197a0002c0002t0002g0200a0002c0002t0002g0202others(8): Show | 11 | HG01243.hp1 HG02080.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-63759_68-63757d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485555 | A | ATTTT | 6 | a0002c0002t0002g0236a0002c0002t0011g0245a0003c0003t0003g0185others(3): Show | 6 | HG01074.hp1 HG03540.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-63760_68-63757d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485555 | A | ATTTTT | 6 | a0001c0001t0001g0079a0002c0002t0002g0062a0002c0002t0002g0232others(3): Show | 6 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-63761_68-63757d others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485555 | A | ATTTTTT | 17 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(14): Show | 17 | HG01358.hp1 HG01934.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-63762_68-63757d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485555 | A | ATTTTTTT | 7 | a0001c0001t0001g0074a0001c0001t0004g0076a0001c0001t0004g0077others(4): Show | 7 | HG00408.hp2 HG01928.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-63763_68-63757d others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485555 | A | ATTTTTTT others(1): Show |
5 | a0001c0001t0004g0066a0001c0001t0004g0069a0001c0001t0004g0089others(2): Show | 5 | HG01123.hp2 HG02622.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-63764_68-63757d others(10): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485555 | AT | A | 5 | a0001c0001t0001g0147a0001c0001t0001g0153a0002c0002t0002g0033others(2): Show | 5 | HG00621.hp1 HG02735.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-63757delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485555 | ||||||
| chr6:136485585 | C | T | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-63786G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485585 | ||||||
| chr6:136485853 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-64054G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485853 | ||||||
| chr6:136485896 | T | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | NA18940.hp1 NA18949.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-64097A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485896 | ||||||
| chr6:136485960 | GACAA | G | 5 | a0004c0004t0001g0096a0004c0004t0001g0118a0004c0004t0001g0119others(2): Show | 5 | HG02723.hp2 HG02809.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-64165_68-64162d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136485960 | ||||||
| chr6:136486181 | G | C | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+64161C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136486181 | ||||||
| chr6:136486198 | T | C | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+64144A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136486198 | ||||||
| chr6:136486789 | A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0117 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.67+63553T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136486789 | ||||||
| chr6:136486909 | T | C | 3 | a0001c0001t0008g0094a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | HG02922.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.67+63433A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136486909 | ||||||
| chr6:136486975 | AGAAAG | A | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+63362_67+63366d others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136486975 | ||||||
| chr6:136486998 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.67+63344A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136486998 | ||||||
| chr6:136487014 | T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.67+63328A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136487014 | ||||||
| chr6:136487576 | G | A | 2 | a0001c0001t0001g0145a0010c0011t0001g0028 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+62766C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136487576 | ||||||
| chr6:136487700 | C | T | 13 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(10): Show | 13 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.67+62642G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136487700 | ||||||
| chr6:136487712 | G | GA | 46 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(43): Show | 46 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+62629dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136487712 | ||||||
| chr6:136487814 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.67+62528C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136487814 | ||||||
| chr6:136488031 | T | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+62311A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488031 | ||||||
| chr6:136488070 | T | C | 1 | a0002c0002t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.67+62272A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488070 | ||||||
| chr6:136488118 | G | A | 1 | a0002c0002t0002g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.67+62224C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488118 | ||||||
| chr6:136488130 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67+62212A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488130 | ||||||
| chr6:136488321 | C | A | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+62021G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488321 | ||||||
| chr6:136488386 | A | G | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+61956T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488386 | ||||||
| chr6:136488444 | C | CT | 23 | a0001c0001t0001g0043a0001c0001t0012g0132a0002c0002t0002g0001others(20): Show | 23 | HG01074.hp1 HG01934.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.67+61897dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488444 | ||||||
| chr6:136488444 | CTTT | C | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+61895_67+61897d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488444 | ||||||
| chr6:136488724 | T | C | 1 | a0002c0002t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67+61618A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488724 | ||||||
| chr6:136488733 | A | T | 1 | a0001c0001t0004g0078 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.67+61609T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488733 | ||||||
| chr6:136488861 | C | T | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+61481G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136488861 | ||||||
| chr6:136489117 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67+61225G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489117 | ||||||
| chr6:136489172 | AT | A | 157 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.67+61169delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489172 | ||||||
| chr6:136489182 | T | A | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+61160A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489182 | ||||||
| chr6:136489331 | T | C | 1 | a0002c0002t0003g0049 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.67+61011A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489331 | ||||||
| chr6:136489378 | G | C | 153 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.67+60964C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489378 | ||||||
| chr6:136489400 | T | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+60942A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489400 | ||||||
| chr6:136489439 | C | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+60903G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489439 | ||||||
| chr6:136489523 | T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.67+60819A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489523 | ||||||
| chr6:136489526 | C | CT | 108 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(105): Show | 108 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.67+60815dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489526 | ||||||
| chr6:136489526 | C | CTT | 10 | a0001c0001t0004g0076a0001c0001t0004g0088a0001c0001t0004g0178others(7): Show | 10 | HG00621.hp2 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+60814_67+60815d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489526 | ||||||
| chr6:136489526 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0145a0002c0002t0002g0202a0010c0011t0001g0028 | 3 | HG02109.hp1 NA19010.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+60806_67+60815d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489526 | ||||||
| chr6:136489533 | T | G | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+60809A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489533 | ||||||
| chr6:136489675 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.67+60667C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489675 | ||||||
| chr6:136489809 | G | A | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+60533C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136489809 | ||||||
| chr6:136490317 | C | T | 153 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.67+60025G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136490317 | ||||||
| chr6:136490463 | A | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+59879T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136490463 | ||||||
| chr6:136490498 | A | AC | 153 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.67+59843dupG | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136490498 | ||||||
| chr6:136490577 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.67+59765C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136490577 | ||||||
| chr6:136490631 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.67+59711G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136490631 | ||||||
| chr6:136491177 | T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0091others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.67+59165A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136491177 | ||||||
| chr6:136491308 | T | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+59034A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136491308 | ||||||
| chr6:136491476 | T | C | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+58866A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136491476 | ||||||
| chr6:136491855 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.67+58487G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136491855 | ||||||
| chr6:136492302 | T | G | 5 | a0004c0004t0001g0096a0004c0004t0001g0118a0004c0004t0001g0119others(2): Show | 5 | HG02723.hp2 HG02809.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+58040A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136492302 | ||||||
| chr6:136492399 | G | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0116others(1): Show | 4 | HG02135.hp2 NA18974.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+57943C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136492399 | ||||||
| chr6:136492463 | G | C | 37 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(34): Show | 37 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.67+57879C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136492463 | ||||||
| chr6:136492916 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+57426A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136492916 | ||||||
| chr6:136493121 | C | CT | 40 | a0001c0001t0001g0129a0001c0001t0004g0016a0001c0001t0013g0179others(37): Show | 40 | HG00408.hp1 HG01106.hp1 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.67+57220dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493121 | ||||||
| chr6:136493121 | C | CTTTT | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG01074.hp1 HG02615.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+57217_67+57220d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493121 | ||||||
| chr6:136493121 | C | CTTTTT | 29 | a0001c0001t0001g0063a0001c0001t0001g0134a0001c0001t0001g0135others(26): Show | 29 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.67+57216_67+57220d others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493121 | ||||||
| chr6:136493121 | C | CTTTTTT | 10 | a0001c0001t0004g0248a0002c0002t0002g0062a0003c0003t0003g0031others(7): Show | 10 | HG02055.hp1 HG02280.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+57215_67+57220d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493121 | ||||||
| chr6:136493121 | C | CTTTTTTT others(3): Show |
1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67+57211_67+57220d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493121 | ||||||
| chr6:136493145 | C | T | 45 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+57197G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493145 | ||||||
| chr6:136493160 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.67+57182C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493160 | ||||||
| chr6:136493170 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.67+57172G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493170 | ||||||
| chr6:136493404 | T | C | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+56938A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493404 | ||||||
| chr6:136493469 | G | A | 1 | a0009c0013t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.67+56873C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493469 | ||||||
| chr6:136493962 | C | T | 45 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+56380G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136493962 | ||||||
| chr6:136494035 | A | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+56307T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136494035 | ||||||
| chr6:136494387 | T | C | 155 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(152): Show | 155 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.67+55955A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136494387 | ||||||
| chr6:136494456 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.67+55886A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136494456 | ||||||
| chr6:136494460 | A | C | 1 | a0002c0002t0002g0244 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.67+55882T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136494460 | ||||||
| chr6:136494518 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67+55824T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136494518 | ||||||
| chr6:136494519 | T | G | 45 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+55823A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136494519 | ||||||
| chr6:136494966 | G | A | 1 | a0001c0001t0001g0172 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.67+55376C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136494966 | ||||||
| chr6:136494980 | T | C | 1 | a0002c0002t0002g0235 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.67+55362A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136494980 | ||||||
| chr6:136495064 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67+55278T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136495064 | ||||||
| chr6:136495453 | T | TAC | 15 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0139others(12): Show | 15 | HG00323.hp1 HG01934.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+54887_67+54888d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136495453 | ||||||
| chr6:136495453 | T | TACAC | 27 | a0002c0002t0003g0009a0002c0002t0003g0012a0002c0002t0003g0024others(24): Show | 27 | HG00408.hp1 HG01106.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.67+54885_67+54888d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136495453 | ||||||
| chr6:136495453 | T | TACACAC | 9 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0017others(6): Show | 9 | HG00639.hp1 HG01433.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+54883_67+54888d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136495453 | ||||||
| chr6:136495453 | TAC | T | 19 | a0002c0002t0002g0001a0002c0002t0002g0032a0002c0002t0002g0033others(16): Show | 19 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.67+54887_67+54888d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136495453 | ||||||
| chr6:136495453 | TACAC | T | 69 | a0001c0001t0001g0100a0001c0001t0001g0134a0001c0001t0001g0135others(66): Show | 69 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.67+54885_67+54888d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136495453 | ||||||
| chr6:136495453 | TACACAC | T | 8 | a0001c0001t0001g0043a0002c0002t0002g0193a0002c0002t0002g0194others(5): Show | 8 | HG02074.hp1 HG03579.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+54883_67+54888d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136495453 | ||||||
| chr6:136495632 | T | C | 1 | a0009c0013t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.67+54710A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136495632 | ||||||
| chr6:136496135 | ACCC | A | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+54204_67+54206d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496135 | ||||||
| chr6:136496154 | G | A | 4 | a0002c0002t0002g0208a0002c0002t0002g0212a0002c0002t0002g0213others(1): Show | 4 | HG02074.hp1 NA18944.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+54188C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496154 | ||||||
| chr6:136496279 | G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0117 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.67+54063C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496279 | ||||||
| chr6:136496350 | A | G | 174 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0063others(171): Show | 174 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.67+53992T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496350 | ||||||
| chr6:136496381 | GTGAAAAC others(3727): Show |
G | 4 | a0001c0001t0013g0179a0006c0006t0006g0180a0006c0006t0006g0181others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+50227_67+53960d others(2): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496381 | ||||||
| chr6:136496427 | T | C | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+53915A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496427 | ||||||
| chr6:136496484 | A | C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+53858T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496484 | ||||||
| chr6:136496630 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.67+53712C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496630 | ||||||
| chr6:136496687 | T | G | 1 | a0001c0001t0004g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.67+53655A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496687 | ||||||
| chr6:136496761 | G | C | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+53581C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496761 | ||||||
| chr6:136496777 | T | TA | 57 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0103others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+53564dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496777 | ||||||
| chr6:136496777 | T | TAA | 16 | a0001c0001t0001g0029a0001c0001t0001g0145a0001c0001t0001g0175others(13): Show | 16 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+53563_67+53564d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496777 | ||||||
| chr6:136496777 | TA | T | 35 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(32): Show | 35 | HG01074.hp1 HG01123.hp2 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.67+53564delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496777 | ||||||
| chr6:136496777 | TAA | T | 34 | a0001c0001t0004g0016a0001c0001t0004g0065a0002c0002t0003g0006others(31): Show | 34 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.67+53563_67+53564d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496777 | ||||||
| chr6:136496777 | TAAA | T | 5 | a0002c0002t0003g0049a0002c0002t0005g0005a0002c0002t0005g0008others(2): Show | 5 | HG02015.hp1 HG02965.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+53562_67+53564d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496777 | ||||||
| chr6:136496910 | C | T | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+53432G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496910 | ||||||
| chr6:136496982 | G | A | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+53360C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136496982 | ||||||
| chr6:136497075 | G | A | 45 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+53267C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497075 | ||||||
| chr6:136497339 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.67+53003A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497339 | ||||||
| chr6:136497375 | T | C | 1 | a0002c0002t0002g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.67+52967A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497375 | ||||||
| chr6:136497447 | C | A | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+52895G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497447 | ||||||
| chr6:136497525 | T | TAA | 42 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(39): Show | 42 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.67+52815_67+52816d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497525 | ||||||
| chr6:136497538 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.67+52804T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497538 | ||||||
| chr6:136497576 | A | G | 155 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(152): Show | 155 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.67+52766T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497576 | ||||||
| chr6:136497723 | C | G | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+52619G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497723 | ||||||
| chr6:136497724 | G | A | 45 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+52618C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497724 | ||||||
| chr6:136497730 | T | C | 1 | a0002c0002t0002g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.67+52612A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497730 | ||||||
| chr6:136497754 | G | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+52588C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497754 | ||||||
| chr6:136497766 | T | TC | 45 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+52575dupG | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497766 | ||||||
| chr6:136497797 | C | CA | 30 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0101others(27): Show | 30 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.67+52544dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497797 | ||||||
| chr6:136497797 | CA | C | 49 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(46): Show | 49 | HG01074.hp1 HG01123.hp2 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.67+52544delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136497797 | ||||||
| chr6:136498229 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.67+52113A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498229 | ||||||
| chr6:136498315 | G | T | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.67+52027C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498315 | ||||||
| chr6:136498342 | G | C | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+52000C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498342 | ||||||
| chr6:136498535 | T | G | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.67+51807A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498535 | ||||||
| chr6:136498664 | T | C | 1 | a0002c0002t0002g0197 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.67+51678A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498664 | ||||||
| chr6:136498706 | C | A | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+51636G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498706 | ||||||
| chr6:136498749 | A | ATG | 20 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0130others(17): Show | 20 | HG00639.hp2 HG02055.hp2 HG03453.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+51591_67+51592d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498749 | ||||||
| chr6:136498749 | ATG | A | 46 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(43): Show | 46 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+51591_67+51592d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498749 | ||||||
| chr6:136498940 | ACT | A | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+51400_67+51401d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136498940 | ||||||
| chr6:136499013 | A | G | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+51329T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136499013 | ||||||
| chr6:136499165 | C | A | 1 | a0002c0002t0002g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.67+51177G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136499165 | ||||||
| chr6:136499449 | AGAGGTTA others(7): Show |
A | 2 | a0001c0001t0001g0097a0001c0001t0001g0117 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.67+50879_67+50892d others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136499449 | ||||||
| chr6:136499732 | C | T | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+50610G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136499732 | ||||||
| chr6:136499841 | T | C | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+50501A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136499841 | ||||||
| chr6:136500079 | T | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+50263A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136500079 | ||||||
| chr6:136500104 | C | T | 11 | a0002c0002t0002g0032a0002c0002t0002g0033a0002c0002t0002g0034others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.67+50238G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136500104 | ||||||
| chr6:136500394 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.67+49948A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136500394 | ||||||
| chr6:136500464 | G | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+49878C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136500464 | ||||||
| chr6:136500761 | T | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+49581A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136500761 | ||||||
| chr6:136500785 | A | C | 45 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+49557T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136500785 | ||||||
| chr6:136500950 | A | G | 3 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.67+49392T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136500950 | ||||||
| chr6:136500957 | G | GA | 56 | a0001c0001t0001g0159a0002c0002t0002g0193a0002c0002t0002g0194others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+49384dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136500957 | ||||||
| chr6:136501118 | GAACT | G | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+49220_67+49223d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136501118 | ||||||
| chr6:136501146 | A | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+49196T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136501146 | ||||||
| chr6:136501242 | A | G | 35 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(32): Show | 35 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.67+49100T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136501242 | ||||||
| chr6:136501374 | T | C | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+48968A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136501374 | ||||||
| chr6:136501443 | G | A | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+48899C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136501443 | ||||||
| chr6:136501674 | T | A | 1 | a0002c0002t0002g0244 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.67+48668A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136501674 | ||||||
| chr6:136501785 | C | G | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.67+48557G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136501785 | ||||||
| chr6:136501921 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+48421G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136501921 | ||||||
| chr6:136502743 | T | C | 1 | a0002c0002t0002g0197 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.67+47599A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136502743 | ||||||
| chr6:136502902 | T | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+47440A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136502902 | ||||||
| chr6:136502925 | T | C | 42 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(39): Show | 42 | HG00408.hp2 HG01074.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.67+47417A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136502925 | ||||||
| chr6:136502955 | T | C | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+47387A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136502955 | ||||||
| chr6:136503201 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67+47141G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136503201 | ||||||
| chr6:136503211 | C | T | 1 | a0002c0002t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+47131G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136503211 | ||||||
| chr6:136503254 | T | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+47088A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136503254 | ||||||
| chr6:136503293 | T | A | 3 | a0002c0002t0007g0205a0002c0002t0007g0206a0002c0002t0007g0207 | 3 | HG02723.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.67+47049A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136503293 | ||||||
| chr6:136503401 | A | G | 18 | a0001c0001t0013g0179a0002c0002t0002g0001a0002c0002t0002g0032others(15): Show | 18 | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.67+46941T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136503401 | ||||||
| chr6:136503449 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.67+46893G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136503449 | ||||||
| chr6:136503472 | A | G | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+46870T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136503472 | ||||||
| chr6:136503609 | G | A | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+46733C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136503609 | ||||||
| chr6:136504180 | T | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+46162A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136504180 | ||||||
| chr6:136504307 | G | A | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.67+46035C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136504307 | ||||||
| chr6:136504654 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.67+45688T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136504654 | ||||||
| chr6:136504740 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.67+45602C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136504740 | ||||||
| chr6:136504880 | A | G | 1 | a0002c0002t0003g0048 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.67+45462T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136504880 | ||||||
| chr6:136504983 | A | G | 43 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(40): Show | 43 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+45359T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136504983 | ||||||
| chr6:136505159 | A | G | 18 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0114others(15): Show | 18 | HG00423.hp1 HG00544.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.67+45183T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505159 | ||||||
| chr6:136505206 | T | C | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.67+45136A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505206 | ||||||
| chr6:136505241 | T | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+45101A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505241 | ||||||
| chr6:136505251 | A | ATG | 3 | a0001c0001t0001g0161a0004c0004t0001g0120a0010c0011t0001g0028 | 3 | HG00639.hp2 HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.67+45089_67+45090d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505251 | ||||||
| chr6:136505251 | A | G | 1 | a0001c0001t0013g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.67+45091T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505251 | ||||||
| chr6:136505251 | ATG | A | 8 | a0001c0001t0001g0099a0001c0001t0001g0136a0001c0001t0001g0152others(5): Show | 8 | HG00423.hp1 HG01943.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+45089_67+45090d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505251 | ||||||
| chr6:136505251 | ATGTG | A | 11 | a0001c0001t0001g0103a0001c0001t0001g0141a0001c0001t0001g0150others(8): Show | 11 | HG00544.hp1 HG01358.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+45087_67+45090d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505251 | ||||||
| chr6:136505251 | ATGTGTG | A | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 15 | HG00733.hp1 HG00735.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+45085_67+45090d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505251 | ||||||
| chr6:136505267 | GTGTGTGT others(17): Show |
G | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+45051_67+45074d others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505267 | ||||||
| chr6:136505267 | GTGTGTGT others(19): Show |
G | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+45049_67+45074d others(28): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505267 | ||||||
| chr6:136505269 | GTGTGTGT others(13): Show |
G | 3 | a0003c0003t0003g0185a0003c0003t0003g0187a0003c0003t0003g0188 | 3 | NA19060.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.67+45053_67+45072d others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505269 | ||||||
| chr6:136505271 | G | A | 2 | a0002c0002t0003g0003a0002c0002t0003g0177 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.67+45071C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505271 | ||||||
| chr6:136505271 | G | GTA | 6 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0116others(3): Show | 6 | HG02135.hp2 NA18747.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+45070_67+45071i others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505271 | ||||||
| chr6:136505271 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.67+45070_67+45071i others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505271 | ||||||
| chr6:136505271 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0095 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.67+45070_67+45071i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505271 | ||||||
| chr6:136505271 | GTGTGTGT others(11): Show |
G | 1 | a0003c0003t0003g0191 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.67+45053_67+45070d others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505271 | ||||||
| chr6:136505271 | GTGTGTGT others(13): Show |
G | 4 | a0003c0003t0003g0186a0003c0003t0003g0189a0003c0003t0003g0192others(1): Show | 4 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+45051_67+45070d others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505271 | ||||||
| chr6:136505273 | G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0098others(9): Show | 12 | HG01243.hp2 HG02135.hp2 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+45069C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATA | 19 | a0002c0002t0002g0196a0002c0002t0002g0197a0002c0002t0002g0198others(16): Show | 19 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.67+45068_67+45069i others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATA | 8 | a0002c0002t0002g0212a0002c0002t0002g0214a0002c0002t0002g0216others(5): Show | 8 | HG00642.hp1 HG02074.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+45068_67+45069i others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATAT others(1): Show |
6 | a0002c0002t0002g0200a0002c0002t0002g0202a0002c0002t0002g0225others(3): Show | 6 | HG01243.hp1 HG02165.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+45068_67+45069i others(10): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATAT others(3): Show |
2 | a0002c0002t0002g0210a0002c0002t0002g0236 | 2 | NA18956.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.67+45068_67+45069i others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATAT others(5): Show |
5 | a0002c0002t0002g0203a0002c0002t0002g0221a0002c0002t0002g0222others(2): Show | 5 | HG02083.hp2 HG04199.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+45068_67+45069i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATAT others(7): Show |
1 | a0002c0002t0002g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.67+45068_67+45069i others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATAT others(9): Show |
1 | a0002c0002t0002g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.67+45068_67+45069i others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATAT others(13): Show |
1 | a0002c0002t0002g0193 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.67+45068_67+45069i others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATAT others(15): Show |
1 | a0002c0002t0002g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67+45068_67+45069i others(24): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | G | GTATATAT others(19): Show |
1 | a0002c0002t0002g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.67+45068_67+45069i others(28): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505273 | GTGTGTAT others(9): Show |
G | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+45053_67+45068d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505273 | ||||||
| chr6:136505275 | G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0098others(64): Show | 67 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.67+45067C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505275 | ||||||
| chr6:136505275 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.67+45066_67+45067i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505275 | ||||||
| chr6:136505275 | G | GTATATAT others(7): Show |
1 | a0002c0002t0002g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.67+45066_67+45067i others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505275 | ||||||
| chr6:136505275 | G | GTATATAT others(13): Show |
2 | a0001c0001t0004g0061a0001c0001t0013g0179 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+45066_67+45067i others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505275 | ||||||
| chr6:136505275 | G | GTATATAT others(15): Show |
2 | a0002c0002t0002g0217a0003c0003t0003g0031 | 2 | HG01257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.67+45066_67+45067i others(24): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505275 | ||||||
| chr6:136505275 | GTGTATAT others(7): Show |
G | 3 | a0002c0002t0007g0205a0002c0002t0007g0206a0002c0002t0007g0207 | 3 | HG02723.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.67+45053_67+45066d others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505275 | ||||||
| chr6:136505277 | G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0098others(87): Show | 90 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.67+45065C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTA | 15 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0117others(12): Show | 15 | HG00621.hp1 HG01928.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+45063_67+45064d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTATA | 8 | a0001c0001t0001g0043a0001c0001t0001g0101a0001c0001t0001g0109others(5): Show | 8 | HG01192.hp1 HG02132.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+45061_67+45064d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTATATAT others(5): Show |
1 | a0001c0001t0004g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.67+45053_67+45064d others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTATATAT others(9): Show |
1 | a0001c0001t0004g0067 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.67+45049_67+45064d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTATATAT others(11): Show |
2 | a0001c0001t0004g0068a0001c0001t0004g0178 | 2 | HG02155.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.67+45047_67+45064d others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTATATAT others(13): Show |
2 | a0006c0006t0006g0180a0006c0006t0006g0182 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.67+45045_67+45064d others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTATATAT others(15): Show |
2 | a0002c0002t0003g0085a0006c0006t0006g0181 | 2 | HG01358.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.67+45043_67+45064d others(24): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(3): Show |
3 | a0001c0001t0004g0077a0001c0001t0014g0060a0002c0002t0002g0001 | 3 | HG02273.hp2 HG02965.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.67+45064_67+45065i others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(5): Show |
2 | a0001c0001t0001g0079a0004c0004t0001g0080 | 2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.67+45064_67+45065i others(14): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(7): Show |
2 | a0001c0001t0004g0084a0001c0001t0008g0094 | 2 | HG01934.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.67+45064_67+45065i others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(9): Show |
3 | a0001c0001t0001g0073a0001c0001t0004g0066a0001c0001t0004g0088 | 3 | HG01928.hp1 NA18994.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.67+45064_67+45065i others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67+45064_67+45065i others(20): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(13): Show |
1 | a0001c0001t0004g0078 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.67+45064_67+45065i others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(15): Show |
5 | a0001c0001t0001g0063a0001c0001t0004g0064a0001c0001t0004g0081others(2): Show | 5 | HG01123.hp2 HG02040.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+45064_67+45065i others(24): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(17): Show |
7 | a0001c0001t0004g0065a0001c0001t0004g0069a0001c0001t0004g0070others(4): Show | 7 | HG00408.hp2 HG02055.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+45064_67+45065i others(26): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTATAT others(19): Show |
1 | a0001c0001t0004g0076 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.67+45064_67+45065i others(28): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | G | GTGTGTAT others(13): Show |
3 | a0001c0001t0004g0071a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | HG02135.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.67+45064_67+45065i others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | GTATATA | G | 11 | a0002c0002t0002g0032a0002c0002t0002g0033a0002c0002t0002g0034others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.67+45059_67+45064d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505277 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+45049_67+45064d others(18): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505277 | ||||||
| chr6:136505279 | A | G | 3 | a0001c0001t0001g0072a0004c0004t0001g0096a0004c0004t0001g0118 | 3 | HG02723.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.67+45063T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505279 | ||||||
| chr6:136505281 | A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0145 | 3 | HG02896.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+45061T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505281 | ||||||
| chr6:136505285 | A | G | 2 | a0002c0002t0002g0033a0002c0002t0002g0044 | 2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+45057T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505285 | ||||||
| chr6:136505824 | C | T | 3 | a0003c0003t0003g0185a0003c0003t0003g0187a0003c0003t0003g0188 | 3 | NA19060.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.67+44518G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505824 | ||||||
| chr6:136505922 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.67+44420T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505922 | ||||||
| chr6:136505989 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.67+44353A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136505989 | ||||||
| chr6:136506009 | T | C | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+44333A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506009 | ||||||
| chr6:136506111 | T | C | 8 | a0003c0003t0003g0185a0003c0003t0003g0186a0003c0003t0003g0187others(5): Show | 8 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+44231A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506111 | ||||||
| chr6:136506124 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.67+44218A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506124 | ||||||
| chr6:136506127 | CCTAGAAA others(21): Show |
C | 1 | a0001c0001t0001g0170 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.67+44187_67+44214d others(30): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506127 | ||||||
| chr6:136506285 | C | T | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+44057G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506285 | ||||||
| chr6:136506437 | G | A | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+43905C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506437 | ||||||
| chr6:136506456 | T | C | 1 | a0001c0001t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+43886A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506456 | ||||||
| chr6:136506756 | T | C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+43586A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506756 | ||||||
| chr6:136506777 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.67+43565G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136506777 | ||||||
| chr6:136507018 | C | T | 153 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.67+43324G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507018 | ||||||
| chr6:136507264 | T | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+43078A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507264 | ||||||
| chr6:136507282 | C | T | 3 | a0002c0002t0002g0216a0002c0002t0002g0218a0002c0002t0002g0234 | 3 | HG00642.hp1 HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.67+43060G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507282 | ||||||
| chr6:136507353 | G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0110 | 3 | HG01243.hp2 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.67+42989C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507353 | ||||||
| chr6:136507475 | C | CA | 51 | a0001c0001t0001g0145a0002c0002t0002g0193a0002c0002t0002g0194others(48): Show | 51 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+42866dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507475 | ||||||
| chr6:136507475 | C | CAA | 6 | a0002c0002t0002g0204a0002c0002t0002g0213a0002c0002t0003g0003others(3): Show | 6 | HG02723.hp1 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+42865_67+42866d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507475 | ||||||
| chr6:136507475 | CA | C | 96 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(93): Show | 96 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.67+42866delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507475 | ||||||
| chr6:136507544 | G | A | 153 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.67+42798C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507544 | ||||||
| chr6:136507558 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.67+42784T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507558 | ||||||
| chr6:136507559 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.67+42783T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507559 | ||||||
| chr6:136507711 | T | C | 4 | a0001c0001t0013g0179a0006c0006t0006g0180a0006c0006t0006g0181others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+42631A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136507711 | ||||||
| chr6:136508161 | G | A | 95 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(92): Show | 95 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.67+42181C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508161 | ||||||
| chr6:136508170 | C | T | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+42172G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508170 | ||||||
| chr6:136508240 | G | A | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+42102C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508240 | ||||||
| chr6:136508258 | G | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+42084C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508258 | ||||||
| chr6:136508263 | C | T | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+42079G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508263 | ||||||
| chr6:136508519 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.67+41823T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508519 | ||||||
| chr6:136508552 | G | A | 1 | a0002c0002t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.67+41790C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508552 | ||||||
| chr6:136508778 | C | T | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+41564G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508778 | ||||||
| chr6:136508794 | A | C | 56 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+41548T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508794 | ||||||
| chr6:136508795 | T | C | 1 | a0001c0001t0004g0088 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.67+41547A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508795 | ||||||
| chr6:136508849 | G | A | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.67+41493C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508849 | ||||||
| chr6:136508851 | G | A | 3 | a0002c0002t0002g0227a0002c0002t0009g0223a0002c0002t0009g0224 | 3 | HG00733.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.67+41491C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508851 | ||||||
| chr6:136508892 | T | C | 2 | a0001c0001t0001g0150a0001c0010t0001g0151 | 2 | HG01358.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.67+41450A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508892 | ||||||
| chr6:136508927 | C | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+41415G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508927 | ||||||
| chr6:136508975 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.67+41367G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136508975 | ||||||
| chr6:136509303 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.67+41039G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509303 | ||||||
| chr6:136509313 | C | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+41029G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509313 | ||||||
| chr6:136509416 | A | ATT | 159 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(156): Show | 159 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.67+40924_67+40925d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509416 | ||||||
| chr6:136509479 | T | C | 38 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.67+40863A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509479 | ||||||
| chr6:136509554 | C | T | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+40788G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509554 | ||||||
| chr6:136509599 | C | T | 22 | a0001c0001t0001g0063a0001c0001t0004g0064a0001c0001t0004g0065others(19): Show | 22 | HG00408.hp2 HG01123.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+40743G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509599 | ||||||
| chr6:136509624 | T | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+40718A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509624 | ||||||
| chr6:136509627 | T | C | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+40715A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509627 | ||||||
| chr6:136509918 | T | C | 157 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.67+40424A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509918 | ||||||
| chr6:136509928 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.67+40414C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136509928 | ||||||
| chr6:136510063 | G | A | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+40279C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136510063 | ||||||
| chr6:136510157 | G | A | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+40185C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136510157 | ||||||
| chr6:136510873 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+39469G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136510873 | ||||||
| chr6:136510887 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.67+39455C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136510887 | ||||||
| chr6:136510982 | G | A | 151 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(148): Show | 151 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.67+39360C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136510982 | ||||||
| chr6:136510999 | A | G | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+39343T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136510999 | ||||||
| chr6:136511024 | T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0145a0010c0011t0001g0028 | 3 | HG02109.hp1 HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+39318A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136511024 | ||||||
| chr6:136511196 | A | G | 1 | a0002c0002t0002g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.67+39146T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136511196 | ||||||
| chr6:136511505 | G | GA | 151 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(148): Show | 151 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.67+38836_67+38837i others(3): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136511505 | ||||||
| chr6:136511658 | A | G | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+38684T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136511658 | ||||||
| chr6:136511873 | A | G | 1 | a0003c0003t0003g0186 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.67+38469T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136511873 | ||||||
| chr6:136511889 | A | G | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+38453T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136511889 | ||||||
| chr6:136511996 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+38346A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136511996 | ||||||
| chr6:136512043 | G | A | 3 | a0002c0002t0007g0205a0002c0002t0007g0206a0002c0002t0007g0207 | 3 | HG02723.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.67+38299C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512043 | ||||||
| chr6:136512202 | T | C | 94 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(91): Show | 94 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.67+38140A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512202 | ||||||
| chr6:136512438 | C | G | 93 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.67+37904G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512438 | ||||||
| chr6:136512618 | G | A | 2 | a0001c0001t0001g0079a0004c0004t0001g0080 | 2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.67+37724C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512618 | ||||||
| chr6:136512622 | C | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+37720G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512622 | ||||||
| chr6:136512707 | G | A | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.67+37635C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512707 | ||||||
| chr6:136512736 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.67+37606A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512736 | ||||||
| chr6:136512835 | CCTTT | C | 35 | a0001c0001t0004g0016a0002c0002t0003g0009a0002c0002t0003g0012others(32): Show | 35 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.67+37503_67+37506d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512835 | ||||||
| chr6:136512998 | G | GGTTTTGT others(3): Show |
51 | a0001c0001t0001g0043a0001c0001t0004g0016a0002c0002t0002g0001others(48): Show | 51 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+37334_67+37343d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512998 | ||||||
| chr6:136512998 | G | GGTTTTGT others(8): Show |
41 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(38): Show | 41 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.67+37329_67+37343d others(17): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512998 | ||||||
| chr6:136512998 | G | GGTTTTGT others(13): Show |
1 | a0001c0001t0004g0077 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.67+37324_67+37343d others(22): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136512998 | ||||||
| chr6:136513146 | C | T | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+37196G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136513146 | ||||||
| chr6:136513365 | G | A | 159 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(156): Show | 159 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.67+36977C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136513365 | ||||||
| chr6:136513385 | C | G | 1 | a0001c0001t0004g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.67+36957G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136513385 | ||||||
| chr6:136513474 | T | A | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+36868A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136513474 | ||||||
| chr6:136514132 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+36210A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514132 | ||||||
| chr6:136514225 | T | C | 1 | a0002c0002t0007g0207 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.67+36117A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514225 | ||||||
| chr6:136514237 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67+36105G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514237 | ||||||
| chr6:136514246 | T | C | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+36096A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514246 | ||||||
| chr6:136514554 | C | T | 1 | a0002c0002t0003g0006 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.67+35788G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514554 | ||||||
| chr6:136514580 | C | CA | 14 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0100others(11): Show | 14 | HG00423.hp1 HG01123.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+35761dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514580 | ||||||
| chr6:136514580 | C | CAAAAAAA others(7): Show |
1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+35748_67+35761d others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514580 | ||||||
| chr6:136514580 | CA | C | 46 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0109others(43): Show | 46 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.67+35761delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514580 | ||||||
| chr6:136514580 | CAA | C | 25 | a0001c0001t0001g0043a0001c0001t0001g0147a0001c0001t0004g0076others(22): Show | 25 | HG02109.hp2 HG02155.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.67+35760_67+35761d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514580 | ||||||
| chr6:136514580 | CAAA | C | 28 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(25): Show | 28 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+35759_67+35761d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514580 | ||||||
| chr6:136514580 | CAAAAAA | C | 48 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(45): Show | 48 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.67+35756_67+35761d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514580 | ||||||
| chr6:136514580 | CAAAAAAA | C | 9 | a0001c0001t0013g0179a0002c0002t0002g0216a0002c0002t0002g0227others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+35755_67+35761d others(9): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514580 | ||||||
| chr6:136514721 | G | A | 2 | a0001c0001t0001g0163a0001c0012t0001g0174 | 2 | NA18969.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.67+35621C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514721 | ||||||
| chr6:136514860 | A | G | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.67+35482T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136514860 | ||||||
| chr6:136515354 | A | G | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+34988T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136515354 | ||||||
| chr6:136515634 | G | C | 1 | a0002c0002t0002g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.67+34708C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136515634 | ||||||
| chr6:136515825 | T | C | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+34517A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136515825 | ||||||
| chr6:136516102 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67+34240T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516102 | ||||||
| chr6:136516164 | AT | A | 56 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(53): Show | 56 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+34177delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516164 | ||||||
| chr6:136516385 | T | G | 1 | a0002c0002t0007g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67+33957A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516385 | ||||||
| chr6:136516395 | T | C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+33947A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516395 | ||||||
| chr6:136516629 | G | A | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+33713C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516629 | ||||||
| chr6:136516648 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.67+33694C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516648 | ||||||
| chr6:136516777 | G | C | 1 | a0001c0001t0004g0078 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.67+33565C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516777 | ||||||
| chr6:136516829 | A | G | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+33513T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516829 | ||||||
| chr6:136516923 | T | C | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+33419A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516923 | ||||||
| chr6:136516975 | C | CA | 166 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0063others(163): Show | 166 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.67+33366dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136516975 | ||||||
| chr6:136517282 | C | A | 1 | a0002c0002t0002g0215 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.67+33060G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517282 | ||||||
| chr6:136517332 | G | A | 1 | a0002c0002t0002g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.67+33010C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517332 | ||||||
| chr6:136517337 | G | GAAATT | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+33004_67+33005i others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517337 | ||||||
| chr6:136517385 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67+32957T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517385 | ||||||
| chr6:136517502 | A | T | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+32840T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517502 | ||||||
| chr6:136517538 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.67+32804A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517538 | ||||||
| chr6:136517580 | T | C | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+32762A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517580 | ||||||
| chr6:136517590 | C | T | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+32752G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517590 | ||||||
| chr6:136517763 | T | C | 52 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.67+32579A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517763 | ||||||
| chr6:136517766 | A | AC | 153 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.67+32575dupG | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517766 | ||||||
| chr6:136517778 | T | C | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+32564A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517778 | ||||||
| chr6:136517786 | G | A | 3 | a0002c0002t0003g0046a0002c0002t0003g0054a0002c0002t0003g0055 | 3 | NA18995.hp1 NA19001.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.67+32556C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136517786 | ||||||
| chr6:136518050 | G | A | 56 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+32292C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518050 | ||||||
| chr6:136518078 | T | C | 157 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.67+32264A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518078 | ||||||
| chr6:136518094 | C | T | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+32248G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518094 | ||||||
| chr6:136518449 | A | G | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+31893T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518449 | ||||||
| chr6:136518600 | T | C | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+31742A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518600 | ||||||
| chr6:136518652 | T | C | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+31690A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518652 | ||||||
| chr6:136518655 | C | T | 1 | a0010c0011t0001g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+31687G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518655 | ||||||
| chr6:136518657 | C | G | 157 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.67+31685G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518657 | ||||||
| chr6:136518789 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+31553C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518789 | ||||||
| chr6:136518836 | G | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+31506C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136518836 | ||||||
| chr6:136519067 | A | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+31275T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136519067 | ||||||
| chr6:136519153 | A | T | 10 | a0002c0002t0002g0200a0002c0002t0002g0204a0002c0002t0002g0216others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+31189T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136519153 | ||||||
| chr6:136519555 | C | G | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+30787G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136519555 | ||||||
| chr6:136519704 | G | A | 1 | a0002c0002t0002g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.67+30638C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136519704 | ||||||
| chr6:136519861 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.67+30481T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136519861 | ||||||
| chr6:136519877 | C | T | 1 | a0002c0002t0002g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.67+30465G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136519877 | ||||||
| chr6:136520199 | CA | C | 22 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(19): Show | 22 | HG02109.hp2 HG02155.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.67+30142delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520199 | ||||||
| chr6:136520215 | A | G | 1 | a0002c0002t0002g0208 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.67+30127T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520215 | ||||||
| chr6:136520216 | A | AG | 34 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(31): Show | 34 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.67+30125dupC | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520216 | ||||||
| chr6:136520216 | A | G | 71 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0004g0016others(68): Show | 71 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.67+30126T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520216 | ||||||
| chr6:136520298 | A | C | 1 | a0002c0002t0002g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.67+30044T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520298 | ||||||
| chr6:136520399 | A | G | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+29943T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520399 | ||||||
| chr6:136520493 | T | C | 1 | a0002c0002t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67+29849A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520493 | ||||||
| chr6:136520515 | C | T | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+29827G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520515 | ||||||
| chr6:136520580 | T | C | 2 | a0001c0001t0008g0111a0001c0001t0008g0112 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.67+29762A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520580 | ||||||
| chr6:136520673 | T | C | 1 | a0002c0002t0002g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+29669A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520673 | ||||||
| chr6:136520859 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.67+29483G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136520859 | ||||||
| chr6:136521289 | T | C | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+29053A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136521289 | ||||||
| chr6:136521345 | C | T | 1 | a0002c0014t0002g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.67+28997G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136521345 | ||||||
| chr6:136521547 | G | C | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+28795C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136521547 | ||||||
| chr6:136521743 | C | T | 33 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.67+28599G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136521743 | ||||||
| chr6:136521779 | A | G | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+28563T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136521779 | ||||||
| chr6:136522253 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.67+28089G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136522253 | ||||||
| chr6:136522253 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+28089G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136522253 | ||||||
| chr6:136522493 | A | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+27849T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136522493 | ||||||
| chr6:136522606 | G | A | 1 | a0002c0002t0003g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.67+27736C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136522606 | ||||||
| chr6:136522615 | T | C | 1 | a0002c0002t0002g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.67+27727A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136522615 | ||||||
| chr6:136522658 | G | A | 1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67+27684C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136522658 | ||||||
| chr6:136522669 | G | A | 1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67+27673C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136522669 | ||||||
| chr6:136522949 | C | T | 1 | a0002c0002t0003g0006 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.67+27393G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136522949 | ||||||
| chr6:136523119 | T | C | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+27223A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136523119 | ||||||
| chr6:136523185 | C | T | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+27157G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136523185 | ||||||
| chr6:136523283 | C | T | 2 | a0001c0001t0001g0145a0010c0011t0001g0028 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+27059G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136523283 | ||||||
| chr6:136523734 | A | T | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+26608T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136523734 | ||||||
| chr6:136523749 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.67+26593C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136523749 | ||||||
| chr6:136523843 | C | A | 95 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(92): Show | 95 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.67+26499G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136523843 | ||||||
| chr6:136524286 | T | TG | 3 | a0001c0001t0001g0029a0001c0001t0001g0145a0010c0011t0001g0028 | 3 | HG02109.hp1 HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+26055dupC | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136524286 | ||||||
| chr6:136524363 | A | G | 97 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(94): Show | 97 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.67+25979T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136524363 | ||||||
| chr6:136524611 | G | A | 56 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+25731C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136524611 | ||||||
| chr6:136524754 | C | T | 2 | a0001c0001t0001g0145a0010c0011t0001g0028 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+25588G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136524754 | ||||||
| chr6:136525333 | G | C | 8 | a0003c0003t0003g0185a0003c0003t0003g0186a0003c0003t0003g0187others(5): Show | 8 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+25009C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136525333 | ||||||
| chr6:136525369 | C | T | 1 | a0002c0002t0003g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.67+24973G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136525369 | ||||||
| chr6:136525479 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.67+24863C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136525479 | ||||||
| chr6:136525706 | G | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+24636C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136525706 | ||||||
| chr6:136525903 | A | C | 1 | a0001c0001t0004g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.67+24439T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136525903 | ||||||
| chr6:136525978 | GT | G | 92 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(89): Show | 92 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.67+24363delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136525978 | ||||||
| chr6:136526120 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.67+24222A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526120 | ||||||
| chr6:136526266 | T | C | 93 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.67+24076A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526266 | ||||||
| chr6:136526275 | G | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0110others(2): Show | 5 | HG01243.hp2 HG01258.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+24067C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526275 | ||||||
| chr6:136526277 | G | GCA | 46 | a0001c0001t0001g0152a0001c0001t0004g0016a0002c0002t0002g0232others(43): Show | 46 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.67+24063_67+24064d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526277 | ||||||
| chr6:136526277 | G | GCACA | 31 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(28): Show | 31 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.67+24061_67+24064d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526277 | ||||||
| chr6:136526277 | G | GCACACA | 17 | a0001c0001t0001g0043a0001c0001t0001g0079a0002c0002t0002g0001others(14): Show | 17 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+24059_67+24064d others(8): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526277 | ||||||
| chr6:136526277 | G | GCACACAC others(3): Show |
1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+24055_67+24064d others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526277 | ||||||
| chr6:136526277 | G | GCGCACAC others(3): Show |
1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+24064_67+24065i others(12): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526277 | ||||||
| chr6:136526277 | GCA | G | 56 | a0001c0001t0001g0103a0001c0001t0013g0179a0002c0002t0002g0193others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+24063_67+24064d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526277 | ||||||
| chr6:136526279 | A | G | 5 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0008g0094others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+24063T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526279 | ||||||
| chr6:136526405 | T | C | 60 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(57): Show | 60 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+23937A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526405 | ||||||
| chr6:136526451 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.67+23891G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526451 | ||||||
| chr6:136526478 | C | A | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+23864G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526478 | ||||||
| chr6:136526510 | C | A | 1 | a0001c0001t0014g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.67+23832G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526510 | ||||||
| chr6:136526584 | G | A | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+23758C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526584 | ||||||
| chr6:136526610 | G | T | 3 | a0001c0001t0008g0094a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | HG02922.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.67+23732C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526610 | ||||||
| chr6:136526786 | G | A | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+23556C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526786 | ||||||
| chr6:136526802 | AGGCAT | A | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+23535_67+23539d others(7): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526802 | ||||||
| chr6:136526978 | T | C | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+23364A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136526978 | ||||||
| chr6:136527032 | T | C | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+23310A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527032 | ||||||
| chr6:136527089 | C | T | 3 | a0002c0002t0007g0205a0002c0002t0007g0206a0002c0002t0007g0207 | 3 | HG02723.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.67+23253G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527089 | ||||||
| chr6:136527091 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+23251A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527091 | ||||||
| chr6:136527103 | G | A | 1 | a0002c0002t0002g0232 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.67+23239C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527103 | ||||||
| chr6:136527203 | A | C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+23139T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527203 | ||||||
| chr6:136527242 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.67+23100T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527242 | ||||||
| chr6:136527314 | T | C | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+23028A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527314 | ||||||
| chr6:136527358 | T | C | 1 | a0002c0002t0003g0056 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.67+22984A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527358 | ||||||
| chr6:136527375 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+22967A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527375 | ||||||
| chr6:136527447 | A | G | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+22895T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527447 | ||||||
| chr6:136527470 | G | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+22872C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136527470 | ||||||
| chr6:136528129 | A | G | 3 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.67+22213T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136528129 | ||||||
| chr6:136528146 | C | T | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+22196G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136528146 | ||||||
| chr6:136528466 | T | A | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.67+21876A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136528466 | ||||||
| chr6:136528745 | T | C | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+21597A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136528745 | ||||||
| chr6:136528773 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67+21569G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136528773 | ||||||
| chr6:136528883 | T | TAAGACAT others(306): Show |
1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+21458_67+21459i others(315): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136528883 | ||||||
| chr6:136529151 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.67+21191C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529151 | ||||||
| chr6:136529156 | C | T | 1 | a0001c0001t0004g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.67+21186G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529156 | ||||||
| chr6:136529281 | AT | A | 171 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(168): Show | 171 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.67+21060delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529281 | ||||||
| chr6:136529312 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67+21030C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529312 | ||||||
| chr6:136529355 | A | G | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+20987T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529355 | ||||||
| chr6:136529405 | G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG00735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.67+20937C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529405 | ||||||
| chr6:136529461 | G | C | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.67+20881C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529461 | ||||||
| chr6:136529549 | A | G | 153 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.67+20793T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529549 | ||||||
| chr6:136529648 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+20694A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529648 | ||||||
| chr6:136529853 | C | A | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+20489G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529853 | ||||||
| chr6:136529976 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.67+20366A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136529976 | ||||||
| chr6:136530044 | T | C | 34 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(31): Show | 34 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.67+20298A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136530044 | ||||||
| chr6:136530168 | C | T | 4 | a0001c0001t0013g0179a0006c0006t0006g0180a0006c0006t0006g0181others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+20174G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136530168 | ||||||
| chr6:136530455 | A | C | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+19887T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136530455 | ||||||
| chr6:136530490 | C | T | 1 | a0001c0001t0008g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.67+19852G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136530490 | ||||||
| chr6:136530537 | ATCAAACA others(1241): Show |
A | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+18557_67+19804d others(2): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136530537 | ||||||
| chr6:136530563 | G | T | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+19779C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136530563 | ||||||
| chr6:136530738 | T | A | 1 | a0002c0002t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67+19604A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136530738 | ||||||
| chr6:136530899 | A | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+19443T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136530899 | ||||||
| chr6:136531147 | G | A | 56 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+19195C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136531147 | ||||||
| chr6:136532074 | T | TA | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+18267dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136532074 | ||||||
| chr6:136532139 | A | C | 1 | a0002c0002t0002g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.67+18203T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136532139 | ||||||
| chr6:136532228 | G | A | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+18114C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136532228 | ||||||
| chr6:136532264 | G | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+18078C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136532264 | ||||||
| chr6:136532617 | G | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+17725C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136532617 | ||||||
| chr6:136532623 | A | AT | 109 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(106): Show | 109 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.67+17718dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136532623 | ||||||
| chr6:136532936 | G | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+17406C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136532936 | ||||||
| chr6:136533006 | T | C | 58 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(55): Show | 58 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+17336A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136533006 | ||||||
| chr6:136533043 | C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0175a0005c0005t0001g0104 | 3 | HG00423.hp1 NA19006.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.67+17299G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136533043 | ||||||
| chr6:136533070 | C | T | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+17272G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136533070 | ||||||
| chr6:136533220 | C | T | 1 | a0003c0003t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+17122G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136533220 | ||||||
| chr6:136533518 | T | G | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+16824A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136533518 | ||||||
| chr6:136533641 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67+16701C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136533641 | ||||||
| chr6:136533666 | G | A | 58 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(55): Show | 58 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+16676C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136533666 | ||||||
| chr6:136533831 | C | G | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+16511G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136533831 | ||||||
| chr6:136534076 | A | G | 1 | a0002c0002t0002g0244 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.67+16266T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136534076 | ||||||
| chr6:136534158 | T | C | 58 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(55): Show | 58 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+16184A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136534158 | ||||||
| chr6:136534554 | G | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+15788C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136534554 | ||||||
| chr6:136534764 | G | C | 1 | a0002c0002t0002g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.67+15578C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136534764 | ||||||
| chr6:136534959 | G | A | 1 | a0002c0002t0003g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.67+15383C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136534959 | ||||||
| chr6:136534974 | CATGAGAA others(7): Show |
C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+15354_67+15367d others(16): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136534974 | ||||||
| chr6:136535684 | T | C | 1 | a0002c0002t0002g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.67+14658A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136535684 | ||||||
| chr6:136535714 | C | CT | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+14627dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136535714 | ||||||
| chr6:136535902 | C | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0110others(7): Show | 10 | HG00733.hp1 HG01243.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+14440G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136535902 | ||||||
| chr6:136535961 | T | C | 22 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(19): Show | 22 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+14381A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136535961 | ||||||
| chr6:136536249 | G | T | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+14093C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136536249 | ||||||
| chr6:136536630 | C | T | 4 | a0001c0001t0013g0179a0006c0006t0006g0180a0006c0006t0006g0181others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+13712G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136536630 | ||||||
| chr6:136536688 | T | A | 1 | a0002c0002t0002g0243 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.67+13654A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136536688 | ||||||
| chr6:136536824 | T | A | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+13518A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136536824 | ||||||
| chr6:136537139 | CTCTT | C | 3 | a0001c0001t0001g0097a0008c0008t0006g0026a0008c0008t0006g0027 | 3 | HG02965.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.67+13199_67+13202d others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537139 | ||||||
| chr6:136537145 | CT | C | 56 | a0001c0001t0001g0161a0001c0001t0001g0183a0002c0002t0002g0193others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+13196delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537145 | ||||||
| chr6:136537150 | T | C | 1 | a0002c0002t0010g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+13192A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537150 | ||||||
| chr6:136537214 | T | C | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+13128A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537214 | ||||||
| chr6:136537232 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.67+13110G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537232 | ||||||
| chr6:136537275 | C | G | 1 | a0002c0002t0003g0047 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.67+13067G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537275 | ||||||
| chr6:136537693 | G | A | 58 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(55): Show | 58 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+12649C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537693 | ||||||
| chr6:136537788 | A | AT | 11 | a0001c0001t0001g0097a0001c0001t0001g0116a0001c0001t0001g0117others(8): Show | 11 | HG02572.hp1 HG02723.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+12553dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537788 | ||||||
| chr6:136537788 | AT | A | 61 | a0001c0001t0001g0100a0001c0001t0001g0162a0001c0001t0001g0173others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.67+12553delA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537788 | ||||||
| chr6:136537885 | G | A | 1 | a0002c0002t0002g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+12457C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537885 | ||||||
| chr6:136537895 | C | T | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+12447G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136537895 | ||||||
| chr6:136538016 | G | A | 1 | a0006c0006t0006g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.67+12326C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538016 | ||||||
| chr6:136538146 | G | T | 1 | a0001c0001t0004g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.67+12196C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538146 | ||||||
| chr6:136538329 | G | A | 1 | a0003c0003t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+12013C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538329 | ||||||
| chr6:136538415 | G | A | 38 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.67+11927C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538415 | ||||||
| chr6:136538462 | T | C | 58 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(55): Show | 58 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+11880A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538462 | ||||||
| chr6:136538513 | C | T | 10 | a0002c0002t0003g0177a0003c0003t0003g0059a0003c0003t0003g0185others(7): Show | 10 | HG02155.hp2 NA18522.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+11829G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538513 | ||||||
| chr6:136538646 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.67+11696G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538646 | ||||||
| chr6:136538798 | C | CA | 41 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0091others(38): Show | 41 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.67+11543dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538798 | ||||||
| chr6:136538798 | C | CAA | 39 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(36): Show | 39 | HG01074.hp1 HG02040.hp2 HG02132.hp2 others(36): Show |
intron_variant | MODIFIER | c.67+11542_67+11543d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538798 | ||||||
| chr6:136538798 | C | CAAA | 10 | a0001c0001t0004g0084a0001c0001t0004g0086a0001c0001t0004g0087others(7): Show | 10 | HG00408.hp2 HG01123.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+11541_67+11543d others(5): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538798 | ||||||
| chr6:136538798 | CA | C | 5 | a0001c0001t0013g0179a0002c0002t0002g0236a0002c0002t0002g0237others(2): Show | 5 | NA18906.hp2 NA18979.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+11543delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538798 | ||||||
| chr6:136538798 | CAA | C | 51 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(48): Show | 51 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+11542_67+11543d others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538798 | ||||||
| chr6:136538798 | CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+11533_67+11543d others(13): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136538798 | ||||||
| chr6:136539071 | T | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+11271A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539071 | ||||||
| chr6:136539231 | C | T | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+11111G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539231 | ||||||
| chr6:136539232 | G | A | 1 | a0002c0002t0002g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.67+11110C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539232 | ||||||
| chr6:136539279 | A | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+11063T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539279 | ||||||
| chr6:136539439 | C | T | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+10903G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539439 | ||||||
| chr6:136539593 | T | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0103a0001c0001t0001g0106others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+10749A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539593 | ||||||
| chr6:136539635 | C | T | 1 | a0002c0002t0002g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.67+10707G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539635 | ||||||
| chr6:136539796 | T | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+10546A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539796 | ||||||
| chr6:136539865 | G | A | 1 | a0002c0002t0002g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.67+10477C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136539865 | ||||||
| chr6:136540090 | C | T | 1 | a0002c0002t0002g0062 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.67+10252G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540090 | ||||||
| chr6:136540139 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.67+10203G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540139 | ||||||
| chr6:136540261 | T | C | 9 | a0003c0003t0003g0059a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+10081A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540261 | ||||||
| chr6:136540266 | T | C | 37 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(34): Show | 37 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.67+10076A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540266 | ||||||
| chr6:136540437 | C | A | 153 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.67+9905G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540437 | ||||||
| chr6:136540438 | A | AAAAG | 152 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(149): Show | 152 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.67+9900_67+9903dup others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540438 | ||||||
| chr6:136540545 | A | C | 58 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(55): Show | 58 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+9797T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540545 | ||||||
| chr6:136540659 | A | G | 37 | a0001c0001t0004g0016a0002c0002t0003g0003a0002c0002t0003g0006others(34): Show | 37 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.67+9683T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540659 | ||||||
| chr6:136540749 | A | C | 2 | a0002c0002t0007g0246a0002c0002t0011g0245 | 2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.67+9593T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540749 | ||||||
| chr6:136540891 | C | G | 1 | a0002c0002t0002g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.67+9451G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540891 | ||||||
| chr6:136540944 | G | C | 157 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.67+9398C>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540944 | ||||||
| chr6:136540958 | A | C | 33 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.67+9384T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136540958 | ||||||
| chr6:136541005 | C | T | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+9337G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136541005 | ||||||
| chr6:136541046 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.67+9296G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136541046 | ||||||
| chr6:136541166 | A | C | 1 | a0001c0001t0001g0095 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.67+9176T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136541166 | ||||||
| chr6:136541322 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67+9020T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136541322 | ||||||
| chr6:136541392 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+8950A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136541392 | ||||||
| chr6:136541585 | T | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+8757A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136541585 | ||||||
| chr6:136541952 | G | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+8390C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136541952 | ||||||
| chr6:136542303 | A | T | 4 | a0001c0001t0001g0176a0001c0001t0008g0094a0001c0001t0008g0111others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+8039T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542303 | ||||||
| chr6:136542374 | G | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+7968C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542374 | ||||||
| chr6:136542379 | A | G | 14 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+7963T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542379 | ||||||
| chr6:136542486 | A | G | 157 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.67+7856T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542486 | ||||||
| chr6:136542589 | A | G | 57 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(54): Show | 57 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+7753T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542589 | ||||||
| chr6:136542719 | T | TA | 56 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+7622dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542719 | ||||||
| chr6:136542720 | A | T | 1 | a0001c0001t0014g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.67+7622T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542720 | ||||||
| chr6:136542730 | A | G | 56 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(53): Show | 56 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+7612T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542730 | ||||||
| chr6:136542826 | T | G | 56 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+7516A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136542826 | ||||||
| chr6:136543321 | A | T | 56 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+7021T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136543321 | ||||||
| chr6:136543414 | T | C | 157 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0072others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.67+6928A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136543414 | ||||||
| chr6:136543543 | G | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+6799C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136543543 | ||||||
| chr6:136543582 | G | A | 1 | a0002c0002t0002g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+6760C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136543582 | ||||||
| chr6:136543649 | G | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+6693C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136543649 | ||||||
| chr6:136543861 | T | C | 1 | a0002c0002t0002g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.67+6481A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136543861 | ||||||
| chr6:136543925 | C | A | 1 | a0002c0002t0002g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.67+6417G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136543925 | ||||||
| chr6:136544007 | C | G | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+6335G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136544007 | ||||||
| chr6:136544403 | G | A | 1 | a0002c0002t0003g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+5939C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136544403 | ||||||
| chr6:136544442 | C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0110 | 3 | HG01243.hp2 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.67+5900G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136544442 | ||||||
| chr6:136544658 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+5684A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136544658 | ||||||
| chr6:136544888 | A | G | 36 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(33): Show | 36 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+5454T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136544888 | ||||||
| chr6:136544923 | G | A | 1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67+5419C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136544923 | ||||||
| chr6:136545096 | T | A | 3 | a0006c0006t0006g0180a0006c0006t0006g0181a0006c0006t0006g0182 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.67+5246A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545096 | ||||||
| chr6:136545109 | C | G | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+5233G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545109 | ||||||
| chr6:136545318 | G | GA | 19 | a0001c0001t0001g0176a0002c0002t0002g0242a0002c0002t0002g0243others(16): Show | 19 | HG02280.hp2 NA18939.hp2 NA18948.hp1 others(16): Show |
intron_variant | MODIFIER | c.67+5023dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545318 | ||||||
| chr6:136545318 | GA | G | 16 | a0001c0001t0001g0109a0001c0001t0001g0184a0001c0001t0004g0061others(13): Show | 16 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+5023delT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545318 | ||||||
| chr6:136545488 | T | C | 1 | a0002c0002t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+4854A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545488 | ||||||
| chr6:136545758 | A | ATTT | 51 | a0001c0001t0001g0043a0001c0001t0004g0016a0002c0002t0002g0001others(48): Show | 51 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+4581_67+4583dup others(3): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545758 | ||||||
| chr6:136545758 | A | ATTTT | 94 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0072others(91): Show | 94 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.67+4583_67+4584ins others(4): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545758 | ||||||
| chr6:136545762 | A | T | 51 | a0001c0001t0001g0043a0001c0001t0004g0016a0002c0002t0002g0001others(48): Show | 51 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+4580T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545762 | ||||||
| chr6:136545764 | T | A | 51 | a0001c0001t0001g0043a0001c0001t0004g0016a0002c0002t0002g0001others(48): Show | 51 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+4578A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545764 | ||||||
| chr6:136545869 | G | A | 2 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+4473C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136545869 | ||||||
| chr6:136546312 | C | CT | 16 | a0001c0001t0001g0043a0002c0002t0002g0001a0002c0002t0002g0032others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+4029dupA | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136546312 | ||||||
| chr6:136546362 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.67+3980G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136546362 | ||||||
| chr6:136546386 | A | G | 33 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.67+3956T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136546386 | ||||||
| chr6:136546578 | C | A | 57 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+3764G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136546578 | ||||||
| chr6:136546846 | T | G | 2 | a0002c0002t0007g0246a0002c0002t0011g0245 | 2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.67+3496A>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136546846 | ||||||
| chr6:136546901 | C | T | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+3441G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136546901 | ||||||
| chr6:136547239 | T | C | 1 | a0008c0008t0006g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67+3103A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136547239 | ||||||
| chr6:136547440 | C | T | 33 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.67+2902G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136547440 | ||||||
| chr6:136547535 | C | T | 3 | a0001c0001t0001g0002a0002c0002t0003g0003a0008c0008t0006g0027 | 3 | HG03453.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+2807G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136547535 | ||||||
| chr6:136547683 | T | C | 2 | a0001c0001t0001g0002a0002c0002t0003g0003 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.67+2659A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136547683 | ||||||
| chr6:136547698 | G | GAAGATA | 154 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0063others(151): Show | 154 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.67+2643_67+2644ins others(6): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136547698 | ||||||
| chr6:136547791 | G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0063others(151): Show | 154 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.67+2551C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136547791 | ||||||
| chr6:136548087 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67+2255G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548087 | ||||||
| chr6:136548097 | A | AC | 21 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 21 | HG00423.hp1 HG00642.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+2244dupG | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548097 | ||||||
| chr6:136548098 | C | A | 1 | a0003c0003t0003g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.67+2244G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548098 | ||||||
| chr6:136548099 | C | CA | 3 | a0001c0001t0014g0060a0002c0002t0003g0030a0002c0002t0005g0004 | 3 | NA18978.hp2 NA19002.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.67+2242_67+2243ins others(1): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548099 | ||||||
| chr6:136548100 | C | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0063others(138): Show | 141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.67+2242G>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548100 | ||||||
| chr6:136548174 | G | A | 1 | a0001c0001t0004g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.67+2168C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548174 | ||||||
| chr6:136548605 | A | T | 1 | a0002c0002t0002g0199 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.67+1737T>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548605 | ||||||
| chr6:136548652 | G | A | 3 | a0001c0001t0001g0002a0002c0002t0003g0003a0008c0008t0006g0027 | 3 | HG03453.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+1690C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548652 | ||||||
| chr6:136548753 | T | C | 33 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00408.hp2 HG01074.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.67+1589A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548753 | ||||||
| chr6:136548827 | A | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0063others(142): Show | 145 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.67+1515T>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548827 | ||||||
| chr6:136548842 | G | A | 8 | a0003c0003t0003g0185a0003c0003t0003g0186a0003c0003t0003g0187others(5): Show | 8 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+1500C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136548842 | ||||||
| chr6:136549230 | A | G | 2 | a0001c0001t0001g0029a0010c0011t0001g0028 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.67+1112T>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549230 | ||||||
| chr6:136549332 | C | T | 3 | a0001c0001t0001g0002a0002c0002t0003g0003a0008c0008t0006g0027 | 3 | HG03453.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+1010G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549332 | ||||||
| chr6:136549431 | G | GA | 5 | a0001c0001t0004g0178a0001c0001t0013g0179a0006c0006t0006g0180others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+910dupT | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549431 | ||||||
| chr6:136549539 | C | T | 1 | a0008c0008t0006g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+803G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549539 | ||||||
| chr6:136549552 | C | T | 22 | a0001c0001t0004g0016a0002c0002t0003g0006a0002c0002t0003g0009others(19): Show | 22 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+790G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549552 | ||||||
| chr6:136549564 | C | T | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+778G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549564 | ||||||
| chr6:136549584 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.67+758C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549584 | ||||||
| chr6:136549587 | T | A | 1 | a0003c0003t0003g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.67+755A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549587 | ||||||
| chr6:136549606 | T | C | 8 | a0003c0003t0003g0185a0003c0003t0003g0186a0003c0003t0003g0187others(5): Show | 8 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+736A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549606 | ||||||
| chr6:136549679 | C | G | 7 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(4): Show | 7 | NA18940.hp2 NA18945.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+663G>C | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549679 | ||||||
| chr6:136549973 | G | A | 1 | a0002c0002t0002g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.67+369C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549973 | ||||||
| chr6:136549991 | C | T | 2 | a0001c0001t0001g0002a0002c0002t0003g0003 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.67+351G>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136549991 | ||||||
| chr6:136550001 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.67+341A>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136550001 | ||||||
| chr6:136550112 | G | T | 1 | a0002c0002t0002g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+230C>A | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136550112 | ||||||
| chr6:136550207 | G | A | 8 | a0003c0003t0003g0185a0003c0003t0003g0186a0003c0003t0003g0187others(5): Show | 8 | HG02155.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+135C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136550207 | ||||||
| chr6:136550216 | T | C | 55 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+126A>G | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136550216 | ||||||
| chr6:136550220 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.67+122C>T | MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | 136550220 |