Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4233 |
|---|---|
| ensemblid | ENSG00000105976.16 |
| hgncid | 7029 |
| symbol | MET |
| name | MET proto-oncogene, receptor tyrosine kinase |
| refseq_nuc | NM_000245.4 |
| refseq_prot | NP_000236.2 |
| ensembl_nuc | ENST00000397752.8 |
| ensembl_prot | ENSP00000380860.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 116672196 |
| end | 116798377 |
| strand | + |
| ver | v1.2 |
| region | chr7:116672196-116798377 |
| region5000 | chr7:116667196-116803377 |
| regionname0 | MET_chr7_116672196_116798377 |
| regionname5000 | MET_chr7_116667196_116803377 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1390 | 316 | 82 | 58 | 129 | 9 | 36 | 91 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0002 | 0/0 | 1390 | 9 | 0 | 2 | 7 | 0 | 0 | 4 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0003 | 0/0 | 1390 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0004 | 0/0 | 1390 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0005 | 0/0 | 1390 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0006 | 0/0 | 1390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0007 | 0/0 | 1390 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0008 | 0/0 | 1390 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0009 | 0/0 | 1390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0010 | 0/0 | 1390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0011 | 0/0 | 1390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0012 | 0/0 | 1390 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4173 | 108 | 32 | 24 | 36 | 2 | 12 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0002 | 0/0 | 4173 | 103 | 5 | 22 | 55 | 4 | 17 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0003 | 0/0 | 4173 | 55 | 4 | 9 | 34 | 2 | 6 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0004 | 0/0 | 4173 | 20 | 20 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0005 | 0/0 | 4173 | 15 | 14 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0006 | 0/0 | 4173 | 6 | 0 | 2 | 4 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0007 | 0/0 | 4173 | 5 | 5 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0008 | 0/0 | 4173 | 4 | 1 | 2 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0009 | 0/0 | 4173 | 4 | 4 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0010 | 0/0 | 4173 | 3 | 0 | 0 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0011 | 0/0 | 4173 | 2 | 0 | 0 | 2 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0012 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0013 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0014 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0015 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0016 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0017 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0018 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0019 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0020 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0021 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0022 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0023 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0024 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| c0025 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2650 | 61 | 4 | 10 | 38 | 2 | 7 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0002 | 1/1 | 2650 | 51 | 25 | 8 | 12 | 1 | 3 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0003 | 0/0 | 2650 | 48 | 9 | 5 | 26 | 3 | 5 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0004 | 0/0 | 2650 | 45 | 1 | 11 | 20 | 2 | 11 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0005 | 0/0 | 2650 | 38 | 6 | 11 | 17 | 1 | 3 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0006 | 0/0 | 2650 | 25 | 14 | 2 | 8 | 0 | 1 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0007 | 0/0 | 2650 | 20 | 8 | 5 | 5 | 0 | 2 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0008 | 0/0 | 2650 | 18 | 2 | 5 | 7 | 0 | 4 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0009 | 0/0 | 2650 | 7 | 7 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0010 | 0/0 | 2650 | 3 | 3 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0011 | 0/0 | 2650 | 3 | 0 | 0 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0012 | 0/0 | 2650 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0013 | 0/0 | 2650 | 2 | 0 | 0 | 2 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0014 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0015 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0016 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0017 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0018 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0019 | 0/0 | 2650 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0020 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0021 | 0/0 | 2650 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0022 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0023 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0024 | 0/0 | 2650 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0025 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0026 | 0/0 | 2650 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0027 | 0/0 | 2650 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0028 | 0/0 | 2650 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0029 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| t0030 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0294 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4173 | 108 | 32 | 24 | 36 | 2 | 12 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0002 | 0/0 | 4173 | 103 | 5 | 22 | 55 | 4 | 17 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0003 | 0/0 | 4173 | 55 | 4 | 9 | 34 | 2 | 6 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004 | 0/0 | 4173 | 20 | 20 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0005 | 0/0 | 4173 | 15 | 14 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0007 | 0/0 | 4173 | 5 | 5 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0008 | 0/0 | 4173 | 4 | 1 | 2 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0015 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0017 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0018 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0019 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0022 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0025 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0002c0006 | 0/0 | 4173 | 6 | 0 | 2 | 4 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0002c0010 | 0/0 | 4173 | 3 | 0 | 0 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0003c0009 | 0/0 | 4173 | 4 | 4 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0004c0011 | 0/0 | 4173 | 2 | 0 | 0 | 2 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0005c0012 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0006c0013 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0007c0016 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0008c0014 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0009c0020 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0010c0021 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0011c0023 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0012c0024 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 6822 | 40 | 18 | 6 | 11 | 0 | 3 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0003 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0005 | 0/0 | 6822 | 35 | 4 | 11 | 16 | 1 | 3 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0006 | 0/0 | 6822 | 3 | 3 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0007 | 0/0 | 6822 | 14 | 4 | 4 | 4 | 0 | 2 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0008 | 0/0 | 6822 | 11 | 0 | 3 | 4 | 0 | 4 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0015 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0020 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0026 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0001t0027 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0002t0001 | 0/0 | 6822 | 56 | 4 | 10 | 34 | 2 | 6 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0002t0004 | 0/0 | 6822 | 44 | 1 | 11 | 19 | 2 | 11 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0002t0013 | 0/0 | 6822 | 2 | 0 | 0 | 2 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0002t0028 | 0/0 | 6822 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0003t0003 | 0/0 | 6822 | 35 | 0 | 5 | 23 | 2 | 5 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0003t0006 | 0/0 | 6822 | 12 | 1 | 2 | 8 | 0 | 1 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0003t0009 | 0/0 | 6822 | 3 | 3 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0003t0011 | 0/0 | 6822 | 3 | 0 | 0 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0003t0021 | 0/0 | 6822 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0003t0024 | 0/0 | 6822 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0002 | 0/0 | 6822 | 4 | 4 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0003 | 0/0 | 6822 | 7 | 7 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0005 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0008 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0012 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0018 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0022 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0023 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0029 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0004t0030 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0005t0002 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0005t0006 | 0/0 | 6822 | 8 | 8 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0005t0007 | 0/0 | 6822 | 2 | 1 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0005t0010 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0005t0016 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0005t0025 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0007t0009 | 0/0 | 6822 | 4 | 4 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0007t0014 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0008t0002 | 0/0 | 6822 | 3 | 0 | 2 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0008t0005 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0015t0003 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0017t0003 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0018t0017 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0019t0001 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0022t0004 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0001c0025t0005 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0002c0006t0007 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0002c0006t0008 | 0/0 | 6822 | 5 | 0 | 2 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0002c0010t0001 | 0/0 | 6822 | 3 | 0 | 0 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0003c0009t0007 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0003c0009t0008 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0003c0009t0010 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0004c0011t0002 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0004c0011t0019 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0005c0012t0006 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0006c0013t0002 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0007c0016t0003 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0008c0014t0001 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0009c0020t0003 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0010c0021t0002 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0011c0023t0007 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| a0012c0024t0003 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | copy fasta | chr7 | 116667196 | 116803377 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0294 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0015g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0020g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0026g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0027g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0013g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0028g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0009g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0011g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0021g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0024g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0012g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0012g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0018g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0022g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0023g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0029g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0030g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0016g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0025g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0007t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0007t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0007t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0007t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0007t0014g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0008t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0008t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0008t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0008t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0015t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0017t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0018t0017g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0019t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0022t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0025t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0008g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0010t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0010t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0010t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0003c0009t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0003c0009t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0003c0009t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0003c0009t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0004c0011t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0004c0011t0019g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0005c0012t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0005c0012t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0006c0013t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0007c0016t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0008c0014t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0009c0020t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0010c0021t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0011c0023t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0012c0024t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0007 | c0016 | t0003 | g0059 | EUR | GBR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00099 | hp2 | a0001 | c0001 | t0027 | g0123 | EUR | GBR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0078 | EUR | GBR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0335 | EUR | GBR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00280 | hp1 | a0001 | c0008 | t0002 | g0030 | EUR | FIN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0125 | EUR | FIN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0209 | EUR | FIN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0183 | EUR | FIN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00408 | hp2 | a0001 | c0003 | t0003 | g0069 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00438 | hp1 | a0002 | c0010 | t0001 | g0116 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00544 | hp1 | a0002 | c0006 | t0008 | g0233 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00597 | hp1 | a0001 | c0002 | t0004 | g0316 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00597 | hp2 | a0001 | c0003 | t0003 | g0082 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00609 | hp2 | a0001 | c0003 | t0011 | g0039 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00621 | hp1 | a0001 | c0003 | t0006 | g0001 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0302 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00639 | hp1 | a0001 | c0003 | t0006 | g0239 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0132 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00642 | hp2 | a0001 | c0008 | t0002 | g0242 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00673 | hp2 | a0001 | c0001 | t0007 | g0284 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00733 | hp2 | a0001 | c0002 | t0004 | g0244 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00738 | hp1 | a0001 | c0003 | t0021 | g0236 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0193 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0079 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0065 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0288 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0075 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0287 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0091 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0051 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01099 | hp2 | a0001 | c0002 | t0004 | g0177 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01168 | hp2 | a0001 | c0002 | t0004 | g0245 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0291 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0220 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0034 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01243 | hp1 | a0001 | c0005 | t0007 | g0146 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0234 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0286 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01256 | hp2 | a0001 | c0008 | t0002 | g0241 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01257 | hp1 | a0001 | c0002 | t0004 | g0243 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0268 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0192 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01346 | hp1 | a0001 | c0003 | t0006 | g0173 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0223 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01358 | hp2 | a0001 | c0002 | t0004 | g0176 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01361 | hp1 | a0002 | c0006 | t0008 | g0124 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0224 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01433 | hp1 | a0001 | c0003 | t0024 | g0187 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0263 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01496 | hp2 | a0001 | c0002 | t0004 | g0310 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01891 | hp1 | a0001 | c0004 | t0018 | g0256 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01891 | hp2 | a0001 | c0007 | t0009 | g0253 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01934 | hp1 | a0002 | c0006 | t0008 | g0114 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01978 | hp1 | a0001 | c0002 | t0004 | g0290 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01978 | hp2 | a0001 | c0002 | t0028 | g0267 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0081 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02015 | hp1 | a0001 | c0001 | t0008 | g0058 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02027 | hp2 | a0001 | c0003 | t0003 | g0080 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02040 | hp1 | a0001 | c0003 | t0006 | g0320 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02055 | hp1 | a0001 | c0007 | t0009 | g0251 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0339 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02074 | hp1 | a0001 | c0003 | t0006 | g0340 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0297 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02083 | hp1 | a0001 | c0002 | t0004 | g0312 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0164 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0100 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0228 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02135 | hp2 | a0001 | c0002 | t0004 | g0318 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | CDX | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | CDX | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0261 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0156 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0026 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0221 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0062 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0282 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02451 | hp1 | a0001 | c0005 | t0006 | g0135 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0145 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02523 | hp1 | a0002 | c0010 | t0001 | g0115 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02523 | hp2 | a0001 | c0003 | t0003 | g0103 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02572 | hp1 | a0001 | c0004 | t0003 | g0049 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0309 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02615 | hp1 | a0010 | c0021 | t0002 | g0258 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02615 | hp2 | a0001 | c0005 | t0010 | g0136 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02622 | hp1 | a0001 | c0005 | t0016 | g0147 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02630 | hp1 | a0001 | c0004 | t0022 | g0255 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02630 | hp2 | a0001 | c0007 | t0014 | g0252 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02647 | hp1 | a0003 | c0009 | t0007 | g0009 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02647 | hp2 | a0001 | c0004 | t0003 | g0048 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0231 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02683 | hp2 | a0001 | c0001 | t0008 | g0188 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02717 | hp1 | a0001 | c0004 | t0003 | g0050 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0262 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02723 | hp2 | a0001 | c0005 | t0006 | g0007 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0169 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02809 | hp1 | a0001 | c0003 | t0009 | g0265 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02818 | hp2 | a0005 | c0012 | t0006 | g0028 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02886 | hp1 | a0001 | c0004 | t0005 | g0032 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02886 | hp2 | a0001 | c0005 | t0010 | g0289 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02896 | hp2 | a0003 | c0009 | t0007 | g0008 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02922 | hp2 | a0005 | c0012 | t0006 | g0257 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02965 | hp1 | a0001 | c0004 | t0003 | g0046 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02970 | hp1 | a0001 | c0005 | t0006 | g0142 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02970 | hp2 | a0001 | c0005 | t0006 | g0138 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02976 | hp2 | a0001 | c0004 | t0029 | g0189 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0311 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03098 | hp2 | a0001 | c0003 | t0009 | g0264 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03130 | hp1 | a0001 | c0005 | t0002 | g0143 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03139 | hp2 | a0001 | c0005 | t0007 | g0247 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0260 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03209 | hp2 | a0001 | c0003 | t0006 | g0198 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0016 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03225 | hp2 | a0001 | c0005 | t0025 | g0181 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03239 | hp1 | a0001 | c0003 | t0006 | g0159 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03239 | hp2 | a0001 | c0002 | t0004 | g0133 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03453 | hp1 | a0001 | c0004 | t0023 | g0027 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03486 | hp1 | a0001 | c0005 | t0006 | g0155 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03486 | hp2 | a0001 | c0007 | t0009 | g0254 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0017 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0269 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03492 | hp1 | a0001 | c0002 | t0004 | g0338 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0271 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03516 | hp1 | a0006 | c0013 | t0002 | g0006 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0194 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03540 | hp1 | a0001 | c0004 | t0008 | g0190 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03579 | hp1 | a0001 | c0018 | t0017 | g0029 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03579 | hp2 | a0009 | c0020 | t0003 | g0191 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0131 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0077 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0130 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0165 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0085 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03704 | hp2 | a0001 | c0002 | t0004 | g0314 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0063 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0235 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0185 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03942 | hp1 | a0001 | c0019 | t0001 | g0170 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03942 | hp2 | a0001 | c0002 | t0004 | g0337 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0168 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04115 | hp2 | a0001 | c0002 | t0004 | g0283 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0052 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04184 | hp2 | a0001 | c0002 | t0004 | g0292 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04204 | hp1 | a0001 | c0001 | t0008 | g0167 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0313 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04228 | hp2 | a0001 | c0002 | t0004 | g0240 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18522 | hp2 | a0001 | c0004 | t0012 | g0128 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | CHB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18612 | hp2 | a0001 | c0003 | t0006 | g0321 | EAS | CHB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18747 | hp1 | a0004 | c0011 | t0019 | g0330 | EAS | CHB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | CHB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18906 | hp1 | a0003 | c0009 | t0008 | g0035 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18906 | hp2 | a0001 | c0004 | t0002 | g0158 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0298 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18941 | hp2 | a0001 | c0002 | t0004 | g0279 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0315 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18943 | hp2 | a0012 | c0024 | t0003 | g0072 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18950 | hp1 | a0001 | c0002 | t0004 | g0278 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18951 | hp1 | a0001 | c0003 | t0003 | g0067 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18953 | hp1 | a0001 | c0003 | t0003 | g0206 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18953 | hp2 | a0001 | c0001 | t0007 | g0331 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18954 | hp1 | a0001 | c0003 | t0003 | g0068 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18964 | hp1 | a0001 | c0002 | t0013 | g0107 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18965 | hp1 | a0001 | c0003 | t0006 | g0299 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18968 | hp1 | a0002 | c0006 | t0008 | g0112 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18969 | hp2 | a0001 | c0015 | t0003 | g0061 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18970 | hp2 | a0001 | c0003 | t0003 | g0073 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18973 | hp1 | a0001 | c0003 | t0006 | g0153 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18973 | hp2 | a0004 | c0011 | t0002 | g0319 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18974 | hp1 | a0001 | c0002 | t0004 | g0277 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0084 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18978 | hp1 | a0001 | c0003 | t0003 | g0070 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18979 | hp1 | a0001 | c0003 | t0003 | g0066 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18983 | hp2 | a0001 | c0003 | t0011 | g0104 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18985 | hp1 | a0001 | c0003 | t0003 | g0064 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18985 | hp2 | a0001 | c0002 | t0004 | g0276 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0281 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0336 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18994 | hp1 | a0001 | c0002 | t0004 | g0150 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0161 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18995 | hp2 | a0001 | c0003 | t0006 | g0148 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19000 | hp1 | a0001 | c0003 | t0003 | g0227 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19000 | hp2 | a0008 | c0014 | t0001 | g0217 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19005 | hp1 | a0001 | c0025 | t0005 | g0106 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19005 | hp2 | a0002 | c0006 | t0008 | g0113 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19009 | hp1 | a0001 | c0001 | t0008 | g0200 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19009 | hp2 | a0001 | c0003 | t0003 | g0226 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19010 | hp1 | a0001 | c0003 | t0006 | g0285 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19011 | hp1 | a0001 | c0003 | t0003 | g0076 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19011 | hp2 | a0002 | c0006 | t0007 | g0003 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0225 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19030 | hp1 | a0001 | c0003 | t0009 | g0266 | AFR | LWK | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19030 | hp2 | a0001 | c0004 | t0003 | g0047 | AFR | LWK | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19043 | hp1 | a0001 | c0007 | t0009 | g0259 | AFR | LWK | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19055 | hp1 | a0002 | c0010 | t0001 | g0086 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19055 | hp2 | a0001 | c0002 | t0004 | g0301 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19063 | hp2 | a0001 | c0017 | t0003 | g0083 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0071 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19068 | hp1 | a0001 | c0022 | t0004 | g0151 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19068 | hp2 | a0001 | c0003 | t0003 | g0043 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19074 | hp1 | a0001 | c0003 | t0011 | g0074 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19076 | hp1 | a0001 | c0003 | t0003 | g0232 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19078 | hp1 | a0001 | c0003 | t0003 | g0207 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19078 | hp2 | a0001 | c0002 | t0013 | g0057 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0149 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19084 | hp1 | a0001 | c0003 | t0003 | g0110 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19087 | hp1 | a0001 | c0002 | t0004 | g0300 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19089 | hp1 | a0001 | c0002 | t0004 | g0152 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19089 | hp2 | a0001 | c0001 | t0026 | g0205 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19091 | hp1 | a0001 | c0002 | t0004 | g0275 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19240 | hp1 | a0011 | c0023 | t0007 | g0246 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19240 | hp2 | a0001 | c0005 | t0006 | g0139 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20129 | hp1 | a0001 | c0005 | t0006 | g0129 | AFR | ASW | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20129 | hp2 | a0001 | c0005 | t0006 | g0154 | AFR | ASW | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20752 | hp1 | a0001 | c0003 | t0003 | g0270 | EUR | TSI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0237 | EUR | TSI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0248 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02109 | hp2 | a0001 | c0004 | t0003 | g0195 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02559 | hp1 | a0001 | c0008 | t0005 | g0060 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0157 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03471 | hp1 | a0001 | c0004 | t0030 | g0197 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03471 | hp2 | a0003 | c0009 | t0010 | g0010 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG06807 | hp1 | a0001 | c0004 | t0012 | g0127 | AFR | USA | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0238 | AFR | USA | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | USA | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | USA | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0294 | REF | REF | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0295 | REF | REF | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116699218
|
A | G | 1 | a0012 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.134A>G | p.Asn45Ser | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 530/6822 | 134/4173 | 45/1390 | chr7 | 116699218 | ||
| chr7:116699227
|
C | T | 1 | a0011 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.143C>T | p.Ala48Val | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 539/6822 | 143/4173 | 48/1390 | chr7 | 116699227 | ||
| chr7:116700032
|
A | G | 1 | a0003 | 4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
missense_variant | MODERATE | c.948A>G | p.Ile316Met | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 1344/6822 | 948/4173 | 316/1390 | chr7 | 116700032 | ||
| chr7:116700169
|
T | C | 1 | a0005 | 2 | HG02818.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.1085T>C | p.Met362Thr | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 1481/6822 | 1085/4173 | 362/1390 | chr7 | 116700169 | ||
| chr7:116700208
|
A | G | 2 | a0002a0010 | 10 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(7): Show |
missense_variant | MODERATE | c.1124A>G | p.Asn375Ser | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 1520/6822 | 1124/4173 | 375/1390 | chr7 | 116700208 | ||
| chr7:116755368
|
G | A | 2 | a0006a0010 | 2 | HG02615.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.1715G>A | p.Ser572Asn | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/21 | 2111/6822 | 1715/4173 | 572/1390 | chr7 | 116755368 | ||
| chr7:116769723
|
C | T | 1 | a0009 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.2662C>T | p.His888Tyr | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/21 | 3058/6822 | 2662/4173 | 888/1390 | chr7 | 116769723 | ||
| chr7:116771936
|
C | T | 1 | a0007 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.2975C>T | p.Thr992Ile | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/21 | 3371/6822 | 2975/4173 | 992/1390 | chr7 | 116771936 | ||
| chr7:116774917
|
G | A | 1 | a0008 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.3065G>A | p.Arg1022Gln | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/21 | 3461/6822 | 3065/4173 | 1022/1390 | chr7 | 116774917 | ||
| chr7:116796038
|
G | A | 1 | a0004 | 2 | NA18747.hp1 NA18973.hp2 |
missense_variant | MODERATE | c.4087G>A | p.Ala1363Thr | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 4483/6822 | 4087/4173 | 1363/1390 | chr7 | 116796038 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116699120
|
C | T | 1 | a0001c0025 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.36C>T | p.Leu12Leu | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 432/6822 | 36/4173 | 12/1390 | chr7 | 116699120 | ||
| chr7:116699228
|
G | A | 1 | a0001c0008 | 4 | HG00280.hp1 HG00642.hp2 HG01256.hp2 others(1): Show |
synonymous_variant | LOW | c.144G>A | p.Ala48Ala | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 540/6822 | 144/4173 | 48/1390 | chr7 | 116699228 | ||
| chr7:116699474
|
C | T | 1 | a0005c0012 | 2 | HG02818.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.390C>T | p.Leu130Leu | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 786/6822 | 390/4173 | 130/1390 | chr7 | 116699474 | ||
| chr7:116699489
|
C | T | 1 | a0001c0022 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.405C>T | p.Ser135Ser | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 801/6822 | 405/4173 | 135/1390 | chr7 | 116699489 | ||
| chr7:116699618
|
C | T | 6 | a0001c0004a0001c0019a0002c0006others(3): Show | 32 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(29): Show |
synonymous_variant | LOW | c.534C>T | p.Ser178Ser | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 930/6822 | 534/4173 | 178/1390 | chr7 | 116699618 | ||
| chr7:116700215
|
C | T | 3 | a0001c0005a0001c0007a0011c0023 | 21 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
synonymous_variant | LOW | c.1131C>T | p.Ile377Ile | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 1527/6822 | 1131/4173 | 377/1390 | chr7 | 116700215 | ||
| chr7:116700275
|
C | T | 1 | a0001c0018 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1191C>T | p.Cys397Cys | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/21 | 1587/6822 | 1191/4173 | 397/1390 | chr7 | 116700275 | ||
| chr7:116740908
|
A | G | 1 | a0001c0017 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.1584A>G | p.Gln528Gln | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/21 | 1980/6822 | 1584/4173 | 528/1390 | chr7 | 116740908 | ||
| chr7:116757518
|
A | G | 6 | a0001c0003a0001c0007a0001c0015others(3): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(61): Show |
synonymous_variant | LOW | c.1944A>G | p.Gln648Gln | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 7/21 | 2340/6822 | 1944/4173 | 648/1390 | chr7 | 116757518 | ||
| chr7:116783373
|
C | T | 1 | a0001c0015 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.3702C>T | p.Tyr1234Tyr | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/21 | 4098/6822 | 3702/4173 | 1234/1390 | chr7 | 116783373 | ||
| chr7:116795714
|
C | T | 5 | a0001c0002a0001c0019a0001c0022others(2): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
synonymous_variant | LOW | c.3858C>T | p.Asp1286Asp | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 20/21 | 4254/6822 | 3858/4173 | 1286/1390 | chr7 | 116795714 | ||
| chr7:116795968
|
G | A | 5 | a0001c0002a0001c0019a0001c0022others(2): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
synonymous_variant | LOW | c.4017G>A | p.Ala1339Ala | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 4413/6822 | 4017/4173 | 1339/1390 | chr7 | 116795968 | ||
| chr7:116796043
|
G | A | 5 | a0001c0002a0001c0019a0001c0022others(2): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
synonymous_variant | LOW | c.4092G>A | p.Pro1364Pro | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 4488/6822 | 4092/4173 | 1364/1390 | chr7 | 116796043 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116672385
|
C | G | 29 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(26): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
5_prime_UTR_variant | MODIFIER | c.-207C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/21 | 26700 | chr7 | 116672385 | |||||
| chr7:116672525
|
C | A | 1 | a0001c0007t0014 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-67C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/21 | 26560 | chr7 | 116672525 | |||||
| chr7:116796325
|
C | T | 2 | a0001c0004t0023a0001c0004t0030 | 2 | HG03453.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*201C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 201 | chr7 | 116796325 | |||||
| chr7:116796339
|
G | A | 1 | a0001c0001t0015 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*215G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 215 | chr7 | 116796339 | |||||
| chr7:116796340
|
C | A | 4 | a0001c0003t0009a0001c0003t0024a0001c0007t0009others(1): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*216C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 216 | chr7 | 116796340 | |||||
| chr7:116796355
|
T | G | 1 | a0001c0005t0016 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 231 | chr7 | 116796355 | |||||
| chr7:116796407
|
T | C | 1 | a0001c0018t0017 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*283T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 283 | chr7 | 116796407 | |||||
| chr7:116796571
|
T | C | 1 | a0001c0004t0018 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 447 | chr7 | 116796571 | |||||
| chr7:116796726
|
C | T | 1 | a0001c0003t0011 | 3 | HG00609.hp2 NA18983.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*602C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 602 | chr7 | 116796726 | |||||
| chr7:116796744
|
G | A | 1 | a0004c0011t0019 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 620 | chr7 | 116796744 | |||||
| chr7:116796808
|
G | A | 10 | a0001c0001t0007a0001c0001t0008a0001c0001t0020others(7): Show | 39 | HG00544.hp1 HG00673.hp2 HG01070.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*684G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 684 | chr7 | 116796808 | |||||
| chr7:116796911
|
G | A | 1 | a0001c0005t0016 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*787G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 787 | chr7 | 116796911 | |||||
| chr7:116797134
|
G | T | 2 | a0001c0004t0022a0001c0004t0029 | 2 | HG02630.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1010G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1010 | chr7 | 116797134 | |||||
| chr7:116797152
|
A | G | 8 | a0001c0002t0001a0001c0002t0004a0001c0002t0013others(5): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1028A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1028 | chr7 | 116797152 | |||||
| chr7:116797165
|
G | T | 1 | a0001c0001t0027 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1041G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1041 | chr7 | 116797165 | |||||
| chr7:116797344
|
G | A | 1 | a0001c0004t0012 | 2 | HG06807.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1220G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1220 | chr7 | 116797344 | |||||
| chr7:116797348
|
C | T | 1 | a0001c0003t0021 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1224C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1224 | chr7 | 116797348 | |||||
| chr7:116797368
|
G | A | 1 | a0001c0002t0013 | 2 | NA18964.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1244 | chr7 | 116797368 | |||||
| chr7:116797450
|
A | G | 8 | a0001c0002t0001a0001c0002t0004a0001c0002t0013others(5): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1326A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1326 | chr7 | 116797450 | |||||
| chr7:116797552
|
G | A | 45 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(42): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1428G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1428 | chr7 | 116797552 | |||||
| chr7:116798031
|
G | T | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1907 | chr7 | 116798031 | |||||
| chr7:116798032
|
T | G | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1908T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1908 | chr7 | 116798032 | |||||
| chr7:116798111
|
C | T | 4 | a0001c0004t0018a0001c0005t0010a0001c0005t0025others(1): Show | 5 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1987C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 1987 | chr7 | 116798111 | |||||
| chr7:116798224
|
C | T | 2 | a0001c0004t0023a0001c0004t0030 | 2 | HG03453.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2100C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 2100 | chr7 | 116798224 | |||||
| chr7:116798326
|
G | A | 1 | a0001c0002t0028 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2202G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 2202 | chr7 | 116798326 | |||||
| chr7:116798364
|
G | A | 8 | a0001c0002t0001a0001c0002t0004a0001c0002t0013others(5): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2240G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 21/21 | 2240 | chr7 | 116798364 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116672737
|
G | A | 2 | a0001c0001t0002g0002a0001c0003t0006g0001 | 2 | HG00621.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-15+160G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116672737 | ||||||
| chr7:116672813
|
GA | G | 25 | a0001c0001t0002g0317a0001c0001t0002g0322a0001c0001t0002g0323others(22): Show | 25 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+237delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116672813 | ||||||
| chr7:116672879
|
G | C | 1 | a0002c0006t0007g0003 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-15+302G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116672879 | ||||||
| chr7:116672911
|
C | T | 1 | a0001c0001t0005g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-15+334C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116672911 | ||||||
| chr7:116672932
|
T | C | 299 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-15+355T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116672932 | ||||||
| chr7:116673056
|
G | A | 13 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(10): Show | 13 | HG02622.hp2 HG02647.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+479G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673056 | ||||||
| chr7:116673080
|
C | G | 7 | a0001c0001t0005g0268a0001c0002t0001g0272a0001c0002t0001g0273others(4): Show | 7 | HG00738.hp2 HG01106.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+503C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673080 | ||||||
| chr7:116673083
|
A | G | 3 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266 | 3 | HG02809.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+506A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673083 | ||||||
| chr7:116673145
|
C | T | 3 | a0001c0001t0006g0261a0001c0001t0007g0262a0001c0001t0007g0263 | 3 | HG01496.hp1 HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-15+568C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673145 | ||||||
| chr7:116673272
|
T | C | 1 | a0001c0002t0004g0017 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-15+695T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673272 | ||||||
| chr7:116673313
|
G | T | 1 | a0001c0001t0007g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+736G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673313 | ||||||
| chr7:116673407
|
C | T | 1 | a0001c0001t0007g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+830C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673407 | ||||||
| chr7:116673492
|
T | C | 7 | a0001c0001t0005g0024a0001c0002t0001g0018a0001c0002t0001g0019others(4): Show | 7 | HG01255.hp2 HG01261.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+915T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673492 | ||||||
| chr7:116673573
|
A | T | 1 | a0001c0002t0004g0314 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-15+996A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116673573 | ||||||
| chr7:116674083
|
T | C | 1 | a0001c0001t0007g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+1506T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674083 | ||||||
| chr7:116674144
|
C | G | 11 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0004t0018g0256others(8): Show | 11 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+1567C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674144 | ||||||
| chr7:116674273
|
A | C | 290 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-15+1696A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674273 | ||||||
| chr7:116674351
|
G | A | 104 | a0001c0001t0003g0033a0001c0001t0005g0034a0001c0001t0005g0036others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.-15+1774G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674351 | ||||||
| chr7:116674425
|
TA | T | 6 | a0001c0001t0002g0031a0001c0001t0007g0260a0001c0003t0009g0264others(3): Show | 6 | HG00280.hp1 HG02698.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+1857delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116674425 | |||||
| chr7:116674542
|
T | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0134a0001c0001t0002g0137others(74): Show | 77 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-15+1965T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674542 | ||||||
| chr7:116674647
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0006c0013t0002g0006 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-15+2070G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674647 | ||||||
| chr7:116674666
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15+2089G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674666 | ||||||
| chr7:116674755
|
T | C | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-15+2178T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674755 | ||||||
| chr7:116674814
|
G | A | 70 | a0001c0001t0002g0134a0001c0001t0002g0137a0001c0001t0002g0140others(67): Show | 70 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+2237G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674814 | ||||||
| chr7:116674859
|
C | T | 3 | a0001c0004t0002g0248a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG02109.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+2282C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116674859 | ||||||
| chr7:116675121
|
T | C | 3 | a0001c0004t0002g0248a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG02109.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+2544T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116675121 | ||||||
| chr7:116675151
|
T | C | 96 | a0001c0001t0002g0002a0001c0001t0002g0134a0001c0001t0002g0137others(93): Show | 96 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-15+2574T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116675151 | ||||||
| chr7:116675429
|
T | A | 2 | a0001c0001t0002g0171a0001c0001t0007g0172 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-15+2852T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116675429 | ||||||
| chr7:116675430
|
T | A | 3 | a0001c0001t0002g0171a0001c0001t0007g0172a0001c0003t0006g0173 | 3 | HG01346.hp1 HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-15+2853T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116675430 | ||||||
| chr7:116675754
|
C | CT | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0004t0002g0248others(3): Show | 6 | HG00280.hp2 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+3189dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116675754 | |||||
| chr7:116675754
|
CT | C | 99 | a0001c0001t0002g0031a0001c0001t0002g0134a0001c0001t0002g0137others(96): Show | 99 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-15+3189delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116675754 | |||||
| chr7:116675873
|
G | A | 2 | a0001c0002t0001g0178a0001c0002t0001g0179 | 2 | NA18968.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-15+3296G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116675873 | ||||||
| chr7:116675874
|
T | G | 1 | a0001c0002t0001g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-15+3297T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116675874 | ||||||
| chr7:116675895
|
C | T | 3 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266 | 3 | HG02809.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+3318C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116675895 | ||||||
| chr7:116675908
|
G | A | 1 | a0001c0002t0001g0180 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-15+3331G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116675908 | ||||||
| chr7:116676121
|
T | C | 2 | a0001c0004t0023g0027a0005c0012t0006g0028 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-15+3544T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116676121 | ||||||
| chr7:116676181
|
G | A | 1 | a0001c0005t0006g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+3604G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116676181 | ||||||
| chr7:116676354
|
G | A | 3 | a0001c0004t0002g0248a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG02109.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+3777G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116676354 | ||||||
| chr7:116676430
|
C | T | 1 | a0001c0001t0007g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-15+3853C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116676430 | ||||||
| chr7:116676555
|
A | G | 1 | a0001c0002t0004g0245 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-15+3978A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116676555 | ||||||
| chr7:116676735
|
A | G | 1 | a0001c0004t0003g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-15+4158A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116676735 | ||||||
| chr7:116676809
|
A | T | 3 | a0001c0004t0002g0248a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG02109.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+4232A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116676809 | ||||||
| chr7:116676960
|
G | A | 1 | a0001c0003t0003g0043 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-15+4383G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116676960 | ||||||
| chr7:116676960
|
GGAA | G | 4 | a0001c0001t0006g0311a0001c0003t0009g0264a0001c0003t0009g0265others(1): Show | 4 | HG02809.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+4392_-15+4394d others(5): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116676960 | |||||
| chr7:116676988
|
G | GT | 21 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0171others(18): Show | 21 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+4422dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116676988 | |||||
| chr7:116676988
|
GT | G | 97 | a0001c0001t0005g0045a0001c0001t0005g0052a0001c0001t0005g0062others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-15+4422delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116676988 | |||||
| chr7:116677000
|
G | T | 1 | a0001c0002t0004g0177 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-15+4423G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677000 | ||||||
| chr7:116677003
|
T | TTTTTG | 8 | a0001c0002t0001g0175a0001c0002t0004g0149a0001c0002t0004g0150others(5): Show | 8 | HG02735.hp1 NA18945.hp1 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+4452_-15+4456d others(7): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116677003 | |||||
| chr7:116677026
|
T | C | 2 | a0001c0001t0002g0171a0001c0001t0007g0172 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-15+4449T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677026 | ||||||
| chr7:116677038
|
C | T | 2 | a0001c0001t0002g0171a0001c0001t0007g0172 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-15+4461C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677038 | ||||||
| chr7:116677265
|
G | A | 2 | a0001c0005t0006g0154a0001c0005t0006g0155 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+4688G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677265 | ||||||
| chr7:116677589
|
G | C | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15+5012G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677589 | ||||||
| chr7:116677608
|
C | T | 4 | a0001c0001t0002g0162a0001c0004t0002g0248a0001c0005t0007g0247others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5031C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677608 | ||||||
| chr7:116677797
|
C | T | 1 | a0001c0001t0007g0339 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-15+5220C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677797 | ||||||
| chr7:116677823
|
G | A | 286 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-15+5246G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677823 | ||||||
| chr7:116677855
|
A | G | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15+5278A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116677855 | ||||||
| chr7:116677969
|
T | TTCTC | 3 | a0001c0004t0002g0248a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG02109.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+5406_-15+5409d others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116677969 | |||||
| chr7:116677973
|
CTCTCTCT others(7): Show |
C | 220 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(217): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-15+5410_-15+5423d others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116677973 | |||||
| chr7:116678036
|
G | A | 6 | a0001c0002t0004g0275a0001c0002t0004g0276a0001c0002t0004g0277others(3): Show | 6 | NA18941.hp2 NA18950.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+5459G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116678036 | ||||||
| chr7:116678247
|
G | A | 1 | a0001c0001t0005g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-15+5670G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116678247 | ||||||
| chr7:116678432
|
GT | G | 223 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(220): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-15+5864delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116678432 | |||||
| chr7:116678441
|
T | A | 4 | a0001c0001t0002g0162a0001c0001t0007g0260a0001c0001t0007g0281others(1): Show | 4 | HG01255.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5864T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116678441 | ||||||
| chr7:116678688
|
T | C | 12 | a0001c0001t0002g0002a0001c0001t0007g0130a0001c0002t0001g0175others(9): Show | 12 | HG00639.hp2 HG03239.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15+6111T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116678688 | ||||||
| chr7:116678711
|
CTTGGGAC others(5): Show |
C | 223 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(220): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-15+6145_-15+6156d others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116678711 | |||||
| chr7:116678780
|
G | A | 1 | a0001c0002t0004g0316 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-15+6203G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116678780 | ||||||
| chr7:116678948
|
A | G | 223 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(220): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-15+6371A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116678948 | ||||||
| chr7:116679074
|
G | C | 1 | a0001c0002t0001g0199 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-15+6497G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679074 | ||||||
| chr7:116679157
|
C | T | 222 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(219): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-15+6580C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679157 | ||||||
| chr7:116679160
|
C | T | 217 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(214): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-15+6583C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679160 | ||||||
| chr7:116679208
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-15+6631G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679208 | ||||||
| chr7:116679213
|
A | G | 1 | a0001c0005t0016g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-15+6636A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679213 | ||||||
| chr7:116679471
|
A | G | 1 | a0001c0001t0007g0313 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-15+6894A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679471 | ||||||
| chr7:116679499
|
C | T | 1 | a0001c0003t0003g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-15+6922C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679499 | ||||||
| chr7:116679558
|
G | A | 1 | a0001c0001t0007g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+6981G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679558 | ||||||
| chr7:116679750
|
G | A | 22 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(19): Show | 22 | HG02055.hp2 HG02572.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15+7173G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679750 | ||||||
| chr7:116679838
|
A | C | 1 | a0001c0001t0027g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15+7261A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679838 | ||||||
| chr7:116679872
|
A | G | 70 | a0001c0001t0002g0308a0001c0001t0005g0105a0001c0001t0005g0223others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+7295A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116679872 | ||||||
| chr7:116680016
|
G | C | 1 | a0001c0004t0012g0127 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15+7439G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680016 | ||||||
| chr7:116680086
|
C | T | 1 | a0001c0001t0005g0038 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-15+7509C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680086 | ||||||
| chr7:116680105
|
T | C | 1 | a0001c0005t0025g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-15+7528T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680105 | ||||||
| chr7:116680128
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-15+7551A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680128 | ||||||
| chr7:116680161
|
A | G | 1 | a0001c0003t0011g0104 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-15+7584A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680161 | ||||||
| chr7:116680212
|
T | C | 12 | a0001c0001t0003g0033a0001c0001t0005g0034a0001c0001t0005g0036others(9): Show | 12 | HG01192.hp2 HG01496.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+7635T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680212 | ||||||
| chr7:116680351
|
T | A | 79 | a0001c0001t0002g0308a0001c0001t0005g0052a0001c0001t0008g0200others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-15+7774T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680351 | ||||||
| chr7:116680452
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-15+7875T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680452 | ||||||
| chr7:116680708
|
A | G | 1 | a0001c0007t0009g0259 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15+8131A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680708 | ||||||
| chr7:116680759
|
T | C | 19 | a0001c0001t0002g0162a0001c0001t0002g0308a0001c0001t0005g0160others(16): Show | 19 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-15+8182T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680759 | ||||||
| chr7:116680810
|
C | T | 214 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(211): Show | 214 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-15+8233C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680810 | ||||||
| chr7:116680832
|
C | T | 122 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0171others(119): Show | 122 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.-15+8255C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680832 | ||||||
| chr7:116680854
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-15+8277A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680854 | ||||||
| chr7:116680891
|
G | A | 1 | a0001c0003t0003g0051 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-15+8314G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680891 | ||||||
| chr7:116680951
|
G | A | 1 | a0007c0016t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-15+8374G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680951 | ||||||
| chr7:116680985
|
T | C | 141 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0162others(138): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-15+8408T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116680985 | ||||||
| chr7:116681137
|
G | T | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15+8560G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116681137 | ||||||
| chr7:116681331
|
AGGTTTTA others(21): Show |
A | 1 | a0001c0002t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-15+8755_-15+8782d others(30): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116681331 | ||||||
| chr7:116681360
|
A | T | 1 | a0001c0002t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-15+8783A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116681360 | ||||||
| chr7:116681742
|
C | G | 27 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0171others(24): Show | 27 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+9165C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116681742 | ||||||
| chr7:116681748
|
A | G | 213 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(210): Show | 213 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-15+9171A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116681748 | ||||||
| chr7:116681938
|
CA | C | 61 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0162others(58): Show | 61 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+9372delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116681938 | |||||
| chr7:116682131
|
A | G | 61 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0162others(58): Show | 61 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+9554A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116682131 | ||||||
| chr7:116682569
|
A | G | 10 | a0001c0001t0002g0171a0001c0001t0003g0033a0001c0001t0005g0034others(7): Show | 10 | HG01192.hp2 HG01496.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+9992A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116682569 | ||||||
| chr7:116682737
|
A | C | 61 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0162others(58): Show | 61 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+10160A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116682737 | ||||||
| chr7:116682999
|
G | T | 43 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0171others(40): Show | 43 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.-15+10422G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116682999 | ||||||
| chr7:116683018
|
A | G | 12 | a0001c0001t0002g0308a0001c0001t0007g0130a0001c0001t0007g0281others(9): Show | 12 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+10441A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683018 | ||||||
| chr7:116683090
|
T | G | 61 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0162others(58): Show | 61 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+10513T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683090 | ||||||
| chr7:116683110
|
G | C | 1 | a0001c0001t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-15+10533G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683110 | ||||||
| chr7:116683137
|
G | A | 1 | a0001c0001t0007g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-15+10560G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683137 | ||||||
| chr7:116683259
|
G | C | 18 | a0001c0001t0002g0162a0001c0001t0002g0308a0001c0001t0005g0160others(15): Show | 18 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+10682G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683259 | ||||||
| chr7:116683275
|
C | T | 18 | a0001c0001t0002g0162a0001c0001t0002g0308a0001c0001t0005g0160others(15): Show | 18 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+10698C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683275 | ||||||
| chr7:116683276
|
G | A | 1 | a0001c0005t0006g0135 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-15+10699G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683276 | ||||||
| chr7:116683444
|
C | G | 3 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266 | 3 | HG02809.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+10867C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683444 | ||||||
| chr7:116683460
|
T | G | 1 | a0004c0011t0002g0319 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-15+10883T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683460 | ||||||
| chr7:116683490
|
C | T | 18 | a0001c0001t0002g0162a0001c0001t0002g0308a0001c0001t0005g0160others(15): Show | 18 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+10913C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683490 | ||||||
| chr7:116683882
|
G | T | 43 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0171others(40): Show | 43 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.-15+11305G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116683882 | ||||||
| chr7:116684447
|
T | C | 10 | a0001c0001t0002g0171a0001c0001t0003g0033a0001c0001t0005g0034others(7): Show | 10 | HG01192.hp2 HG01496.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+11870T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116684447 | ||||||
| chr7:116684477
|
C | T | 304 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-15+11900C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116684477 | ||||||
| chr7:116684640
|
C | A | 43 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0171others(40): Show | 43 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.-15+12063C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116684640 | ||||||
| chr7:116684691
|
T | A | 6 | a0001c0001t0002g0031a0001c0001t0005g0192a0001c0001t0005g0193others(3): Show | 6 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+12114T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116684691 | ||||||
| chr7:116684763
|
G | A | 4 | a0001c0001t0005g0174a0001c0001t0005g0183a0001c0001t0005g0184others(1): Show | 4 | HG00323.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+12186G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116684763 | ||||||
| chr7:116684908
|
G | C | 1 | a0001c0005t0006g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+12331G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116684908 | ||||||
| chr7:116684933
|
G | A | 1 | a0001c0005t0010g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15+12356G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116684933 | ||||||
| chr7:116685081
|
G | A | 1 | a0001c0015t0003g0061 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-15+12504G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116685081 | ||||||
| chr7:116685089
|
G | A | 16 | a0001c0004t0002g0145a0001c0004t0002g0157a0001c0004t0002g0158others(13): Show | 16 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+12512G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116685089 | ||||||
| chr7:116685095
|
G | A | 43 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0171others(40): Show | 43 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.-15+12518G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116685095 | ||||||
| chr7:116685272
|
T | C | 334 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(331): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-15+12695T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116685272 | ||||||
| chr7:116685465
|
G | A | 43 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0171others(40): Show | 43 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.-15+12888G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116685465 | ||||||
| chr7:116685744
|
A | T | 1 | a0001c0002t0001g0018 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-15+13167A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116685744 | ||||||
| chr7:116685948
|
C | T | 3 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266 | 3 | HG02809.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-14-13123C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116685948 | ||||||
| chr7:116685949
|
G | A | 1 | a0001c0002t0004g0017 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-14-13122G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116685949 | ||||||
| chr7:116686111
|
C | T | 1 | a0001c0003t0006g0321 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-14-12960C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116686111 | ||||||
| chr7:116686122
|
AATCCCCC others(265): Show |
A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-12947_-14-1267 others(4): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116686122 | |||||
| chr7:116686344
|
C | T | 1 | a0001c0001t0008g0058 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-14-12727C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116686344 | ||||||
| chr7:116686375
|
CT | C | 11 | a0001c0001t0002g0171a0001c0001t0003g0033a0001c0001t0005g0034others(8): Show | 11 | HG01192.hp2 HG01496.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-12694delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116686375 | |||||
| chr7:116686547
|
A | G | 1 | a0001c0004t0003g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14-12524A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116686547 | ||||||
| chr7:116686554
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-12517G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116686554 | ||||||
| chr7:116686696
|
G | T | 2 | a0001c0004t0022g0255a0001c0004t0029g0189 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-14-12375G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116686696 | ||||||
| chr7:116686754
|
C | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-12317C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116686754 | ||||||
| chr7:116687059
|
G | C | 8 | a0001c0002t0004g0275a0001c0002t0004g0276a0001c0002t0004g0277others(5): Show | 8 | HG02080.hp1 NA18940.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-12012G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116687059 | ||||||
| chr7:116687172
|
A | G | 1 | a0001c0001t0002g0334 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-14-11899A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116687172 | ||||||
| chr7:116687364
|
C | T | 2 | a0001c0004t0022g0255a0001c0004t0029g0189 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-14-11707C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116687364 | ||||||
| chr7:116687376
|
C | G | 110 | a0001c0001t0002g0134a0001c0001t0002g0308a0001c0001t0005g0052others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-14-11695C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116687376 | ||||||
| chr7:116687387
|
C | G | 18 | a0001c0005t0002g0143a0001c0005t0006g0007a0001c0005t0006g0129others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14-11684C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116687387 | ||||||
| chr7:116687658
|
G | A | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14-11413G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116687658 | ||||||
| chr7:116687978
|
C | T | 31 | a0001c0004t0002g0145a0001c0004t0002g0157a0001c0004t0002g0158others(28): Show | 31 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.-14-11093C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116687978 | ||||||
| chr7:116688509
|
G | A | 3 | a0001c0005t0002g0143a0001c0005t0006g0142a0001c0005t0016g0147 | 3 | HG02622.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-14-10562G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116688509 | ||||||
| chr7:116688600
|
G | T | 2 | a0005c0012t0006g0028a0005c0012t0006g0257 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-14-10471G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116688600 | ||||||
| chr7:116688606
|
T | C | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG01169.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-14-10465T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116688606 | ||||||
| chr7:116688712
|
G | A | 1 | a0001c0001t0005g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-14-10359G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116688712 | ||||||
| chr7:116689105
|
G | GAAATTTC others(4): Show |
90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-9961_-14-9951d others(13): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116689105 | |||||
| chr7:116689116
|
T | C | 1 | a0001c0001t0008g0165 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-14-9955T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116689116 | ||||||
| chr7:116689119
|
A | G | 1 | a0001c0002t0001g0222 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-14-9952A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116689119 | ||||||
| chr7:116689347
|
G | T | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-9724G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116689347 | ||||||
| chr7:116689559
|
C | CT | 26 | a0001c0001t0002g0307a0001c0001t0002g0333a0001c0001t0005g0045others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.-14-9485dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116689559 | |||||
| chr7:116689559
|
CT | C | 18 | a0001c0001t0002g0011a0001c0001t0002g0303a0001c0001t0005g0037others(15): Show | 18 | HG00323.hp2 HG01169.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.-14-9485delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116689559 | |||||
| chr7:116689559
|
CTT | C | 10 | a0001c0004t0002g0145a0001c0004t0002g0248a0001c0004t0003g0195others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-9486_-14-9485d others(4): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116689559 | |||||
| chr7:116689559
|
CTTT | C | 14 | a0001c0004t0002g0157a0001c0004t0002g0158a0001c0004t0008g0190others(11): Show | 14 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-14-9487_-14-9485d others(5): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116689559 | |||||
| chr7:116689559
|
CTTTT | C | 10 | a0001c0001t0005g0085a0001c0001t0007g0025a0001c0001t0007g0172others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-9488_-14-9485d others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116689559 | |||||
| chr7:116689559
|
CTTTTT | C | 78 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0003g0033others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.-14-9489_-14-9485d others(7): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116689559 | |||||
| chr7:116689603
|
C | T | 3 | a0001c0003t0003g0084a0001c0003t0006g0153a0001c0017t0003g0083 | 3 | NA18973.hp1 NA18974.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-14-9468C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116689603 | ||||||
| chr7:116689802
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-14-9269G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116689802 | ||||||
| chr7:116689929
|
C | T | 28 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0005g0192others(25): Show | 28 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14-9142C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116689929 | ||||||
| chr7:116689965
|
G | A | 32 | a0001c0004t0002g0145a0001c0004t0002g0157a0001c0004t0002g0158others(29): Show | 32 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-9106G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116689965 | ||||||
| chr7:116690053
|
T | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-9018T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116690053 | ||||||
| chr7:116690106
|
C | A | 6 | a0001c0001t0007g0025a0001c0001t0007g0172a0001c0001t0007g0260others(3): Show | 6 | HG01496.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8965C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116690106 | ||||||
| chr7:116690305
|
G | A | 1 | a0001c0002t0004g0276 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-14-8766G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116690305 | ||||||
| chr7:116690505
|
G | C | 2 | a0001c0004t0002g0157a0001c0004t0002g0158 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-14-8566G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116690505 | ||||||
| chr7:116690756
|
CCTGTTAT others(3): Show |
C | 1 | a0001c0001t0015g0156 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-14-8313_-14-8304d others(12): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116690756 | |||||
| chr7:116690824
|
C | T | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-8247C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116690824 | ||||||
| chr7:116690978
|
C | T | 2 | a0001c0002t0001g0272a0001c0002t0001g0273 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-14-8093C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116690978 | ||||||
| chr7:116691047
|
C | A | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-8024C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116691047 | ||||||
| chr7:116691316
|
C | T | 108 | a0001c0001t0002g0134a0001c0001t0005g0052a0001c0001t0008g0220others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-14-7755C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116691316 | ||||||
| chr7:116691458
|
C | T | 1 | a0001c0003t0006g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-14-7613C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116691458 | ||||||
| chr7:116691475
|
A | T | 2 | a0001c0002t0001g0122a0001c0002t0001g0126 | 2 | HG02735.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-14-7596A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116691475 | ||||||
| chr7:116691835
|
C | G | 32 | a0001c0004t0002g0145a0001c0004t0002g0157a0001c0004t0002g0158others(29): Show | 32 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-7236C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116691835 | ||||||
| chr7:116691975
|
G | A | 4 | a0001c0001t0002g0274a0001c0001t0002g0322a0001c0001t0002g0323others(1): Show | 4 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-7096G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116691975 | ||||||
| chr7:116692091
|
G | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-6980G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692091 | ||||||
| chr7:116692143
|
A | G | 123 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.-14-6928A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692143 | ||||||
| chr7:116692177
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-6894T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692177 | ||||||
| chr7:116692178
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-6893G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692178 | ||||||
| chr7:116692194
|
A | G | 2 | a0001c0003t0009g0264a0001c0003t0009g0265 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-6877A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692194 | ||||||
| chr7:116692228
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-6843G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692228 | ||||||
| chr7:116692262
|
A | G | 2 | a0001c0001t0005g0160a0008c0014t0001g0217 | 2 | HG02965.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-14-6809A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692262 | ||||||
| chr7:116692270
|
T | A | 91 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.-14-6801T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692270 | ||||||
| chr7:116692355
|
G | A | 1 | a0001c0005t0007g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-6716G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692355 | ||||||
| chr7:116692433
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-6638A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692433 | ||||||
| chr7:116692485
|
C | G | 255 | a0001c0001t0002g0031a0001c0001t0002g0134a0001c0001t0002g0162others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-14-6586C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692485 | ||||||
| chr7:116692739
|
C | G | 5 | a0001c0001t0005g0174a0001c0001t0005g0183a0001c0001t0005g0184others(2): Show | 5 | HG00323.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-6332C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116692739 | ||||||
| chr7:116693105
|
G | T | 1 | a0001c0001t0005g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-14-5966G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693105 | ||||||
| chr7:116693283
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-5788C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693283 | ||||||
| chr7:116693333
|
G | A | 32 | a0001c0004t0002g0145a0001c0004t0002g0157a0001c0004t0002g0158others(29): Show | 32 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-5738G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693333 | ||||||
| chr7:116693435
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-5636A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693435 | ||||||
| chr7:116693565
|
C | G | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG01169.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-14-5506C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693565 | ||||||
| chr7:116693655
|
A | G | 4 | a0001c0002t0001g0090a0001c0002t0004g0238a0001c0002t0004g0245others(1): Show | 4 | HG01168.hp2 HG01433.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-5416A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693655 | ||||||
| chr7:116693725
|
T | A | 1 | a0001c0004t0002g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14-5346T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693725 | ||||||
| chr7:116693744
|
G | C | 1 | a0001c0005t0010g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-14-5327G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693744 | ||||||
| chr7:116693953
|
A | G | 1 | a0001c0019t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-14-5118A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693953 | ||||||
| chr7:116693990
|
G | T | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-5081G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116693990 | ||||||
| chr7:116694004
|
G | A | 91 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.-14-5067G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694004 | ||||||
| chr7:116694078
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-4993A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694078 | ||||||
| chr7:116694085
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-14-4986G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694085 | ||||||
| chr7:116694255
|
T | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-4816T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694255 | ||||||
| chr7:116694623
|
C | T | 10 | a0001c0002t0004g0152a0001c0002t0004g0275a0001c0002t0004g0276others(7): Show | 10 | HG00621.hp2 HG02080.hp1 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-4448C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694623 | ||||||
| chr7:116694639
|
A | G | 1 | a0001c0002t0004g0291 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-14-4432A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694639 | ||||||
| chr7:116694690
|
T | C | 5 | a0001c0007t0009g0251a0001c0007t0009g0253a0001c0007t0009g0254others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-4381T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694690 | ||||||
| chr7:116694734
|
T | C | 1 | a0002c0006t0007g0003 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-14-4337T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694734 | ||||||
| chr7:116694921
|
G | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-14-4150G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116694921 | ||||||
| chr7:116695004
|
G | T | 4 | a0001c0001t0008g0220a0001c0001t0008g0221a0001c0002t0001g0019others(1): Show | 4 | HG00558.hp2 HG01192.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-4067G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695004 | ||||||
| chr7:116695023
|
G | A | 1 | a0001c0005t0010g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-14-4048G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695023 | ||||||
| chr7:116695055
|
G | A | 18 | a0001c0005t0002g0143a0001c0005t0006g0007a0001c0005t0006g0129others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14-4016G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695055 | ||||||
| chr7:116695140
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-3931A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695140 | ||||||
| chr7:116695154
|
A | G | 1 | a0001c0001t0005g0228 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-14-3917A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695154 | ||||||
| chr7:116695308
|
C | A | 12 | a0001c0004t0003g0195a0001c0004t0018g0256a0002c0006t0007g0003others(9): Show | 12 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.-14-3763C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695308 | ||||||
| chr7:116695414
|
C | G | 1 | a0001c0002t0001g0056 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-14-3657C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695414 | ||||||
| chr7:116695447
|
C | A | 1 | a0011c0023t0007g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-14-3624C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695447 | ||||||
| chr7:116695455
|
G | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-3616G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695455 | ||||||
| chr7:116695594
|
C | T | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-3477C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695594 | ||||||
| chr7:116695615
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-3456G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695615 | ||||||
| chr7:116695713
|
C | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-3358C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695713 | ||||||
| chr7:116695752
|
T | G | 1 | a0001c0002t0004g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-14-3319T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695752 | ||||||
| chr7:116695757
|
A | T | 28 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0005g0192others(25): Show | 28 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14-3314A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695757 | ||||||
| chr7:116695774
|
G | C | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-14-3297G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695774 | ||||||
| chr7:116695959
|
G | A | 55 | a0001c0001t0005g0085a0001c0001t0005g0228a0001c0001t0008g0081others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.-14-3112G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116695959 | ||||||
| chr7:116696050
|
G | A | 5 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-3021G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696050 | ||||||
| chr7:116696062
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-3009G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696062 | ||||||
| chr7:116696263
|
A | ACCCACTG others(3): Show |
1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-2806_-14-2805i others(12): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr7 | 116696263 | |||||
| chr7:116696329
|
G | A | 1 | a0001c0002t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-14-2742G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696329 | ||||||
| chr7:116696544
|
C | A | 2 | a0001c0001t0007g0313a0001c0001t0008g0188 | 2 | HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-14-2527C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696544 | ||||||
| chr7:116696548
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-2523A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696548 | ||||||
| chr7:116696648
|
C | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-2423C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696648 | ||||||
| chr7:116696768
|
G | A | 1 | a0001c0002t0004g0238 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2303G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696768 | ||||||
| chr7:116696789
|
A | G | 5 | a0001c0001t0002g0162a0003c0009t0007g0008a0003c0009t0007g0009others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-2282A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696789 | ||||||
| chr7:116696826
|
T | C | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-2245T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696826 | ||||||
| chr7:116696893
|
C | T | 105 | a0001c0001t0002g0134a0001c0001t0005g0052a0001c0001t0008g0220others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-14-2178C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696893 | ||||||
| chr7:116696894
|
G | A | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-2177G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116696894 | ||||||
| chr7:116697090
|
G | A | 91 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.-14-1981G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697090 | ||||||
| chr7:116697200
|
G | A | 1 | a0001c0004t0003g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-14-1871G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697200 | ||||||
| chr7:116697298
|
T | G | 123 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.-14-1773T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697298 | ||||||
| chr7:116697448
|
T | C | 1 | a0001c0002t0001g0099 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-14-1623T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697448 | ||||||
| chr7:116697595
|
G | A | 20 | a0001c0002t0001g0090a0001c0002t0001g0122a0001c0002t0001g0126others(17): Show | 20 | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-1476G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697595 | ||||||
| chr7:116697627
|
T | C | 1 | a0001c0001t0008g0058 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-14-1444T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697627 | ||||||
| chr7:116697728
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-1343C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697728 | ||||||
| chr7:116697925
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-1146A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697925 | ||||||
| chr7:116697943
|
C | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0249a0001c0001t0002g0250others(38): Show | 41 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-14-1128C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697943 | ||||||
| chr7:116697943
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-1128C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116697943 | ||||||
| chr7:116698266
|
A | C | 1 | a0001c0005t0006g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-14-805A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116698266 | ||||||
| chr7:116698604
|
A | G | 32 | a0001c0004t0002g0145a0001c0004t0002g0157a0001c0004t0002g0158others(29): Show | 32 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-467A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116698604 | ||||||
| chr7:116698973
|
G | A | 1 | a0001c0001t0005g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-14-98G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116698973 | ||||||
| chr7:116699067
|
G | A | 2 | a0001c0004t0002g0157a0001c0004t0002g0158 | 2 | HG02559.hp2 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.-14-4G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 1/20 | chr7 | 116699067 | ||||||
| chr7:116700477
|
A | AT | 91 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1200+193_1200+194i others(3): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116700477 | ||||||
| chr7:116700528
|
A | C | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1200+244A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116700528 | ||||||
| chr7:116700761
|
T | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+477T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116700761 | ||||||
| chr7:116700773
|
T | A | 3 | a0001c0005t0006g0154a0001c0005t0006g0155a0001c0005t0007g0146 | 3 | HG01243.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1200+489T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116700773 | ||||||
| chr7:116701043
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+759G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701043 | ||||||
| chr7:116701247
|
C | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+963C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701247 | ||||||
| chr7:116701267
|
T | C | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1200+983T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701267 | ||||||
| chr7:116701329
|
A | G | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1200+1045A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701329 | ||||||
| chr7:116701434
|
G | A | 91 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1200+1150G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701434 | ||||||
| chr7:116701700
|
T | G | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1200+1416T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701700 | ||||||
| chr7:116701857
|
A | G | 3 | a0001c0002t0004g0235a0001c0002t0004g0337a0001c0002t0004g0338 | 3 | HG03492.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1200+1573A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701857 | ||||||
| chr7:116701935
|
G | A | 1 | a0001c0002t0004g0245 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1200+1651G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701935 | ||||||
| chr7:116701995
|
A | T | 2 | a0001c0004t0023g0027a0001c0004t0030g0197 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1200+1711A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116701995 | ||||||
| chr7:116702125
|
G | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+1841G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702125 | ||||||
| chr7:116702226
|
G | A | 28 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0005g0192others(25): Show | 28 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1200+1942G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702226 | ||||||
| chr7:116702285
|
G | A | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1200+2001G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702285 | ||||||
| chr7:116702363
|
A | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+2079A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702363 | ||||||
| chr7:116702419
|
C | G | 1 | a0001c0001t0002g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1200+2135C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702419 | ||||||
| chr7:116702537
|
T | C | 15 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(12): Show | 15 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1200+2253T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702537 | ||||||
| chr7:116702543
|
G | A | 1 | a0001c0003t0003g0051 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1200+2259G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702543 | ||||||
| chr7:116702573
|
G | T | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1200+2289G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702573 | ||||||
| chr7:116702921
|
C | T | 2 | a0001c0003t0003g0164a0001c0003t0006g0340 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1200+2637C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702921 | ||||||
| chr7:116702934
|
CCTGA | C | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0004g0161 | 3 | NA18968.hp2 NA18995.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1200+2653_1200+265 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116702934 | |||||
| chr7:116702940
|
T | C | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0004g0161 | 3 | NA18968.hp2 NA18995.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1200+2656T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702940 | ||||||
| chr7:116702948
|
T | C | 1 | a0002c0006t0008g0113 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1200+2664T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116702948 | ||||||
| chr7:116703086
|
G | A | 32 | a0001c0004t0002g0145a0001c0004t0002g0157a0001c0004t0002g0158others(29): Show | 32 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1200+2802G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703086 | ||||||
| chr7:116703141
|
T | A | 2 | a0005c0012t0006g0028a0005c0012t0006g0257 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1200+2857T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703141 | ||||||
| chr7:116703263
|
G | C | 2 | a0001c0001t0002g0249a0001c0001t0002g0250 | 2 | HG01433.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1200+2979G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703263 | ||||||
| chr7:116703284
|
A | C | 111 | a0001c0001t0002g0134a0001c0001t0002g0308a0001c0001t0002g0332others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1200+3000A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703284 | ||||||
| chr7:116703378
|
CT | C | 3 | a0001c0004t0002g0248a0001c0004t0023g0027a0001c0004t0030g0197 | 3 | HG02109.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1200+3097delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116703378 | |||||
| chr7:116703459
|
T | C | 5 | a0001c0002t0004g0237a0001c0002t0004g0240a0001c0002t0004g0283others(2): Show | 5 | HG00639.hp1 HG03704.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+3175T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703459 | ||||||
| chr7:116703462
|
A | G | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1200+3178A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703462 | ||||||
| chr7:116703467
|
A | T | 1 | a0001c0003t0003g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1200+3183A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703467 | ||||||
| chr7:116703591
|
T | C | 1 | a0001c0002t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1200+3307T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703591 | ||||||
| chr7:116703705
|
A | T | 1 | a0001c0007t0009g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1200+3421A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703705 | ||||||
| chr7:116703812
|
T | G | 32 | a0001c0004t0002g0145a0001c0004t0002g0157a0001c0004t0002g0158others(29): Show | 32 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1200+3528T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116703812 | ||||||
| chr7:116704044
|
T | C | 92 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1200+3760T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704044 | ||||||
| chr7:116704256
|
C | T | 25 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0005g0192others(22): Show | 25 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1200+3972C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704256 | ||||||
| chr7:116704305
|
T | A | 2 | a0005c0012t0006g0028a0005c0012t0006g0257 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1200+4021T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704305 | ||||||
| chr7:116704384
|
G | A | 3 | a0001c0001t0002g0308a0001c0002t0001g0163a0001c0003t0003g0169 | 3 | HG02602.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1200+4100G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704384 | ||||||
| chr7:116704395
|
T | A | 1 | a0001c0003t0003g0063 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1200+4111T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704395 | ||||||
| chr7:116704490
|
G | A | 2 | a0001c0004t0003g0195a0001c0004t0018g0256 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1200+4206G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704490 | ||||||
| chr7:116704529
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+4245G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704529 | ||||||
| chr7:116704639
|
TA | T | 91 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1200+4356delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704639 | ||||||
| chr7:116704657
|
G | A | 90 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0171others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1200+4373G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704657 | ||||||
| chr7:116704709
|
G | T | 1 | a0001c0001t0002g0296 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1200+4425G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704709 | ||||||
| chr7:116704846
|
G | T | 1 | a0001c0003t0006g0299 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1200+4562G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704846 | ||||||
| chr7:116704994
|
G | A | 7 | a0001c0005t0010g0136a0001c0005t0010g0289a0001c0007t0009g0251others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+4710G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116704994 | ||||||
| chr7:116705120
|
T | C | 1 | a0001c0002t0001g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1200+4836T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705120 | ||||||
| chr7:116705253
|
C | T | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1200+4969C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705253 | ||||||
| chr7:116705506
|
T | C | 1 | a0001c0001t0005g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1200+5222T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705506 | ||||||
| chr7:116705722
|
A | C | 49 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0308others(46): Show | 49 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1200+5438A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705722 | ||||||
| chr7:116705742
|
T | C | 8 | a0001c0005t0006g0007a0001c0005t0006g0129a0001c0005t0006g0135others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+5458T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705742 | ||||||
| chr7:116705749
|
C | A | 1 | a0001c0004t0003g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1200+5465C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705749 | ||||||
| chr7:116705777
|
C | T | 2 | a0005c0012t0006g0028a0005c0012t0006g0257 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1200+5493C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705777 | ||||||
| chr7:116705782
|
G | A | 2 | a0001c0004t0002g0157a0001c0004t0002g0158 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1200+5498G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705782 | ||||||
| chr7:116705835
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+5551C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705835 | ||||||
| chr7:116705905
|
G | A | 4 | a0001c0001t0002g0031a0001c0001t0005g0192a0001c0001t0005g0193others(1): Show | 4 | HG00099.hp2 HG00741.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5621G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705905 | ||||||
| chr7:116705964
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+5680C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116705964 | ||||||
| chr7:116706060
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1200+5776A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116706060 | ||||||
| chr7:116706218
|
C | T | 15 | a0001c0001t0008g0165a0001c0001t0008g0168a0001c0005t0010g0136others(12): Show | 15 | HG00438.hp1 HG00544.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1200+5934C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116706218 | ||||||
| chr7:116706469
|
T | C | 1 | a0001c0002t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1200+6185T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116706469 | ||||||
| chr7:116706535
|
T | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+6251T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116706535 | ||||||
| chr7:116706549
|
G | A | 114 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1200+6265G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116706549 | ||||||
| chr7:116706687
|
C | G | 1 | a0001c0002t0001g0230 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1200+6403C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116706687 | ||||||
| chr7:116706800
|
G | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+6516G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116706800 | ||||||
| chr7:116706888
|
A | AT | 125 | a0001c0001t0002g0162a0001c0001t0002g0308a0001c0001t0005g0097others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1200+6623dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116706888 | |||||
| chr7:116706888
|
A | ATT | 7 | a0001c0001t0007g0025a0001c0001t0007g0260a0001c0001t0007g0262others(4): Show | 7 | HG01496.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+6622_1200+662 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116706888 | |||||
| chr7:116706888
|
AT | A | 20 | a0001c0001t0002g0031a0001c0001t0002g0141a0001c0001t0002g0325others(17): Show | 20 | HG00609.hp1 HG01069.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1200+6623delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116706888 | |||||
| chr7:116706888
|
ATT | A | 6 | a0001c0001t0002g0334a0001c0005t0010g0136a0001c0005t0010g0289others(3): Show | 6 | HG02615.hp2 HG02886.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+6622_1200+662 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116706888 | |||||
| chr7:116706929
|
A | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+6645A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116706929 | ||||||
| chr7:116707102
|
T | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+6818T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707102 | ||||||
| chr7:116707194
|
A | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+6910A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707194 | ||||||
| chr7:116707213
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+6929C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707213 | ||||||
| chr7:116707290
|
C | CA | 5 | a0001c0001t0005g0166a0001c0001t0005g0192a0001c0001t0008g0168others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+7015dupA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116707290 | |||||
| chr7:116707357
|
A | C | 3 | a0001c0001t0002g0141a0001c0004t0002g0157a0001c0004t0002g0158 | 3 | HG02559.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1200+7073A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707357 | ||||||
| chr7:116707426
|
A | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+7142A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707426 | ||||||
| chr7:116707625
|
T | C | 1 | a0001c0001t0008g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1200+7341T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707625 | ||||||
| chr7:116707644
|
T | C | 1 | a0001c0001t0008g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1200+7360T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707644 | ||||||
| chr7:116707646
|
C | T | 1 | a0001c0001t0008g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1200+7362C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707646 | ||||||
| chr7:116707791
|
G | A | 3 | a0001c0005t0007g0146a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG01243.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1200+7507G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707791 | ||||||
| chr7:116707960
|
T | G | 1 | a0001c0001t0008g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1200+7676T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116707960 | ||||||
| chr7:116708053
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1200+7769T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116708053 | ||||||
| chr7:116708256
|
C | T | 3 | a0001c0004t0002g0248a0001c0004t0023g0027a0001c0004t0030g0197 | 3 | HG02109.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1200+7972C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116708256 | ||||||
| chr7:116708375
|
C | A | 1 | a0001c0001t0002g0249 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1200+8091C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116708375 | ||||||
| chr7:116708781
|
A | T | 1 | a0001c0001t0008g0168 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1200+8497A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116708781 | ||||||
| chr7:116708861
|
G | A | 2 | a0001c0003t0003g0225a0001c0003t0006g0299 | 2 | NA18965.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1200+8577G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116708861 | ||||||
| chr7:116709062
|
G | T | 1 | a0001c0005t0010g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1200+8778G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116709062 | ||||||
| chr7:116709317
|
A | G | 1 | a0001c0001t0002g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1200+9033A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116709317 | ||||||
| chr7:116709428
|
A | G | 1 | a0001c0002t0004g0292 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1200+9144A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116709428 | ||||||
| chr7:116709653
|
T | G | 2 | a0001c0002t0001g0272a0001c0002t0001g0273 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1200+9369T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116709653 | ||||||
| chr7:116709704
|
G | T | 1 | a0001c0007t0009g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1200+9420G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116709704 | ||||||
| chr7:116710590
|
T | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+10306T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116710590 | ||||||
| chr7:116710647
|
C | T | 1 | a0007c0016t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1200+10363C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116710647 | ||||||
| chr7:116711078
|
G | A | 15 | a0001c0001t0002g0004a0001c0001t0005g0105a0001c0001t0005g0111others(12): Show | 15 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1200+10794G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116711078 | ||||||
| chr7:116711164
|
C | T | 4 | a0001c0003t0003g0084a0001c0003t0006g0153a0001c0003t0006g0285others(1): Show | 4 | NA18973.hp1 NA18974.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+10880C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116711164 | ||||||
| chr7:116711279
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1200+10995T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116711279 | ||||||
| chr7:116711388
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+11104T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116711388 | ||||||
| chr7:116711869
|
G | A | 1 | a0001c0004t0002g0248 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1200+11585G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116711869 | ||||||
| chr7:116712585
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1200+12301C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116712585 | ||||||
| chr7:116713024
|
T | A | 1 | a0001c0001t0005g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1200+12740T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713024 | ||||||
| chr7:116713075
|
G | A | 1 | a0001c0002t0004g0017 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1200+12791G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713075 | ||||||
| chr7:116713159
|
G | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+12875G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713159 | ||||||
| chr7:116713160
|
C | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+12876C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713160 | ||||||
| chr7:116713222
|
C | T | 3 | a0001c0001t0008g0220a0001c0002t0001g0019a0001c0002t0001g0216 | 3 | HG00558.hp2 HG01192.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1200+12938C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713222 | ||||||
| chr7:116713301
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+13017A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713301 | ||||||
| chr7:116713311
|
C | A | 19 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(16): Show | 19 | HG00673.hp2 HG01256.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1200+13027C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713311 | ||||||
| chr7:116713311
|
C | T | 1 | a0004c0011t0002g0319 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1200+13027C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713311 | ||||||
| chr7:116713373
|
C | T | 1 | a0001c0001t0008g0208 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1200+13089C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713373 | ||||||
| chr7:116713394
|
C | CA | 25 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(22): Show | 25 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.1200+13126dupA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116713394 | |||||
| chr7:116713394
|
CA | C | 14 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0014others(11): Show | 14 | HG02055.hp2 HG02258.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1200+13126delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116713394 | |||||
| chr7:116713740
|
G | A | 1 | a0001c0001t0007g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1200+13456G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713740 | ||||||
| chr7:116713791
|
A | C | 1 | a0001c0002t0001g0199 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1200+13507A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713791 | ||||||
| chr7:116713809
|
G | A | 3 | a0001c0002t0001g0199a0001c0002t0001g0209a0001c0002t0001g0211 | 3 | HG00323.hp1 HG00408.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1200+13525G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116713809 | ||||||
| chr7:116714158
|
C | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+13874C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116714158 | ||||||
| chr7:116714365
|
A | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+14081A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116714365 | ||||||
| chr7:116714471
|
T | A | 146 | a0001c0001t0002g0162a0001c0001t0002g0308a0001c0001t0006g0144others(143): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1200+14187T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116714471 | ||||||
| chr7:116714587
|
C | T | 8 | a0001c0005t0006g0007a0001c0005t0006g0129a0001c0005t0006g0135others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+14303C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116714587 | ||||||
| chr7:116714745
|
G | GCA | 154 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(151): Show | 154 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1200+14492_1200+14 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116714745 | |||||
| chr7:116714745
|
G | GCACA | 17 | a0001c0001t0007g0025a0001c0001t0007g0260a0001c0001t0007g0262others(14): Show | 17 | HG01243.hp1 HG01496.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1200+14490_1200+14 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116714745 | |||||
| chr7:116714745
|
GCA | G | 5 | a0001c0001t0002g0332a0001c0001t0006g0311a0001c0002t0001g0210others(2): Show | 5 | HG00733.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+14492_1200+14 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116714745 | |||||
| chr7:116714745
|
GCACA | G | 5 | a0001c0001t0005g0052a0001c0004t0003g0048a0001c0004t0003g0050others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+14490_1200+14 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116714745 | |||||
| chr7:116714747
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+14463A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116714747 | ||||||
| chr7:116714983
|
A | G | 1 | a0001c0002t0004g0316 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1200+14699A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116714983 | ||||||
| chr7:116715050
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+14766T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715050 | ||||||
| chr7:116715242
|
T | C | 109 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1200+14958T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715242 | ||||||
| chr7:116715428
|
G | C | 1 | a0001c0003t0009g0264 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1200+15144G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715428 | ||||||
| chr7:116715474
|
T | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+15190T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715474 | ||||||
| chr7:116715558
|
A | AC | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1200+15275dupC | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116715558 | |||||
| chr7:116715562
|
T | A | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1200+15278T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715562 | ||||||
| chr7:116715563
|
C | T | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1200+15279C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715563 | ||||||
| chr7:116715564
|
C | T | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1200+15280C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715564 | ||||||
| chr7:116715565
|
A | T | 22 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(19): Show | 22 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1200+15281A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715565 | ||||||
| chr7:116715688
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+15404G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715688 | ||||||
| chr7:116715712
|
C | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200+15428C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715712 | ||||||
| chr7:116715873
|
C | T | 2 | a0001c0001t0002g0004a0001c0004t0002g0145 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1200+15589C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116715873 | ||||||
| chr7:116716022
|
G | C | 261 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(258): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1201-15646G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716022 | ||||||
| chr7:116716026
|
G | A | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(13): Show | 16 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1201-15642G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716026 | ||||||
| chr7:116716150
|
G | A | 15 | a0001c0001t0002g0004a0001c0001t0005g0105a0001c0001t0005g0111others(12): Show | 15 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1201-15518G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716150 | ||||||
| chr7:116716274
|
AGGGAGAG others(3): Show |
A | 1 | a0001c0008t0005g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1201-15392_1201-15 others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716274 | |||||
| chr7:116716276
|
G | GGAGAGAG others(13): Show |
1 | a0001c0002t0001g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1201-15385_1201-15 others(26): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716276 | |||||
| chr7:116716283
|
GGGAGAGA others(4): Show |
G | 1 | a0001c0005t0006g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1201-15383_1201-15 others(17): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716283 | |||||
| chr7:116716284
|
G | A | 3 | a0001c0001t0002g0296a0001c0001t0002g0308a0001c0002t0001g0163 | 3 | HG02602.hp1 HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1201-15384G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716284 | ||||||
| chr7:116716284
|
G | GAGAGAGA others(10): Show |
1 | a0001c0001t0002g0005 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1201-15384_1201-15 others(23): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716284 | ||||||
| chr7:116716284
|
G | GGA | 33 | a0001c0001t0002g0031a0001c0001t0002g0305a0001c0001t0005g0038others(30): Show | 33 | HG00323.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1201-15331_1201-15 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGAGA | 34 | a0001c0001t0002g0141a0001c0001t0002g0249a0001c0001t0002g0250others(31): Show | 34 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.1201-15333_1201-15 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGAGAGA | 20 | a0001c0001t0002g0328a0001c0001t0005g0045a0001c0001t0005g0062others(17): Show | 20 | HG00741.hp1 HG01361.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.1201-15335_1201-15 others(12): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGAGAGAG others(1): Show |
10 | a0001c0001t0005g0036a0001c0001t0005g0194a0001c0003t0003g0065others(7): Show | 10 | HG01069.hp2 HG01070.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1201-15337_1201-15 others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGAGAGAG others(3): Show |
5 | a0001c0002t0001g0088a0001c0002t0004g0131a0001c0003t0003g0076others(2): Show | 5 | HG03654.hp1 NA18612.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-15339_1201-15 others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGAGAGAG others(5): Show |
4 | a0001c0002t0001g0222a0001c0003t0003g0077a0001c0003t0003g0103others(1): Show | 4 | HG02040.hp1 HG02523.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-15341_1201-15 others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGAGAGAG others(7): Show |
2 | a0001c0002t0001g0089a0001c0003t0003g0078 | 2 | HG00140.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1201-15343_1201-15 others(20): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGAGAGAG others(9): Show |
2 | a0001c0001t0005g0192a0001c0003t0003g0079 | 2 | HG00741.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1201-15345_1201-15 others(22): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGAGAGAG others(13): Show |
1 | a0001c0003t0003g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1201-15349_1201-15 others(26): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGGGAGAG others(7): Show |
3 | a0001c0003t0003g0084a0001c0003t0006g0285a0001c0017t0003g0083 | 3 | NA18974.hp2 NA19010.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1201-15383_1201-15 others(20): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
G | GGGGAGAG others(17): Show |
1 | a0001c0003t0006g0153 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1201-15383_1201-15 others(30): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGA | G | 33 | a0001c0001t0002g0002a0001c0001t0002g0140a0001c0001t0002g0324others(30): Show | 33 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1201-15331_1201-15 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGA | G | 35 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0304others(32): Show | 35 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1201-15333_1201-15 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGAGA | G | 21 | a0001c0001t0002g0317a0001c0001t0002g0329a0001c0001t0005g0105others(18): Show | 21 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1201-15335_1201-15 others(12): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGAGAG others(1): Show |
G | 18 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0162others(15): Show | 18 | HG01433.hp1 HG02451.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-15337_1201-15 others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGAGAG others(3): Show |
G | 4 | a0001c0001t0008g0058a0001c0002t0001g0054a0001c0002t0001g0179others(1): Show | 4 | HG02015.hp1 HG03139.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-15339_1201-15 others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGAGAG others(5): Show |
G | 10 | a0001c0001t0002g0004a0001c0001t0002g0332a0001c0001t0005g0160others(7): Show | 10 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1201-15341_1201-15 others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGAGAG others(7): Show |
G | 12 | a0001c0001t0002g0137a0001c0001t0002g0325a0001c0001t0002g0326others(9): Show | 12 | HG00280.hp1 HG00642.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-15343_1201-15 others(20): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGAGAG others(9): Show |
G | 7 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1201-15345_1201-15 others(22): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGAGAG others(11): Show |
G | 4 | a0001c0004t0003g0195a0001c0005t0025g0181a0003c0009t0010g0010others(1): Show | 4 | HG02109.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-15347_1201-15 others(24): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716284
|
GGAGAGAG others(15): Show |
G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-15351_1201-15 others(28): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716284 | |||||
| chr7:116716286
|
A | G | 1 | a0001c0005t0006g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1201-15382A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716286 | ||||||
| chr7:116716327
|
GAGAGAGA others(5): Show |
G | 3 | a0001c0001t0003g0033a0001c0001t0006g0261a0001c0001t0015g0156 | 3 | HG02145.hp2 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1201-15339_1201-15 others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716327 | |||||
| chr7:116716334
|
A | AGAGAGAG others(3): Show |
1 | a0001c0003t0003g0080 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1201-15330_1201-15 others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716334 | |||||
| chr7:116716337
|
GA | G | 5 | a0001c0001t0002g0296a0001c0001t0005g0096a0001c0001t0005g0098others(2): Show | 5 | HG00438.hp2 HG02698.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1201-15327delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716337 | |||||
| chr7:116716338
|
A | AG | 3 | a0001c0001t0002g0306a0001c0001t0008g0200a0001c0003t0006g0239 | 3 | HG00639.hp1 HG02896.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1201-15330_1201-15 others(7): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716338 | ||||||
| chr7:116716338
|
A | AGAGAGAG others(10): Show |
1 | a0006c0013t0002g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1201-15330_1201-15 others(23): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716338 | ||||||
| chr7:116716339
|
A | G | 1 | a0001c0005t0006g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1201-15329A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716339 | ||||||
| chr7:116716346
|
C | T | 1 | a0001c0003t0003g0270 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1201-15322C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716346 | ||||||
| chr7:116716467
|
G | A | 2 | a0001c0002t0001g0215a0001c0004t0012g0127 | 2 | HG06807.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1201-15201G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716467 | ||||||
| chr7:116716467
|
G | GAGAA | 41 | a0001c0001t0002g0012a0001c0001t0002g0031a0001c0001t0002g0141others(38): Show | 41 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1201-15132_1201-15 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716467
|
G | GAGAAAGA others(1): Show |
8 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0089others(5): Show | 8 | HG00639.hp2 HG01346.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201-15136_1201-15 others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716467
|
GAGAA | G | 78 | a0001c0001t0002g0004a0001c0001t0002g0293a0001c0001t0002g0294others(75): Show | 78 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1201-15132_1201-15 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716467
|
GAGAAAGA others(1): Show |
G | 63 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(60): Show | 63 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1201-15136_1201-15 others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716467
|
GAGAAAGA others(5): Show |
G | 33 | a0001c0001t0002g0015a0001c0001t0002g0137a0001c0001t0002g0140others(30): Show | 33 | HG00323.hp2 HG00673.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1201-15140_1201-15 others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716467
|
GAGAAAGA others(9): Show |
G | 12 | a0001c0001t0002g0303a0001c0001t0002g0306a0001c0001t0005g0034others(9): Show | 12 | HG00280.hp2 HG00609.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-15144_1201-15 others(22): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716467
|
GAGAAAGA others(13): Show |
G | 7 | a0001c0001t0002g0005a0001c0001t0007g0331a0001c0001t0026g0205others(4): Show | 7 | HG02135.hp2 HG03516.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1201-15148_1201-15 others(26): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716467
|
GAGAAAGA others(17): Show |
G | 3 | a0001c0001t0005g0174a0001c0001t0005g0184a0002c0010t0001g0116 | 3 | HG00438.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1201-15152_1201-15 others(30): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716467
|
GAGAAAGA others(25): Show |
G | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1201-15160_1201-15 others(38): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716467 | |||||
| chr7:116716471
|
A | G | 1 | a0001c0001t0007g0286 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1201-15197A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716471 | ||||||
| chr7:116716521
|
G | GAAAGAA | 3 | a0001c0001t0005g0085a0001c0003t0003g0063a0001c0003t0003g0169 | 3 | HG02735.hp1 HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1201-15145_1201-15 others(12): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116716521 | |||||
| chr7:116716543
|
A | G | 1 | a0001c0001t0008g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1201-15125A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716543 | ||||||
| chr7:116716624
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-15044G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716624 | ||||||
| chr7:116716659
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-15009T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716659 | ||||||
| chr7:116716902
|
C | T | 1 | a0001c0002t0004g0318 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1201-14766C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716902 | ||||||
| chr7:116716913
|
C | T | 1 | a0002c0006t0008g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1201-14755C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716913 | ||||||
| chr7:116716936
|
A | G | 1 | a0001c0002t0004g0297 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1201-14732A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116716936 | ||||||
| chr7:116717157
|
C | T | 103 | a0001c0001t0002g0308a0001c0001t0008g0220a0001c0002t0001g0018others(100): Show | 103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1201-14511C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116717157 | ||||||
| chr7:116717244
|
A | G | 4 | a0001c0001t0003g0033a0001c0001t0006g0261a0001c0001t0015g0156others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-14424A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116717244 | ||||||
| chr7:116717314
|
A | G | 94 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1201-14354A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116717314 | ||||||
| chr7:116717481
|
T | C | 5 | a0001c0005t0006g0007a0001c0005t0006g0129a0001c0005t0006g0135others(2): Show | 5 | HG02451.hp1 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-14187T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116717481 | ||||||
| chr7:116717486
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1201-14182A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116717486 | ||||||
| chr7:116717705
|
C | T | 3 | a0001c0003t0003g0269a0001c0003t0003g0270a0001c0003t0003g0271 | 3 | HG03490.hp2 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1201-13963C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116717705 | ||||||
| chr7:116717795
|
C | G | 1 | a0001c0001t0002g0137 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1201-13873C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116717795 | ||||||
| chr7:116717990
|
A | G | 146 | a0001c0001t0002g0162a0001c0001t0002g0308a0001c0001t0006g0144others(143): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1201-13678A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116717990 | ||||||
| chr7:116718059
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-13609C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116718059 | ||||||
| chr7:116718180
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-13488G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116718180 | ||||||
| chr7:116718258
|
G | A | 1 | a0001c0001t0006g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1201-13410G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116718258 | ||||||
| chr7:116718364
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-13304G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116718364 | ||||||
| chr7:116718381
|
C | A | 2 | a0001c0003t0003g0164a0001c0003t0006g0340 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1201-13287C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116718381 | ||||||
| chr7:116718433
|
T | A | 261 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(258): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1201-13235T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116718433 | ||||||
| chr7:116718506
|
T | A | 1 | a0001c0002t0004g0292 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1201-13162T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116718506 | ||||||
| chr7:116718928
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1201-12740T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116718928 | ||||||
| chr7:116719021
|
C | T | 1 | a0001c0003t0003g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1201-12647C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719021 | ||||||
| chr7:116719249
|
A | G | 2 | a0004c0011t0002g0319a0004c0011t0019g0330 | 2 | NA18747.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1201-12419A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719249 | ||||||
| chr7:116719313
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-12355A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719313 | ||||||
| chr7:116719319
|
C | T | 1 | a0001c0003t0006g0321 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1201-12349C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719319 | ||||||
| chr7:116719409
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-12259G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719409 | ||||||
| chr7:116719475
|
C | T | 2 | a0001c0002t0004g0300a0001c0002t0004g0301 | 2 | NA19055.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1201-12193C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719475 | ||||||
| chr7:116719499
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-12169T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719499 | ||||||
| chr7:116719528
|
C | T | 1 | a0001c0002t0004g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1201-12140C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719528 | ||||||
| chr7:116719663
|
T | C | 1 | a0001c0002t0004g0336 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1201-12005T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719663 | ||||||
| chr7:116719702
|
C | A | 2 | a0001c0002t0004g0318a0001c0018t0017g0029 | 2 | HG02135.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1201-11966C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719702 | ||||||
| chr7:116719805
|
T | C | 3 | a0001c0003t0003g0269a0001c0003t0003g0270a0001c0003t0003g0271 | 3 | HG03490.hp2 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1201-11863T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719805 | ||||||
| chr7:116719893
|
C | G | 8 | a0001c0005t0006g0007a0001c0005t0006g0129a0001c0005t0006g0135others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-11775C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719893 | ||||||
| chr7:116719893
|
C | T | 1 | a0001c0004t0002g0248 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1201-11775C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719893 | ||||||
| chr7:116719922
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-11746G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719922 | ||||||
| chr7:116719965
|
C | T | 1 | a0001c0001t0005g0034 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1201-11703C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719965 | ||||||
| chr7:116719971
|
G | A | 1 | a0001c0003t0003g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1201-11697G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116719971 | ||||||
| chr7:116720044
|
T | G | 1 | a0001c0002t0004g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1201-11624T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720044 | ||||||
| chr7:116720067
|
A | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-11601A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720067 | ||||||
| chr7:116720097
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-11571C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720097 | ||||||
| chr7:116720155
|
T | C | 15 | a0001c0002t0001g0087a0001c0002t0001g0088a0001c0002t0001g0089others(12): Show | 15 | HG00673.hp1 HG02040.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1201-11513T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720155 | ||||||
| chr7:116720159
|
C | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-11509C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720159 | ||||||
| chr7:116720161
|
T | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-11507T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720161 | ||||||
| chr7:116720260
|
G | A | 1 | a0001c0001t0007g0281 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1201-11408G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720260 | ||||||
| chr7:116720451
|
A | T | 8 | a0001c0005t0006g0007a0001c0005t0006g0129a0001c0005t0006g0135others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-11217A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720451 | ||||||
| chr7:116720492
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-11176G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720492 | ||||||
| chr7:116720508
|
A | G | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1201-11160A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720508 | ||||||
| chr7:116720789
|
T | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-10879T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720789 | ||||||
| chr7:116720799
|
C | T | 3 | a0001c0002t0001g0090a0001c0002t0004g0238a0001c0002t0004g0245 | 3 | HG01168.hp2 HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1201-10869C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720799 | ||||||
| chr7:116720910
|
G | A | 57 | a0001c0001t0005g0085a0001c0002t0001g0042a0001c0002t0001g0272others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1201-10758G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116720910 | ||||||
| chr7:116721022
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-10646T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721022 | ||||||
| chr7:116721037
|
A | T | 1 | a0001c0022t0004g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1201-10631A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721037 | ||||||
| chr7:116721094
|
C | T | 2 | a0001c0001t0005g0194a0010c0021t0002g0258 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1201-10574C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721094 | ||||||
| chr7:116721184
|
C | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-10484C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721184 | ||||||
| chr7:116721319
|
G | C | 1 | a0001c0002t0001g0018 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1201-10349G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721319 | ||||||
| chr7:116721401
|
C | T | 15 | a0001c0001t0002g0004a0001c0001t0005g0105a0001c0001t0005g0111others(12): Show | 15 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1201-10267C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721401 | ||||||
| chr7:116721402
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1201-10266G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721402 | ||||||
| chr7:116721519
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-10149T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721519 | ||||||
| chr7:116721659
|
C | A | 10 | a0001c0001t0007g0281a0001c0001t0007g0284a0001c0001t0007g0286others(7): Show | 10 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1201-10009C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721659 | ||||||
| chr7:116721696
|
G | A | 9 | a0001c0002t0001g0022a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG01952.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1201-9972G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721696 | ||||||
| chr7:116721790
|
C | T | 1 | a0001c0002t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1201-9878C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721790 | ||||||
| chr7:116721791
|
G | A | 1 | a0001c0002t0001g0175 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1201-9877G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721791 | ||||||
| chr7:116721906
|
T | A | 1 | a0007c0016t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1201-9762T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116721906 | ||||||
| chr7:116722057
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-9611G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722057 | ||||||
| chr7:116722182
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1201-9486A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722182 | ||||||
| chr7:116722450
|
G | A | 1 | a0001c0001t0008g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1201-9218G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722450 | ||||||
| chr7:116722500
|
A | T | 1 | a0001c0004t0003g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1201-9168A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722500 | ||||||
| chr7:116722527
|
A | T | 1 | a0001c0004t0003g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1201-9141A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722527 | ||||||
| chr7:116722558
|
T | C | 1 | a0001c0001t0005g0268 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1201-9110T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722558 | ||||||
| chr7:116722570
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1201-9098C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722570 | ||||||
| chr7:116722610
|
C | T | 3 | a0001c0002t0004g0235a0001c0002t0004g0337a0001c0002t0004g0338 | 3 | HG03492.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1201-9058C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722610 | ||||||
| chr7:116722611
|
G | A | 4 | a0001c0004t0003g0026a0001c0004t0003g0046a0001c0004t0003g0047others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-9057G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722611 | ||||||
| chr7:116722812
|
C | T | 1 | a0001c0001t0005g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1201-8856C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722812 | ||||||
| chr7:116722888
|
G | A | 1 | a0006c0013t0002g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1201-8780G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116722888 | ||||||
| chr7:116723020
|
C | G | 1 | a0001c0003t0003g0043 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1201-8648C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723020 | ||||||
| chr7:116723127
|
C | T | 1 | a0001c0002t0004g0318 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1201-8541C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723127 | ||||||
| chr7:116723191
|
T | C | 1 | a0001c0001t0005g0223 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1201-8477T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723191 | ||||||
| chr7:116723270
|
G | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0003g0033others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-8398G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723270 | ||||||
| chr7:116723414
|
T | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-8254T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723414 | ||||||
| chr7:116723436
|
C | T | 103 | a0001c0001t0002g0308a0001c0001t0008g0220a0001c0002t0001g0018others(100): Show | 103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1201-8232C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723436 | ||||||
| chr7:116723458
|
A | G | 3 | a0001c0003t0011g0039a0001c0003t0011g0074a0001c0003t0011g0104 | 3 | HG00609.hp2 NA18983.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1201-8210A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723458 | ||||||
| chr7:116723533
|
G | T | 1 | a0001c0003t0003g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1201-8135G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723533 | ||||||
| chr7:116723665
|
T | A | 1 | a0001c0002t0001g0023 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1201-8003T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723665 | ||||||
| chr7:116723704
|
C | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7964C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723704 | ||||||
| chr7:116723721
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1201-7947A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723721 | ||||||
| chr7:116723732
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1201-7936G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723732 | ||||||
| chr7:116723737
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1201-7931C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723737 | ||||||
| chr7:116723757
|
G | C | 1 | a0001c0001t0007g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1201-7911G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723757 | ||||||
| chr7:116723781
|
C | T | 1 | a0001c0019t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1201-7887C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723781 | ||||||
| chr7:116723829
|
A | C | 2 | a0001c0002t0001g0212a0001c0003t0011g0104 | 2 | HG03710.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1201-7839A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723829 | ||||||
| chr7:116723838
|
A | G | 1 | a0001c0002t0004g0338 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1201-7830A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723838 | ||||||
| chr7:116723858
|
A | G | 2 | a0001c0002t0001g0102a0001c0002t0004g0338 | 2 | HG00673.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1201-7810A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723858 | ||||||
| chr7:116723864
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1201-7804G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723864 | ||||||
| chr7:116723904
|
T | C | 2 | a0001c0002t0004g0300a0001c0002t0004g0301 | 2 | NA19055.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1201-7764T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723904 | ||||||
| chr7:116723905
|
T | C | 2 | a0001c0002t0004g0300a0001c0002t0004g0301 | 2 | NA19055.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1201-7763T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723905 | ||||||
| chr7:116723956
|
G | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7712G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723956 | ||||||
| chr7:116723997
|
C | G | 2 | a0001c0005t0002g0143a0001c0018t0017g0029 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1201-7671C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116723997 | ||||||
| chr7:116724026
|
A | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7642A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724026 | ||||||
| chr7:116724090
|
C | T | 1 | a0001c0003t0003g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1201-7578C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724090 | ||||||
| chr7:116724123
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7545G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724123 | ||||||
| chr7:116724133
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7535G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724133 | ||||||
| chr7:116724189
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7479G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724189 | ||||||
| chr7:116724257
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7411T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724257 | ||||||
| chr7:116724258
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7410G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724258 | ||||||
| chr7:116724287
|
T | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7381T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724287 | ||||||
| chr7:116724342
|
G | A | 1 | a0001c0002t0004g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1201-7326G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724342 | ||||||
| chr7:116724367
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-7301C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724367 | ||||||
| chr7:116724435
|
C | T | 1 | a0005c0012t0006g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1201-7233C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724435 | ||||||
| chr7:116724475
|
G | A | 1 | a0001c0005t0002g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1201-7193G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724475 | ||||||
| chr7:116724666
|
A | T | 1 | a0001c0001t0005g0183 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1201-7002A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724666 | ||||||
| chr7:116724718
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-6950G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724718 | ||||||
| chr7:116724749
|
T | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-6919T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724749 | ||||||
| chr7:116724769
|
CA | C | 103 | a0001c0001t0002g0308a0001c0001t0008g0220a0001c0002t0001g0018others(100): Show | 103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1201-6898delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724769 | ||||||
| chr7:116724810
|
C | G | 1 | a0001c0001t0005g0034 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1201-6858C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724810 | ||||||
| chr7:116724972
|
A | G | 4 | a0001c0002t0004g0152a0001c0002t0004g0276a0001c0002t0004g0277others(1): Show | 4 | NA18941.hp2 NA18974.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-6696A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116724972 | ||||||
| chr7:116725164
|
A | G | 1 | a0001c0002t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1201-6504A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725164 | ||||||
| chr7:116725168
|
T | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-6500T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725168 | ||||||
| chr7:116725356
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-6312C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725356 | ||||||
| chr7:116725359
|
T | C | 261 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(258): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1201-6309T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725359 | ||||||
| chr7:116725385
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-6283G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725385 | ||||||
| chr7:116725461
|
T | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-6207T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725461 | ||||||
| chr7:116725463
|
T | C | 1 | a0002c0006t0008g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1201-6205T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725463 | ||||||
| chr7:116725465
|
C | CAT | 64 | a0001c0001t0002g0004a0001c0001t0002g0162a0001c0001t0005g0105others(61): Show | 64 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1201-6183_1201-618 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116725465 | |||||
| chr7:116725465
|
C | CATAT | 100 | a0001c0001t0002g0308a0001c0001t0008g0167a0001c0001t0008g0220others(97): Show | 100 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1201-6185_1201-618 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116725465 | |||||
| chr7:116725465
|
C | CATATAT | 8 | a0001c0002t0001g0216a0001c0002t0001g0219a0001c0002t0004g0240others(5): Show | 8 | HG00438.hp1 HG00558.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201-6187_1201-618 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116725465 | |||||
| chr7:116725485
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-6183T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725485 | ||||||
| chr7:116725511
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-6157G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725511 | ||||||
| chr7:116725784
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-5884A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725784 | ||||||
| chr7:116725925
|
A | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-5743A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116725925 | ||||||
| chr7:116726141
|
A | ATATATAT others(95): Show |
1 | a0001c0005t0006g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1201-5526_1201-552 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726141 | |||||
| chr7:116726141
|
A | ATATATAT others(97): Show |
1 | a0001c0005t0006g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-5526_1201-552 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726141 | |||||
| chr7:116726141
|
A | ATGTATAT others(91): Show |
1 | a0001c0003t0003g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(102): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726141 | |||||
| chr7:116726141
|
A | ATGTATAT others(99): Show |
1 | a0003c0009t0008g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726141 | |||||
| chr7:116726143
|
G | A | 2 | a0001c0005t0006g0154a0001c0005t0006g0155 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1201-5525G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726143 | ||||||
| chr7:116726143
|
G | GTATATAT others(87): Show |
2 | a0001c0003t0006g0148a0001c0003t0006g0321 | 2 | NA18612.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1201-5507_1201-550 others(98): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(95): Show |
2 | a0001c0001t0007g0287a0001c0001t0007g0288 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1201-5503_1201-550 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1201-5503_1201-550 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0003c0009t0010g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
1 | a0001c0005t0025g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
2 | a0001c0002t0004g0292a0001c0002t0004g0300 | 2 | HG04184.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1201-5499_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0002t0004g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0002t0004g0301 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(89): Show |
1 | a0005c0012t0006g0028 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(100): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(93): Show |
1 | a0001c0005t0006g0135 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(104): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(95): Show |
1 | a0001c0003t0003g0043 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(93): Show |
1 | a0001c0002t0001g0087 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(104): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
2 | a0001c0002t0001g0122a0001c0002t0004g0314 | 2 | HG02895.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1201-5499_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0002t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(93): Show |
1 | a0001c0001t0002g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(104): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(91): Show |
1 | a0001c0001t0005g0045 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(102): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0005t0010g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(91): Show |
1 | a0001c0005t0016g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(102): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(93): Show |
2 | a0001c0002t0001g0272a0001c0002t0001g0273 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(104): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
7 | a0001c0003t0003g0066a0001c0003t0003g0084a0001c0003t0003g0270others(4): Show | 7 | HG02970.hp2 NA18974.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
9 | a0001c0002t0001g0117a0001c0002t0001g0119a0001c0002t0001g0120others(6): Show | 9 | HG02723.hp2 HG03239.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0002t0001g0118 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(95): Show |
1 | a0001c0001t0002g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
5 | a0001c0002t0001g0125a0001c0002t0001g0163a0001c0002t0001g0213others(2): Show | 5 | HG00280.hp2 HG03654.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
9 | a0001c0001t0008g0220a0001c0002t0001g0109a0001c0002t0001g0202others(6): Show | 9 | HG00621.hp2 HG01192.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
17 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0180others(14): Show | 17 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(14): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
17 | a0001c0002t0001g0019a0001c0002t0001g0023a0001c0002t0001g0056others(14): Show | 17 | HG00558.hp2 HG00639.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
7 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0088others(4): Show | 7 | HG01346.hp2 HG02004.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
4 | a0001c0002t0001g0214a0001c0002t0004g0152a0001c0002t0004g0276others(1): Show | 4 | HG02027.hp1 NA18941.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
3 | a0001c0002t0004g0149a0001c0002t0004g0150a0008c0014t0001g0217 | 3 | NA18994.hp1 NA19000.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
3 | a0001c0002t0004g0235a0001c0002t0004g0238a0001c0003t0003g0232 | 3 | HG03834.hp1 HG06807.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
3 | a0001c0002t0001g0175a0001c0002t0004g0290a0001c0002t0028g0267 | 3 | HG01978.hp1 HG01978.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(89): Show |
1 | a0001c0001t0005g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(100): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(91): Show |
3 | a0001c0001t0002g0013a0001c0001t0005g0034a0001c0001t0005g0194 | 3 | HG01192.hp2 HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(102): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(93): Show |
8 | a0001c0001t0002g0014a0001c0001t0002g0140a0001c0001t0002g0303others(5): Show | 8 | HG00099.hp2 HG00642.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(104): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(95): Show |
9 | a0001c0001t0002g0005a0001c0001t0002g0171a0001c0001t0002g0249others(6): Show | 9 | HG00323.hp2 HG01257.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
6 | a0001c0001t0002g0296a0001c0001t0005g0024a0001c0001t0005g0062others(3): Show | 6 | HG01256.hp2 HG01952.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
1 | a0001c0001t0002g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
3 | a0001c0001t0002g0141a0001c0001t0005g0174a0001c0001t0005g0184 | 3 | HG01168.hp1 HG01169.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
1 | a0001c0004t0002g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0004t0002g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0001t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0005t0002g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(95): Show |
1 | a0001c0003t0021g0236 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
1 | a0001c0004t0003g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
12 | a0001c0001t0002g0137a0001c0003t0003g0064a0001c0003t0003g0065others(9): Show | 12 | HG00140.hp1 HG00408.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
11 | a0001c0002t0001g0042a0001c0003t0003g0051a0001c0003t0003g0068others(8): Show | 11 | HG00597.hp2 HG00639.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
2 | a0001c0003t0003g0164a0001c0003t0006g0340 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
2 | a0001c0003t0003g0080a0012c0024t0003g0072 | 2 | HG02027.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
2 | a0001c0003t0003g0225a0007c0016t0003g0059 | 2 | HG00099.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
2 | a0001c0001t0005g0085a0001c0003t0003g0063 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(95): Show |
1 | a0001c0004t0008g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
1 | a0001c0002t0004g0244 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0002t0001g0222 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
2 | a0001c0002t0001g0229a0001c0002t0004g0133 | 2 | HG02071.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
2 | a0001c0002t0004g0283a0001c0003t0006g0001 | 2 | HG00621.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(109): Show |
1 | a0001c0002t0001g0219 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(120): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
1 | a0001c0002t0001g0230 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0007t0014g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
2 | a0001c0001t0002g0307a0001c0008t0002g0030 | 2 | HG00280.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1201-5495_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0001t0002g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(95): Show |
1 | a0001c0003t0003g0073 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
2 | a0001c0004t0003g0046a0001c0004t0003g0047 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
4 | a0001c0001t0002g0134a0001c0003t0003g0067a0001c0004t0003g0026others(1): Show | 4 | HG02280.hp2 HG02818.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
7 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0003t0003g0103others(4): Show | 7 | HG00609.hp2 HG02523.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
1 | a0001c0003t0003g0071 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
1 | a0001c0003t0003g0169 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0002t0004g0297 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0003t0003g0076 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
3 | a0001c0002t0001g0054a0001c0002t0001g0055a0001c0002t0004g0161 | 3 | NA18612.hp1 NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
1 | a0001c0002t0004g0298 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(109): Show |
1 | a0001c0002t0001g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(120): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
6 | a0001c0003t0009g0264a0001c0003t0024g0187a0001c0004t0003g0195others(3): Show | 6 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
1 | a0001c0003t0009g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
7 | a0001c0001t0002g0317a0001c0001t0002g0327a0001c0001t0002g0329others(4): Show | 7 | HG00558.hp1 HG02135.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
6 | a0001c0001t0002g0274a0001c0001t0002g0324a0001c0001t0002g0325others(3): Show | 6 | HG00733.hp1 HG01106.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
2 | a0001c0001t0002g0322a0001c0001t0002g0323 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0025t0005g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(97): Show |
2 | a0001c0001t0026g0205a0001c0002t0001g0204 | 2 | NA18983.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
1 | a0001c0005t0006g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0001t0003g0033 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
2 | a0001c0001t0006g0261a0001c0001t0015g0156 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1201-5491_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0003t0003g0070 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0002t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
1 | a0011c0023t0007g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
2 | a0001c0001t0007g0339a0001c0001t0008g0168 | 2 | HG02071.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1201-5491_1201-549 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
2 | a0003c0009t0007g0008a0003c0009t0007g0009 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1201-5491_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0007t0009g0259 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(99): Show |
1 | a0001c0001t0005g0037 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(101): Show |
1 | a0001c0001t0005g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
2 | a0001c0001t0005g0040a0001c0001t0005g0166 | 2 | HG00609.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1201-5491_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0001t0007g0313 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1201-5491_1201-549 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
1 | a0001c0001t0005g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
2 | a0001c0001t0008g0058a0002c0006t0008g0113 | 2 | HG02015.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1201-5490_1201-548 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(109): Show |
4 | a0001c0001t0007g0260a0001c0001t0007g0331a0002c0010t0001g0086others(1): Show | 4 | HG00438.hp1 HG03195.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-5490_1201-548 others(120): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(111): Show |
3 | a0001c0005t0007g0146a0002c0006t0008g0112a0002c0006t0008g0233 | 3 | HG00544.hp1 HG01243.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1201-5490_1201-548 others(122): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
1 | a0001c0003t0009g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
6 | a0001c0001t0002g0002a0001c0001t0005g0093a0001c0001t0005g0094others(3): Show | 6 | HG00438.hp2 NA18941.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-5490_1201-548 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(105): Show |
1 | a0001c0001t0005g0097 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(116): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(117): Show |
1 | a0001c0001t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(128): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
1 | a0001c0004t0005g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(109): Show |
2 | a0001c0001t0008g0081a0002c0006t0007g0003 | 2 | HG02004.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1201-5490_1201-548 others(120): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(111): Show |
2 | a0001c0001t0007g0130a0001c0005t0007g0247 | 2 | HG03139.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1201-5490_1201-548 others(122): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(113): Show |
1 | a0002c0006t0008g0114 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(124): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(103): Show |
1 | a0001c0001t0008g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(111): Show |
1 | a0001c0001t0008g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(122): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(109): Show |
1 | a0002c0010t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(120): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(111): Show |
2 | a0001c0001t0008g0165a0001c0001t0008g0208 | 2 | HG03688.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1201-5490_1201-548 others(122): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(111): Show |
1 | a0001c0001t0008g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(122): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(113): Show |
1 | a0001c0001t0008g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(124): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(107): Show |
1 | a0001c0004t0003g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(118): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(113): Show |
1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(124): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(109): Show |
1 | a0001c0004t0003g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(120): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(115): Show |
1 | a0001c0001t0008g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(126): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(115): Show |
1 | a0001c0001t0007g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(126): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(117): Show |
1 | a0001c0001t0007g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(128): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(115): Show |
1 | a0001c0001t0007g0281 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(126): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATATAT others(119): Show |
1 | a0001c0001t0007g0286 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(130): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATGTAT others(95): Show |
1 | a0001c0001t0005g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1201-5522_1201-552 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATGTAT others(91): Show |
1 | a0001c0019t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1201-5522_1201-552 others(102): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATGTAT others(93): Show |
1 | a0001c0004t0002g0248 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1201-5522_1201-552 others(104): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATGTAT others(95): Show |
5 | a0001c0001t0005g0223a0001c0004t0012g0127a0001c0004t0012g0128others(2): Show | 5 | HG01358.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-5522_1201-552 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATGTAT others(97): Show |
5 | a0001c0001t0005g0105a0001c0001t0005g0111a0001c0001t0005g0224others(2): Show | 5 | HG01361.hp2 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1201-5522_1201-552 others(108): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATGTAT others(103): Show |
1 | a0001c0001t0002g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1201-5522_1201-552 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTATGTAT others(103): Show |
1 | a0001c0004t0002g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1201-5522_1201-552 others(114): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTGTATAT others(99): Show |
1 | a0001c0002t0001g0215 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1201-5524_1201-552 others(110): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTGTATAT others(95): Show |
2 | a0001c0001t0005g0192a0001c0001t0005g0193 | 2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1201-5524_1201-552 others(106): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726143
|
G | GTGTATAT others(113): Show |
1 | a0002c0006t0008g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1201-5524_1201-552 others(124): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726143 | |||||
| chr7:116726145
|
A | ATATATAT others(79): Show |
1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-5513_1201-551 others(90): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726145 | |||||
| chr7:116726145
|
A | ATATATAT others(101): Show |
1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(112): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726145 | |||||
| chr7:116726147
|
A | ATATATAT others(83): Show |
1 | a0005c0012t0006g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(94): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726147 | |||||
| chr7:116726147
|
A | ATATATAT others(85): Show |
1 | a0001c0002t0001g0126 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1201-5499_1201-549 others(96): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726147 | |||||
| chr7:116726147
|
A | ATATATAT others(87): Show |
1 | a0001c0002t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(98): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726147 | |||||
| chr7:116726149
|
A | ATATATAT others(85): Show |
3 | a0001c0002t0001g0053a0001c0002t0013g0057a0001c0002t0013g0107 | 3 | NA18964.hp1 NA19012.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1201-5497_1201-549 others(96): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726149 | |||||
| chr7:116726151
|
A | ATATATAT others(79): Show |
1 | a0001c0001t0005g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(90): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726151 | |||||
| chr7:116726157
|
A | ATATATAT others(77): Show |
1 | a0001c0005t0010g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(88): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726157 | |||||
| chr7:116726157
|
A | ATATATAT others(77): Show |
1 | a0001c0003t0003g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1201-5495_1201-549 others(88): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726157 | |||||
| chr7:116726159
|
A | ATATATAT others(75): Show |
1 | a0001c0002t0001g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1201-5497_1201-549 others(86): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726159 | |||||
| chr7:116726161
|
A | ATATATAT others(73): Show |
2 | a0004c0011t0002g0319a0004c0011t0019g0330 | 2 | NA18747.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1201-5493_1201-549 others(84): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726161 | |||||
| chr7:116726163
|
A | ATATATAT others(83): Show |
1 | a0001c0001t0006g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(94): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726163 | |||||
| chr7:116726166
|
T | C | 1 | a0002c0006t0008g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1201-5502T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726166 | ||||||
| chr7:116726171
|
A | ATATACAC others(63): Show |
1 | a0001c0002t0001g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1201-5493_1201-549 others(74): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116726171 | |||||
| chr7:116726178
|
T | TACACACA others(109): Show |
1 | a0001c0001t0020g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(120): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726178 | ||||||
| chr7:116726178
|
T | TATATACA others(109): Show |
1 | a0001c0001t0007g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(120): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726178 | ||||||
| chr7:116726178
|
T | TATATACA others(115): Show |
1 | a0001c0001t0007g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(126): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726178 | ||||||
| chr7:116726178
|
T | TATATATA others(115): Show |
1 | a0001c0001t0007g0263 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1201-5490_1201-548 others(126): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726178 | ||||||
| chr7:116726179
|
G | A | 1 | a0001c0002t0004g0309 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1201-5489G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726179 | ||||||
| chr7:116726180
|
G | T | 1 | a0001c0002t0004g0309 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1201-5488G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726180 | ||||||
| chr7:116726252
|
T | G | 2 | a0001c0002t0001g0088a0001c0002t0001g0089 | 2 | HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1201-5416T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726252 | ||||||
| chr7:116726253
|
A | T | 2 | a0001c0002t0001g0088a0001c0002t0001g0089 | 2 | HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1201-5415A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726253 | ||||||
| chr7:116726254
|
T | C | 2 | a0001c0002t0001g0088a0001c0002t0001g0089 | 2 | HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1201-5414T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726254 | ||||||
| chr7:116726333
|
G | A | 1 | a0001c0004t0002g0248 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1201-5335G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726333 | ||||||
| chr7:116726402
|
T | A | 1 | a0001c0005t0006g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1201-5266T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726402 | ||||||
| chr7:116726437
|
G | A | 5 | a0001c0001t0007g0025a0001c0001t0007g0260a0001c0001t0007g0262others(2): Show | 5 | HG01496.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-5231G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726437 | ||||||
| chr7:116726525
|
G | A | 2 | a0001c0004t0002g0157a0001c0004t0002g0158 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1201-5143G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726525 | ||||||
| chr7:116726883
|
G | A | 1 | a0001c0005t0006g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1201-4785G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726883 | ||||||
| chr7:116726887
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-4781T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116726887 | ||||||
| chr7:116727118
|
G | A | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1201-4550G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116727118 | ||||||
| chr7:116727237
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-4431G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116727237 | ||||||
| chr7:116727248
|
T | A | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1201-4420T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116727248 | ||||||
| chr7:116727273
|
AG | A | 3 | a0003c0009t0007g0008a0003c0009t0007g0009a0003c0009t0008g0035 | 3 | HG02647.hp1 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1201-4393delG | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116727273 | |||||
| chr7:116727275
|
G | A | 1 | a0001c0001t0005g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1201-4393G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116727275 | ||||||
| chr7:116727479
|
CCCTT | C | 4 | a0001c0005t0010g0136a0001c0005t0010g0289a0001c0005t0025g0181others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-4172_1201-416 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr7 | 116727479 | |||||
| chr7:116727633
|
G | A | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1201-4035G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116727633 | ||||||
| chr7:116727644
|
C | T | 1 | a0001c0001t0005g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1201-4024C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116727644 | ||||||
| chr7:116728272
|
C | T | 1 | a0001c0002t0004g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1201-3396C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116728272 | ||||||
| chr7:116728314
|
A | G | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1201-3354A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116728314 | ||||||
| chr7:116728336
|
T | C | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1201-3332T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116728336 | ||||||
| chr7:116728834
|
C | T | 2 | a0001c0004t0003g0048a0001c0004t0003g0050 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1201-2834C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116728834 | ||||||
| chr7:116729128
|
C | T | 1 | a0001c0003t0003g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1201-2540C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116729128 | ||||||
| chr7:116729132
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1201-2536C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116729132 | ||||||
| chr7:116729133
|
G | A | 8 | a0001c0005t0006g0007a0001c0005t0006g0129a0001c0005t0006g0135others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-2535G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116729133 | ||||||
| chr7:116729606
|
T | A | 1 | a0001c0003t0006g0321 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1201-2062T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116729606 | ||||||
| chr7:116729800
|
C | T | 1 | a0001c0002t0004g0237 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1201-1868C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116729800 | ||||||
| chr7:116730010
|
G | T | 1 | a0001c0002t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1201-1658G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116730010 | ||||||
| chr7:116730233
|
G | T | 145 | a0001c0001t0002g0162a0001c0001t0002g0308a0001c0001t0005g0315others(142): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1201-1435G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116730233 | ||||||
| chr7:116730322
|
A | G | 1 | a0001c0002t0004g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1201-1346A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116730322 | ||||||
| chr7:116730675
|
G | A | 1 | a0001c0001t0005g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1201-993G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116730675 | ||||||
| chr7:116730772
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1201-896G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116730772 | ||||||
| chr7:116730911
|
G | A | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1201-757G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116730911 | ||||||
| chr7:116730957
|
A | G | 32 | a0001c0001t0007g0025a0001c0001t0007g0130a0001c0001t0007g0172others(29): Show | 32 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1201-711A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116730957 | ||||||
| chr7:116730966
|
A | C | 1 | a0001c0001t0002g0249 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1201-702A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116730966 | ||||||
| chr7:116731175
|
T | C | 4 | a0001c0005t0010g0136a0001c0005t0010g0289a0001c0005t0025g0181others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-493T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116731175 | ||||||
| chr7:116731182
|
T | C | 1 | a0001c0002t0004g0336 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1201-486T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116731182 | ||||||
| chr7:116731347
|
T | C | 15 | a0001c0001t0002g0004a0001c0001t0002g0171a0001c0001t0005g0105others(12): Show | 15 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1201-321T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116731347 | ||||||
| chr7:116731377
|
A | G | 1 | a0001c0003t0003g0227 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1201-291A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116731377 | ||||||
| chr7:116731421
|
T | C | 15 | a0001c0001t0002g0004a0001c0001t0002g0171a0001c0001t0005g0105others(12): Show | 15 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1201-247T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 2/20 | chr7 | 116731421 | ||||||
| chr7:116731892
|
C | G | 2 | a0001c0001t0005g0315a0001c0002t0001g0056 | 2 | HG02129.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1392+33C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116731892 | ||||||
| chr7:116731977
|
T | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1392+118T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116731977 | ||||||
| chr7:116732135
|
G | C | 8 | a0001c0005t0006g0007a0001c0005t0006g0129a0001c0005t0006g0135others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392+276G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116732135 | ||||||
| chr7:116732308
|
T | C | 1 | a0001c0003t0011g0074 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1392+449T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116732308 | ||||||
| chr7:116732388
|
A | T | 12 | a0001c0001t0003g0033a0001c0001t0006g0144a0001c0001t0006g0261others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1392+529A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116732388 | ||||||
| chr7:116732500
|
G | A | 2 | a0001c0002t0001g0087a0001c0002t0001g0229 | 2 | HG02071.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1392+641G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116732500 | ||||||
| chr7:116732524
|
T | G | 1 | a0001c0002t0004g0291 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1392+665T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116732524 | ||||||
| chr7:116732605
|
A | G | 1 | a0001c0003t0003g0067 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1392+746A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116732605 | ||||||
| chr7:116732908
|
C | A | 1 | a0009c0020t0003g0191 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1392+1049C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116732908 | ||||||
| chr7:116732981
|
G | C | 2 | a0001c0002t0001g0088a0001c0002t0001g0089 | 2 | HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1392+1122G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116732981 | ||||||
| chr7:116733133
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1392+1274C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116733133 | ||||||
| chr7:116733145
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1392+1286T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116733145 | ||||||
| chr7:116733360
|
T | A | 2 | a0001c0001t0002g0171a0001c0004t0002g0145 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1392+1501T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116733360 | ||||||
| chr7:116733725
|
T | C | 1 | a0001c0004t0023g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1392+1866T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116733725 | ||||||
| chr7:116733727
|
T | A | 1 | a0001c0004t0002g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1392+1868T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116733727 | ||||||
| chr7:116733728
|
A | T | 1 | a0001c0001t0002g0317 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1392+1869A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116733728 | ||||||
| chr7:116734036
|
C | G | 336 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1392+2177C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734036 | ||||||
| chr7:116734046
|
C | G | 4 | a0001c0001t0005g0085a0001c0003t0003g0063a0001c0003t0003g0169others(1): Show | 4 | HG00099.hp1 HG02735.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1392+2187C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734046 | ||||||
| chr7:116734116
|
G | A | 4 | a0001c0008t0002g0030a0001c0008t0002g0241a0001c0008t0002g0242others(1): Show | 4 | HG00280.hp1 HG00642.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+2257G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734116 | ||||||
| chr7:116734198
|
A | T | 4 | a0001c0001t0002g0162a0003c0009t0007g0008a0003c0009t0007g0009others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+2339A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734198 | ||||||
| chr7:116734224
|
AT | A | 9 | a0001c0001t0002g0162a0001c0002t0004g0152a0001c0004t0008g0190others(6): Show | 9 | HG01243.hp1 HG02647.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1392+2373delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 116734224 | |||||
| chr7:116734545
|
G | A | 1 | a0001c0002t0004g0244 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1392+2686G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734545 | ||||||
| chr7:116734692
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1392+2833G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734692 | ||||||
| chr7:116734748
|
G | A | 2 | a0001c0003t0003g0077a0001c0003t0003g0078 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1392+2889G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734748 | ||||||
| chr7:116734759
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1392+2900C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734759 | ||||||
| chr7:116734974
|
C | T | 2 | a0001c0004t0023g0027a0001c0004t0030g0197 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1392+3115C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116734974 | ||||||
| chr7:116735075
|
G | T | 4 | a0001c0005t0010g0136a0001c0005t0010g0289a0001c0005t0025g0181others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+3216G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116735075 | ||||||
| chr7:116735148
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1392+3289A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116735148 | ||||||
| chr7:116735218
|
C | T | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1392+3359C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116735218 | ||||||
| chr7:116735221
|
C | T | 1 | a0003c0009t0010g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1392+3362C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116735221 | ||||||
| chr7:116735490
|
C | T | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1392+3631C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116735490 | ||||||
| chr7:116735779
|
C | CT | 98 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(95): Show | 98 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1392+3937dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 116735779 | |||||
| chr7:116735779
|
CT | C | 72 | a0001c0001t0002g0141a0001c0001t0002g0322a0001c0001t0002g0333others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1392+3937delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 116735779 | |||||
| chr7:116735860
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1392+4001C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116735860 | ||||||
| chr7:116736213
|
T | C | 2 | a0001c0002t0004g0292a0001c0019t0001g0170 | 2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1393-3737T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116736213 | ||||||
| chr7:116736353
|
CA | C | 6 | a0001c0001t0002g0332a0001c0001t0005g0045a0001c0001t0005g0184others(3): Show | 6 | HG01168.hp1 HG01168.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-3583delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 116736353 | |||||
| chr7:116736411
|
A | G | 45 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1393-3539A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116736411 | ||||||
| chr7:116736577
|
G | A | 1 | a0001c0002t0004g0177 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1393-3373G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116736577 | ||||||
| chr7:116736634
|
C | T | 1 | a0002c0010t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1393-3316C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116736634 | ||||||
| chr7:116736753
|
C | T | 36 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(33): Show | 36 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1393-3197C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116736753 | ||||||
| chr7:116736759
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1393-3191A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116736759 | ||||||
| chr7:116736831
|
A | G | 1 | a0001c0004t0029g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1393-3119A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116736831 | ||||||
| chr7:116736972
|
T | C | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1393-2978T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116736972 | ||||||
| chr7:116737456
|
A | G | 10 | a0001c0003t0006g0198a0001c0003t0009g0264a0001c0003t0009g0265others(7): Show | 10 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1393-2494A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116737456 | ||||||
| chr7:116737646
|
C | T | 2 | a0001c0002t0004g0300a0001c0002t0004g0301 | 2 | NA19055.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1393-2304C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116737646 | ||||||
| chr7:116737649
|
T | C | 1 | a0001c0002t0004g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1393-2301T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116737649 | ||||||
| chr7:116737744
|
CAT | C | 53 | a0001c0002t0001g0042a0001c0002t0001g0121a0001c0003t0003g0043others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1393-2203_1393-220 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 116737744 | |||||
| chr7:116737795
|
G | C | 1 | a0001c0001t0002g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1393-2155G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116737795 | ||||||
| chr7:116737982
|
T | C | 7 | a0001c0004t0018g0256a0001c0005t0006g0154a0001c0005t0006g0155others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393-1968T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116737982 | ||||||
| chr7:116737987
|
C | T | 1 | a0001c0001t0005g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1393-1963C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116737987 | ||||||
| chr7:116738076
|
G | C | 1 | a0001c0001t0002g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1393-1874G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738076 | ||||||
| chr7:116738172
|
GT | G | 12 | a0001c0001t0003g0033a0001c0001t0006g0144a0001c0001t0006g0261others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1393-1773delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 116738172 | |||||
| chr7:116738326
|
A | G | 2 | a0001c0002t0001g0042a0001c0003t0003g0232 | 2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1393-1624A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738326 | ||||||
| chr7:116738499
|
C | A | 9 | a0001c0001t0002g0162a0001c0004t0008g0190a0001c0005t0007g0146others(6): Show | 9 | HG01243.hp1 HG02647.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1393-1451C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738499 | ||||||
| chr7:116738608
|
CATT | C | 14 | a0001c0001t0007g0331a0001c0001t0007g0339a0001c0001t0008g0081others(11): Show | 14 | HG00438.hp1 HG00544.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1393-1340_1393-133 others(7): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 116738608 | |||||
| chr7:116738789
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1393-1161C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738789 | ||||||
| chr7:116738841
|
T | C | 1 | a0001c0002t0001g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1393-1109T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738841 | ||||||
| chr7:116738862
|
G | A | 1 | a0001c0003t0006g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1393-1088G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738862 | ||||||
| chr7:116738887
|
G | A | 1 | a0001c0002t0004g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1393-1063G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738887 | ||||||
| chr7:116738981
|
C | T | 1 | a0005c0012t0006g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1393-969C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738981 | ||||||
| chr7:116738984
|
T | C | 1 | a0001c0004t0003g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1393-966T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116738984 | ||||||
| chr7:116739040
|
C | T | 109 | a0001c0001t0005g0315a0001c0001t0026g0205a0001c0002t0001g0018others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1393-910C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116739040 | ||||||
| chr7:116739086
|
G | A | 1 | a0001c0002t0004g0302 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1393-864G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116739086 | ||||||
| chr7:116739108
|
A | G | 1 | a0001c0002t0004g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1393-842A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116739108 | ||||||
| chr7:116739398
|
T | TA | 14 | a0001c0001t0002g0004a0001c0001t0002g0171a0001c0001t0005g0105others(11): Show | 14 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1393-545dupA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 116739398 | |||||
| chr7:116739501
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1393-449T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116739501 | ||||||
| chr7:116739690
|
C | T | 7 | a0001c0004t0018g0256a0001c0005t0006g0154a0001c0005t0006g0155others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393-260C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 3/20 | chr7 | 116739690 | ||||||
| chr7:116740135
|
A | G | 2 | a0001c0002t0004g0292a0001c0019t0001g0170 | 2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1527+51A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 4/20 | chr7 | 116740135 | ||||||
| chr7:116741050
|
A | G | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1701+25A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116741050 | ||||||
| chr7:116741067
|
G | GT | 13 | a0001c0001t0002g0162a0001c0001t0002g0333a0001c0001t0007g0331others(10): Show | 13 | HG01081.hp1 HG01243.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1701+58dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116741067 | |||||
| chr7:116741321
|
G | A | 1 | a0001c0008t0002g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1701+296G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116741321 | ||||||
| chr7:116741697
|
A | T | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1701+672A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116741697 | ||||||
| chr7:116741721
|
C | T | 2 | a0001c0004t0003g0046a0001c0004t0003g0047 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1701+696C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116741721 | ||||||
| chr7:116741980
|
T | A | 40 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(37): Show | 40 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1701+955T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116741980 | ||||||
| chr7:116742186
|
G | A | 1 | a0001c0005t0007g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1701+1161G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116742186 | ||||||
| chr7:116742204
|
C | T | 5 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(2): Show | 5 | HG01255.hp2 HG01346.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1701+1179C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116742204 | ||||||
| chr7:116742205
|
G | A | 1 | a0001c0002t0004g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1701+1180G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116742205 | ||||||
| chr7:116742592
|
C | T | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1701+1567C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116742592 | ||||||
| chr7:116742815
|
A | G | 45 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1701+1790A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116742815 | ||||||
| chr7:116742931
|
C | T | 1 | a0001c0001t0007g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1701+1906C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116742931 | ||||||
| chr7:116742939
|
G | T | 2 | a0001c0002t0004g0297a0001c0002t0004g0298 | 2 | HG02080.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1701+1914G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116742939 | ||||||
| chr7:116743087
|
A | C | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1701+2062A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116743087 | ||||||
| chr7:116743191
|
A | G | 45 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1701+2166A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116743191 | ||||||
| chr7:116743231
|
G | A | 1 | a0001c0001t0005g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1701+2206G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116743231 | ||||||
| chr7:116743655
|
C | A | 1 | a0001c0002t0013g0107 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1701+2630C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116743655 | ||||||
| chr7:116743789
|
T | C | 45 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1701+2764T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116743789 | ||||||
| chr7:116743944
|
G | A | 45 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1701+2919G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116743944 | ||||||
| chr7:116743973
|
C | A | 2 | a0001c0004t0002g0157a0001c0004t0002g0158 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1701+2948C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116743973 | ||||||
| chr7:116744220
|
T | G | 45 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1701+3195T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116744220 | ||||||
| chr7:116744305
|
G | A | 6 | a0001c0002t0001g0087a0001c0002t0001g0088a0001c0002t0001g0089others(3): Show | 6 | HG02071.hp2 HG02074.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1701+3280G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116744305 | ||||||
| chr7:116744767
|
A | C | 5 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0002g0327others(2): Show | 5 | NA18955.hp2 NA18992.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.1701+3742A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116744767 | ||||||
| chr7:116744785
|
G | A | 2 | a0001c0005t0006g0154a0001c0005t0006g0155 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1701+3760G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116744785 | ||||||
| chr7:116744944
|
G | A | 2 | a0001c0002t0004g0300a0001c0002t0004g0301 | 2 | NA19055.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1701+3919G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116744944 | ||||||
| chr7:116744974
|
A | T | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1701+3949A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116744974 | ||||||
| chr7:116745074
|
A | G | 2 | a0001c0002t0001g0099a0001c0002t0004g0312 | 2 | HG02083.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1701+4049A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116745074 | ||||||
| chr7:116745278
|
G | C | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1701+4253G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116745278 | ||||||
| chr7:116745643
|
G | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1701+4618G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116745643 | ||||||
| chr7:116745758
|
A | G | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1701+4733A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116745758 | ||||||
| chr7:116746023
|
T | C | 4 | a0001c0003t0003g0077a0001c0003t0003g0078a0001c0003t0003g0079others(1): Show | 4 | HG00140.hp1 HG00741.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1701+4998T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746023 | ||||||
| chr7:116746222
|
G | A | 2 | a0001c0002t0004g0292a0001c0019t0001g0170 | 2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1701+5197G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746222 | ||||||
| chr7:116746359
|
G | T | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1701+5334G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746359 | ||||||
| chr7:116746383
|
G | A | 1 | a0001c0002t0004g0237 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1701+5358G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746383 | ||||||
| chr7:116746454
|
C | T | 1 | a0001c0003t0003g0051 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1701+5429C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746454 | ||||||
| chr7:116746578
|
T | C | 1 | a0001c0002t0001g0018 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1701+5553T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746578 | ||||||
| chr7:116746579
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1701+5554G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746579 | ||||||
| chr7:116746692
|
A | G | 2 | a0001c0004t0022g0255a0001c0004t0029g0189 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1701+5667A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746692 | ||||||
| chr7:116746696
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1701+5671C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746696 | ||||||
| chr7:116746739
|
G | A | 1 | a0001c0001t0007g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1701+5714G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746739 | ||||||
| chr7:116746768
|
C | T | 1 | a0001c0001t0005g0183 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1701+5743C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746768 | ||||||
| chr7:116746769
|
G | A | 4 | a0001c0001t0008g0165a0001c0001t0008g0167a0001c0001t0008g0168others(1): Show | 4 | HG02809.hp1 HG03688.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1701+5744G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746769 | ||||||
| chr7:116746771
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1701+5746G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746771 | ||||||
| chr7:116746888
|
C | T | 1 | a0001c0003t0003g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1701+5863C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746888 | ||||||
| chr7:116746969
|
C | G | 1 | a0001c0002t0004g0314 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1701+5944C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116746969 | ||||||
| chr7:116747364
|
G | A | 1 | a0001c0004t0030g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1701+6339G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116747364 | ||||||
| chr7:116747514
|
C | T | 2 | a0001c0002t0004g0176a0001c0002t0004g0177 | 2 | HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1701+6489C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116747514 | ||||||
| chr7:116747709
|
C | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0171a0001c0004t0002g0145 | 3 | HG02451.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1701+6684C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116747709 | ||||||
| chr7:116747750
|
T | A | 7 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0007t0009g0251others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+6725T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116747750 | ||||||
| chr7:116747752
|
AACTCGGC others(5): Show |
A | 7 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0007t0009g0251others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+6730_1701+674 others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116747752 | |||||
| chr7:116747887
|
C | T | 1 | a0001c0002t0004g0282 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1701+6862C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116747887 | ||||||
| chr7:116747967
|
C | T | 106 | a0001c0001t0005g0315a0001c0002t0001g0018a0001c0002t0001g0019others(103): Show | 106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1701+6942C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116747967 | ||||||
| chr7:116747984
|
G | A | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1701+6959G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116747984 | ||||||
| chr7:116748016
|
C | T | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1701+6991C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748016 | ||||||
| chr7:116748020
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1701+6995C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748020 | ||||||
| chr7:116748137
|
G | A | 1 | a0002c0006t0008g0233 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1701+7112G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748137 | ||||||
| chr7:116748200
|
C | T | 2 | a0001c0001t0002g0013a0001c0001t0002g0014 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1702-7155C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748200 | ||||||
| chr7:116748315
|
T | G | 1 | a0002c0006t0008g0114 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1702-7040T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748315 | ||||||
| chr7:116748341
|
G | A | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1702-7014G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748341 | ||||||
| chr7:116748753
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1702-6602G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748753 | ||||||
| chr7:116748812
|
A | C | 34 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0134others(31): Show | 34 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1702-6543A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748812 | ||||||
| chr7:116748864
|
A | G | 3 | a0001c0008t0002g0030a0001c0008t0002g0242a0001c0008t0005g0060 | 3 | HG00280.hp1 HG00642.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1702-6491A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116748864 | ||||||
| chr7:116749009
|
C | T | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1702-6346C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749009 | ||||||
| chr7:116749267
|
A | G | 1 | a0001c0017t0003g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1702-6088A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749267 | ||||||
| chr7:116749325
|
A | G | 2 | a0001c0001t0007g0313a0001c0001t0008g0188 | 2 | HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1702-6030A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749325 | ||||||
| chr7:116749410
|
C | G | 1 | a0001c0005t0006g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1702-5945C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749410 | ||||||
| chr7:116749469
|
A | G | 12 | a0001c0001t0003g0033a0001c0001t0006g0144a0001c0001t0006g0261others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1702-5886A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749469 | ||||||
| chr7:116749675
|
G | C | 1 | a0001c0001t0005g0040 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1702-5680G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749675 | ||||||
| chr7:116749753
|
C | T | 1 | a0001c0005t0007g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1702-5602C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749753 | ||||||
| chr7:116749779
|
A | G | 4 | a0001c0001t0026g0205a0001c0002t0001g0119a0001c0002t0001g0203others(1): Show | 4 | NA18983.hp1 NA18993.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702-5576A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749779 | ||||||
| chr7:116749901
|
A | G | 2 | a0004c0011t0002g0319a0004c0011t0019g0330 | 2 | NA18747.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1702-5454A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749901 | ||||||
| chr7:116749999
|
A | G | 1 | a0001c0002t0004g0161 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1702-5356A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116749999 | ||||||
| chr7:116750050
|
T | C | 1 | a0001c0002t0001g0023 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1702-5305T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116750050 | ||||||
| chr7:116750800
|
G | A | 63 | a0001c0001t0005g0315a0001c0001t0026g0205a0001c0002t0001g0019others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1702-4555G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116750800 | ||||||
| chr7:116751071
|
GGTATATA others(5): Show |
G | 1 | a0001c0003t0003g0207 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1702-4283_1702-427 others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116751071 | ||||||
| chr7:116751170
|
C | T | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1702-4185C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116751170 | ||||||
| chr7:116751295
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1702-4060C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116751295 | ||||||
| chr7:116751551
|
T | G | 1 | a0001c0003t0003g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1702-3804T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116751551 | ||||||
| chr7:116751769
|
T | C | 1 | a0001c0015t0003g0061 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1702-3586T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116751769 | ||||||
| chr7:116751783
|
C | G | 1 | a0001c0004t0003g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1702-3572C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116751783 | ||||||
| chr7:116751954
|
G | A | 1 | a0001c0002t0004g0292 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1702-3401G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116751954 | ||||||
| chr7:116752071
|
A | G | 2 | a0001c0003t0003g0077a0001c0003t0003g0078 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1702-3284A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116752071 | ||||||
| chr7:116752135
|
C | T | 8 | a0001c0001t0002g0162a0001c0004t0008g0190a0001c0005t0007g0146others(5): Show | 8 | HG01243.hp1 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1702-3220C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116752135 | ||||||
| chr7:116752136
|
A | G | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1702-3219A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116752136 | ||||||
| chr7:116752191
|
G | A | 3 | a0001c0005t0007g0146a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG01243.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1702-3164G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116752191 | ||||||
| chr7:116752457
|
C | T | 2 | a0001c0003t0003g0077a0001c0003t0003g0078 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1702-2898C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116752457 | ||||||
| chr7:116752854
|
G | A | 6 | a0001c0001t0003g0033a0001c0001t0006g0261a0001c0001t0015g0156others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1702-2501G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116752854 | ||||||
| chr7:116752958
|
T | G | 2 | a0001c0002t0004g0292a0001c0019t0001g0170 | 2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1702-2397T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116752958 | ||||||
| chr7:116752965
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1702-2390G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116752965 | ||||||
| chr7:116753153
|
G | A | 7 | a0001c0002t0001g0272a0001c0002t0001g0273a0001c0002t0004g0017others(4): Show | 7 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-2202G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753153 | ||||||
| chr7:116753173
|
G | C | 4 | a0001c0005t0010g0136a0001c0005t0010g0289a0001c0005t0025g0181others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702-2182G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753173 | ||||||
| chr7:116753264
|
T | C | 31 | a0001c0001t0007g0025a0001c0001t0007g0130a0001c0001t0007g0172others(28): Show | 31 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1702-2091T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753264 | ||||||
| chr7:116753342
|
T | C | 1 | a0002c0006t0008g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1702-2013T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753342 | ||||||
| chr7:116753477
|
G | C | 1 | a0001c0005t0016g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1702-1878G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753477 | ||||||
| chr7:116753489
|
G | A | 1 | a0001c0003t0006g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1702-1866G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753489 | ||||||
| chr7:116753516
|
TA | T | 7 | a0001c0004t0018g0256a0001c0005t0006g0154a0001c0005t0006g0155others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-1838delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753516 | ||||||
| chr7:116753538
|
A | G | 1 | a0001c0003t0003g0103 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1702-1817A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753538 | ||||||
| chr7:116753588
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1702-1767A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753588 | ||||||
| chr7:116753638
|
T | C | 1 | a0001c0001t0002g0333 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1702-1717T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753638 | ||||||
| chr7:116753677
|
A | G | 2 | a0001c0004t0003g0048a0001c0004t0003g0050 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1702-1678A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753677 | ||||||
| chr7:116753725
|
A | T | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-1630A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116753725 | ||||||
| chr7:116754032
|
G | A | 2 | a0001c0004t0022g0255a0001c0004t0029g0189 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1702-1323G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754032 | ||||||
| chr7:116754044
|
A | C | 1 | a0001c0001t0002g0005 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1702-1311A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754044 | ||||||
| chr7:116754062
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0002g0014 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1702-1293G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754062 | ||||||
| chr7:116754139
|
G | A | 9 | a0001c0001t0002g0162a0001c0004t0008g0190a0001c0005t0007g0146others(6): Show | 9 | HG01243.hp1 HG02647.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1702-1216G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754139 | ||||||
| chr7:116754475
|
C | T | 2 | a0001c0002t0004g0290a0001c0002t0028g0267 | 2 | HG01978.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1702-880C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754475 | ||||||
| chr7:116754635
|
C | T | 1 | a0001c0003t0006g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1702-720C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754635 | ||||||
| chr7:116754659
|
A | G | 4 | a0001c0001t0026g0205a0001c0002t0001g0119a0001c0002t0001g0203others(1): Show | 4 | NA18983.hp1 NA18993.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702-696A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754659 | ||||||
| chr7:116754728
|
G | A | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1702-627G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754728 | ||||||
| chr7:116754885
|
GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0002g0296 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1702-462_1702-451d others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754885 | |||||
| chr7:116754893
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1702-462G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754893 | ||||||
| chr7:116754893
|
G | GAGAA | 63 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0013others(60): Show | 63 | HG00408.hp2 HG00597.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1702-406_1702-403d others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
G | GAGAAAGA others(1): Show |
29 | a0001c0001t0002g0012a0001c0001t0002g0293a0001c0001t0002g0304others(26): Show | 29 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1702-410_1702-403d others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
G | GAGAAAGA others(5): Show |
10 | a0001c0001t0002g0014a0001c0001t0002g0303a0001c0001t0005g0062others(7): Show | 10 | HG00609.hp2 HG01099.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1702-414_1702-403d others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
G | GAGAAAGA others(9): Show |
3 | a0001c0003t0003g0079a0002c0006t0008g0113a0003c0009t0007g0008 | 3 | HG00741.hp2 HG02896.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1702-418_1702-403d others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
G | GAGAAGAA others(4): Show |
2 | a0001c0004t0003g0049a0001c0007t0009g0254 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1702-458_1702-457i others(13): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
GAGAA | G | 41 | a0001c0001t0002g0015a0001c0001t0002g0162a0001c0001t0002g0250others(38): Show | 41 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1702-406_1702-403d others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
GAGAAAGA others(1): Show |
G | 43 | a0001c0001t0002g0249a0001c0001t0002g0325a0001c0001t0002g0326others(40): Show | 43 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1702-410_1702-403d others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
GAGAAAGA others(5): Show |
G | 31 | a0001c0002t0001g0020a0001c0002t0001g0022a0001c0002t0001g0056others(28): Show | 31 | HG00140.hp2 HG00558.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1702-414_1702-403d others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
GAGAAAGA others(9): Show |
G | 34 | a0001c0001t0002g0004a0001c0001t0005g0111a0001c0001t0005g0223others(31): Show | 34 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1702-418_1702-403d others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
GAGAAAGA others(13): Show |
G | 8 | a0001c0002t0001g0099a0001c0002t0001g0108a0001c0002t0001g0215others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1702-422_1702-403d others(22): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
GAGAAAGA others(17): Show |
G | 1 | a0001c0001t0005g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1702-426_1702-403d others(26): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754893
|
GAGAAAGA others(21): Show |
G | 2 | a0001c0001t0002g0171a0001c0004t0002g0145 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1702-430_1702-403d others(30): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754893 | |||||
| chr7:116754897
|
A | G | 1 | a0001c0002t0004g0244 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1702-458A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754897 | ||||||
| chr7:116754939
|
G | GAAAGAAA others(9): Show |
1 | a0001c0001t0005g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1702-403_1702-402i others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754939 | |||||
| chr7:116754949
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-406A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754949 | ||||||
| chr7:116754951
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-404G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754951 | ||||||
| chr7:116754952
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-403A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754952 | ||||||
| chr7:116754956
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-399A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754956 | ||||||
| chr7:116754970
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-385G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754970 | ||||||
| chr7:116754974
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-381G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754974 | ||||||
| chr7:116754975
|
C | G | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-380C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754975 | ||||||
| chr7:116754977
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1702-378G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754977 | ||||||
| chr7:116754983
|
G | GAAAGAAA others(4): Show |
1 | a0002c0006t0008g0113 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1702-372_1702-371i others(13): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754983 | ||||||
| chr7:116754983
|
G | GAAAGAAA others(16): Show |
1 | a0001c0002t0001g0099 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1702-372_1702-371i others(25): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116754983 | ||||||
| chr7:116754983
|
G | GGAAA | 41 | a0001c0001t0002g0031a0001c0001t0002g0304a0001c0001t0002g0322others(38): Show | 41 | HG00280.hp2 HG00673.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.1702-315_1702-312d others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
G | GGAAAGAA others(1): Show |
52 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0015others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1702-319_1702-312d others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
G | GGAAAGAA others(5): Show |
83 | a0001c0001t0002g0014a0001c0001t0002g0305a0001c0001t0002g0325others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.1702-323_1702-312d others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
G | GGAAAGAA others(9): Show |
50 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1702-327_1702-312d others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
G | GGAAAGAA others(13): Show |
41 | a0001c0001t0002g0134a0001c0001t0002g0326a0001c0001t0002g0327others(38): Show | 41 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1702-331_1702-312d others(22): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
G | GGAAAGAA others(17): Show |
10 | a0001c0001t0002g0249a0001c0001t0005g0093a0001c0002t0001g0102others(7): Show | 10 | HG00673.hp1 HG01099.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1702-335_1702-312d others(26): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
G | GGAAAGAA others(21): Show |
1 | a0001c0002t0001g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1702-339_1702-312d others(30): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
G | GGAAAGAA others(25): Show |
2 | a0001c0002t0001g0055a0001c0002t0001g0175 | 2 | NA18945.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1702-343_1702-312d others(34): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
G | GGAAGAAA others(12): Show |
1 | a0001c0001t0008g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1702-369_1702-368i others(21): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
GGAAA | G | 6 | a0001c0001t0005g0045a0001c0003t0003g0080a0001c0003t0003g0226others(3): Show | 6 | HG02027.hp2 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1702-315_1702-312d others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754983
|
GGAAAGAA others(9): Show |
G | 1 | a0001c0008t0002g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1702-327_1702-312d others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754983 | |||||
| chr7:116754994
|
A | AAGAAAGA others(3): Show |
4 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0021others(1): Show | 4 | HG01255.hp2 HG01346.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1702-359_1702-350d others(12): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116754994 | |||||
| chr7:116755036
|
G | GAAAGAAA others(6): Show |
1 | a0001c0003t0003g0164 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1702-312_1702-311i others(15): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755036 | |||||
| chr7:116755036
|
G | GAAAGAAA others(10): Show |
1 | a0001c0003t0006g0340 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1702-312_1702-311i others(19): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755036 | |||||
| chr7:116755041
|
A | AAAGAAAG others(4): Show |
1 | a0001c0002t0004g0298 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1702-312_1702-311i others(13): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755041 | |||||
| chr7:116755041
|
A | AAAGAAAG others(8): Show |
1 | a0003c0009t0010g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1702-312_1702-311i others(17): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755041 | |||||
| chr7:116755041
|
A | AAAGAAAG others(12): Show |
2 | a0001c0002t0004g0177a0001c0002t0004g0244 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1702-312_1702-311i others(21): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755041 | |||||
| chr7:116755041
|
A | AAAGAAAG others(16): Show |
1 | a0001c0001t0005g0184 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1702-312_1702-311i others(25): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755041 | |||||
| chr7:116755041
|
A | AAAGAAAG others(7): Show |
1 | a0001c0002t0013g0057 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1702-312_1702-311i others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755041 | |||||
| chr7:116755042
|
A | AAGAAAGA others(3): Show |
1 | a0001c0002t0004g0336 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1702-312_1702-311i others(12): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755042 | |||||
| chr7:116755042
|
A | AAGAAAGA others(11): Show |
1 | a0001c0001t0008g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1702-312_1702-311i others(20): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr7 | 116755042 | |||||
| chr7:116755043
|
A | AGAAAGAA others(14): Show |
1 | a0001c0005t0016g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1702-312_1702-311i others(23): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116755043 | ||||||
| chr7:116755203
|
C | T | 333 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1702-152C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 5/20 | chr7 | 116755203 | ||||||
| chr7:116755583
|
C | A | 1 | a0001c0003t0024g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1862+68C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116755583 | ||||||
| chr7:116756179
|
CT | C | 5 | a0001c0001t0006g0144a0001c0004t0003g0026a0001c0004t0003g0046others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1862+665delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116756179 | ||||||
| chr7:116756294
|
ATAAT | A | 9 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1862+780_1862+783d others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116756294 | ||||||
| chr7:116756299
|
A | C | 9 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1862+784A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116756299 | ||||||
| chr7:116756574
|
C | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0230a0001c0002t0004g0149others(1): Show | 4 | NA18945.hp1 NA18994.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1863-863C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116756574 | ||||||
| chr7:116756930
|
A | G | 2 | a0001c0001t0007g0331a0001c0001t0007g0339 | 2 | HG02071.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1863-507A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116756930 | ||||||
| chr7:116757044
|
C | T | 1 | a0001c0005t0010g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1863-393C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116757044 | ||||||
| chr7:116757059
|
T | C | 6 | a0001c0001t0006g0144a0001c0004t0003g0026a0001c0004t0003g0046others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1863-378T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116757059 | ||||||
| chr7:116757066
|
C | CA | 7 | a0001c0001t0002g0334a0001c0001t0006g0311a0001c0002t0001g0231others(4): Show | 7 | HG00621.hp1 HG02602.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1863-356dupA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 116757066 | |||||
| chr7:116757173
|
C | T | 1 | a0001c0003t0003g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1863-264C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116757173 | ||||||
| chr7:116757215
|
A | G | 1 | a0001c0003t0003g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1863-222A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 6/20 | chr7 | 116757215 | ||||||
| chr7:116758229
|
A | G | 2 | a0001c0002t0001g0108a0001c0022t0004g0151 | 2 | NA18954.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2103-230A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 8/20 | chr7 | 116758229 | ||||||
| chr7:116758267
|
A | G | 1 | a0001c0002t0004g0291 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2103-192A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 8/20 | chr7 | 116758267 | ||||||
| chr7:116758709
|
C | T | 40 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(37): Show | 40 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2264+89C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 9/20 | chr7 | 116758709 | ||||||
| chr7:116759076
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2265-315C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 9/20 | chr7 | 116759076 | ||||||
| chr7:116759077
|
G | A | 82 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.2265-314G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 9/20 | chr7 | 116759077 | ||||||
| chr7:116759099
|
C | G | 1 | a0001c0001t0020g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2265-292C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 9/20 | chr7 | 116759099 | ||||||
| chr7:116759132
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2265-259T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 9/20 | chr7 | 116759132 | ||||||
| chr7:116759163
|
G | A | 2 | a0001c0005t0007g0247a0011c0023t0007g0246 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2265-228G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 9/20 | chr7 | 116759163 | ||||||
| chr7:116759220
|
T | C | 1 | a0001c0003t0003g0100 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2265-171T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 9/20 | chr7 | 116759220 | ||||||
| chr7:116759644
|
C | G | 1 | a0001c0001t0007g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2364+154C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116759644 | ||||||
| chr7:116759869
|
C | T | 2 | a0001c0005t0006g0138a0001c0005t0006g0139 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2364+379C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116759869 | ||||||
| chr7:116759887
|
C | T | 4 | a0001c0001t0003g0033a0001c0001t0006g0261a0001c0001t0015g0156others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2364+397C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116759887 | ||||||
| chr7:116759967
|
A | T | 14 | a0001c0001t0002g0004a0001c0001t0002g0013a0001c0001t0002g0171others(11): Show | 14 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2364+477A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116759967 | ||||||
| chr7:116760080
|
G | A | 1 | a0001c0003t0006g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2364+590G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116760080 | ||||||
| chr7:116760982
|
G | T | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2364+1492G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116760982 | ||||||
| chr7:116761375
|
G | A | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2365-1675G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116761375 | ||||||
| chr7:116761615
|
G | T | 9 | a0001c0001t0002g0162a0001c0004t0008g0190a0001c0005t0007g0146others(6): Show | 9 | HG01243.hp1 HG02647.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-1435G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116761615 | ||||||
| chr7:116761851
|
T | C | 1 | a0001c0001t0008g0058 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2365-1199T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116761851 | ||||||
| chr7:116761902
|
T | C | 1 | a0001c0002t0001g0215 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2365-1148T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116761902 | ||||||
| chr7:116761920
|
T | C | 12 | a0001c0001t0003g0033a0001c0001t0006g0144a0001c0001t0006g0261others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2365-1130T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116761920 | ||||||
| chr7:116762039
|
T | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0140others(8): Show | 11 | HG02055.hp2 HG02258.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2365-1011T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116762039 | ||||||
| chr7:116762046
|
CTA | C | 11 | a0001c0001t0007g0130a0001c0001t0007g0281a0001c0001t0007g0284others(8): Show | 11 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2365-1002_2365-100 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 116762046 | |||||
| chr7:116762069
|
A | C | 8 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2365-981A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116762069 | ||||||
| chr7:116762455
|
A | T | 7 | a0001c0004t0018g0256a0001c0005t0006g0154a0001c0005t0006g0155others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2365-595A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116762455 | ||||||
| chr7:116762679
|
A | G | 40 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(37): Show | 40 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2365-371A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116762679 | ||||||
| chr7:116762976
|
G | T | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2365-74G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116762976 | ||||||
| chr7:116763012
|
G | A | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2365-38G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 10/20 | chr7 | 116763012 | ||||||
| chr7:116763369
|
A | G | 1 | a0001c0005t0016g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2583+101A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116763369 | ||||||
| chr7:116763499
|
G | A | 1 | a0001c0002t0004g0316 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2583+231G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116763499 | ||||||
| chr7:116763688
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2583+420A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116763688 | ||||||
| chr7:116763865
|
T | C | 1 | a0001c0003t0006g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2583+597T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116763865 | ||||||
| chr7:116764592
|
A | G | 12 | a0001c0001t0003g0033a0001c0001t0006g0144a0001c0001t0006g0261others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2583+1324A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116764592 | ||||||
| chr7:116765018
|
A | G | 40 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(37): Show | 40 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2583+1750A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116765018 | ||||||
| chr7:116765027
|
C | T | 1 | a0001c0003t0021g0236 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2583+1759C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116765027 | ||||||
| chr7:116765286
|
C | CA | 104 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0140others(101): Show | 104 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.2583+2040dupA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116765286 | |||||
| chr7:116765286
|
C | CAA | 14 | a0001c0001t0002g0162a0001c0001t0007g0130a0001c0001t0007g0281others(11): Show | 14 | HG00438.hp1 HG00673.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2583+2039_2583+204 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116765286 | |||||
| chr7:116765333
|
T | C | 230 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2583+2065T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116765333 | ||||||
| chr7:116765370
|
C | G | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2583+2102C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116765370 | ||||||
| chr7:116766022
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2583+2754A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116766022 | ||||||
| chr7:116766156
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2583+2888A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116766156 | ||||||
| chr7:116766324
|
A | G | 6 | a0001c0002t0001g0213a0001c0002t0004g0275a0001c0002t0004g0276others(3): Show | 6 | NA18941.hp2 NA18950.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2583+3056A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116766324 | ||||||
| chr7:116766363
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2583+3095C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116766363 | ||||||
| chr7:116766497
|
C | T | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2584-3148C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116766497 | ||||||
| chr7:116766812
|
T | G | 1 | a0001c0001t0002g0333 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2584-2833T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116766812 | ||||||
| chr7:116766853
|
A | C | 1 | a0007c0016t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2584-2792A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116766853 | ||||||
| chr7:116767222
|
C | T | 3 | a0001c0002t0004g0017a0001c0002t0004g0243a0001c0002t0004g0335 | 3 | HG00140.hp2 HG01257.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.2584-2423C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767222 | ||||||
| chr7:116767386
|
G | A | 1 | a0001c0001t0027g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2584-2259G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767386 | ||||||
| chr7:116767507
|
C | A | 1 | a0001c0002t0004g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2584-2138C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767507 | ||||||
| chr7:116767829
|
T | C | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2584-1816T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767829 | ||||||
| chr7:116767838
|
T | C | 1 | a0001c0002t0004g0309 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2584-1807T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767838 | ||||||
| chr7:116767961
|
C | CAT | 93 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0162others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2584-1671_2584-167 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116767961 | |||||
| chr7:116767974
|
A | ATATG | 3 | a0001c0004t0023g0027a0001c0004t0030g0197a0001c0018t0017g0029 | 3 | HG03453.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2584-1670_2584-166 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116767974 | |||||
| chr7:116767974
|
A | ATG | 79 | a0001c0001t0026g0205a0001c0002t0001g0019a0001c0002t0001g0042others(76): Show | 79 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.2584-1639_2584-163 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116767974 | |||||
| chr7:116767974
|
A | ATGTG | 9 | a0001c0002t0001g0053a0001c0002t0001g0219a0001c0002t0013g0057others(6): Show | 9 | HG02451.hp1 HG02723.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2584-1641_2584-163 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116767974 | |||||
| chr7:116767974
|
A | G | 1 | a0001c0004t0003g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2584-1671A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767974 | ||||||
| chr7:116767974
|
ATG | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(75): Show | 78 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2584-1639_2584-163 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116767974 | |||||
| chr7:116767974
|
ATGTG | A | 5 | a0001c0001t0002g0303a0001c0001t0002g0306a0001c0001t0005g0034others(2): Show | 5 | HG00280.hp1 HG01192.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2584-1641_2584-163 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116767974 | |||||
| chr7:116767976
|
G | A | 20 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0249others(17): Show | 20 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.2584-1669G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767976 | ||||||
| chr7:116767978
|
G | A | 67 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(64): Show | 67 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.2584-1667G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767978 | ||||||
| chr7:116767980
|
G | A | 3 | a0001c0001t0002g0303a0001c0001t0002g0306a0001c0001t0005g0034 | 3 | HG01192.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2584-1665G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767980 | ||||||
| chr7:116767982
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2584-1663G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116767982 | ||||||
| chr7:116768026
|
G | GTA | 17 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0014others(14): Show | 17 | HG01891.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2584-1602_2584-160 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116768026 | |||||
| chr7:116768028
|
A | G | 2 | a0001c0002t0001g0212a0002c0010t0001g0116 | 2 | HG00438.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2584-1617A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116768028 | ||||||
| chr7:116768043
|
T | A | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2584-1602T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116768043 | ||||||
| chr7:116768065
|
T | C | 1 | a0001c0004t0018g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2584-1580T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116768065 | ||||||
| chr7:116768191
|
T | C | 7 | a0001c0001t0002g0317a0001c0001t0002g0329a0001c0001t0002g0332others(4): Show | 7 | HG00558.hp1 HG02135.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.2584-1454T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116768191 | ||||||
| chr7:116768760
|
A | G | 12 | a0001c0001t0003g0033a0001c0001t0006g0144a0001c0001t0006g0261others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2584-885A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116768760 | ||||||
| chr7:116769011
|
A | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2584-634A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116769011 | ||||||
| chr7:116769546
|
T | A | 1 | a0001c0003t0003g0051 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2584-99T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | chr7 | 116769546 | ||||||
| chr7:116769621
|
C | CT | 12 | a0001c0001t0007g0313a0001c0003t0003g0232a0001c0004t0003g0047others(9): Show | 12 | HG01891.hp1 HG01934.hp1 HG02615.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.2584-9dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116769621 | |||||
| chr7:116769621
|
CT | C | 97 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(94): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2584-9delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr7 | 116769621 | |||||
| chr7:116769826
|
A | C | 1 | a0001c0003t0003g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2730+35A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116769826 | ||||||
| chr7:116769981
|
G | A | 2 | a0001c0001t0008g0167a0001c0001t0008g0168 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2730+190G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116769981 | ||||||
| chr7:116770039
|
C | T | 1 | a0001c0002t0004g0316 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2730+248C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116770039 | ||||||
| chr7:116770067
|
A | G | 7 | a0001c0004t0018g0256a0001c0005t0006g0154a0001c0005t0006g0155others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2730+276A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116770067 | ||||||
| chr7:116770076
|
G | A | 2 | a0001c0002t0004g0176a0001c0002t0004g0177 | 2 | HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2730+285G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116770076 | ||||||
| chr7:116770487
|
C | T | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2730+696C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116770487 | ||||||
| chr7:116770508
|
A | G | 2 | a0006c0013t0002g0006a0010c0021t0002g0258 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2730+717A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116770508 | ||||||
| chr7:116770749
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2731-749C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116770749 | ||||||
| chr7:116770921
|
T | C | 1 | a0001c0002t0001g0022 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2731-577T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116770921 | ||||||
| chr7:116771071
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2731-427C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116771071 | ||||||
| chr7:116771106
|
C | T | 12 | a0001c0001t0003g0033a0001c0001t0006g0144a0001c0001t0006g0261others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2731-392C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116771106 | ||||||
| chr7:116771221
|
A | G | 1 | a0001c0001t0008g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2731-277A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116771221 | ||||||
| chr7:116771387
|
T | C | 1 | a0001c0002t0004g0238 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2731-111T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 12/20 | chr7 | 116771387 | ||||||
| chr7:116771724
|
G | A | 9 | a0001c0001t0002g0162a0001c0004t0008g0190a0001c0005t0007g0146others(6): Show | 9 | HG01243.hp1 HG02647.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2887+70G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 13/20 | chr7 | 116771724 | ||||||
| chr7:116771764
|
C | T | 1 | a0007c0016t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2888-85C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 13/20 | chr7 | 116771764 | ||||||
| chr7:116771794
|
C | CCT | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2888-54_2888-53dup others(2): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr7 | 116771794 | |||||
| chr7:116771813
|
G | A | 3 | a0001c0001t0005g0111a0001c0001t0005g0223a0001c0001t0005g0224 | 3 | HG01358.hp1 HG01361.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2888-36G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 13/20 | chr7 | 116771813 | ||||||
| chr7:116772236
|
A | C | 1 | a0001c0004t0002g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3028+247A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116772236 | ||||||
| chr7:116772511
|
A | G | 2 | a0001c0004t0003g0048a0001c0004t0003g0050 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3028+522A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116772511 | ||||||
| chr7:116772705
|
T | C | 4 | a0001c0002t0001g0087a0001c0002t0001g0119a0001c0002t0001g0204others(1): Show | 4 | HG02071.hp2 NA18983.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.3028+716T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116772705 | ||||||
| chr7:116773071
|
GA | G | 9 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3028+1091delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 116773071 | |||||
| chr7:116773325
|
C | T | 1 | a0001c0003t0011g0074 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3028+1336C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116773325 | ||||||
| chr7:116773541
|
C | A | 2 | a0001c0004t0022g0255a0001c0004t0029g0189 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3029-1340C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116773541 | ||||||
| chr7:116773565
|
C | T | 2 | a0001c0003t0003g0164a0001c0003t0006g0340 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.3029-1316C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116773565 | ||||||
| chr7:116773732
|
C | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3029-1149C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116773732 | ||||||
| chr7:116774316
|
G | A | 1 | a0001c0008t0002g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3029-565G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116774316 | ||||||
| chr7:116774841
|
T | C | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3029-40T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 14/20 | chr7 | 116774841 | ||||||
| chr7:116775296
|
T | C | 1 | a0001c0002t0001g0121 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3259+185T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116775296 | ||||||
| chr7:116775430
|
G | A | 4 | a0001c0003t0003g0084a0001c0003t0006g0153a0001c0003t0006g0285others(1): Show | 4 | NA18973.hp1 NA18974.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.3259+319G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116775430 | ||||||
| chr7:116775824
|
G | C | 1 | a0001c0002t0004g0161 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3259+713G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116775824 | ||||||
| chr7:116775956
|
G | T | 231 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.3259+845G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116775956 | ||||||
| chr7:116775973
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3259+862G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116775973 | ||||||
| chr7:116776273
|
C | T | 66 | a0001c0001t0006g0311a0001c0001t0026g0205a0001c0003t0003g0043others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3260-1116C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116776273 | ||||||
| chr7:116776369
|
G | A | 2 | a0001c0002t0004g0238a0001c0002t0004g0245 | 2 | HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3260-1020G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116776369 | ||||||
| chr7:116776827
|
T | C | 1 | a0001c0003t0003g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3260-562T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116776827 | ||||||
| chr7:116776896
|
A | G | 6 | a0001c0001t0006g0144a0001c0004t0003g0026a0001c0004t0003g0046others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3260-493A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116776896 | ||||||
| chr7:116777051
|
T | A | 1 | a0001c0005t0006g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3260-338T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116777051 | ||||||
| chr7:116777052
|
A | G | 2 | a0001c0001t0006g0311a0001c0003t0006g0198 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3260-337A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116777052 | ||||||
| chr7:116777156
|
T | C | 9 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3260-233T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116777156 | ||||||
| chr7:116777186
|
T | C | 6 | a0001c0001t0007g0025a0001c0001t0007g0172a0001c0001t0007g0260others(3): Show | 6 | HG01496.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3260-203T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 15/20 | chr7 | 116777186 | ||||||
| chr7:116777794
|
G | C | 97 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(94): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.3340+325G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 16/20 | chr7 | 116777794 | ||||||
| chr7:116778031
|
G | A | 1 | a0001c0001t0006g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3340+562G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 16/20 | chr7 | 116778031 | ||||||
| chr7:116778679
|
G | A | 1 | a0001c0002t0001g0020 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3341-97G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 16/20 | chr7 | 116778679 | ||||||
| chr7:116779208
|
T | C | 12 | a0001c0001t0003g0033a0001c0001t0006g0144a0001c0001t0006g0261others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3522+251T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116779208 | ||||||
| chr7:116779285
|
G | A | 1 | a0001c0002t0004g0297 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3522+328G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116779285 | ||||||
| chr7:116779576
|
C | T | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3522+619C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116779576 | ||||||
| chr7:116780504
|
C | A | 66 | a0001c0001t0006g0311a0001c0001t0026g0205a0001c0003t0003g0043others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3523-1484C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116780504 | ||||||
| chr7:116780520
|
TG | T | 3 | a0001c0005t0007g0146a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG01243.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3523-1466delG | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr7 | 116780520 | |||||
| chr7:116780597
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3523-1391C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116780597 | ||||||
| chr7:116781140
|
C | T | 2 | a0001c0002t0004g0176a0001c0002t0004g0177 | 2 | HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.3523-848C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116781140 | ||||||
| chr7:116781747
|
C | T | 6 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3523-241C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116781747 | ||||||
| chr7:116781771
|
T | A | 8 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3523-217T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116781771 | ||||||
| chr7:116781825
|
G | A | 8 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3523-163G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116781825 | ||||||
| chr7:116781913
|
T | C | 231 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.3523-75T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 17/20 | chr7 | 116781913 | ||||||
| chr7:116782160
|
C | T | 9 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3632+63C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 18/20 | chr7 | 116782160 | ||||||
| chr7:116782231
|
G | A | 1 | a0001c0003t0003g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3632+134G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 18/20 | chr7 | 116782231 | ||||||
| chr7:116782241
|
C | G | 1 | a0001c0004t0008g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3632+144C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 18/20 | chr7 | 116782241 | ||||||
| chr7:116782563
|
T | C | 9 | a0001c0004t0003g0195a0001c0005t0006g0007a0001c0005t0006g0129others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3632+466T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 18/20 | chr7 | 116782563 | ||||||
| chr7:116782956
|
T | C | 2 | a0001c0003t0003g0076a0001c0003t0003g0080 | 2 | HG02027.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3633-348T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 18/20 | chr7 | 116782956 | ||||||
| chr7:116783107
|
G | A | 55 | a0001c0001t0026g0205a0001c0003t0003g0043a0001c0003t0003g0051others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.3633-197G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 18/20 | chr7 | 116783107 | ||||||
| chr7:116783266
|
A | G | 9 | a0001c0003t0009g0264a0001c0003t0009g0265a0001c0003t0009g0266others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3633-38A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 18/20 | chr7 | 116783266 | ||||||
| chr7:116783277
|
G | T | 2 | a0001c0002t0001g0099a0001c0002t0004g0312 | 2 | HG02083.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.3633-27G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 18/20 | chr7 | 116783277 | ||||||
| chr7:116783544
|
T | C | 1 | a0001c0003t0006g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3798+75T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116783544 | ||||||
| chr7:116783660
|
T | C | 2 | a0001c0001t0002g0012a0001c0004t0002g0145 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3798+191T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116783660 | ||||||
| chr7:116783729
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3798+260G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116783729 | ||||||
| chr7:116783947
|
T | G | 14 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0013others(11): Show | 14 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3798+478T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116783947 | ||||||
| chr7:116784101
|
T | C | 1 | a0001c0003t0003g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3798+632T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784101 | ||||||
| chr7:116784139
|
C | A | 1 | a0001c0003t0003g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3798+670C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784139 | ||||||
| chr7:116784419
|
A | G | 1 | a0001c0001t0007g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3798+950A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784419 | ||||||
| chr7:116784645
|
C | A | 3 | a0001c0005t0007g0146a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG01243.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3798+1176C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784645 | ||||||
| chr7:116784808
|
A | T | 2 | a0001c0001t0007g0313a0001c0001t0008g0188 | 2 | HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3798+1339A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784808 | ||||||
| chr7:116784877
|
C | G | 2 | a0001c0001t0002g0249a0001c0001t0002g0250 | 2 | HG01433.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3798+1408C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784877 | ||||||
| chr7:116784884
|
C | A | 1 | a0002c0006t0008g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3798+1415C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784884 | ||||||
| chr7:116784933
|
C | T | 1 | a0001c0002t0004g0297 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3798+1464C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784933 | ||||||
| chr7:116784971
|
C | T | 1 | a0001c0002t0004g0314 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3798+1502C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116784971 | ||||||
| chr7:116785186
|
G | A | 1 | a0001c0003t0003g0110 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3798+1717G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116785186 | ||||||
| chr7:116785199
|
G | A | 1 | a0001c0005t0016g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3798+1730G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116785199 | ||||||
| chr7:116785439
|
G | A | 231 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.3798+1970G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116785439 | ||||||
| chr7:116785574
|
CA | C | 5 | a0001c0002t0001g0054a0001c0002t0001g0055a0001c0002t0001g0178others(2): Show | 5 | HG00597.hp1 NA18612.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798+2106delA | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116785574 | ||||||
| chr7:116785601
|
A | G | 4 | a0001c0001t0003g0033a0001c0001t0006g0261a0001c0001t0015g0156others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3798+2132A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116785601 | ||||||
| chr7:116785831
|
CT | C | 5 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0002g0327others(2): Show | 5 | NA18955.hp2 NA18992.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798+2363delT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116785831 | ||||||
| chr7:116785907
|
C | A | 11 | a0001c0001t0006g0311a0001c0003t0006g0198a0001c0003t0009g0264others(8): Show | 11 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3798+2438C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116785907 | ||||||
| chr7:116785959
|
C | A | 1 | a0001c0002t0004g0237 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3798+2490C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116785959 | ||||||
| chr7:116786170
|
C | T | 11 | a0001c0001t0006g0311a0001c0003t0006g0198a0001c0003t0009g0264others(8): Show | 11 | HG01433.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3798+2701C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116786170 | ||||||
| chr7:116786235
|
A | T | 1 | a0001c0001t0005g0062 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3798+2766A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116786235 | ||||||
| chr7:116786259
|
G | A | 1 | a0002c0006t0008g0233 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3798+2790G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116786259 | ||||||
| chr7:116786621
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3798+3152G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116786621 | ||||||
| chr7:116786965
|
A | G | 55 | a0001c0001t0026g0205a0001c0003t0003g0043a0001c0003t0003g0051others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.3798+3496A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116786965 | ||||||
| chr7:116787023
|
C | T | 1 | a0001c0002t0001g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3798+3554C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116787023 | ||||||
| chr7:116787247
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0329a0001c0001t0005g0038others(10): Show | 13 | HG00438.hp2 HG02135.hp1 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.3798+3778T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116787247 | ||||||
| chr7:116787593
|
C | T | 7 | a0001c0004t0018g0256a0001c0005t0006g0154a0001c0005t0006g0155others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798+4124C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116787593 | ||||||
| chr7:116787680
|
T | C | 1 | a0001c0005t0007g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3798+4211T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116787680 | ||||||
| chr7:116787881
|
C | T | 1 | a0001c0001t0008g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3798+4412C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116787881 | ||||||
| chr7:116787911
|
C | A | 1 | a0001c0003t0003g0169 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3798+4442C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116787911 | ||||||
| chr7:116788266
|
C | G | 3 | a0001c0004t0002g0157a0001c0008t0002g0030a0001c0008t0002g0242 | 3 | HG00280.hp1 HG00642.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3798+4797C>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116788266 | ||||||
| chr7:116788337
|
G | A | 2 | a0001c0003t0003g0063a0001c0003t0003g0169 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.3798+4868G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116788337 | ||||||
| chr7:116788428
|
G | A | 1 | a0001c0005t0006g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3798+4959G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116788428 | ||||||
| chr7:116788519
|
A | C | 291 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.3798+5050A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116788519 | ||||||
| chr7:116788543
|
C | T | 1 | a0001c0004t0002g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3798+5074C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116788543 | ||||||
| chr7:116788765
|
A | G | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3798+5296A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116788765 | ||||||
| chr7:116788791
|
A | G | 5 | a0001c0001t0002g0140a0001c0001t0002g0303a0001c0001t0002g0304others(2): Show | 5 | HG02258.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798+5322A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116788791 | ||||||
| chr7:116789180
|
G | C | 39 | a0001c0001t0002g0162a0001c0001t0007g0025a0001c0001t0007g0130others(36): Show | 39 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.3798+5711G>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116789180 | ||||||
| chr7:116789317
|
A | T | 1 | a0001c0003t0003g0071 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3798+5848A>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116789317 | ||||||
| chr7:116789759
|
T | C | 1 | a0001c0002t0004g0310 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3799-5896T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116789759 | ||||||
| chr7:116789993
|
C | A | 2 | a0001c0002t0004g0301a0002c0010t0001g0115 | 2 | HG02523.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.3799-5662C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116789993 | ||||||
| chr7:116790211
|
A | G | 66 | a0001c0001t0006g0311a0001c0001t0026g0205a0001c0003t0003g0043others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3799-5444A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116790211 | ||||||
| chr7:116790308
|
T | C | 231 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.3799-5347T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116790308 | ||||||
| chr7:116790561
|
C | T | 1 | a0001c0002t0004g0338 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3799-5094C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116790561 | ||||||
| chr7:116790598
|
C | T | 14 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0013others(11): Show | 14 | HG01358.hp1 HG01361.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3799-5057C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116790598 | ||||||
| chr7:116790607
|
A | C | 1 | a0001c0005t0006g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3799-5048A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116790607 | ||||||
| chr7:116790646
|
T | C | 61 | a0001c0002t0001g0019a0001c0002t0001g0042a0001c0002t0001g0044others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.3799-5009T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116790646 | ||||||
| chr7:116790647
|
C | A | 61 | a0001c0002t0001g0019a0001c0002t0001g0042a0001c0002t0001g0044others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.3799-5008C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116790647 | ||||||
| chr7:116790921
|
A | C | 1 | a0001c0001t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3799-4734A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116790921 | ||||||
| chr7:116791216
|
G | T | 1 | a0010c0021t0002g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3799-4439G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116791216 | ||||||
| chr7:116791373
|
C | T | 255 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0013others(252): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.3799-4282C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116791373 | ||||||
| chr7:116791894
|
T | G | 55 | a0001c0001t0026g0205a0001c0003t0003g0043a0001c0003t0003g0051others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.3799-3761T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116791894 | ||||||
| chr7:116791944
|
G | A | 1 | a0001c0004t0003g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3799-3711G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116791944 | ||||||
| chr7:116791952
|
T | C | 333 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.3799-3703T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116791952 | ||||||
| chr7:116792037
|
T | G | 2 | a0001c0004t0003g0048a0001c0004t0003g0050 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3799-3618T>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116792037 | ||||||
| chr7:116792085
|
A | AT | 108 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3799-3562dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792085 | |||||
| chr7:116792161
|
T | C | 1 | a0001c0003t0009g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3799-3494T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116792161 | ||||||
| chr7:116792406
|
A | C | 1 | a0001c0001t0007g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3799-3249A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116792406 | ||||||
| chr7:116792420
|
T | C | 1 | a0001c0001t0026g0205 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3799-3235T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116792420 | ||||||
| chr7:116792456
|
G | GAC | 59 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0162others(56): Show | 59 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.3799-3154_3799-315 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
G | GACAC | 25 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324others(22): Show | 25 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.3799-3156_3799-315 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
G | GACACAC | 31 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0005g0085others(28): Show | 31 | HG00621.hp1 HG00673.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.3799-3158_3799-315 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
G | GACACACA others(3): Show |
6 | a0001c0001t0007g0331a0001c0001t0007g0339a0001c0005t0007g0146others(3): Show | 6 | HG00544.hp1 HG01243.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3799-3162_3799-315 others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
G | GACACACA others(5): Show |
6 | a0001c0001t0007g0130a0001c0003t0006g0198a0001c0004t0008g0190others(3): Show | 6 | HG03209.hp2 HG03540.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.3799-3164_3799-315 others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
G | GACACACA others(7): Show |
3 | a0001c0001t0008g0165a0001c0005t0007g0247a0011c0023t0007g0246 | 3 | HG03139.hp2 HG03688.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3799-3166_3799-315 others(18): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
G | GACACACA others(9): Show |
2 | a0003c0009t0007g0008a0003c0009t0007g0009 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3799-3168_3799-315 others(20): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
G | GACACACA others(13): Show |
1 | a0001c0001t0008g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3799-3172_3799-315 others(24): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
GAC | G | 10 | a0001c0001t0002g0011a0001c0001t0002g0171a0001c0001t0005g0183others(7): Show | 10 | HG00323.hp2 HG00741.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.3799-3154_3799-315 others(6): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
GACAC | G | 6 | a0001c0001t0002g0329a0001c0001t0005g0174a0001c0001t0005g0184others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.3799-3156_3799-315 others(8): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
GACACAC | G | 23 | a0001c0001t0002g0134a0001c0001t0015g0156a0001c0002t0001g0179others(20): Show | 23 | HG00323.hp1 HG00408.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.3799-3158_3799-315 others(10): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
GACACACA others(1): Show |
G | 99 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.3799-3160_3799-315 others(12): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
GACACACA others(3): Show |
G | 1 | a0001c0002t0004g0244 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3799-3162_3799-315 others(14): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792456
|
GACACACA others(5): Show |
G | 1 | a0001c0004t0003g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3799-3164_3799-315 others(16): Show |
MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116792456 | |||||
| chr7:116792472
|
C | T | 4 | a0001c0002t0001g0272a0001c0002t0001g0273a0001c0002t0004g0131others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.3799-3183C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116792472 | ||||||
| chr7:116792735
|
A | G | 5 | a0001c0005t0006g0007a0001c0005t0006g0129a0001c0005t0006g0135others(2): Show | 5 | HG02451.hp1 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3799-2920A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116792735 | ||||||
| chr7:116792841
|
A | C | 1 | a0001c0002t0004g0243 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3799-2814A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116792841 | ||||||
| chr7:116792913
|
A | G | 1 | a0001c0004t0003g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3799-2742A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116792913 | ||||||
| chr7:116793109
|
A | C | 1 | a0001c0001t0005g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3799-2546A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793109 | ||||||
| chr7:116793177
|
C | CT | 71 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0013others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.3799-2463dupT | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 116793177 | |||||
| chr7:116793198
|
G | A | 1 | a0001c0002t0001g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3799-2457G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793198 | ||||||
| chr7:116793342
|
T | C | 1 | a0001c0001t0007g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3799-2313T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793342 | ||||||
| chr7:116793420
|
C | T | 2 | a0001c0003t0003g0065a0001c0003t0003g0075 | 2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.3799-2235C>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793420 | ||||||
| chr7:116793428
|
G | A | 1 | a0001c0003t0003g0100 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3799-2227G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793428 | ||||||
| chr7:116793473
|
T | C | 108 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3799-2182T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793473 | ||||||
| chr7:116793576
|
G | A | 108 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3799-2079G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793576 | ||||||
| chr7:116793886
|
G | A | 1 | a0008c0014t0001g0217 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3799-1769G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793886 | ||||||
| chr7:116793927
|
A | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0140others(8): Show | 11 | HG02055.hp2 HG02258.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.3799-1728A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116793927 | ||||||
| chr7:116794248
|
A | C | 4 | a0001c0001t0002g0274a0001c0001t0002g0322a0001c0001t0002g0323others(1): Show | 4 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.3799-1407A>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116794248 | ||||||
| chr7:116794284
|
G | A | 109 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.3799-1371G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116794284 | ||||||
| chr7:116794411
|
A | G | 1 | a0001c0001t0005g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3799-1244A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116794411 | ||||||
| chr7:116794739
|
C | A | 109 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.3799-916C>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116794739 | ||||||
| chr7:116794862
|
G | A | 1 | a0001c0002t0004g0301 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3799-793G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116794862 | ||||||
| chr7:116794897
|
T | C | 1 | a0001c0001t0015g0156 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3799-758T>C | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116794897 | ||||||
| chr7:116795069
|
A | G | 73 | a0001c0001t0006g0311a0001c0001t0026g0205a0001c0003t0003g0043others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.3799-586A>G | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116795069 | ||||||
| chr7:116795268
|
G | T | 1 | a0001c0018t0017g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3799-387G>T | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116795268 | ||||||
| chr7:116795314
|
G | A | 1 | a0001c0003t0006g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3799-341G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116795314 | ||||||
| chr7:116795362
|
G | A | 109 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.3799-293G>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116795362 | ||||||
| chr7:116795371
|
T | A | 1 | a0001c0003t0003g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3799-284T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116795371 |