Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0002 | 0/0 | 1390 | 9 | 0 | 2 | 7 | 0 | 0 | 4 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0003 | 0/0 | 1390 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0004 | 0/0 | 1390 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0005 | 0/0 | 1390 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0006 | 0/0 | 1390 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0007 | 0/0 | 1390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0008 | 0/0 | 1390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0009 | 0/0 | 1390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0010 | 0/0 | 1390 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0011 | 0/0 | 1390 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| a0012 | 0/0 | 1390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | MKAPA others(1385): Show |
chr7 | 116667196 | 116803377 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4170 | 108 | 32 | 24 | 36 | 2 | 12 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0002 | 0/0 | 4170 | 103 | 5 | 22 | 55 | 4 | 17 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0003 | 0/0 | 4170 | 55 | 4 | 9 | 34 | 2 | 6 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0004 | 0/0 | 4170 | 20 | 20 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0005 | 0/0 | 4170 | 15 | 14 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0007 | 0/0 | 4170 | 5 | 5 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0008 | 0/0 | 4170 | 4 | 1 | 2 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0015 | 0/0 | 4170 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0017 | 0/0 | 4170 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0018 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0019 | 0/0 | 4170 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0022 | 0/0 | 4170 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0001c0025 | 0/0 | 4170 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0002c0006 | 0/0 | 4170 | 6 | 0 | 2 | 4 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0002c0010 | 0/0 | 4170 | 3 | 0 | 0 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0003c0009 | 0/0 | 4170 | 4 | 4 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0004c0012 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0005c0011 | 0/0 | 4170 | 2 | 0 | 0 | 2 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0006c0016 | 0/0 | 4170 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0007c0021 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0008c0013 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0009c0020 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0010c0024 | 0/0 | 4170 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0011c0014 | 0/0 | 4170 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
chr7 | 116667196 | 116803377 | ||
| a0012c0023 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | ATGAA others(4165): Show |
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 | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0003 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0005 | 0/0 | 6822 | 35 | 4 | 11 | 16 | 1 | 3 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0006 | 0/0 | 6822 | 3 | 3 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0007 | 0/0 | 6822 | 14 | 4 | 4 | 4 | 0 | 2 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0008 | 0/0 | 6822 | 11 | 0 | 3 | 4 | 0 | 4 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0015 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0020 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0026 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0001t0027 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0002t0001 | 0/0 | 6822 | 56 | 4 | 10 | 34 | 2 | 6 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0002t0004 | 0/0 | 6822 | 44 | 1 | 11 | 19 | 2 | 11 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0002t0013 | 0/0 | 6822 | 2 | 0 | 0 | 2 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0002t0028 | 0/0 | 6822 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0003t0003 | 0/0 | 6822 | 35 | 0 | 5 | 23 | 2 | 5 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0003t0006 | 0/0 | 6822 | 12 | 1 | 2 | 8 | 0 | 1 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0003t0009 | 0/0 | 6822 | 3 | 3 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0003t0011 | 0/0 | 6822 | 3 | 0 | 0 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0003t0021 | 0/0 | 6822 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0003t0024 | 0/0 | 6822 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0002 | 0/0 | 6822 | 4 | 4 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0003 | 0/0 | 6822 | 7 | 7 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0005 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0008 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0012 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0018 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0022 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0023 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0029 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0004t0030 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0005t0002 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0005t0006 | 0/0 | 6822 | 8 | 8 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0005t0007 | 0/0 | 6822 | 2 | 1 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0005t0010 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0005t0016 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0005t0025 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0007t0009 | 0/0 | 6822 | 4 | 4 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0007t0014 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0008t0002 | 0/0 | 6822 | 3 | 0 | 2 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0008t0005 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0015t0003 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0017t0003 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0018t0017 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0019t0001 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0022t0004 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0001c0025t0005 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0002c0006t0007 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0002c0006t0008 | 0/0 | 6822 | 5 | 0 | 2 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0002c0010t0001 | 0/0 | 6822 | 3 | 0 | 0 | 3 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0003c0009t0007 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0003c0009t0008 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0003c0009t0010 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0004c0012t0006 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0005c0011t0002 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0005c0011t0019 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0006c0016t0003 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0007c0021t0002 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0008c0013t0002 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0009c0020t0003 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0010c0024t0003 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0011c0014t0001 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| a0012c0023t0007 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | AGACA others(6817): Show |
chr7 | 116667196 | 116803377 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0009 | 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 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0138 | 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 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0187 | 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 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0007g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0166 | 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 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0008g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0026g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0001t0027g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 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 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0047 | 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 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0100 | 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 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0200 | 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 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0223 | 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 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0013g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0002t0028g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0003t0003g0072 | 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 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0003g0208 | 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 |
| a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0003t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0003t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0021g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0003t0024g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0002g0146 | 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 |
| a0001c0004t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0029 | 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 |
| a0001c0004t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0008g0191 | 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 |
| a0001c0004t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0018g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0022g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0023g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0029g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0004t0030g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0136 | 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 |
| a0001c0005t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0006g0143 | 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 |
| a0001c0005t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0007g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0005t0025g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0007t0009g0252 | 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 |
| a0001c0007t0009g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0007t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0007t0014g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0008t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0008t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0008t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0015t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0017t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0018t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0019t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0022t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0001c0025t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0007g0006 | 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 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0008g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0006t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0002c0010t0001g0089 | 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 |
| a0002c0010t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0003c0009t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0003c0009t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0003c0009t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0003c0009t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0004c0012t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0004c0012t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0005c0011t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0005c0011t0019g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0006c0016t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0007c0021t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0008c0013t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0009c0020t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0010c0024t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0011c0014t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| a0012c0023t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 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 | a0006 | c0016 | t0003 | g0062 | EUR | GBR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00099 | hp2 | a0001 | c0001 | t0027 | g0124 | EUR | GBR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0081 | EUR | GBR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0332 | EUR | GBR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00280 | hp1 | a0001 | c0008 | t0002 | g0033 | EUR | FIN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0126 | EUR | FIN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0210 | EUR | FIN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0184 | EUR | FIN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00408 | hp2 | a0001 | c0003 | t0003 | g0070 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00438 | hp1 | a0002 | c0010 | t0001 | g0117 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0099 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00544 | hp1 | a0002 | c0006 | t0008 | g0234 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00597 | hp1 | a0001 | c0002 | t0004 | g0313 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00597 | hp2 | a0001 | c0003 | t0003 | g0085 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00609 | hp2 | a0001 | c0003 | t0011 | g0042 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00621 | hp1 | a0001 | c0003 | t0006 | g0004 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0299 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00639 | hp1 | a0001 | c0003 | t0006 | g0240 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0133 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00642 | hp2 | a0001 | c0008 | t0002 | g0243 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00673 | hp2 | a0001 | c0001 | t0007 | g0281 | EAS | CHS | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00733 | hp2 | a0001 | c0002 | t0004 | g0245 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00738 | hp1 | a0001 | c0003 | t0021 | g0237 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0194 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0076 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0068 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0285 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0077 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0284 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0094 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0054 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01099 | hp2 | a0001 | c0002 | t0004 | g0178 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01168 | hp2 | a0001 | c0002 | t0004 | g0246 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0175 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0288 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0221 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0037 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01243 | hp1 | a0001 | c0005 | t0007 | g0147 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0235 | AMR | PUR | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0187 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0283 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01256 | hp2 | a0001 | c0008 | t0002 | g0242 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01257 | hp1 | a0001 | c0002 | t0004 | g0244 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0269 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0193 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01346 | hp1 | a0001 | c0003 | t0006 | g0174 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0225 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01358 | hp2 | a0001 | c0002 | t0004 | g0177 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01361 | hp1 | a0002 | c0006 | t0008 | g0125 | 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 | g0188 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0264 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01496 | hp2 | a0001 | c0002 | t0004 | g0307 | AMR | CLM | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01891 | hp1 | a0001 | c0004 | t0018 | g0257 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01891 | hp2 | a0001 | c0007 | t0009 | g0254 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01934 | hp1 | a0002 | c0006 | t0008 | g0115 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01978 | hp1 | a0001 | c0002 | t0004 | g0287 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG01978 | hp2 | a0001 | c0002 | t0028 | g0268 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0084 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02015 | hp1 | a0001 | c0001 | t0008 | g0061 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02027 | hp2 | a0001 | c0003 | t0003 | g0078 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02040 | hp1 | a0001 | c0003 | t0006 | g0317 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02055 | hp1 | a0001 | c0007 | t0009 | g0252 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0336 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02074 | hp1 | a0001 | c0003 | t0006 | g0337 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0294 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02083 | hp1 | a0001 | c0002 | t0004 | g0309 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0165 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0101 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0229 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02135 | hp2 | a0001 | c0002 | t0004 | g0315 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | CDX | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | CDX | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0262 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0173 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0157 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0029 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0222 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0065 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0279 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PEL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02451 | hp1 | a0001 | c0005 | t0006 | g0136 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0146 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02523 | hp1 | a0002 | c0010 | t0001 | g0116 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02523 | hp2 | a0001 | c0003 | t0003 | g0104 | EAS | KHV | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02572 | hp1 | a0001 | c0004 | t0003 | g0052 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0306 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02615 | hp1 | a0007 | c0021 | t0002 | g0259 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02615 | hp2 | a0001 | c0005 | t0010 | g0137 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02622 | hp1 | a0001 | c0005 | t0016 | g0148 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02630 | hp1 | a0001 | c0004 | t0022 | g0256 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02630 | hp2 | a0001 | c0007 | t0014 | g0253 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02647 | hp1 | a0003 | c0009 | t0007 | g0011 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02647 | hp2 | a0001 | c0004 | t0003 | g0051 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02683 | hp2 | a0001 | c0001 | t0008 | g0189 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02717 | hp1 | a0001 | c0004 | t0003 | g0053 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0263 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02723 | hp2 | a0001 | c0005 | t0006 | g0010 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0170 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02809 | hp1 | a0001 | c0003 | t0009 | g0266 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02818 | hp2 | a0004 | c0012 | t0006 | g0031 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02886 | hp1 | a0001 | c0004 | t0005 | g0035 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02886 | hp2 | a0001 | c0005 | t0010 | g0286 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02896 | hp2 | a0003 | c0009 | t0007 | g0012 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02922 | hp2 | a0004 | c0012 | t0006 | g0258 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02965 | hp1 | a0001 | c0004 | t0003 | g0049 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02970 | hp1 | a0001 | c0005 | t0006 | g0143 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02970 | hp2 | a0001 | c0005 | t0006 | g0139 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02976 | hp2 | a0001 | c0004 | t0029 | g0190 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0308 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03098 | hp2 | a0001 | c0003 | t0009 | g0265 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03130 | hp1 | a0001 | c0005 | t0002 | g0144 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03139 | hp2 | a0001 | c0005 | t0007 | g0248 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0261 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03209 | hp2 | a0001 | c0003 | t0006 | g0199 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03225 | hp2 | a0001 | c0005 | t0025 | g0182 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03239 | hp1 | a0001 | c0003 | t0006 | g0160 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03239 | hp2 | a0001 | c0002 | t0004 | g0134 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03453 | hp1 | a0001 | c0004 | t0023 | g0030 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03486 | hp1 | a0001 | c0005 | t0006 | g0156 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03486 | hp2 | a0001 | c0007 | t0009 | g0255 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0020 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0002 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03492 | hp1 | a0001 | c0002 | t0004 | g0335 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0002 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03516 | hp1 | a0008 | c0013 | t0002 | g0008 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | ESN | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03540 | hp1 | a0001 | c0004 | t0008 | g0191 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03579 | hp1 | a0001 | c0018 | t0017 | g0032 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03579 | hp2 | a0009 | c0020 | t0003 | g0192 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0132 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0079 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0131 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0166 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0088 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03704 | hp2 | a0001 | c0002 | t0004 | g0311 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0066 | SAS | PJL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0236 | 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 | g0171 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03942 | hp2 | a0001 | c0002 | t0004 | g0334 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0169 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04115 | hp2 | a0001 | c0002 | t0004 | g0280 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0055 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04184 | hp2 | a0001 | c0002 | t0004 | g0289 | SAS | BEB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04204 | hp1 | a0001 | c0001 | t0008 | g0168 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0310 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG04228 | hp2 | a0001 | c0002 | t0004 | g0241 | SAS | STU | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18522 | hp2 | a0001 | c0004 | t0012 | g0129 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | CHB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18612 | hp2 | a0001 | c0003 | t0006 | g0318 | EAS | CHB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18747 | hp1 | a0005 | c0011 | t0019 | g0327 | EAS | CHB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | CHB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18906 | hp1 | a0003 | c0009 | t0008 | g0038 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18906 | hp2 | a0001 | c0004 | t0002 | g0159 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0295 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18941 | hp2 | a0001 | c0002 | t0004 | g0276 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18943 | hp2 | a0010 | c0024 | t0003 | g0074 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18950 | hp1 | a0001 | c0002 | t0004 | g0277 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18951 | hp1 | a0001 | c0003 | t0003 | g0071 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0275 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18953 | hp1 | a0001 | c0003 | t0003 | g0207 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18953 | hp2 | a0001 | c0001 | t0007 | g0328 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18954 | hp1 | a0001 | c0003 | t0003 | g0075 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0202 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18964 | hp1 | a0001 | c0002 | t0013 | g0108 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18965 | hp1 | a0001 | c0003 | t0006 | g0296 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18968 | hp1 | a0002 | c0006 | t0008 | g0113 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18969 | hp2 | a0001 | c0015 | t0003 | g0064 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18970 | hp2 | a0001 | c0003 | t0003 | g0082 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18973 | hp1 | a0001 | c0003 | t0006 | g0154 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18973 | hp2 | a0005 | c0011 | t0002 | g0316 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18974 | hp1 | a0001 | c0002 | t0004 | g0274 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0087 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18978 | hp1 | a0001 | c0003 | t0003 | g0072 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18979 | hp1 | a0001 | c0003 | t0003 | g0069 | 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 | g0205 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18983 | hp2 | a0001 | c0003 | t0011 | g0105 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18985 | hp1 | a0001 | c0003 | t0003 | g0067 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18985 | hp2 | a0001 | c0002 | t0004 | g0273 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0278 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0333 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18994 | hp1 | a0001 | c0002 | t0004 | g0151 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0162 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18995 | hp2 | a0001 | c0003 | t0006 | g0149 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19000 | hp1 | a0001 | c0003 | t0003 | g0228 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19000 | hp2 | a0011 | c0014 | t0001 | g0218 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19005 | hp1 | a0001 | c0025 | t0005 | g0107 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19005 | hp2 | a0002 | c0006 | t0008 | g0114 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19009 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19009 | hp2 | a0001 | c0003 | t0003 | g0227 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19010 | hp1 | a0001 | c0003 | t0006 | g0282 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19011 | hp1 | a0001 | c0003 | t0003 | g0080 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19011 | hp2 | a0002 | c0006 | t0007 | g0006 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0226 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19030 | hp1 | a0001 | c0003 | t0009 | g0267 | AFR | LWK | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19030 | hp2 | a0001 | c0004 | t0003 | g0050 | AFR | LWK | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19043 | hp1 | a0001 | c0007 | t0009 | g0260 | AFR | LWK | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19055 | hp1 | a0002 | c0010 | t0001 | g0089 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19055 | hp2 | a0001 | c0002 | t0004 | g0298 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0209 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19063 | hp2 | a0001 | c0017 | t0003 | g0086 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0073 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19068 | hp1 | a0001 | c0022 | t0004 | g0152 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19068 | hp2 | a0001 | c0003 | t0003 | g0046 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19074 | hp1 | a0001 | c0003 | t0011 | g0083 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19076 | hp1 | a0001 | c0003 | t0003 | g0233 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19078 | hp1 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19078 | hp2 | a0001 | c0002 | t0013 | g0060 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0150 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19084 | hp1 | a0001 | c0003 | t0003 | g0111 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19087 | hp1 | a0001 | c0002 | t0004 | g0297 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19089 | hp1 | a0001 | c0002 | t0004 | g0153 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19089 | hp2 | a0001 | c0001 | t0026 | g0206 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19091 | hp1 | a0001 | c0002 | t0004 | g0272 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19240 | hp1 | a0012 | c0023 | t0007 | g0247 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA19240 | hp2 | a0001 | c0005 | t0006 | g0140 | AFR | YRI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20129 | hp1 | a0001 | c0005 | t0006 | g0130 | AFR | ASW | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20129 | hp2 | a0001 | c0005 | t0006 | g0155 | 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 | g0238 | EUR | TSI | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0249 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02109 | hp2 | a0001 | c0004 | t0003 | g0196 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02559 | hp1 | a0001 | c0008 | t0005 | g0063 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0158 | AFR | ACB | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03471 | hp1 | a0001 | c0004 | t0030 | g0198 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG03471 | hp2 | a0003 | c0009 | t0010 | g0013 | AFR | MSL | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG06807 | hp1 | a0001 | c0004 | t0012 | g0128 | AFR | USA | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0239 | AFR | USA | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | USA | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | USA | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0291 | REF | REF | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0292 | REF | REF | MET_chr7_116667196_116803377 | MET | chr7 | 116667196 | 116803377 |
| view | 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 | a0010 | 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 | a0012 | 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 | a0004 | 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 | a0002 a0007 |
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 | a0007 a0008 |
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 | a0006 | 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 | a0011 | 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 | a0005 | 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 |
| view | 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 | a0004c0012 | 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 | a0001c0004 a0001c0019 a0002c0006 others(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 | a0001c0005 a0001c0007 a0012c0023 |
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 | a0001c0003 a0001c0007 a0001c0015 others(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 | a0001c0002 a0001c0019 a0001c0022 others(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 | a0001c0002 a0001c0019 a0001c0022 others(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 | a0001c0002 a0001c0019 a0001c0022 others(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 |
| view | 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 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(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 | a0001c0004t0023 a0001c0004t0030 |
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 | a0001c0003t0009 a0001c0003t0024 a0001c0007t0009 others(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 | a0005c0011t0019 | 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 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0020 others(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 | a0001c0004t0022 a0001c0004t0029 |
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 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0013 others(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 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0013 others(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 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0004t0018 a0001c0005t0010 a0001c0005t0025 others(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 | a0001c0004t0023 a0001c0004t0030 |
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 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0013 others(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 |
| view | 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 | a0001c0001t0002g0005 a0001c0003t0006g0004 |
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 | a0001c0001t0002g0314 a0001c0001t0002g0319 a0001c0001t0002g0320 others(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 | a0002c0006t0007g0006 | 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 | a0001c0001t0005g0312 | 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 | 296 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(293): 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 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(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 | 5 | a0001c0001t0005g0269 a0001c0002t0001g0003 a0001c0002t0028g0268 others(2): 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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 |
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 | a0001c0001t0006g0262 a0001c0001t0007g0263 a0001c0001t0007g0264 |
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 | a0001c0002t0004g0020 | 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 | a0001c0001t0007g0261 | 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 | a0001c0001t0007g0261 | 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 | a0001c0001t0005g0027 a0001c0002t0001g0021 a0001c0002t0001g0022 others(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 | a0001c0002t0004g0311 | 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 | a0001c0001t0007g0261 | 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 | a0001c0001t0002g0250 a0001c0001t0002g0251 a0001c0004t0018g0257 others(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 | 287 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(284): 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 | 101 | a0001c0001t0003g0036 a0001c0001t0005g0001 a0001c0001t0005g0037 others(98): 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 | a0001c0001t0002g0034 a0001c0001t0007g0261 a0001c0003t0009g0265 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0135 a0001c0001t0002g0138 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0008c0013t0002g0008 |
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 | a0001c0001t0002g0163 | 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 | a0001c0004t0012g0128 a0001c0004t0012g0129 |
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 | a0001c0001t0002g0135 a0001c0001t0002g0138 a0001c0001t0002g0141 others(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 | a0001c0004t0002g0249 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0004t0002g0249 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0135 a0001c0001t0002g0138 others(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 | a0001c0001t0002g0172 a0001c0001t0007g0173 |
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 | a0001c0001t0002g0172 a0001c0001t0007g0173 a0001c0003t0006g0174 |
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 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0004t0002g0249 others(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 | a0001c0001t0002g0034 a0001c0001t0002g0135 a0001c0001t0002g0138 others(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 | a0001c0002t0001g0179 a0001c0002t0001g0180 |
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 | a0001c0002t0001g0045 | 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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 |
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 | a0001c0002t0001g0181 | 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 | a0001c0004t0023g0030 a0004c0012t0006g0031 |
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 | a0001c0005t0006g0130 | 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 | a0001c0004t0002g0249 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0001t0007g0173 | 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 | a0001c0002t0004g0246 | 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 | a0001c0004t0003g0029 | 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 | a0001c0004t0002g0249 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0003t0003g0046 | 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 | a0001c0001t0006g0308 a0001c0003t0009g0265 a0001c0003t0009g0266 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0172 others(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 | 94 | a0001c0001t0005g0001 a0001c0001t0005g0048 a0001c0001t0005g0055 others(91): 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 | a0001c0002t0004g0178 | 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 | a0001c0002t0001g0176 a0001c0002t0004g0150 a0001c0002t0004g0151 others(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 | a0001c0001t0002g0172 a0001c0001t0007g0173 |
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 | a0001c0001t0002g0172 a0001c0001t0007g0173 |
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 | a0001c0005t0006g0155 a0001c0005t0006g0156 |
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 | a0001c0001t0006g0308 | 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 | a0001c0001t0002g0163 a0001c0004t0002g0249 a0001c0005t0007g0248 others(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 | a0001c0001t0007g0336 | 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 | 283 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(280): 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 | a0001c0001t0006g0308 | 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 | a0001c0004t0002g0249 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | 217 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(214): 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 | a0001c0002t0004g0272 a0001c0002t0004g0273 a0001c0002t0004g0274 others(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 | a0001c0001t0005g0112 | 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 | 220 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(217): 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 | a0001c0001t0002g0163 a0001c0001t0007g0261 a0001c0001t0007g0278 others(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 | a0001c0001t0002g0005 a0001c0001t0007g0131 a0001c0002t0001g0176 others(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 | 220 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(217): 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 | a0001c0002t0004g0313 | 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 | 220 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(217): 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 | a0001c0002t0001g0200 | 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 | 219 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(216): 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 | 214 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(211): 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 | a0001c0001t0002g0314 | 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 | a0001c0005t0016g0148 | 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 | a0001c0001t0007g0310 | 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 | a0001c0003t0003g0233 | 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 | a0001c0001t0007g0261 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(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 | a0001c0001t0027g0124 | 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 | a0001c0001t0002g0305 a0001c0001t0005g0106 a0001c0001t0005g0224 others(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 | a0001c0004t0012g0128 | 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 | a0001c0001t0005g0041 | 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 | a0001c0005t0025g0182 | 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 | a0001c0002t0001g0232 | 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 | a0001c0003t0011g0105 | 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 | a0001c0001t0003g0036 a0001c0001t0005g0037 a0001c0001t0005g0039 others(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 | a0001c0001t0002g0305 a0001c0001t0005g0055 a0001c0001t0008g0201 others(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 | a0001c0018t0017g0032 | 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 | a0001c0007t0009g0260 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0305 a0001c0001t0005g0161 others(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 | 213 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(210): 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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0172 others(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 | a0001c0001t0002g0034 | 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 | a0001c0003t0003g0054 | 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 | a0006c0016t0003g0062 | 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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0163 others(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 | a0001c0001t0006g0308 | 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 | a0001c0002t0001g0197 | 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 | a0001c0002t0001g0197 | 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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0172 others(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 | 212 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(209): 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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0163 others(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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0163 others(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 | a0001c0001t0002g0172 a0001c0001t0003g0036 a0001c0001t0005g0037 others(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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0163 others(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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0172 others(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 | a0001c0001t0002g0305 a0001c0001t0007g0131 a0001c0001t0007g0278 others(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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0163 others(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 | a0001c0001t0002g0135 | 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 | a0001c0001t0007g0281 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0305 a0001c0001t0005g0161 others(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 | a0001c0001t0002g0163 a0001c0001t0002g0305 a0001c0001t0005g0161 others(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 | a0001c0005t0006g0136 | 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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 |
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 | a0005c0011t0002g0316 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0305 a0001c0001t0005g0161 others(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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0172 others(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 | a0001c0001t0002g0172 a0001c0001t0003g0036 a0001c0001t0005g0037 others(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 | 301 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(298): 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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0172 others(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 | a0001c0001t0002g0034 a0001c0001t0005g0193 a0001c0001t0005g0194 others(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 | a0001c0001t0005g0175 a0001c0001t0005g0184 a0001c0001t0005g0185 others(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 | a0001c0005t0006g0155 | 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 | a0001c0005t0010g0137 | 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 | a0001c0015t0003g0064 | 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 | a0001c0004t0002g0146 a0001c0004t0002g0158 a0001c0004t0002g0159 others(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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0172 others(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 | 331 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(328): 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 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0172 others(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 | a0001c0002t0001g0021 | 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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 |
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 | a0001c0002t0004g0020 | 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 | a0001c0003t0006g0318 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0008g0061 | 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 | a0001c0001t0002g0172 a0001c0001t0003g0036 a0001c0001t0005g0037 others(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 | a0001c0004t0003g0053 | 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 | a0001c0018t0017g0032 | 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 | a0001c0004t0022g0256 a0001c0004t0029g0190 |
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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0272 a0001c0002t0004g0273 a0001c0002t0004g0274 others(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 | a0001c0001t0002g0331 | 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 | a0001c0004t0022g0256 a0001c0004t0029g0190 |
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 | a0001c0001t0002g0135 a0001c0001t0002g0305 a0001c0001t0005g0055 others(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 | a0001c0005t0002g0144 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0004t0018g0257 | 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 | a0001c0004t0002g0146 a0001c0004t0002g0158 a0001c0004t0002g0159 others(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 | a0001c0005t0002g0144 a0001c0005t0006g0143 a0001c0005t0016g0148 |
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 | a0004c0012t0006g0031 a0004c0012t0006g0258 |
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 | a0001c0002t0004g0287 a0001c0002t0004g0288 |
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 | a0001c0001t0005g0312 | 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 |
88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | a0001c0001t0008g0166 | 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 | a0001c0002t0001g0223 | 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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | a0001c0001t0002g0304 a0001c0001t0002g0330 a0001c0001t0005g0048 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0300 a0001c0001t0005g0040 others(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 | a0001c0004t0002g0146 a0001c0004t0002g0249 a0001c0004t0003g0196 others(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 | a0001c0004t0002g0158 a0001c0004t0002g0159 a0001c0004t0008g0191 others(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 | a0001c0001t0005g0088 a0001c0001t0007g0028 a0001c0001t0007g0173 others(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 | 76 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0003g0036 others(73): 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 | a0001c0003t0003g0087 a0001c0003t0006g0154 a0001c0017t0003g0086 |
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 | a0001c0002t0001g0232 | 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 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0005g0193 others(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 | a0001c0004t0002g0146 a0001c0004t0002g0158 a0001c0004t0002g0159 others(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 | a0001c0018t0017g0032 | 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 | a0001c0001t0007g0028 a0001c0001t0007g0173 a0001c0001t0007g0261 others(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 | a0001c0002t0004g0273 | 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 | a0001c0004t0002g0158 a0001c0004t0002g0159 |
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 | a0001c0001t0015g0157 | 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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | 1 | a0001c0002t0001g0003 | 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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | a0001c0001t0002g0135 a0001c0001t0005g0055 a0001c0001t0008g0221 others(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 | a0001c0003t0006g0160 | 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 | a0001c0002t0001g0123 a0001c0002t0001g0127 |
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 | a0001c0004t0002g0146 a0001c0004t0002g0158 a0001c0004t0002g0159 others(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 | a0001c0001t0002g0271 a0001c0001t0002g0319 a0001c0001t0002g0320 others(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 | a0001c0018t0017g0032 | 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 | 121 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(118): 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0003t0009g0265 a0001c0003t0009g0266 |
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 | a0001c0018t0017g0032 | 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 | a0001c0001t0005g0161 a0011c0014t0001g0218 |
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 | 89 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(86): 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 | a0001c0005t0007g0147 | 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 | a0001c0001t0002g0142 | 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 | 253 | a0001c0001t0002g0034 a0001c0001t0002g0135 a0001c0001t0002g0163 others(250): 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 | a0001c0001t0005g0175 a0001c0001t0005g0184 a0001c0001t0005g0185 others(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 | a0001c0001t0005g0312 | 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 | a0001c0018t0017g0032 | 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 | a0001c0004t0002g0146 a0001c0004t0002g0158 a0001c0004t0002g0159 others(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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0287 a0001c0002t0004g0288 |
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 | a0001c0002t0001g0093 a0001c0002t0004g0239 a0001c0002t0004g0246 others(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 | a0001c0004t0002g0146 | 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 | a0001c0005t0010g0286 | 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 | a0001c0019t0001g0171 | 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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | 89 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(86): 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0153 a0001c0002t0004g0272 a0001c0002t0004g0273 others(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 | a0001c0002t0004g0288 | 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 | a0001c0007t0009g0252 a0001c0007t0009g0254 a0001c0007t0009g0255 others(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 | a0002c0006t0007g0006 | 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
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 | a0001c0001t0008g0221 a0001c0001t0008g0222 a0001c0002t0001g0022 others(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 | a0001c0005t0010g0137 | 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 | a0001c0005t0002g0144 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0018t0017g0032 | 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 | a0001c0001t0005g0229 | 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 | a0001c0004t0003g0196 a0001c0004t0018g0257 a0002c0006t0007g0006 others(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 | a0001c0002t0001g0059 | 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 | a0012c0023t0007g0247 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0334 | 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 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0005g0193 others(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 | a0001c0004t0012g0128 a0001c0004t0012g0129 |
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 | 53 | a0001c0001t0005g0088 a0001c0001t0005g0229 a0001c0001t0008g0084 others(50): 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0001g0047 | 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 | a0001c0001t0007g0310 a0001c0001t0008g0189 |
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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0239 | 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 | a0001c0001t0002g0163 a0003c0009t0007g0011 a0003c0009t0007g0012 others(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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | a0001c0001t0002g0135 a0001c0001t0005g0055 a0001c0001t0008g0221 others(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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | 89 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(86): 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 | a0001c0004t0003g0196 | 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 | 121 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(118): 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 | a0001c0002t0001g0100 | 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 | a0001c0002t0001g0093 a0001c0002t0001g0123 a0001c0002t0001g0127 others(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 | a0001c0001t0008g0061 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | 40 | a0001c0001t0002g0005 a0001c0001t0002g0250 a0001c0001t0002g0251 others(37): 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 | a0001c0018t0017g0032 | 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 | a0001c0005t0006g0010 | 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 | a0001c0004t0002g0146 a0001c0004t0002g0158 a0001c0004t0002g0159 others(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 | a0001c0001t0005g0312 | 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 | a0001c0004t0002g0158 a0001c0004t0002g0159 |
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 | 89 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(86): 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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | a0001c0018t0017g0032 | 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 | a0001c0005t0006g0155 a0001c0005t0006g0156 a0001c0005t0007g0147 |
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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | 89 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(86): 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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | a0001c0002t0004g0236 a0001c0002t0004g0334 a0001c0002t0004g0335 |
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 | a0001c0002t0004g0246 | 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 | a0001c0004t0023g0030 a0001c0004t0030g0198 |
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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0005g0193 others(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 | a0001c0004t0012g0128 a0001c0004t0012g0129 |
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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0142 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(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 | a0001c0003t0003g0054 | 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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | a0001c0003t0003g0165 a0001c0003t0006g0337 |
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 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0004g0162 |
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 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0004g0162 |
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 | a0002c0006t0008g0114 | 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 | a0001c0004t0002g0146 a0001c0004t0002g0158 a0001c0004t0002g0159 others(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 | a0004c0012t0006g0031 a0004c0012t0006g0258 |
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 | a0001c0001t0002g0250 a0001c0001t0002g0251 |
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 | a0001c0001t0002g0135 a0001c0001t0002g0305 a0001c0001t0002g0329 others(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 | a0001c0004t0002g0249 a0001c0004t0023g0030 a0001c0004t0030g0198 |
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 | a0001c0002t0004g0238 a0001c0002t0004g0241 a0001c0002t0004g0280 others(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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0003t0003g0085 | 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 | a0001c0002t0001g0217 | 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 | a0001c0007t0009g0255 | 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 | a0001c0004t0002g0146 a0001c0004t0002g0158 a0001c0004t0002g0159 others(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 | 90 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(87): 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 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0005g0193 others(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 | a0004c0012t0006g0031 a0004c0012t0006g0258 |
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 | a0001c0001t0002g0305 a0001c0002t0001g0164 a0001c0003t0003g0170 |
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 | a0001c0003t0003g0066 | 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 | a0001c0004t0003g0196 a0001c0004t0018g0257 |
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 | a0001c0018t0017g0032 | 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 | 89 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(86): 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 | 88 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0172 others(85): 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 | a0001c0001t0002g0293 | 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 | a0001c0003t0006g0296 | 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 | a0001c0005t0010g0137 a0001c0005t0010g0286 a0001c0007t0009g0252 others(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 | a0001c0002t0001g0210 | 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 | a0001c0001t0006g0308 | 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 | a0001c0001t0005g0187 | 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 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0305 others(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 | a0001c0005t0006g0010 a0001c0005t0006g0130 a0001c0005t0006g0136 others(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 | a0001c0004t0003g0052 | 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 | a0004c0012t0006g0031 a0004c0012t0006g0258 |
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 | a0001c0004t0002g0158 a0001c0004t0002g0159 |
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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0034 a0001c0001t0005g0193 a0001c0001t0005g0194 others(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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0163 | 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 | a0001c0001t0008g0166 a0001c0001t0008g0169 a0001c0005t0010g0137 others(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 | a0001c0002t0001g0047 | 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 | a0001c0018t0017g0032 | 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 | 112 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(109): 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 | a0001c0002t0001g0231 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0305 a0001c0001t0005g0098 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0261 a0001c0001t0007g0263 others(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 | a0001c0001t0002g0034 a0001c0001t0002g0142 a0001c0001t0002g0322 others(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 | a0001c0001t0002g0331 a0001c0005t0010g0137 a0001c0005t0010g0286 others(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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0005g0167 a0001c0001t0005g0193 a0001c0001t0008g0169 others(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 | a0001c0001t0002g0142 a0001c0004t0002g0158 a0001c0004t0002g0159 |
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 | a0001c0018t0017g0032 | 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 | a0001c0001t0008g0189 | 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 | a0001c0001t0008g0189 | 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 | a0001c0001t0008g0189 | 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 | a0001c0005t0007g0147 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0001t0008g0189 | 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 | a0001c0001t0002g0305 | 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 | a0001c0004t0002g0249 a0001c0004t0023g0030 a0001c0004t0030g0198 |
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 | a0001c0001t0002g0250 | 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 | a0001c0001t0008g0169 | 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 | a0001c0003t0003g0226 a0001c0003t0006g0296 |
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 | a0001c0005t0010g0286 | 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 | a0001c0001t0002g0251 | 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 | a0001c0002t0004g0289 | 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 | 1 | a0001c0002t0001g0003 | 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 | a0001c0007t0009g0255 | 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 | a0001c0018t0017g0032 | 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 | a0006c0016t0003g0062 | 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 | a0001c0001t0002g0007 a0001c0001t0005g0106 a0001c0001t0005g0112 others(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 | a0001c0003t0003g0087 a0001c0003t0006g0154 a0001c0003t0006g0282 others(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 | a0001c0001t0002g0250 | 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 | a0001c0018t0017g0032 | 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 | a0001c0004t0002g0249 | 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 | a0001c0002t0001g0047 | 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 | a0001c0001t0005g0195 | 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 | a0001c0002t0004g0020 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0008g0221 a0001c0002t0001g0022 a0001c0002t0001g0217 |
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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0005c0011t0002g0316 | 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 | a0001c0001t0008g0209 | 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0001t0002g0009 a0001c0001t0002g0016 a0001c0001t0002g0017 others(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 | a0001c0001t0007g0173 | 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 | a0001c0002t0001g0200 | 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 | a0001c0002t0001g0200 a0001c0002t0001g0210 a0001c0002t0001g0212 |
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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0305 a0001c0001t0006g0145 others(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 | a0001c0005t0006g0010 a0001c0005t0006g0130 a0001c0005t0006g0136 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0015 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0261 a0001c0001t0007g0263 others(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 | a0001c0001t0002g0329 a0001c0001t0006g0308 a0001c0002t0001g0211 others(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 | a0001c0001t0005g0055 a0001c0004t0003g0051 a0001c0004t0003g0053 others(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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0313 | 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 | a0001c0018t0017g0032 | 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 | 107 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(104): 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 | a0001c0003t0009g0265 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0007 a0001c0004t0002g0146 |
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 | 259 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(256): 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0001t0002g0007 a0001c0001t0005g0106 a0001c0001t0005g0112 others(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 | a0001c0008t0005g0063 | 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 | a0001c0002t0001g0164 | 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 | a0001c0005t0006g0143 | 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 | a0001c0001t0002g0293 a0001c0001t0002g0305 a0001c0002t0001g0164 |
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 | a0001c0001t0002g0009 | 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 | a0001c0001t0002g0034 a0001c0001t0002g0302 a0001c0001t0005g0041 others(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 | a0001c0001t0002g0142 a0001c0001t0002g0250 a0001c0001t0002g0251 others(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 | a0001c0001t0002g0325 a0001c0001t0005g0048 a0001c0001t0005g0065 others(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 | a0001c0001t0005g0039 a0001c0001t0005g0195 a0001c0003t0003g0068 others(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 | a0001c0002t0001g0091 a0001c0002t0004g0132 a0001c0003t0003g0080 others(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 | a0001c0002t0001g0223 a0001c0003t0003g0079 a0001c0003t0003g0104 others(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 | a0001c0002t0001g0092 a0001c0003t0003g0081 |
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 | a0001c0001t0005g0193 a0001c0003t0003g0076 |
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 | a0001c0003t0003g0085 | 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 | a0001c0003t0003g0087 a0001c0003t0006g0282 a0001c0017t0003g0086 |
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 | a0001c0003t0006g0154 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0141 a0001c0001t0002g0321 others(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 | 34 | a0001c0001t0002g0290 a0001c0001t0002g0301 a0001c0001t0002g0319 others(31): Show |
34 | HG00140.hp2 HG00544.hp1 HG00642.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 | GGAGAGA | G | 21 | a0001c0001t0002g0314 a0001c0001t0002g0326 a0001c0001t0005g0106 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0163 others(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 | a0001c0001t0008g0061 a0001c0002t0001g0057 a0001c0002t0001g0180 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0329 a0001c0001t0005g0161 others(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 | a0001c0001t0002g0138 a0001c0001t0002g0322 a0001c0001t0002g0324 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0004t0003g0196 a0001c0005t0025g0182 a0003c0009t0010g0013 others(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 | a0001c0018t0017g0032 | 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 | a0001c0005t0006g0130 | 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 | a0001c0001t0003g0036 a0001c0001t0006g0262 a0001c0001t0015g0157 |
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 | a0001c0003t0003g0078 | 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 | a0001c0001t0002g0293 a0001c0001t0005g0001 a0001c0001t0005g0099 others(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 | a0001c0001t0002g0303 a0001c0001t0008g0201 a0001c0003t0006g0240 |
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 | a0008c0013t0002g0008 | 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 | a0001c0005t0006g0143 | 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 | a0001c0002t0001g0214 a0001c0004t0012g0128 |
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 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0142 others(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 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0092 others(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 | 75 | a0001c0001t0002g0007 a0001c0001t0002g0290 a0001c0001t0002g0293 others(72): Show |
77 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(74): 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 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0017 others(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 | 32 | a0001c0001t0002g0018 a0001c0001t0002g0138 a0001c0001t0002g0141 others(29): 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 | a0001c0001t0002g0300 a0001c0001t0002g0303 a0001c0001t0005g0037 others(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 | a0001c0001t0002g0009 a0001c0001t0007g0328 a0001c0001t0026g0206 others(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 | a0001c0001t0005g0175 a0001c0001t0005g0186 a0002c0010t0001g0117 |
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 | a0001c0004t0018g0257 | 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 | a0001c0001t0007g0283 | 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 | a0001c0001t0005g0088 a0001c0003t0003g0066 a0001c0003t0003g0170 |
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 | a0001c0001t0008g0168 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0315 | 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 | a0002c0006t0008g0125 | 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 | a0001c0002t0004g0294 | 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 | a0001c0001t0002g0305 a0001c0001t0008g0221 a0001c0002t0001g0021 others(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 | a0001c0001t0003g0036 a0001c0001t0006g0262 a0001c0001t0015g0157 others(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 | 92 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(89): 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 | a0001c0005t0006g0010 a0001c0005t0006g0130 a0001c0005t0006g0136 others(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 | a0001c0002t0001g0203 | 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 | 2 | a0001c0003t0003g0002 a0001c0003t0003g0270 |
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 | a0001c0001t0002g0138 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0305 a0001c0001t0006g0145 others(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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0006g0145 | 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 | a0001c0018t0017g0032 | 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 | a0001c0003t0003g0165 a0001c0003t0006g0337 |
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 | 259 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(256): 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 | a0001c0002t0004g0289 | 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 | a0001c0001t0005g0161 | 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 | a0001c0003t0003g0094 | 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 | a0005c0011t0002g0316 a0005c0011t0019g0327 |
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 | a0001c0018t0017g0032 | 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 | a0001c0003t0006g0318 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0297 a0001c0002t0004g0298 |
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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0334 | 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 | a0001c0002t0004g0333 | 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 | a0001c0002t0004g0315 a0001c0018t0017g0032 |
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 | 2 | a0001c0003t0003g0002 a0001c0003t0003g0270 |
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 | a0001c0005t0006g0010 a0001c0005t0006g0130 a0001c0005t0006g0136 others(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 | a0001c0004t0002g0249 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0005g0037 | 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 | a0001c0003t0003g0111 | 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 | a0001c0002t0004g0134 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0001g0090 a0001c0002t0001g0091 a0001c0002t0001g0092 others(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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0007g0278 | 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 | a0001c0005t0006g0010 a0001c0005t0006g0130 a0001c0005t0006g0136 others(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 | a0001c0018t0017g0032 | 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 | a0001c0001t0006g0308 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0001g0093 a0001c0002t0004g0239 a0001c0002t0004g0246 |
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 | 55 | a0001c0001t0005g0088 a0001c0002t0001g0003 a0001c0002t0001g0045 others(52): 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 | a0001c0018t0017g0032 | 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 | a0001c0022t0004g0152 | 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 | a0001c0001t0005g0195 a0007c0021t0002g0259 |
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 | a0001c0018t0017g0032 | 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 | a0001c0002t0001g0021 | 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 | a0001c0001t0002g0007 a0001c0001t0005g0106 a0001c0001t0005g0112 others(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 | a0001c0001t0002g0135 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0007g0278 a0001c0001t0007g0281 a0001c0001t0007g0283 others(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 | a0001c0002t0001g0026 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0002t0001g0126 | 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 | a0001c0002t0001g0176 | 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 | a0006c0016t0003g0062 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0305 | 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 | a0001c0001t0008g0168 | 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 | a0001c0004t0003g0196 | 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 | a0001c0004t0003g0196 | 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 | a0001c0001t0005g0269 | 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 | a0001c0002t0001g0203 | 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 | a0001c0002t0004g0236 a0001c0002t0004g0334 a0001c0002t0004g0335 |
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 | a0001c0004t0003g0029 a0001c0004t0003g0049 a0001c0004t0003g0050 others(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 | a0001c0001t0005g0194 | 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 | a0008c0013t0002g0008 | 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 | a0001c0003t0003g0046 | 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 | a0001c0002t0004g0315 | 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 | a0001c0001t0005g0225 | 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 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0003g0036 others(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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0305 a0001c0001t0008g0221 a0001c0002t0001g0021 others(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 | a0001c0003t0011g0042 a0001c0003t0011g0083 a0001c0003t0011g0105 |
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 | a0001c0003t0003g0085 | 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 | a0001c0002t0001g0025 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0271 | 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 | a0001c0001t0002g0271 | 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 | a0001c0002t0001g0047 | 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 | a0001c0001t0007g0261 | 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 | a0001c0019t0001g0171 | 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 | a0001c0002t0001g0213 a0001c0003t0011g0105 |
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 | a0001c0002t0004g0335 | 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 | a0001c0002t0001g0103 a0001c0002t0004g0335 |
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 | a0001c0002t0001g0213 | 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 | a0001c0002t0004g0297 a0001c0002t0004g0298 |
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 | a0001c0002t0004g0297 a0001c0002t0004g0298 |
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 | a0001c0018t0017g0032 | 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 | a0001c0005t0002g0144 a0001c0018t0017g0032 |
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 | a0001c0018t0017g0032 | 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 | a0001c0003t0003g0094 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0132 | 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 | a0001c0018t0017g0032 | 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 | a0004c0012t0006g0258 | 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 | a0001c0005t0002g0144 | 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 | a0001c0001t0005g0184 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0305 a0001c0001t0008g0221 a0001c0002t0001g0021 others(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 | a0001c0001t0005g0037 | 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 | a0001c0002t0004g0153 a0001c0002t0004g0273 a0001c0002t0004g0274 others(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 | a0001c0002t0001g0180 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | 259 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(256): 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0002c0006t0008g0125 | 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 | 63 | a0001c0001t0002g0007 a0001c0001t0002g0163 a0001c0001t0005g0106 others(60): 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 | a0001c0001t0002g0305 a0001c0001t0008g0168 a0001c0001t0008g0221 others(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 | a0001c0002t0001g0217 a0001c0002t0001g0220 a0001c0002t0004g0241 others(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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0005t0006g0155 | 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 | a0001c0005t0006g0156 | 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 | a0001c0003t0003g0079 | 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 | a0003c0009t0008g0038 | 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 | a0001c0005t0006g0155 a0001c0005t0006g0156 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0318 |
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 | a0001c0001t0007g0284 a0001c0001t0007g0285 |
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 | a0001c0004t0018g0257 | 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 | a0003c0009t0010g0013 | 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 | a0001c0005t0025g0182 | 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 | a0001c0002t0004g0289 a0001c0002t0004g0297 |
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 | a0001c0002t0004g0235 | 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 | a0001c0002t0004g0298 | 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 | a0004c0012t0006g0031 | 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 | a0001c0005t0006g0136 | 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 | a0001c0003t0003g0046 | 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 | a0001c0002t0001g0090 | 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 | a0001c0002t0001g0123 a0001c0002t0004g0311 |
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 | a0001c0002t0001g0047 | 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 | a0001c0001t0002g0034 | 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 | a0001c0001t0005g0048 | 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 | a0001c0005t0010g0137 | 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 | a0001c0005t0016g0148 | 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 |
1 | a0001c0002t0001g0003 | 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 | a0001c0003t0003g0069 a0001c0003t0003g0087 a0001c0003t0003g0270 others(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 |
8 | a0001c0002t0001g0118 a0001c0002t0001g0120 a0001c0002t0001g0121 others(5): 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 | a0001c0002t0001g0119 | 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 | a0001c0001t0002g0305 | 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 | a0001c0002t0001g0126 a0001c0002t0001g0164 a0001c0002t0001g0215 others(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 | a0001c0001t0008g0221 a0001c0002t0001g0110 a0001c0002t0001g0203 others(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 | a0001c0002t0001g0021 a0001c0002t0001g0026 a0001c0002t0001g0181 others(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 | a0001c0002t0001g0022 a0001c0002t0001g0025 a0001c0002t0001g0059 others(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 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0091 others(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 | a0001c0002t0001g0216 a0001c0002t0004g0153 a0001c0002t0004g0273 others(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 | a0001c0002t0004g0150 a0001c0002t0004g0151 a0011c0014t0001g0218 |
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 | a0001c0002t0004g0236 a0001c0002t0004g0239 a0001c0003t0003g0233 |
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 | a0001c0002t0001g0176 a0001c0002t0004g0287 a0001c0002t0028g0268 |
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 | a0001c0001t0005g0039 | 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 | a0001c0001t0002g0017 a0001c0001t0005g0037 a0001c0001t0005g0195 |
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 | a0001c0001t0002g0016 a0001c0001t0002g0141 a0001c0001t0002g0300 others(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 |
8 | a0001c0001t0002g0009 a0001c0001t0002g0172 a0001c0001t0002g0250 others(5): Show |
8 | HG00323.hp2 HG01257.hp2 HG01433.hp2 others(5): 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 | a0001c0001t0002g0293 a0001c0001t0005g0027 a0001c0001t0005g0065 others(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 | a0001c0001t0002g0290 | 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 | a0001c0001t0002g0142 a0001c0001t0005g0175 a0001c0001t0005g0186 |
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 | a0001c0004t0002g0159 | 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 | a0001c0004t0002g0158 | 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 | a0001c0001t0002g0018 | 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 | a0001c0005t0002g0144 | 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 | a0001c0003t0021g0237 | 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 | a0001c0004t0003g0052 | 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 | a0001c0001t0002g0138 a0001c0003t0003g0067 a0001c0003t0003g0068 others(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 | a0001c0002t0001g0045 a0001c0003t0003g0054 a0001c0003t0003g0075 others(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 | a0001c0003t0003g0165 a0001c0003t0006g0337 |
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 | a0001c0003t0003g0078 a0010c0024t0003g0074 |
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 | a0001c0003t0003g0226 a0006c0016t0003g0062 |
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 | a0001c0001t0005g0088 a0001c0003t0003g0066 |
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 | a0001c0004t0008g0191 | 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 | a0001c0002t0004g0245 | 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 | a0001c0002t0001g0223 | 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 | a0001c0002t0001g0230 a0001c0002t0004g0134 |
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 | a0001c0002t0004g0280 a0001c0003t0006g0004 |
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 | a0001c0002t0001g0220 | 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 | a0001c0002t0001g0231 | 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 | a0001c0007t0014g0253 | 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 | a0001c0001t0002g0304 a0001c0008t0002g0033 |
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 | a0001c0001t0002g0325 | 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 | a0001c0003t0003g0082 | 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 | a0001c0004t0003g0049 a0001c0004t0003g0050 |
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 | a0001c0001t0002g0135 a0001c0003t0003g0071 a0001c0004t0003g0029 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0003t0003g0104 others(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 | a0001c0003t0003g0073 | 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 | a0001c0003t0003g0170 | 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 | a0001c0002t0004g0294 | 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 | a0001c0003t0003g0080 | 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 | a0001c0002t0001g0057 a0001c0002t0001g0058 a0001c0002t0004g0162 |
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 | a0001c0002t0004g0295 | 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 | a0001c0002t0001g0179 | 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 | a0001c0003t0009g0265 a0001c0003t0024g0188 a0001c0004t0003g0196 others(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 | a0001c0003t0009g0266 | 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 | a0001c0001t0002g0314 a0001c0001t0002g0323 a0001c0001t0002g0326 others(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 | a0001c0001t0002g0271 a0001c0001t0002g0321 a0001c0001t0002g0322 others(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 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
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 | a0001c0025t0005g0107 | 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 | a0001c0001t0026g0206 a0001c0002t0001g0205 |
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 | a0001c0005t0006g0143 | 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 | a0001c0001t0003g0036 | 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 | a0001c0001t0006g0262 a0001c0001t0015g0157 |
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 | a0001c0003t0003g0072 | 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 | a0001c0002t0001g0180 | 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 | a0012c0023t0007g0247 | 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 | a0001c0001t0007g0336 a0001c0001t0008g0169 |
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 | a0003c0009t0007g0011 a0003c0009t0007g0012 |
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 | a0001c0007t0009g0260 | 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 | a0001c0001t0005g0040 | 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 | a0001c0001t0005g0044 | 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 | a0001c0001t0005g0043 a0001c0001t0005g0167 |
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 | a0001c0001t0007g0310 | 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 | a0001c0001t0005g0161 | 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 | a0001c0001t0008g0061 a0002c0006t0008g0114 |
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 | a0001c0001t0007g0261 a0001c0001t0007g0328 a0002c0010t0001g0089 others(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 | a0001c0005t0007g0147 a0002c0006t0008g0113 a0002c0006t0008g0234 |
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 | a0001c0003t0009g0267 | 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 |
5 | a0001c0001t0002g0005 a0001c0001t0005g0001 a0001c0001t0005g0096 others(2): 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 | a0001c0001t0005g0098 | 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 | a0001c0001t0005g0095 | 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 | a0001c0004t0005g0035 | 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 | a0001c0001t0008g0084 a0002c0006t0007g0006 |
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 | a0001c0001t0007g0131 a0001c0005t0007g0248 |
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 | a0002c0006t0008g0115 | 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 | a0001c0001t0008g0189 | 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 | a0001c0001t0008g0201 | 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 | a0002c0010t0001g0116 | 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 | a0001c0001t0008g0166 a0001c0001t0008g0209 |
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 | a0001c0001t0008g0168 | 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 | a0001c0001t0008g0222 | 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 | a0001c0004t0003g0051 | 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 | a0001c0001t0006g0308 | 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 | a0001c0004t0003g0053 | 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 | a0001c0001t0008g0202 | 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 | a0001c0001t0007g0281 | 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 | a0001c0001t0007g0173 | 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 | a0001c0001t0007g0278 | 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 | a0001c0001t0007g0283 | 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 | a0001c0001t0005g0312 | 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 | a0001c0019t0001g0171 | 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 | a0001c0004t0002g0249 | 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 | a0001c0001t0005g0225 a0001c0004t0012g0128 a0001c0004t0012g0129 others(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 | a0001c0001t0005g0106 a0001c0001t0005g0112 a0001c0001t0005g0224 others(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 | a0001c0001t0002g0007 | 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 | a0001c0004t0002g0146 | 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 | a0001c0002t0001g0214 | 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 | a0001c0001t0005g0193 a0001c0001t0005g0194 |
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 | a0002c0006t0008g0125 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0163 | 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 | a0004c0012t0006g0258 | 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 | a0001c0002t0001g0127 | 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 | a0001c0002t0001g0232 | 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 | a0001c0002t0001g0056 a0001c0002t0013g0060 a0001c0002t0013g0108 |
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 | a0001c0001t0005g0187 | 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 | a0001c0005t0010g0286 | 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 | a0001c0003t0003g0094 | 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 | a0001c0002t0001g0219 | 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 | a0005c0011t0002g0316 a0005c0011t0019g0327 |
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 | a0001c0001t0006g0145 | 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 | a0002c0006t0008g0125 | 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 | a0001c0002t0001g0204 | 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 | a0001c0001t0020g0019 | 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 | a0001c0001t0007g0263 | 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 | a0001c0001t0007g0028 | 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 | a0001c0001t0007g0264 | 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 | a0001c0002t0004g0306 | 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 | a0001c0002t0004g0306 | 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 | a0001c0002t0001g0091 a0001c0002t0001g0092 |
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 | a0001c0002t0001g0091 a0001c0002t0001g0092 |
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 | a0001c0002t0001g0091 a0001c0002t0001g0092 |
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 | a0001c0004t0002g0249 | 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 | a0001c0005t0006g0010 | 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 | a0001c0001t0007g0028 a0001c0001t0007g0261 a0001c0001t0007g0263 others(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 | a0001c0004t0002g0158 a0001c0004t0002g0159 |
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 | a0001c0005t0006g0010 | 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 | a0001c0018t0017g0032 | 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 | a0001c0004t0018g0257 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0001g0183 | 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 | a0003c0009t0007g0011 a0003c0009t0007g0012 a0003c0009t0008g0038 |
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 | a0001c0001t0005g0161 | 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 | a0001c0005t0010g0137 a0001c0005t0010g0286 a0001c0005t0025g0182 others(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 | a0001c0004t0018g0257 | 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 | a0001c0002t0004g0134 | 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 | a0001c0004t0018g0257 | 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 | a0001c0004t0012g0128 a0001c0004t0012g0129 |
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 | a0001c0004t0003g0051 a0001c0004t0003g0053 |
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 | a0001c0003t0003g0111 | 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 | a0001c0002t0001g0127 | 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 | a0001c0005t0006g0010 a0001c0005t0006g0130 a0001c0005t0006g0136 others(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 | a0001c0003t0006g0318 | 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 | a0001c0002t0004g0238 | 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 | a0001c0002t0001g0232 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0305 a0001c0001t0005g0312 others(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 | a0001c0002t0004g0132 | 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 | a0001c0001t0005g0312 | 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 | a0001c0018t0017g0032 | 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 | a0001c0004t0012g0128 a0001c0004t0012g0129 |
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 | a0001c0001t0007g0028 a0001c0001t0007g0131 a0001c0001t0007g0173 others(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 | a0001c0001t0002g0250 | 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 | a0001c0005t0010g0137 a0001c0005t0010g0286 a0001c0005t0025g0182 others(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 | a0001c0002t0004g0333 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0172 a0001c0001t0005g0106 others(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 | a0001c0003t0003g0228 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0172 a0001c0001t0005g0106 others(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 | a0001c0001t0005g0312 a0001c0002t0001g0059 |
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 | a0001c0018t0017g0032 | 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 | a0001c0005t0006g0010 a0001c0005t0006g0130 a0001c0005t0006g0136 others(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 | a0001c0003t0011g0083 | 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 | a0001c0001t0003g0036 a0001c0001t0006g0145 a0001c0001t0006g0262 others(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 | a0001c0002t0001g0090 a0001c0002t0001g0230 |
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 | a0001c0002t0004g0288 | 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 | a0001c0003t0003g0071 | 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 | a0009c0020t0003g0192 | 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 | a0001c0002t0001g0091 a0001c0002t0001g0092 |
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 | a0001c0018t0017g0032 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0172 a0001c0004t0002g0146 |
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 | a0001c0004t0023g0030 | 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 | a0001c0004t0002g0158 | 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 | a0001c0001t0002g0314 | 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 | 333 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(330): 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 | a0001c0001t0005g0088 a0001c0003t0003g0066 a0001c0003t0003g0170 others(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 | a0001c0008t0002g0033 a0001c0008t0002g0242 a0001c0008t0002g0243 others(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 | a0001c0001t0002g0163 a0003c0009t0007g0011 a0003c0009t0007g0012 others(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 | a0001c0001t0002g0163 a0001c0002t0004g0153 a0001c0004t0008g0191 others(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 | a0001c0002t0004g0245 | 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 | a0001c0002t0001g0022 | 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 | a0001c0003t0003g0079 a0001c0003t0003g0081 |
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 | a0001c0002t0001g0203 | 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 | a0001c0004t0023g0030 a0001c0004t0030g0198 |
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 | a0001c0005t0010g0137 a0001c0005t0010g0286 a0001c0005t0025g0182 others(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 | a0001c0018t0017g0032 | 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 | a0001c0001t0006g0308 | 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 | a0003c0009t0010g0013 | 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 | a0001c0004t0012g0128 a0001c0004t0012g0129 |
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 | 97 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(94): 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 | 71 | a0001c0001t0002g0142 a0001c0001t0002g0319 a0001c0001t0002g0330 others(68): 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0004g0289 a0001c0019t0001g0171 |
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 | a0001c0001t0002g0329 a0001c0001t0005g0048 a0001c0001t0005g0186 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0002t0004g0178 | 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 | a0002c0010t0001g0117 | 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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0002t0001g0183 | 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 | a0001c0004t0029g0190 | 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 | a0001c0001t0006g0308 | 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 | a0001c0003t0006g0199 a0001c0003t0009g0265 a0001c0003t0009g0266 others(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 | a0001c0002t0004g0297 a0001c0002t0004g0298 |
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 | a0001c0002t0004g0334 | 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 | 52 | a0001c0002t0001g0045 a0001c0002t0001g0122 a0001c0003t0003g0002 others(49): 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 | a0001c0001t0002g0251 | 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 | a0001c0004t0018g0257 a0001c0005t0006g0155 a0001c0005t0006g0156 others(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 | a0001c0001t0005g0312 | 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 | a0001c0001t0002g0034 | 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 | a0001c0001t0003g0036 a0001c0001t0006g0145 a0001c0001t0006g0262 others(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 | a0001c0002t0001g0045 a0001c0003t0003g0233 |
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 | a0001c0001t0002g0163 a0001c0004t0008g0191 a0001c0005t0007g0147 others(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 | a0001c0001t0007g0328 a0001c0001t0007g0336 a0001c0001t0008g0084 others(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 | a0001c0001t0002g0304 | 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 | a0001c0002t0001g0110 | 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 | a0001c0003t0006g0240 | 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 | a0001c0002t0004g0280 | 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 | a0004c0012t0006g0258 | 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 | a0001c0004t0003g0029 | 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 | 108 | a0001c0001t0005g0312 a0001c0001t0026g0206 a0001c0002t0001g0003 others(105): 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 | a0001c0002t0004g0299 | 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 | a0001c0002t0004g0134 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0172 a0001c0001t0005g0106 others(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 | a0001c0018t0017g0032 | 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 | a0001c0004t0018g0257 a0001c0005t0006g0155 a0001c0005t0006g0156 others(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 | a0001c0002t0004g0289 a0001c0019t0001g0171 |
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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0001t0002g0163 a0001c0001t0002g0330 a0001c0001t0007g0328 others(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 | a0001c0008t0002g0243 | 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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0004t0003g0049 a0001c0004t0003g0050 |
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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0005t0007g0147 | 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 | a0001c0002t0001g0021 a0001c0002t0001g0023 a0001c0002t0001g0024 others(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 | a0001c0002t0004g0134 | 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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0001t0007g0131 | 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 | a0001c0002t0004g0294 a0001c0002t0004g0295 |
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 | a0001c0001t0006g0308 | 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0001t0005g0088 | 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 | a0001c0002t0013g0108 | 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0004t0002g0158 a0001c0004t0002g0159 |
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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0002t0001g0090 a0001c0002t0001g0091 a0001c0002t0001g0092 others(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 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 others(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 | a0001c0005t0006g0155 a0001c0005t0006g0156 |
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 | a0001c0002t0004g0297 a0001c0002t0004g0298 |
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 | a0001c0001t0006g0308 | 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 | a0001c0002t0001g0100 a0001c0002t0004g0309 |
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 | a0001c0001t0006g0308 | 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 | a0001c0018t0017g0032 | 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 | a0001c0004t0018g0257 | 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 | a0001c0003t0003g0076 a0001c0003t0003g0079 a0001c0003t0003g0081 others(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 | a0001c0002t0004g0289 a0001c0019t0001g0171 |
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 | a0001c0001t0002g0163 | 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 | a0001c0002t0004g0238 | 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 | a0001c0003t0003g0054 | 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 | a0001c0002t0001g0021 | 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 | a0001c0002t0001g0021 | 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 | a0001c0004t0022g0256 a0001c0004t0029g0190 |
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 | a0001c0002t0001g0197 | 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 | a0001c0001t0007g0173 | 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 | a0001c0001t0005g0184 | 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 | a0001c0001t0008g0166 a0001c0001t0008g0168 a0001c0001t0008g0169 others(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 | a0001c0002t0001g0123 | 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 | a0001c0003t0003g0085 | 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 | a0001c0002t0004g0311 | 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 | a0001c0004t0030g0198 | 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 | a0001c0002t0004g0177 a0001c0002t0004g0178 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0172 a0001c0004t0002g0146 |
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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0007t0009g0252 others(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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0007t0009g0252 others(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 | a0001c0002t0004g0279 | 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 | 105 | a0001c0001t0005g0312 a0001c0002t0001g0003 a0001c0002t0001g0021 others(102): 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 | a0001c0001t0005g0055 | 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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0001t0002g0163 | 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 | a0002c0006t0008g0234 | 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 | a0001c0001t0002g0016 a0001c0001t0002g0017 |
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 | a0002c0006t0008g0115 | 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 | a0001c0001t0006g0308 | 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 | a0001c0001t0002g0314 | 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0135 others(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 | a0001c0008t0002g0033 a0001c0008t0002g0243 a0001c0008t0005g0063 |
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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0017t0003g0086 | 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 | a0001c0001t0007g0310 a0001c0001t0008g0189 |
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 | a0001c0005t0006g0155 | 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 | a0001c0001t0003g0036 a0001c0001t0006g0145 a0001c0001t0006g0262 others(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 | a0001c0001t0005g0043 | 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 | a0001c0005t0007g0248 | 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 | a0001c0001t0026g0206 a0001c0002t0001g0121 a0001c0002t0001g0204 others(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 | a0005c0011t0002g0316 a0005c0011t0019g0327 |
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 | a0001c0002t0004g0162 | 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 | a0001c0002t0001g0025 | 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 | a0001c0001t0005g0312 a0001c0001t0026g0206 a0001c0002t0001g0022 others(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 | a0001c0003t0003g0208 | 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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0001t0002g0017 | 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 | a0001c0003t0003g0111 | 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 | a0001c0015t0003g0064 | 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 | a0001c0004t0003g0029 | 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 | a0001c0002t0004g0289 | 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 | a0001c0003t0003g0079 a0001c0003t0003g0081 |
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 | a0001c0001t0002g0163 a0001c0004t0008g0191 a0001c0005t0007g0147 others(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 | a0001c0001t0006g0308 | 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 | a0001c0005t0007g0147 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0003t0003g0079 a0001c0003t0003g0081 |
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 | a0001c0001t0003g0036 a0001c0001t0006g0262 a0001c0001t0015g0157 others(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 | a0001c0002t0004g0289 a0001c0019t0001g0171 |
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 | a0001c0002t0001g0213 | 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 | 6 | a0001c0002t0001g0003 a0001c0002t0004g0020 a0001c0002t0004g0132 others(3): 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 | a0001c0005t0010g0137 a0001c0005t0010g0286 a0001c0005t0025g0182 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0131 a0001c0001t0007g0173 others(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 | a0002c0006t0008g0125 | 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 | a0001c0005t0016g0148 | 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 | a0001c0003t0006g0174 | 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 | a0001c0004t0018g0257 a0001c0005t0006g0155 a0001c0005t0006g0156 others(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 | a0001c0003t0003g0104 | 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 | a0001c0001t0002g0016 | 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 | a0001c0001t0002g0330 | 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 | a0001c0004t0003g0051 a0001c0004t0003g0053 |
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 | a0001c0002t0001g0183 | 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 | a0001c0004t0022g0256 a0001c0004t0029g0190 |
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 | a0001c0001t0002g0009 | 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 | a0001c0001t0002g0016 a0001c0001t0002g0017 |
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 | a0001c0001t0002g0163 a0001c0004t0008g0191 a0001c0005t0007g0147 others(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 | a0001c0002t0004g0287 a0001c0002t0028g0268 |
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 | a0001c0003t0006g0240 | 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 | a0001c0001t0026g0206 a0001c0002t0001g0121 a0001c0002t0001g0204 others(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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0001t0002g0293 | 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 | a0001c0001t0002g0141 | 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 | 62 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0017 others(59): 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 | a0001c0001t0002g0015 a0001c0001t0002g0290 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0016 a0001c0001t0002g0300 a0001c0001t0005g0065 others(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 | a0001c0003t0003g0076 a0002c0006t0008g0114 a0003c0009t0007g0012 |
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 | a0001c0004t0003g0052 a0001c0007t0009g0255 |
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 | 40 | a0001c0001t0002g0018 a0001c0001t0002g0163 a0001c0001t0002g0251 others(37): Show |
40 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(37): 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 | a0001c0001t0002g0250 a0001c0001t0002g0322 a0001c0001t0002g0324 others(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 | a0001c0002t0001g0023 a0001c0002t0001g0026 a0001c0002t0001g0059 others(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 | 33 | a0001c0001t0002g0007 a0001c0001t0005g0112 a0001c0001t0005g0224 others(30): 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 | a0001c0002t0001g0100 a0001c0002t0001g0109 a0001c0002t0001g0214 others(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 | a0001c0001t0005g0312 | 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 | a0001c0001t0002g0172 a0001c0004t0002g0146 |
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 | a0001c0002t0004g0245 | 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 | a0001c0001t0005g0187 | 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 | a0001c0002t0001g0183 | 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 | a0001c0002t0001g0183 | 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 | a0001c0002t0001g0183 | 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 | a0001c0002t0001g0183 | 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 | a0001c0002t0001g0183 | 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 | a0001c0002t0001g0183 | 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 | a0001c0002t0001g0183 | 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 | a0001c0002t0001g0183 | 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 | a0002c0006t0008g0114 | 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 | a0001c0002t0001g0100 | 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 | a0001c0001t0002g0034 a0001c0001t0002g0301 a0001c0001t0002g0319 others(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 |
51 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0018 others(48): 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 |
82 | a0001c0001t0002g0016 a0001c0001t0002g0302 a0001c0001t0002g0322 others(79): 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 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0015 others(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 |
40 | a0001c0001t0002g0135 a0001c0001t0002g0323 a0001c0001t0002g0324 others(37): 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 | a0001c0001t0002g0250 a0001c0001t0005g0097 a0001c0002t0001g0103 others(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 | a0001c0002t0001g0179 | 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 | a0001c0002t0001g0058 a0001c0002t0001g0176 |
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 | a0001c0001t0008g0168 | 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 | a0001c0001t0005g0048 a0001c0003t0003g0078 a0001c0003t0003g0227 others(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 | a0001c0008t0002g0243 | 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 | a0001c0002t0001g0021 a0001c0002t0001g0023 a0001c0002t0001g0024 others(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 | a0001c0003t0003g0165 | 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 | a0001c0003t0006g0337 | 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 | a0001c0002t0004g0295 | 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 | a0003c0009t0010g0013 | 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 | a0001c0002t0004g0178 a0001c0002t0004g0245 |
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 | a0001c0001t0005g0186 | 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 | a0001c0002t0013g0060 | 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 | a0001c0002t0004g0333 | 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 | a0001c0001t0008g0222 | 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 | a0001c0005t0016g0148 | 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 | 330 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(327): 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 | a0001c0003t0024g0188 | 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 | a0001c0001t0006g0145 a0001c0004t0003g0029 a0001c0004t0003g0049 others(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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 others(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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 others(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 | a0001c0002t0001g0176 a0001c0002t0001g0231 a0001c0002t0004g0150 others(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 | a0001c0001t0007g0328 a0001c0001t0007g0336 |
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 | a0001c0005t0010g0137 | 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 | a0001c0001t0006g0145 a0001c0004t0003g0029 a0001c0004t0003g0049 others(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 | a0001c0001t0002g0331 a0001c0001t0006g0308 a0001c0002t0001g0232 others(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 | a0001c0003t0003g0233 | 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 | a0001c0003t0003g0070 | 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 | a0001c0002t0001g0109 a0001c0022t0004g0152 |
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 | a0001c0002t0004g0288 | 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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0002t0001g0110 | 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 | 80 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0014 others(77): Show |
81 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(78): 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 | a0001c0001t0020g0019 | 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 | a0001c0001t0002g0138 | 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 | a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0003t0003g0101 | 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 | a0001c0001t0007g0173 | 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 | a0001c0005t0006g0139 a0001c0005t0006g0140 |
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 | a0001c0001t0003g0036 a0001c0001t0006g0262 a0001c0001t0015g0157 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0017 a0001c0001t0002g0172 others(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 | a0001c0003t0006g0174 | 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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0001t0002g0163 a0001c0004t0008g0191 a0001c0005t0007g0147 others(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 | a0001c0001t0008g0061 | 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 | a0001c0002t0001g0214 | 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 | a0001c0001t0003g0036 a0001c0001t0006g0145 a0001c0001t0006g0262 others(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 | a0001c0001t0002g0009 a0001c0001t0002g0016 a0001c0001t0002g0141 others(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 | a0001c0001t0007g0131 a0001c0001t0007g0278 a0001c0001t0007g0281 others(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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 others(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 | a0001c0004t0018g0257 a0001c0005t0006g0155 a0001c0005t0006g0156 others(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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0004t0018g0257 | 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 | a0001c0001t0006g0308 | 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 | a0001c0005t0016g0148 | 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 | a0001c0002t0004g0313 | 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 | a0001c0002t0001g0110 | 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 | a0001c0003t0006g0199 | 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 | a0001c0001t0003g0036 a0001c0001t0006g0145 a0001c0001t0006g0262 others(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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0003t0021g0237 | 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 | 103 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0141 others(100): Show |
103 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(100): 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 | a0001c0001t0002g0163 a0001c0001t0007g0131 a0001c0001t0007g0278 others(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 | 227 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): 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 | a0001c0004t0018g0257 | 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 | a0001c0002t0001g0203 | 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 | a0001c0001t0002g0034 | 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 | a0001c0002t0001g0215 a0001c0002t0004g0272 a0001c0002t0004g0273 others(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 | a0001c0001t0002g0301 | 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 | a0001c0001t0006g0308 | 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 | a0001c0001t0002g0330 | 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 | a0006c0016t0003g0062 | 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 | a0001c0002t0004g0020 a0001c0002t0004g0244 a0001c0002t0004g0332 |
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 | a0001c0001t0027g0124 | 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 | a0001c0002t0004g0334 | 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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0002t0004g0306 | 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 | 92 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0163 others(89): 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 | a0001c0004t0023g0030 a0001c0004t0030g0198 a0001c0018t0017g0032 |
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 | a0001c0001t0026g0206 a0001c0002t0001g0022 a0001c0002t0001g0045 others(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 | a0001c0002t0001g0056 a0001c0002t0001g0220 a0001c0002t0013g0060 others(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 | a0001c0004t0003g0196 | 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 | 76 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0014 others(73): Show |
77 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(74): 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 | a0001c0001t0002g0300 a0001c0001t0002g0303 a0001c0001t0005g0037 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0250 others(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 | 65 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0014 others(62): Show |
66 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(63): 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 | a0001c0001t0002g0300 a0001c0001t0002g0303 a0001c0001t0005g0037 |
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 | a0001c0001t0005g0065 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(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 | a0001c0002t0001g0213 a0002c0010t0001g0117 |
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 | a0001c0018t0017g0032 | 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 | a0001c0004t0018g0257 | 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 | a0001c0001t0002g0314 a0001c0001t0002g0326 a0001c0001t0002g0329 others(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 | a0001c0001t0003g0036 a0001c0001t0006g0145 a0001c0001t0006g0262 others(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 | a0001c0018t0017g0032 | 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 | a0001c0003t0003g0054 | 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 | a0001c0001t0007g0310 a0001c0003t0003g0233 a0001c0004t0003g0050 others(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 | 95 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(92): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): 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 | a0001c0003t0003g0079 | 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 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
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 | a0001c0002t0004g0313 | 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 | a0001c0004t0018g0257 a0001c0005t0006g0155 a0001c0005t0006g0156 others(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 | a0001c0002t0004g0177 a0001c0002t0004g0178 |
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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0007c0021t0002g0259 a0008c0013t0002g0008 |
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 | a0001c0002t0001g0219 | 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 | a0001c0002t0001g0026 | 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 | a0001c0001t0002g0305 | 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 | a0001c0001t0003g0036 a0001c0001t0006g0145 a0001c0001t0006g0262 others(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 | a0001c0001t0008g0189 | 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 | a0001c0002t0004g0239 | 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 | a0001c0001t0002g0163 a0001c0004t0008g0191 a0001c0005t0007g0147 others(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 | a0006c0016t0003g0062 | 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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0001t0005g0112 a0001c0001t0005g0224 a0001c0001t0005g0225 |
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 | a0001c0004t0002g0159 | 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 | a0001c0004t0003g0051 a0001c0004t0003g0053 |
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 | a0001c0002t0001g0090 a0001c0002t0001g0121 a0001c0002t0001g0205 others(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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 others(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 | a0001c0003t0011g0083 | 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 | a0001c0004t0022g0256 a0001c0004t0029g0190 |
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 | a0001c0003t0003g0165 a0001c0003t0006g0337 |
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 | a0001c0018t0017g0032 | 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 | a0001c0008t0002g0033 | 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 | a0001c0018t0017g0032 | 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 | a0001c0002t0001g0122 | 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 | a0001c0003t0003g0087 a0001c0003t0006g0154 a0001c0003t0006g0282 others(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 | a0001c0002t0004g0162 | 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 | 228 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0002t0001g0197 | 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 | 65 | a0001c0001t0006g0308 a0001c0001t0026g0206 a0001c0003t0003g0002 others(62): 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 | a0001c0002t0004g0239 a0001c0002t0004g0246 |
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 | a0001c0003t0003g0111 | 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 | a0001c0001t0006g0145 a0001c0004t0003g0029 a0001c0004t0003g0049 others(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 | a0001c0005t0006g0010 | 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 | a0001c0001t0006g0308 a0001c0003t0006g0199 |
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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 others(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 | a0001c0001t0007g0028 a0001c0001t0007g0173 a0001c0001t0007g0261 others(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 | 95 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(92): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): 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 | a0001c0001t0006g0308 | 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 | a0001c0002t0001g0023 | 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 | a0001c0001t0003g0036 a0001c0001t0006g0145 a0001c0001t0006g0262 others(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 | a0001c0002t0004g0294 | 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 | a0001c0004t0012g0128 a0001c0004t0012g0129 |
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 | 65 | a0001c0001t0006g0308 a0001c0001t0026g0206 a0001c0003t0003g0002 others(62): 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 | a0001c0005t0007g0147 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0002t0001g0219 | 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 | a0001c0002t0004g0177 a0001c0002t0004g0178 |
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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 others(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 | 228 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 others(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 | a0001c0003t0003g0111 | 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 | a0001c0004t0008g0191 | 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 | a0001c0004t0003g0196 a0001c0005t0006g0010 a0001c0005t0006g0130 others(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 | a0001c0003t0003g0078 a0001c0003t0003g0080 |
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 | 54 | a0001c0001t0026g0206 a0001c0003t0003g0002 a0001c0003t0003g0046 others(51): 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 | a0001c0003t0009g0265 a0001c0003t0009g0266 a0001c0003t0009g0267 others(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 | a0001c0002t0001g0100 a0001c0002t0004g0309 |
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 | a0001c0003t0006g0160 | 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 | a0001c0001t0002g0015 a0001c0004t0002g0146 |
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 | a0001c0002t0001g0092 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0017 others(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 | a0001c0003t0003g0085 | 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 | a0001c0003t0003g0081 | 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 | a0001c0001t0007g0173 | 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 | a0001c0005t0007g0147 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0001c0001t0007g0310 a0001c0001t0008g0189 |
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 | a0001c0001t0002g0250 a0001c0001t0002g0251 |
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 | a0002c0006t0008g0125 | 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 | a0001c0002t0004g0294 | 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 | a0001c0002t0004g0311 | 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 | a0001c0003t0003g0111 | 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 | a0001c0005t0016g0148 | 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 | 228 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0002t0001g0057 a0001c0002t0001g0058 a0001c0002t0001g0179 others(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 | a0001c0001t0003g0036 a0001c0001t0006g0262 a0001c0001t0015g0157 others(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 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 others(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 | a0001c0001t0006g0308 a0001c0003t0006g0199 a0001c0003t0009g0265 others(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 | a0001c0002t0004g0238 | 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 | a0001c0001t0006g0308 a0001c0003t0006g0199 a0001c0003t0009g0265 others(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 | a0001c0001t0005g0065 | 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 | a0002c0006t0008g0234 | 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 | a0001c0001t0002g0017 | 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 | 54 | a0001c0001t0026g0206 a0001c0003t0003g0002 a0001c0003t0003g0046 others(51): 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 | a0001c0002t0001g0179 | 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 | 12 | a0001c0001t0002g0005 a0001c0001t0002g0326 a0001c0001t0005g0001 others(9): 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 | a0001c0004t0018g0257 a0001c0005t0006g0155 a0001c0005t0006g0156 others(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 | a0001c0005t0007g0147 | 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 | a0001c0001t0008g0222 | 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 | a0001c0003t0003g0170 | 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 | a0001c0004t0002g0158 a0001c0008t0002g0033 a0001c0008t0002g0243 |
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 | a0001c0003t0003g0066 a0001c0003t0003g0170 |
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 | a0001c0005t0006g0155 | 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 | 288 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): 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 | a0001c0004t0002g0146 | 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 | a0001c0018t0017g0032 | 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 | a0001c0001t0002g0141 a0001c0001t0002g0300 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0163 a0001c0001t0007g0028 a0001c0001t0007g0131 others(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 | a0001c0003t0003g0073 | 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 | a0001c0002t0004g0307 | 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 | a0001c0002t0004g0298 a0002c0010t0001g0116 |
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 | 65 | a0001c0001t0006g0308 a0001c0001t0026g0206 a0001c0003t0003g0002 others(62): 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 | 228 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0002t0004g0335 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0017 others(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 | a0001c0005t0006g0140 | 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 | a0001c0002t0001g0022 a0001c0002t0001g0045 a0001c0002t0001g0047 others(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 | a0001c0002t0001g0022 a0001c0002t0001g0045 a0001c0002t0001g0047 others(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 | a0001c0001t0002g0018 | 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 | a0007c0021t0002g0259 | 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 | 253 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0017 others(250): 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 | 54 | a0001c0001t0026g0206 a0001c0003t0003g0002 a0001c0003t0003g0046 others(51): 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 | a0001c0004t0003g0196 | 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 | 330 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(327): 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 | a0001c0004t0003g0051 a0001c0004t0003g0053 |
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 | 107 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0022 others(104): 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 | a0001c0003t0009g0267 | 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 | a0001c0001t0007g0173 | 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 | a0001c0001t0026g0206 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0163 others(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 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(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 | 30 | a0001c0001t0002g0009 a0001c0001t0002g0017 a0001c0001t0005g0088 others(27): 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 | a0001c0001t0007g0328 a0001c0001t0007g0336 a0001c0005t0007g0147 others(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 | a0001c0001t0007g0131 a0001c0003t0006g0199 a0001c0004t0008g0191 others(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 | a0001c0001t0008g0166 a0001c0005t0007g0248 a0012c0023t0007g0247 |
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 | a0003c0009t0007g0011 a0003c0009t0007g0012 |
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 | a0001c0001t0008g0168 | 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 | a0001c0001t0002g0014 a0001c0001t0002g0172 a0001c0001t0005g0184 others(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 | a0001c0001t0002g0326 a0001c0001t0005g0175 a0001c0001t0005g0186 others(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 | a0001c0001t0002g0135 a0001c0001t0015g0157 a0001c0002t0001g0180 others(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 | 98 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0022 others(95): 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 | a0001c0002t0004g0245 | 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 | a0001c0004t0003g0196 | 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 | 3 | a0001c0002t0001g0003 a0001c0002t0004g0132 a0001c0002t0004g0235 |
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 | a0001c0005t0006g0010 a0001c0005t0006g0130 a0001c0005t0006g0136 others(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 | a0001c0002t0004g0244 | 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 | a0001c0004t0003g0196 | 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 | 70 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0017 others(67): 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 | a0001c0002t0001g0210 | 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 | a0001c0001t0007g0173 | 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 | a0001c0003t0003g0068 a0001c0003t0003g0077 |
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 | a0001c0003t0003g0101 | 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 | 107 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0022 others(104): 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 | 107 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0022 others(104): 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 | a0011c0014t0001g0218 | 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 | a0001c0001t0002g0009 a0001c0001t0002g0016 a0001c0001t0002g0141 others(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 | a0001c0001t0002g0271 a0001c0001t0002g0319 a0001c0001t0002g0320 others(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 | 108 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0022 others(105): 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 | a0001c0001t0005g0112 | 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 | 108 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0022 others(105): 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 | a0001c0002t0004g0298 | 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 | a0001c0001t0015g0157 | 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 | 72 | a0001c0001t0006g0308 a0001c0001t0026g0206 a0001c0003t0003g0002 others(69): 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 | a0001c0018t0017g0032 | 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 | a0001c0003t0006g0160 | 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 | 108 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0022 others(105): 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 | a0001c0003t0003g0233 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3799-284T>A | MET | ENSG00000105976.16 | transcript | ENST00000397752.8 | protein_coding | 19/20 | chr7 | 116795371 |