| geneid | 340267 |
|---|---|
| ensemblid | ENSG00000215018.10 |
| hgncid | 22442 |
| symbol | COL28A1 |
| name | collagen type XXVIII alpha 1 chain |
| refseq_nuc | NM_001037763.3 |
| refseq_prot | NP_001032852.2 |
| ensembl_nuc | ENST00000399429.8 |
| ensembl_prot | ENSP00000382356.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 7357875 |
| end | 7535873 |
| strand | - |
| ver | v1.2 |
| region | chr7:7357875-7535873 |
| region5000 | chr7:7352875-7540873 |
| regionname0 | COL28A1_chr7_7357875_7535873 |
| regionname5000 | COL28A1_chr7_7352875_7540873 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1125 | 81 | 17 | 15 | 24 | 10 | 14 | 18 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002 | 0/0 | 1125 | 33 | 20 | 5 | 3 | 4 | 1 | 2 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0003 | 0/0 | 1125 | 17 | 3 | 7 | 6 | 0 | 1 | 4 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0004 | 0/0 | 1125 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0005 | 0/0 | 1125 | 5 | 4 | 0 | 1 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0006 | 0/0 | 1125 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0007 | 0/0 | 1125 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0008 | 0/0 | 1125 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0009 | 0/0 | 1125 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0010 | 0/0 | 1125 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0011 | 1/0 | 1125 | 3 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0012 | 0/0 | 1125 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0013 | 0/0 | 754 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0014 | 0/0 | 1125 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0015 | 0/0 | 1125 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0016 | 0/0 | 1125 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0017 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0018 | 0/0 | 1125 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0019 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0020 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0021 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0022 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0023 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0024 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0025 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0026 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0027 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0028 | 0/0 | 1125 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0029 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0030 | 0/0 | 1125 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0031 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0032 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0033 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0034 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0035 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3378 | 70 | 10 | 14 | 23 | 8 | 14 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0002 | 0/0 | 3378 | 20 | 8 | 5 | 3 | 4 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0003 | 0/0 | 3378 | 16 | 2 | 7 | 6 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0004 | 0/0 | 3378 | 11 | 11 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0005 | 0/0 | 3378 | 5 | 2 | 1 | 1 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0006 | 0/0 | 3378 | 5 | 5 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0007 | 0/0 | 3378 | 5 | 4 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0008 | 0/0 | 3378 | 4 | 4 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0009 | 0/0 | 3378 | 4 | 4 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0010 | 0/0 | 3378 | 4 | 3 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0011 | 0/0 | 3378 | 3 | 0 | 2 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0012 | 1/0 | 3378 | 2 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0013 | 0/0 | 3378 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0014 | 0/0 | 3378 | 2 | 1 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0015 | 0/0 | 3378 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0016 | 0/0 | 3378 | 2 | 1 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0017 | 0/0 | 3378 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0018 | 0/0 | 3378 | 2 | 0 | 2 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0019 | 0/0 | 3378 | 2 | 1 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0020 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0021 | 0/0 | 3378 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0022 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0023 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0024 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0025 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0026 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0027 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0028 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0029 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0030 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0031 | 0/0 | 3378 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0032 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0033 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0034 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0035 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0036 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0037 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0038 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0039 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0040 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0041 | 0/0 | 3378 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0042 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0043 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0044 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0045 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0046 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0047 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0048 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0049 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0050 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0051 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| c0052 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 920 | 79 | 13 | 17 | 27 | 7 | 15 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0002 | 0/1 | 920 | 60 | 27 | 12 | 11 | 5 | 4 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0003 | 0/0 | 920 | 41 | 38 | 2 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0004 | 0/0 | 920 | 4 | 0 | 4 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0005 | 1/0 | 920 | 3 | 0 | 1 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0006 | 0/0 | 920 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0007 | 0/0 | 920 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0008 | 0/0 | 920 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0009 | 0/0 | 920 | 2 | 0 | 1 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| t0010 | 0/0 | 920 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3378 | 70 | 10 | 14 | 23 | 8 | 14 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0005 | 0/0 | 3378 | 5 | 2 | 1 | 1 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0007 | 0/0 | 3378 | 5 | 4 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0051 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0002 | 0/0 | 3378 | 20 | 8 | 5 | 3 | 4 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0004 | 0/0 | 3378 | 11 | 11 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0031 | 0/0 | 3378 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0049 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0003c0003 | 0/0 | 3378 | 16 | 2 | 7 | 6 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0003c0047 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0004c0006 | 0/0 | 3378 | 5 | 5 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0004c0039 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0005c0010 | 0/0 | 3378 | 4 | 3 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0005c0044 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0006c0015 | 0/0 | 3378 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0006c0019 | 0/0 | 3378 | 2 | 1 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0006c0030 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0007c0008 | 0/0 | 3378 | 4 | 4 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0007c0032 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0008c0009 | 0/0 | 3378 | 4 | 4 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0009c0014 | 0/0 | 3378 | 2 | 1 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0009c0029 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0010c0013 | 0/0 | 3378 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0010c0028 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0011c0012 | 1/0 | 3378 | 2 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0011c0027 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0012c0016 | 0/0 | 3378 | 2 | 1 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0012c0035 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0013c0011 | 0/0 | 3378 | 3 | 0 | 2 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0014c0017 | 0/0 | 3378 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0015c0048 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0015c0052 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0016c0018 | 0/0 | 3378 | 2 | 0 | 2 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0017c0020 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0018c0023 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0019c0024 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0020c0022 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0021c0025 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0022c0026 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0023c0021 | 0/0 | 3378 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0024c0045 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0025c0046 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0026c0043 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0027c0042 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0028c0036 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0029c0037 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0030c0038 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0031c0033 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0032c0034 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0033c0050 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0034c0040 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0035c0041 | 0/0 | 3378 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4297 | 50 | 6 | 11 | 16 | 6 | 11 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0001t0002 | 0/1 | 4297 | 14 | 2 | 1 | 7 | 1 | 2 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0001t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0001t0005 | 0/0 | 4297 | 2 | 0 | 1 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0001t0008 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0001t0009 | 0/0 | 4297 | 2 | 0 | 1 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0005t0001 | 0/0 | 4297 | 3 | 0 | 1 | 1 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0005t0002 | 0/0 | 4297 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0007t0003 | 0/0 | 4297 | 5 | 4 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0001c0051t0008 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0002t0001 | 0/0 | 4297 | 3 | 2 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0002t0002 | 0/0 | 4297 | 16 | 5 | 5 | 2 | 4 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0002t0006 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0004t0003 | 0/0 | 4297 | 11 | 11 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0031t0001 | 0/0 | 4297 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0002c0049t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0003c0003t0001 | 0/0 | 4297 | 11 | 2 | 3 | 5 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0003c0003t0002 | 0/0 | 4297 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0003c0003t0004 | 0/0 | 4297 | 4 | 0 | 4 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0003c0047t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0004c0006t0002 | 0/0 | 4297 | 5 | 5 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0004c0039t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0005c0010t0001 | 0/0 | 4297 | 3 | 2 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0005c0010t0002 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0005c0044t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0006c0015t0002 | 0/0 | 4297 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0006c0019t0002 | 0/0 | 4297 | 2 | 1 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0006c0030t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0007c0008t0003 | 0/0 | 4297 | 3 | 3 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0007c0008t0006 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0007c0032t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0008c0009t0003 | 0/0 | 4297 | 4 | 4 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0009c0014t0001 | 0/0 | 4297 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0009c0014t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0009c0029t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0010c0013t0002 | 0/0 | 4297 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0010c0028t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0011c0012t0002 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0011c0012t0005 | 1/0 | 4297 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0011c0027t0003 | 0/0 | 4297 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0012c0016t0002 | 0/0 | 4297 | 2 | 1 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0012c0035t0002 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0013c0011t0002 | 0/0 | 4297 | 3 | 0 | 2 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0014c0017t0003 | 0/0 | 4297 | 2 | 2 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0015c0048t0002 | 0/0 | 4297 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0015c0052t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0016c0018t0001 | 0/0 | 4297 | 2 | 0 | 2 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0017c0020t0001 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0018c0023t0003 | 0/0 | 4297 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0019c0024t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0020c0022t0002 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0021c0025t0002 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0022c0026t0007 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0023c0021t0002 | 0/0 | 4297 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0024c0045t0001 | 0/0 | 4297 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0025c0046t0001 | 0/0 | 4297 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0026c0043t0007 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0027c0042t0002 | 0/0 | 4297 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0028c0036t0010 | 0/0 | 4297 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0029c0037t0001 | 0/0 | 4297 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0030c0038t0002 | 0/0 | 4297 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0031c0033t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0032c0034t0003 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0033c0050t0002 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0034c0040t0002 | 0/0 | 4297 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| a0035c0041t0001 | 0/0 | 4297 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | copy fasta | chr7 | 7352875 | 7540873 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0005t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0005t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0005t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0007t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0007t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0007t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0007t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0007t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0001c0051t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0002t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0004t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0031t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0002c0049t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0003t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0003c0047t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0004c0006t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0004c0006t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0004c0006t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0004c0006t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0004c0006t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0004c0039t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0005c0010t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0005c0010t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0005c0010t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0005c0010t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0005c0044t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0006c0015t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0006c0015t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0006c0019t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0006c0019t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0006c0030t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0007c0008t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0007c0008t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0007c0008t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0007c0008t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0007c0032t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0008c0009t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0008c0009t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0008c0009t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0008c0009t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0009c0014t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0009c0014t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0009c0029t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0010c0013t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0010c0013t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0010c0028t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0011c0012t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0011c0012t0005g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0011c0027t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0012c0016t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0012c0016t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0012c0035t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0013c0011t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0013c0011t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0013c0011t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0014c0017t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0014c0017t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0015c0048t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0015c0052t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0016c0018t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0016c0018t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0017c0020t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0018c0023t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0019c0024t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0020c0022t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0021c0025t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0022c0026t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0023c0021t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0024c0045t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0025c0046t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0026c0043t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0027c0042t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0028c0036t0010g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0029c0037t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0030c0038t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0031c0033t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0032c0034t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0033c0050t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0034c0040t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| a0035c0041t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0001 | g0099 | EUR | GBR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | GBR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0110 | EUR | GBR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00423 | hp1 | a0024 | c0045 | t0001 | g0087 | EAS | CHS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | CHS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00733 | hp1 | a0030 | c0038 | t0002 | g0114 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0084 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00735 | hp1 | a0003 | c0003 | t0004 | g0194 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00741 | hp1 | a0003 | c0003 | t0004 | g0196 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0077 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01070 | hp1 | a0013 | c0011 | t0002 | g0036 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01070 | hp2 | a0016 | c0018 | t0001 | g0129 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01081 | hp1 | a0018 | c0023 | t0003 | g0165 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01106 | hp2 | a0011 | c0027 | t0003 | g0024 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01109 | hp1 | a0012 | c0016 | t0002 | g0016 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0075 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01167 | hp1 | a0003 | c0003 | t0004 | g0193 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0119 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0118 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01243 | hp1 | a0028 | c0036 | t0010 | g0001 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01243 | hp2 | a0006 | c0019 | t0002 | g0188 | AMR | PUR | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01255 | hp1 | a0001 | c0005 | t0001 | g0100 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0141 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01346 | hp2 | a0015 | c0048 | t0002 | g0017 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01433 | hp1 | a0016 | c0018 | t0001 | g0144 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0131 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0108 | EUR | IBS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0112 | EUR | IBS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0111 | EUR | IBS | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01884 | hp1 | a0020 | c0022 | t0002 | g0163 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01891 | hp1 | a0008 | c0009 | t0003 | g0185 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01891 | hp2 | a0004 | c0006 | t0002 | g0184 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02004 | hp1 | a0003 | c0003 | t0004 | g0195 | AMR | PEL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02004 | hp2 | a0013 | c0011 | t0002 | g0035 | AMR | PEL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02055 | hp1 | a0002 | c0004 | t0003 | g0027 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02055 | hp2 | a0008 | c0009 | t0003 | g0180 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | KHV | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02080 | hp1 | a0001 | c0005 | t0001 | g0098 | EAS | KHV | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02083 | hp1 | a0029 | c0037 | t0001 | g0113 | EAS | KHV | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02145 | hp1 | a0011 | c0012 | t0002 | g0166 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02145 | hp2 | a0002 | c0004 | t0003 | g0032 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02257 | hp1 | a0010 | c0028 | t0003 | g0020 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02257 | hp2 | a0014 | c0017 | t0003 | g0058 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02451 | hp1 | a0002 | c0049 | t0003 | g0189 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02572 | hp1 | a0007 | c0008 | t0003 | g0012 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02572 | hp2 | a0004 | c0006 | t0002 | g0008 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02615 | hp1 | a0002 | c0004 | t0003 | g0070 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0073 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02622 | hp1 | a0001 | c0007 | t0003 | g0175 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0074 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02630 | hp1 | a0032 | c0034 | t0003 | g0038 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02630 | hp2 | a0002 | c0004 | t0003 | g0088 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02647 | hp1 | a0012 | c0035 | t0002 | g0072 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02717 | hp1 | a0007 | c0032 | t0003 | g0014 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02717 | hp2 | a0004 | c0006 | t0002 | g0005 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02723 | hp2 | a0002 | c0004 | t0003 | g0026 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02809 | hp1 | a0004 | c0039 | t0003 | g0071 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02809 | hp2 | a0002 | c0004 | t0003 | g0041 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02818 | hp2 | a0001 | c0005 | t0002 | g0067 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02886 | hp1 | a0033 | c0050 | t0002 | g0190 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02886 | hp2 | a0005 | c0010 | t0001 | g0092 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02897 | hp1 | a0002 | c0004 | t0003 | g0028 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02922 | hp1 | a0026 | c0043 | t0007 | g0029 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02922 | hp2 | a0001 | c0007 | t0003 | g0177 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02965 | hp1 | a0001 | c0005 | t0002 | g0069 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02965 | hp2 | a0006 | c0030 | t0003 | g0065 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02970 | hp1 | a0021 | c0025 | t0002 | g0162 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02970 | hp2 | a0004 | c0006 | t0002 | g0007 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02976 | hp1 | a0031 | c0033 | t0003 | g0031 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02976 | hp2 | a0007 | c0008 | t0003 | g0161 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03017 | hp2 | a0013 | c0011 | t0002 | g0064 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03098 | hp1 | a0005 | c0010 | t0001 | g0105 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03098 | hp2 | a0019 | c0024 | t0003 | g0167 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03130 | hp1 | a0006 | c0015 | t0002 | g0179 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03130 | hp2 | a0002 | c0004 | t0003 | g0033 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03139 | hp2 | a0008 | c0009 | t0003 | g0181 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03195 | hp1 | a0022 | c0026 | t0007 | g0164 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03195 | hp2 | a0002 | c0002 | t0006 | g0002 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03209 | hp1 | a0007 | c0008 | t0006 | g0003 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03209 | hp2 | a0010 | c0013 | t0002 | g0022 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03225 | hp1 | a0002 | c0004 | t0003 | g0030 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03225 | hp2 | a0005 | c0010 | t0002 | g0044 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0059 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03239 | hp2 | a0035 | c0041 | t0001 | g0133 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03453 | hp1 | a0002 | c0004 | t0003 | g0068 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03453 | hp2 | a0006 | c0019 | t0002 | g0187 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0170 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03486 | hp2 | a0006 | c0015 | t0002 | g0101 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03516 | hp1 | a0034 | c0040 | t0002 | g0040 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03516 | hp2 | a0005 | c0044 | t0003 | g0039 | AFR | ESN | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03540 | hp2 | a0002 | c0004 | t0003 | g0186 | AFR | GWD | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | MSL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03654 | hp1 | a0009 | c0014 | t0001 | g0010 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03669 | hp1 | a0002 | c0031 | t0001 | g0115 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0076 | SAS | BEB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03942 | hp1 | a0023 | c0021 | t0002 | g0025 | SAS | BEB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18522 | hp1 | a0001 | c0051 | t0008 | g0192 | AFR | YRI | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18522 | hp2 | a0017 | c0020 | t0001 | g0086 | AFR | YRI | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0079 | EAS | CHB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18612 | hp2 | a0027 | c0042 | t0002 | g0089 | EAS | CHB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18906 | hp1 | a0001 | c0007 | t0003 | g0102 | AFR | YRI | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18906 | hp2 | a0014 | c0017 | t0003 | g0057 | AFR | YRI | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18957 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18968 | hp2 | a0005 | c0010 | t0001 | g0043 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18969 | hp1 | a0025 | c0046 | t0001 | g0142 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19043 | hp1 | a0010 | c0013 | t0002 | g0019 | AFR | LWK | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19043 | hp2 | a0008 | c0009 | t0003 | g0183 | AFR | LWK | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19067 | hp2 | a0003 | c0003 | t0002 | g0159 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA20129 | hp1 | a0001 | c0007 | t0003 | g0176 | AFR | ASW | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA20129 | hp2 | a0007 | c0008 | t0003 | g0013 | AFR | ASW | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA20805 | hp1 | a0001 | c0007 | t0003 | g0148 | EUR | TSI | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA20805 | hp2 | a0001 | c0001 | t0009 | g0136 | EUR | TSI | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02109 | hp1 | a0009 | c0029 | t0003 | g0009 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02109 | hp2 | a0015 | c0052 | t0003 | g0191 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02486 | hp1 | a0003 | c0047 | t0003 | g0045 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0182 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02559 | hp1 | a0012 | c0016 | t0002 | g0123 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| HG02559 | hp2 | a0004 | c0006 | t0002 | g0006 | AFR | ACB | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA20300 | hp1 | a0009 | c0014 | t0003 | g0021 | AFR | USA | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | USA | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0103 | REF | REF | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| homoSapiens_grch38 | hp1 | a0011 | c0012 | t0005 | g0023 | REF | REF | COL28A1_chr7_7352875_7540873 | COL28A1 | chr7 | 7352875 | 7540873 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:7373028
|
A | C | 1 | a0030 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.2878T>G | p.Tyr960Asp | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/35 | 3039/4297 | 2878/3378 | 960/1125 | chr7 | 7373028 | ||
| chr7:7373085
|
T | C | 1 | a0025 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2821A>G | p.Asn941Asp | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/35 | 2982/4297 | 2821/3378 | 941/1125 | chr7 | 7373085 | ||
| chr7:7373177
|
C | T | 2 | a0024a0029 | 2 | HG00423.hp1 HG02083.hp1 |
missense_variant | MODERATE | c.2729G>A | p.Arg910His | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/35 | 2890/4297 | 2729/3378 | 910/1125 | chr7 | 7373177 | ||
| chr7:7373198
|
G | T | 1 | a0028 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2708C>A | p.Thr903Asn | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/35 | 2869/4297 | 2708/3378 | 903/1125 | chr7 | 7373198 | ||
| chr7:7373261
|
T | A | 8 | a0012a0018a0020others(5): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
missense_variant | MODERATE | c.2645A>T | p.Gln882Leu | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/35 | 2806/4297 | 2645/3378 | 882/1125 | chr7 | 7373261 | ||
| chr7:7380805
|
C | A | 1 | a0013 | 3 | HG01070.hp1 HG02004.hp2 HG03017.hp2 |
stop_gained | HIGH | c.2263G>T | p.Glu755* | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 29/35 | 2424/4297 | 2263/3378 | 755/1125 | chr7 | 7380805 | ||
| chr7:7380846
|
C | T | 5 | a0012a0018a0020others(2): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
missense_variant | MODERATE | c.2222G>A | p.Arg741Gln | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 29/35 | 2383/4297 | 2222/3378 | 741/1125 | chr7 | 7380846 | ||
| chr7:7381549
|
G | T | 1 | a0008 | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.2200C>A | p.Gln734Lys | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/35 | 2361/4297 | 2200/3378 | 734/1125 | chr7 | 7381549 | ||
| chr7:7419923
|
G | T | 2 | a0005a0033 | 6 | HG02886.hp1 HG02886.hp2 HG03098.hp1 others(3): Show |
missense_variant | MODERATE | c.2029C>A | p.Pro677Thr | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/35 | 2190/4297 | 2029/3378 | 677/1125 | chr7 | 7419923 | ||
| chr7:7436396
|
T | G | 1 | a0032 | 1 | HG02630.hp1 | missense_variant&splice_region_variant | MODERATE | c.1859A>C | p.Lys620Thr | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/35 | 2020/4297 | 1859/3378 | 620/1125 | chr7 | 7436396 | ||
| chr7:7444474
|
T | C | 1 | a0035 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1525A>G | p.Ile509Val | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/35 | 1686/4297 | 1525/3378 | 509/1125 | chr7 | 7444474 | ||
| chr7:7453466
|
C | G | 9 | a0004a0007a0010others(6): Show | 21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
missense_variant | MODERATE | c.1414G>C | p.Ala472Pro | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/35 | 1575/4297 | 1414/3378 | 472/1125 | chr7 | 7453466 | ||
| chr7:7456061
|
C | A | 1 | a0033 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1354G>T | p.Gly452Trp | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/35 | 1515/4297 | 1354/3378 | 452/1125 | chr7 | 7456061 | ||
| chr7:7456104
|
T | C | 23 | a0002a0003a0005others(20): Show | 89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
missense_variant | MODERATE | c.1311A>G | p.Ile437Met | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/35 | 1472/4297 | 1311/3378 | 437/1125 | chr7 | 7456104 | ||
| chr7:7474604
|
C | G | 25 | a0002a0003a0005others(22): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
missense_variant | MODERATE | c.1299G>C | p.Glu433Asp | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/35 | 1460/4297 | 1299/3378 | 433/1125 | chr7 | 7474604 | ||
| chr7:7506060
|
G | C | 9 | a0003a0005a0009others(6): Show | 34 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(31): Show |
missense_variant | MODERATE | c.980C>G | p.Thr327Ser | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/35 | 1141/4297 | 980/3378 | 327/1125 | chr7 | 7506060 | ||
| chr7:7511128
|
C | A | 1 | a0014 | 2 | HG02257.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.890G>T | p.Arg297Leu | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/35 | 1051/4297 | 890/3378 | 297/1125 | chr7 | 7511128 | ||
| chr7:7520085
|
C | T | 1 | a0023 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.790G>A | p.Glu264Lys | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/35 | 951/4297 | 790/3378 | 264/1125 | chr7 | 7520085 | ||
| chr7:7521949
|
T | C | 1 | a0016 | 2 | HG01070.hp2 HG01433.hp1 |
missense_variant | MODERATE | c.715A>G | p.Ile239Val | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/35 | 876/4297 | 715/3378 | 239/1125 | chr7 | 7521949 | ||
| chr7:7531463
|
G | C | 26 | a0001a0002a0003others(23): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
missense_variant | MODERATE | c.566C>G | p.Ala189Gly | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/35 | 727/4297 | 566/3378 | 189/1125 | chr7 | 7531463 | ||
| chr7:7531724
|
A | G | 1 | a0017 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.305T>C | p.Val102Ala | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/35 | 466/4297 | 305/3378 | 102/1125 | chr7 | 7531724 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:7373014
|
A | G | 2 | a0012c0035a0020c0022 | 2 | HG01884.hp1 HG02647.hp1 |
synonymous_variant | LOW | c.2892T>C | p.Asp964Asp | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/35 | 3053/4297 | 2892/3378 | 964/1125 | chr7 | 7373014 | ||
| chr7:7373518
|
T | C | 15 | a0001c0007a0002c0004a0002c0049others(12): Show | 33 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(30): Show |
synonymous_variant | LOW | c.2388A>G | p.Pro796Pro | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/35 | 2549/4297 | 2388/3378 | 796/1125 | chr7 | 7373518 | ||
| chr7:7432509
|
C | G | 1 | a0033c0050 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.1962G>C | p.Pro654Pro | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/35 | 2123/4297 | 1962/3378 | 654/1125 | chr7 | 7432509 | ||
| chr7:7453491
|
A | G | 2 | a0001c0005a0002c0031 | 6 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(3): Show |
synonymous_variant | LOW | c.1389T>C | p.Ile463Ile | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/35 | 1550/4297 | 1389/3378 | 463/1125 | chr7 | 7453491 | ||
| chr7:7531789
|
T | C | 5 | a0001c0051a0002c0049a0006c0019others(2): Show | 6 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
synonymous_variant | LOW | c.240A>G | p.Gln80Gln | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/35 | 401/4297 | 240/3378 | 80/1125 | chr7 | 7531789 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:7357968
|
G | A | 40 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(37): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*665C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 35/35 | 665 | chr7 | 7357968 | |||||
| chr7:7357985
|
A | G | 17 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(14): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*648T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 35/35 | 648 | chr7 | 7357985 | |||||
| chr7:7358127
|
C | G | 2 | a0001c0001t0008a0001c0051t0008 | 2 | HG03139.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*506G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 35/35 | 506 | chr7 | 7358127 | |||||
| chr7:7358212
|
C | T | 64 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*421G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 35/35 | 421 | chr7 | 7358212 | |||||
| chr7:7358415
|
A | G | 2 | a0022c0026t0007a0026c0043t0007 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*218T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 35/35 | 218 | chr7 | 7358415 | |||||
| chr7:7358479
|
T | G | 1 | a0001c0001t0009 | 2 | HG01433.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*154A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 35/35 | 154 | chr7 | 7358479 | |||||
| chr7:7358522
|
A | C | 2 | a0022c0026t0007a0026c0043t0007 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 35/35 | 111 | chr7 | 7358522 | |||||
| chr7:7535762
|
G | A | 1 | a0003c0003t0004 | 4 | HG00735.hp1 HG00741.hp1 HG01167.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-50C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/35 | 2887 | chr7 | 7535762 | |||||
| chr7:7535860
|
A | G | 3 | a0002c0002t0006a0007c0008t0006a0028c0036t0010 | 3 | HG01243.hp1 HG03195.hp2 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-148T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/35 | 2985 | chr7 | 7535860 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:7358826
|
T | G | 87 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.3206-21A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7358826 | ||||||
| chr7:7358975
|
T | C | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3206-170A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7358975 | ||||||
| chr7:7359006
|
TATTA | T | 87 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.3206-205_3206-202d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359006 | ||||||
| chr7:7359085
|
G | T | 13 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(10): Show | 13 | HG01081.hp1 HG01243.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.3206-280C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359085 | ||||||
| chr7:7359162
|
A | C | 1 | a0003c0003t0001g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3206-357T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359162 | ||||||
| chr7:7359182
|
T | C | 87 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.3206-377A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359182 | ||||||
| chr7:7359252
|
T | C | 2 | a0022c0026t0007g0164a0026c0043t0007g0029 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3206-447A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359252 | ||||||
| chr7:7359253
|
G | A | 1 | a0002c0002t0002g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3206-448C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359253 | ||||||
| chr7:7359290
|
CA | C | 162 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.3206-486delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359290 | ||||||
| chr7:7359348
|
G | C | 12 | a0001c0007t0003g0175a0001c0007t0003g0176a0001c0007t0003g0177others(9): Show | 12 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.3206-543C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359348 | ||||||
| chr7:7359393
|
G | T | 38 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(35): Show | 38 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.3206-588C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359393 | ||||||
| chr7:7359418
|
C | T | 39 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(36): Show | 39 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.3206-613G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359418 | ||||||
| chr7:7359465
|
T | G | 93 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.3206-660A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359465 | ||||||
| chr7:7359514
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0104others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3206-709G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359514 | ||||||
| chr7:7359521
|
T | C | 1 | a0005c0044t0003g0039 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3206-716A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359521 | ||||||
| chr7:7359523
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3206-718C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359523 | ||||||
| chr7:7359543
|
T | C | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3206-738A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359543 | ||||||
| chr7:7359679
|
C | A | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3205+711G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359679 | ||||||
| chr7:7359708
|
T | G | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3205+682A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359708 | ||||||
| chr7:7359718
|
G | C | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3205+672C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359718 | ||||||
| chr7:7359773
|
C | T | 92 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.3205+617G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359773 | ||||||
| chr7:7359843
|
A | G | 145 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.3205+547T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359843 | ||||||
| chr7:7359849
|
T | C | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3205+541A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359849 | ||||||
| chr7:7359885
|
G | A | 6 | a0001c0001t0002g0146a0001c0001t0002g0160a0002c0002t0002g0170others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.3205+505C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359885 | ||||||
| chr7:7359934
|
C | T | 12 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3205+456G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7359934 | ||||||
| chr7:7360090
|
C | T | 1 | a0005c0010t0001g0105 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3205+300G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7360090 | ||||||
| chr7:7360152
|
T | C | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3205+238A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7360152 | ||||||
| chr7:7360171
|
A | C | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3205+219T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7360171 | ||||||
| chr7:7360181
|
C | T | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3205+209G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 34/34 | chr7 | 7360181 | ||||||
| chr7:7360608
|
A | G | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-80T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7360608 | ||||||
| chr7:7360707
|
C | G | 137 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.3067-179G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7360707 | ||||||
| chr7:7360854
|
C | T | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3067-326G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7360854 | ||||||
| chr7:7360855
|
A | G | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3067-327T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7360855 | ||||||
| chr7:7360959
|
G | A | 28 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.3067-431C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7360959 | ||||||
| chr7:7360963
|
T | C | 116 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3067-435A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7360963 | ||||||
| chr7:7361081
|
T | G | 22 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(19): Show | 22 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.3067-553A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361081 | ||||||
| chr7:7361110
|
G | GCAAA | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3067-583_3067-582i others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361110 | ||||||
| chr7:7361115
|
C | CTCTT | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3067-588_3067-587i others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361115 | ||||||
| chr7:7361137
|
A | G | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3067-609T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361137 | ||||||
| chr7:7361169
|
G | A | 2 | a0002c0002t0002g0004a0002c0002t0002g0015 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3067-641C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361169 | ||||||
| chr7:7361188
|
G | C | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3067-660C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361188 | ||||||
| chr7:7361276
|
G | A | 116 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3067-748C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361276 | ||||||
| chr7:7361280
|
C | CAAGA | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3067-756_3067-753d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361280 | ||||||
| chr7:7361296
|
CT | C | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3067-769delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361296 | ||||||
| chr7:7361305
|
T | A | 180 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.3067-777A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361305 | ||||||
| chr7:7361368
|
T | C | 5 | a0012c0016t0002g0016a0012c0035t0002g0072a0020c0022t0002g0163others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3067-840A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361368 | ||||||
| chr7:7361467
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3067-939T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361467 | ||||||
| chr7:7361550
|
G | C | 11 | a0001c0001t0002g0178a0001c0005t0002g0069a0002c0002t0002g0037others(8): Show | 11 | HG01346.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3067-1022C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361550 | ||||||
| chr7:7361572
|
C | T | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1044G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361572 | ||||||
| chr7:7361604
|
G | T | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1076C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361604 | ||||||
| chr7:7361696
|
A | G | 87 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.3067-1168T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361696 | ||||||
| chr7:7361754
|
C | T | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1226G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361754 | ||||||
| chr7:7361768
|
G | C | 1 | a0003c0003t0004g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3067-1240C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361768 | ||||||
| chr7:7361772
|
T | TG | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1245dupC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361772 | ||||||
| chr7:7361793
|
C | G | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3067-1265G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361793 | ||||||
| chr7:7361830
|
C | T | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1302G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361830 | ||||||
| chr7:7361843
|
T | G | 1 | a0002c0002t0006g0002 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3067-1315A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361843 | ||||||
| chr7:7361853
|
T | TA | 5 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024others(2): Show | 5 | HG01106.hp2 HG02109.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3067-1326dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361853 | ||||||
| chr7:7361853
|
T | TAA | 117 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.3067-1327_3067-132 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361853 | ||||||
| chr7:7361854
|
A | AAC | 22 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(19): Show | 22 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.3067-1327_3067-132 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361854 | ||||||
| chr7:7361859
|
C | A | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1331G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7361859 | ||||||
| chr7:7362041
|
C | T | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1513G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362041 | ||||||
| chr7:7362048
|
C | G | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1520G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362048 | ||||||
| chr7:7362069
|
T | C | 2 | a0022c0026t0007g0164a0026c0043t0007g0029 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3067-1541A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362069 | ||||||
| chr7:7362250
|
A | ATTCTTTT | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1729_3067-172 others(11): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362250 | ||||||
| chr7:7362258
|
G | T | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1730C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362258 | ||||||
| chr7:7362306
|
A | G | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3067-1778T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362306 | ||||||
| chr7:7362317
|
G | A | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3067-1789C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362317 | ||||||
| chr7:7362323
|
T | G | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1795A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362323 | ||||||
| chr7:7362350
|
C | CTTGT | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1823_3067-182 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362350 | ||||||
| chr7:7362383
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3067-1855T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362383 | ||||||
| chr7:7362519
|
A | T | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-1991T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362519 | ||||||
| chr7:7362613
|
A | ATT | 142 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.3067-2087_3067-208 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362613 | ||||||
| chr7:7362636
|
T | C | 144 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3067-2108A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362636 | ||||||
| chr7:7362693
|
A | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3067-2165T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362693 | ||||||
| chr7:7362774
|
G | C | 180 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.3067-2246C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362774 | ||||||
| chr7:7362774
|
G | T | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3067-2246C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362774 | ||||||
| chr7:7362945
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0169a0017c0020t0001g0086 | 3 | HG02451.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3067-2417A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362945 | ||||||
| chr7:7362955
|
G | A | 2 | a0009c0029t0003g0009a0011c0027t0003g0024 | 2 | HG01106.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3067-2427C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362955 | ||||||
| chr7:7362959
|
T | C | 145 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.3067-2431A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7362959 | ||||||
| chr7:7363362
|
T | A | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3067-2834A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363362 | ||||||
| chr7:7363384
|
T | C | 115 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.3067-2856A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363384 | ||||||
| chr7:7363417
|
A | T | 12 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0005t0002g0069others(9): Show | 12 | HG01346.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3067-2889T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363417 | ||||||
| chr7:7363482
|
A | G | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3067-2954T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363482 | ||||||
| chr7:7363493
|
G | A | 29 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(26): Show | 29 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.3067-2965C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363493 | ||||||
| chr7:7363618
|
T | C | 4 | a0005c0010t0002g0044a0006c0015t0002g0179a0006c0019t0002g0187others(1): Show | 4 | HG01243.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3067-3090A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363618 | ||||||
| chr7:7363648
|
T | C | 20 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0004others(17): Show | 20 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.3067-3120A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363648 | ||||||
| chr7:7363681
|
G | T | 30 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(27): Show | 30 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.3067-3153C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363681 | ||||||
| chr7:7363742
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3067-3214T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363742 | ||||||
| chr7:7363833
|
T | C | 9 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.3067-3305A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363833 | ||||||
| chr7:7363842
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3067-3314T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363842 | ||||||
| chr7:7363900
|
C | T | 1 | a0001c0005t0001g0100 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3067-3372G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363900 | ||||||
| chr7:7363964
|
C | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3067-3436G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7363964 | ||||||
| chr7:7364001
|
C | T | 1 | a0003c0003t0001g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3067-3473G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364001 | ||||||
| chr7:7364250
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3067-3722A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364250 | ||||||
| chr7:7364275
|
A | T | 13 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(10): Show | 13 | HG01081.hp1 HG01243.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.3067-3747T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364275 | ||||||
| chr7:7364347
|
A | G | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.3067-3819T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364347 | ||||||
| chr7:7364492
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00140.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.3067-3964A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364492 | ||||||
| chr7:7364580
|
T | G | 6 | a0002c0002t0002g0004a0012c0016t0002g0016a0012c0035t0002g0072others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3067-4052A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364580 | ||||||
| chr7:7364609
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3067-4081A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364609 | ||||||
| chr7:7364667
|
T | A | 3 | a0002c0002t0002g0182a0004c0006t0002g0008a0010c0013t0002g0019 | 3 | HG02486.hp2 HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3067-4139A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364667 | ||||||
| chr7:7364683
|
G | A | 28 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(25): Show | 28 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.3067-4155C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364683 | ||||||
| chr7:7364701
|
A | G | 2 | a0022c0026t0007g0164a0026c0043t0007g0029 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3067-4173T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364701 | ||||||
| chr7:7364899
|
C | A | 3 | a0001c0001t0001g0048a0003c0003t0001g0076a0003c0003t0001g0077 | 3 | HG00741.hp2 HG01361.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3067-4371G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7364899 | ||||||
| chr7:7365100
|
T | C | 4 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3067-4572A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365100 | ||||||
| chr7:7365222
|
G | GTACGCAG others(24): Show |
87 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.3067-4725_3067-469 others(35): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365222 | ||||||
| chr7:7365413
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3067-4885G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365413 | ||||||
| chr7:7365438
|
C | T | 87 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.3067-4910G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365438 | ||||||
| chr7:7365669
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3066+5056C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365669 | ||||||
| chr7:7365749
|
G | C | 2 | a0022c0026t0007g0164a0026c0043t0007g0029 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3066+4976C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365749 | ||||||
| chr7:7365768
|
A | G | 6 | a0002c0004t0003g0026a0002c0004t0003g0028a0002c0004t0003g0030others(3): Show | 6 | HG02630.hp1 HG02723.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3066+4957T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365768 | ||||||
| chr7:7365919
|
G | T | 5 | a0012c0016t0002g0016a0012c0035t0002g0072a0020c0022t0002g0163others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3066+4806C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365919 | ||||||
| chr7:7365924
|
T | C | 2 | a0022c0026t0007g0164a0026c0043t0007g0029 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3066+4801A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7365924 | ||||||
| chr7:7366216
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3066+4509G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366216 | ||||||
| chr7:7366266
|
A | C | 114 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.3066+4459T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366266 | ||||||
| chr7:7366339
|
C | A | 1 | a0003c0003t0001g0080 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3066+4386G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366339 | ||||||
| chr7:7366370
|
T | C | 4 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3066+4355A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366370 | ||||||
| chr7:7366396
|
A | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3066+4329T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366396 | ||||||
| chr7:7366450
|
G | C | 180 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.3066+4275C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366450 | ||||||
| chr7:7366472
|
T | A | 9 | a0001c0007t0003g0148a0002c0002t0002g0004a0009c0029t0003g0009others(6): Show | 9 | HG01106.hp2 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.3066+4253A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366472 | ||||||
| chr7:7366660
|
A | T | 1 | a0005c0010t0001g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3066+4065T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366660 | ||||||
| chr7:7366675
|
TAGAA | T | 4 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3066+4046_3066+404 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366675 | ||||||
| chr7:7366797
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3066+3928G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366797 | ||||||
| chr7:7366804
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3066+3921C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366804 | ||||||
| chr7:7366938
|
C | T | 12 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3066+3787G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366938 | ||||||
| chr7:7366969
|
T | C | 88 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.3066+3756A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366969 | ||||||
| chr7:7366971
|
T | C | 88 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.3066+3754A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366971 | ||||||
| chr7:7366973
|
T | C | 88 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.3066+3752A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366973 | ||||||
| chr7:7366980
|
G | A | 29 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(26): Show | 29 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.3066+3745C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7366980 | ||||||
| chr7:7367113
|
G | A | 12 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3066+3612C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7367113 | ||||||
| chr7:7367125
|
T | A | 12 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3066+3600A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7367125 | ||||||
| chr7:7367485
|
G | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3066+3240C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7367485 | ||||||
| chr7:7367521
|
A | G | 89 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.3066+3204T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7367521 | ||||||
| chr7:7367614
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3066+3111G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7367614 | ||||||
| chr7:7367815
|
T | TA | 100 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.3066+2909dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7367815 | ||||||
| chr7:7368165
|
G | C | 1 | a0009c0014t0001g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3066+2560C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368165 | ||||||
| chr7:7368234
|
C | G | 1 | a0028c0036t0010g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3066+2491G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368234 | ||||||
| chr7:7368389
|
G | GT | 39 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.3066+2335dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368389 | ||||||
| chr7:7368389
|
G | GTT | 106 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.3066+2334_3066+233 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368389 | ||||||
| chr7:7368389
|
G | GTTTTTTT others(8): Show |
1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3066+2335_3066+233 others(19): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368389 | ||||||
| chr7:7368389
|
G | GTTTTTTT others(9): Show |
28 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(25): Show | 28 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.3066+2335_3066+233 others(20): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368389 | ||||||
| chr7:7368389
|
G | GTTTTTTT others(8): Show |
4 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3066+2335_3066+233 others(19): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368389 | ||||||
| chr7:7368398
|
G | T | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3066+2327C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368398 | ||||||
| chr7:7368420
|
C | T | 2 | a0001c0001t0001g0120a0003c0003t0001g0074 | 2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3066+2305G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368420 | ||||||
| chr7:7368603
|
A | G | 5 | a0002c0002t0002g0015a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3066+2122T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368603 | ||||||
| chr7:7368730
|
C | A | 1 | a0020c0022t0002g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3066+1995G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368730 | ||||||
| chr7:7368872
|
T | C | 7 | a0012c0016t0002g0016a0012c0016t0002g0123a0012c0035t0002g0072others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.3066+1853A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368872 | ||||||
| chr7:7368932
|
T | A | 4 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3066+1793A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368932 | ||||||
| chr7:7368948
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3066+1777T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7368948 | ||||||
| chr7:7369097
|
G | C | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3066+1628C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369097 | ||||||
| chr7:7369199
|
C | G | 1 | a0003c0047t0003g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3066+1526G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369199 | ||||||
| chr7:7369239
|
A | G | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3066+1486T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369239 | ||||||
| chr7:7369420
|
C | T | 45 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(42): Show | 45 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(42): Show |
intron_variant | MODIFIER | c.3066+1305G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369420 | ||||||
| chr7:7369488
|
G | A | 180 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.3066+1237C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369488 | ||||||
| chr7:7369668
|
G | C | 89 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.3066+1057C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369668 | ||||||
| chr7:7369691
|
T | C | 40 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(37): Show | 40 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.3066+1034A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369691 | ||||||
| chr7:7369747
|
G | A | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3066+978C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369747 | ||||||
| chr7:7369747
|
G | C | 4 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3066+978C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369747 | ||||||
| chr7:7369840
|
C | T | 88 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.3066+885G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369840 | ||||||
| chr7:7369898
|
A | T | 28 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(25): Show | 28 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.3066+827T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7369898 | ||||||
| chr7:7370170
|
A | G | 1 | a0035c0041t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3066+555T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7370170 | ||||||
| chr7:7370336
|
G | C | 1 | a0001c0007t0003g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3066+389C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7370336 | ||||||
| chr7:7370354
|
G | A | 5 | a0002c0002t0002g0015a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3066+371C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7370354 | ||||||
| chr7:7370471
|
T | G | 6 | a0002c0002t0002g0004a0012c0016t0002g0016a0012c0035t0002g0072others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3066+254A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 33/34 | chr7 | 7370471 | ||||||
| chr7:7371012
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0104others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2909-130G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371012 | ||||||
| chr7:7371063
|
T | A | 7 | a0012c0016t0002g0016a0012c0016t0002g0123a0012c0035t0002g0072others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2909-181A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371063 | ||||||
| chr7:7371161
|
C | T | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2909-279G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371161 | ||||||
| chr7:7371237
|
C | T | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2909-355G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371237 | ||||||
| chr7:7371357
|
T | C | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2909-475A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371357 | ||||||
| chr7:7371873
|
C | T | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2909-991G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371873 | ||||||
| chr7:7371886
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0104others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2909-1004C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371886 | ||||||
| chr7:7371894
|
A | G | 6 | a0002c0002t0002g0004a0012c0016t0002g0016a0012c0035t0002g0072others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2909-1012T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371894 | ||||||
| chr7:7371911
|
T | C | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2909-1029A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371911 | ||||||
| chr7:7371942
|
T | C | 46 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(43): Show | 46 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.2908+1056A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371942 | ||||||
| chr7:7371945
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2908+1053C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371945 | ||||||
| chr7:7371957
|
C | T | 1 | a0003c0003t0001g0081 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2908+1041G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371957 | ||||||
| chr7:7371958
|
G | T | 11 | a0001c0001t0002g0178a0001c0005t0002g0069a0002c0002t0002g0037others(8): Show | 11 | HG01346.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2908+1040C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7371958 | ||||||
| chr7:7372141
|
T | G | 1 | a0012c0016t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2908+857A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372141 | ||||||
| chr7:7372171
|
G | A | 30 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(27): Show | 30 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.2908+827C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372171 | ||||||
| chr7:7372256
|
G | A | 1 | a0005c0044t0003g0039 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2908+742C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372256 | ||||||
| chr7:7372266
|
G | A | 27 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(24): Show | 27 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2908+732C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372266 | ||||||
| chr7:7372271
|
T | C | 46 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(43): Show | 46 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.2908+727A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372271 | ||||||
| chr7:7372337
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2908+661A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372337 | ||||||
| chr7:7372392
|
C | T | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2908+606G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372392 | ||||||
| chr7:7372398
|
A | AAAAT | 77 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0046others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.2908+596_2908+599d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372398 | ||||||
| chr7:7372398
|
A | AAAATAAA others(1): Show |
19 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0138others(16): Show | 19 | HG01070.hp1 HG01106.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.2908+592_2908+599d others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372398 | ||||||
| chr7:7372398
|
A | AAAATAAA others(5): Show |
4 | a0001c0001t0002g0135a0001c0001t0002g0152a0002c0002t0002g0139others(1): Show | 4 | HG00438.hp1 NA18612.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.2908+588_2908+599d others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372398 | ||||||
| chr7:7372398
|
A | AAAATAAA others(9): Show |
2 | a0002c0002t0002g0110a0002c0002t0002g0112 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2908+584_2908+599d others(18): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372398 | ||||||
| chr7:7372398
|
A | AAATAAAT others(8): Show |
2 | a0001c0007t0003g0102a0014c0017t0003g0057 | 2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2908+599_2908+600i others(17): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372398 | ||||||
| chr7:7372398
|
AAAAT | A | 12 | a0001c0001t0001g0047a0001c0001t0001g0124a0001c0007t0003g0175others(9): Show | 12 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2908+596_2908+599d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372398 | ||||||
| chr7:7372398
|
AAAATAAA others(1): Show |
A | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2908+592_2908+599d others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372398 | ||||||
| chr7:7372398
|
AAAATAAA others(5): Show |
A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2908+588_2908+599d others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372398 | ||||||
| chr7:7372442
|
T | A | 19 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.2908+556A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372442 | ||||||
| chr7:7372442
|
T | TAAAA | 11 | a0002c0002t0002g0004a0002c0004t0003g0026a0002c0004t0003g0028others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2908+555_2908+556i others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372442 | ||||||
| chr7:7372442
|
T | TAAATAAA others(1): Show |
6 | a0002c0004t0003g0027a0002c0004t0003g0186a0004c0039t0003g0071others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2908+555_2908+556i others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372442 | ||||||
| chr7:7372486
|
C | T | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2908+512G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372486 | ||||||
| chr7:7372753
|
G | A | 89 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2908+245C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372753 | ||||||
| chr7:7372865
|
C | T | 1 | a0003c0003t0004g0195 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2908+133G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372865 | ||||||
| chr7:7372941
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2908+57A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372941 | ||||||
| chr7:7372989
|
C | T | 27 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(24): Show | 27 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2908+9G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 32/34 | chr7 | 7372989 | ||||||
| chr7:7373705
|
C | CT | 95 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.2360-160dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7373705 | ||||||
| chr7:7373735
|
G | A | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2360-189C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7373735 | ||||||
| chr7:7373737
|
C | T | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2360-191G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7373737 | ||||||
| chr7:7373738
|
G | A | 5 | a0012c0016t0002g0016a0012c0035t0002g0072a0020c0022t0002g0163others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2360-192C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7373738 | ||||||
| chr7:7373762
|
G | C | 2 | a0001c0001t0009g0131a0001c0001t0009g0136 | 2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2360-216C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7373762 | ||||||
| chr7:7373911
|
A | G | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | HG00438.hp1 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.2360-365T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7373911 | ||||||
| chr7:7373988
|
C | T | 2 | a0002c0049t0003g0189a0007c0008t0003g0161 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2360-442G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7373988 | ||||||
| chr7:7373994
|
C | T | 9 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(6): Show | 9 | HG01243.hp2 HG02717.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2360-448G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7373994 | ||||||
| chr7:7374024
|
T | TA | 12 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0001g0094others(9): Show | 12 | HG00423.hp1 HG00741.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-479dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374024 | ||||||
| chr7:7374034
|
A | ATATAT | 2 | a0001c0007t0003g0148a0009c0029t0003g0009 | 2 | HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2360-489_2360-488i others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374034 | ||||||
| chr7:7374034
|
A | T | 2 | a0001c0001t0001g0054a0011c0027t0003g0024 | 2 | HG00438.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2360-488T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374034 | ||||||
| chr7:7374036
|
A | AAT | 26 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0048others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.2360-491_2360-490i others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374036 | ||||||
| chr7:7374036
|
A | AATAT | 5 | a0001c0001t0001g0085a0001c0001t0001g0128a0001c0001t0001g0154others(2): Show | 5 | HG01515.hp2 HG03490.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.2360-491_2360-490i others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374036 | ||||||
| chr7:7374036
|
A | AT | 9 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(6): Show | 9 | HG01255.hp2 HG01361.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2360-491_2360-490i others(3): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374036 | ||||||
| chr7:7374036
|
A | ATAT | 5 | a0001c0001t0001g0106a0001c0001t0001g0137a0001c0001t0001g0157others(2): Show | 5 | HG02083.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2360-491_2360-490i others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374036 | ||||||
| chr7:7374036
|
A | T | 7 | a0001c0001t0001g0054a0001c0001t0001g0140a0001c0007t0003g0148others(4): Show | 7 | HG00438.hp2 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.2360-490T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374036 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(42): Show |
1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2360-493_2360-492i others(51): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(11): Show |
2 | a0022c0026t0007g0164a0026c0043t0007g0029 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2360-493_2360-492i others(20): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(13): Show |
1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(22): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(19): Show |
2 | a0012c0035t0002g0072a0020c0022t0002g0163 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2360-493_2360-492i others(28): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(10): Show |
1 | a0031c0033t0003g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(19): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(23): Show |
1 | a0034c0040t0002g0040 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(32): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(29): Show |
1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(38): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(18): Show |
1 | a0021c0025t0002g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(27): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(9): Show |
3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2360-493_2360-492i others(18): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(13): Show |
1 | a0002c0002t0006g0002 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2360-493_2360-492i others(22): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(10): Show |
5 | a0001c0005t0002g0067a0006c0015t0002g0101a0006c0019t0002g0187others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2360-493_2360-492i others(19): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(12): Show |
1 | a0006c0015t0002g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(21): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(9): Show |
1 | a0005c0010t0002g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2360-493_2360-492i others(18): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(20): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAATA others(3): Show |
1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AAAAAATA others(5): Show |
1 | a0012c0016t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2360-493_2360-492i others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | AT | 23 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0090others(20): Show | 23 | HG00280.hp2 HG00423.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.2360-493_2360-492i others(3): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | ATAT | 4 | a0001c0001t0001g0124a0001c0001t0001g0138a0001c0001t0002g0146others(1): Show | 4 | HG02056.hp1 HG03654.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-493_2360-492i others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
A | T | 54 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0046others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.2360-492T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374038
|
AAT | A | 27 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(24): Show | 27 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.2360-494_2360-493d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374038 | ||||||
| chr7:7374039
|
AT | A | 12 | a0001c0007t0003g0175a0001c0007t0003g0176a0001c0007t0003g0177others(9): Show | 12 | HG00140.hp2 HG01516.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-494delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374039 | ||||||
| chr7:7374039
|
ATAT | A | 4 | a0002c0002t0002g0141a0005c0044t0003g0039a0013c0011t0002g0036others(1): Show | 4 | HG01070.hp1 HG01346.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-496_2360-494d others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374039 | ||||||
| chr7:7374040
|
T | A | 16 | a0001c0007t0003g0102a0002c0004t0003g0026a0002c0004t0003g0027others(13): Show | 16 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.2360-494A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374040 | ||||||
| chr7:7374042
|
T | A | 52 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.2360-496A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374042 | ||||||
| chr7:7374044
|
T | A | 47 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(44): Show | 47 | HG00140.hp2 HG00438.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.2360-498A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374044 | ||||||
| chr7:7374046
|
T | A | 12 | a0001c0007t0003g0175a0001c0007t0003g0176a0001c0007t0003g0177others(9): Show | 12 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-500A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374046 | ||||||
| chr7:7374054
|
T | TA | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2360-509dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374054 | ||||||
| chr7:7374060
|
T | C | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2360-514A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374060 | ||||||
| chr7:7374109
|
G | A | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2360-563C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374109 | ||||||
| chr7:7374185
|
T | C | 90 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2360-639A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374185 | ||||||
| chr7:7374216
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2360-670G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374216 | ||||||
| chr7:7374282
|
A | G | 9 | a0001c0007t0003g0102a0002c0004t0003g0027a0002c0004t0003g0186others(6): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2360-736T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374282 | ||||||
| chr7:7374542
|
T | A | 10 | a0012c0016t0002g0016a0012c0016t0002g0123a0012c0035t0002g0072others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2359+919A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374542 | ||||||
| chr7:7374651
|
G | C | 1 | a0009c0014t0001g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2359+810C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374651 | ||||||
| chr7:7374667
|
A | C | 1 | a0001c0001t0002g0146 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2359+794T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374667 | ||||||
| chr7:7374890
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2359+571A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374890 | ||||||
| chr7:7374999
|
T | C | 45 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(42): Show | 45 | HG01081.hp1 HG01106.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.2359+462A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7374999 | ||||||
| chr7:7375122
|
T | C | 7 | a0012c0016t0002g0016a0012c0016t0002g0123a0012c0035t0002g0072others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2359+339A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7375122 | ||||||
| chr7:7375183
|
C | T | 1 | a0028c0036t0010g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2359+278G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7375183 | ||||||
| chr7:7375231
|
G | A | 1 | a0001c0005t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2359+230C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7375231 | ||||||
| chr7:7375292
|
C | T | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2359+169G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 31/34 | chr7 | 7375292 | ||||||
| chr7:7375586
|
C | T | 140 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.2323-89G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7375586 | ||||||
| chr7:7375629
|
A | G | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2323-132T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7375629 | ||||||
| chr7:7375725
|
C | A | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2323-228G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7375725 | ||||||
| chr7:7375746
|
G | A | 8 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(5): Show | 8 | HG01081.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2323-249C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7375746 | ||||||
| chr7:7375765
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2323-268C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7375765 | ||||||
| chr7:7375788
|
C | G | 27 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(24): Show | 27 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2323-291G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7375788 | ||||||
| chr7:7375848
|
T | C | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2323-351A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7375848 | ||||||
| chr7:7375897
|
T | G | 5 | a0012c0016t0002g0016a0012c0035t0002g0072a0020c0022t0002g0163others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2323-400A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7375897 | ||||||
| chr7:7376069
|
C | T | 4 | a0001c0001t0002g0127a0001c0007t0003g0148a0009c0029t0003g0009others(1): Show | 4 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2323-572G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376069 | ||||||
| chr7:7376070
|
G | A | 5 | a0012c0016t0002g0016a0012c0035t0002g0072a0020c0022t0002g0163others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2323-573C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376070 | ||||||
| chr7:7376137
|
T | C | 1 | a0028c0036t0010g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2323-640A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376137 | ||||||
| chr7:7376199
|
AG | A | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2323-703delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376199 | ||||||
| chr7:7376228
|
A | G | 47 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(44): Show | 47 | HG01081.hp1 HG01106.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.2323-731T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376228 | ||||||
| chr7:7376339
|
A | T | 1 | a0017c0020t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2323-842T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376339 | ||||||
| chr7:7376513
|
A | G | 8 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(5): Show | 8 | HG01081.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2323-1016T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376513 | ||||||
| chr7:7376606
|
C | T | 8 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(5): Show | 8 | HG01081.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2323-1109G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376606 | ||||||
| chr7:7376661
|
A | G | 2 | a0021c0025t0002g0162a0034c0040t0002g0040 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2323-1164T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376661 | ||||||
| chr7:7376698
|
T | C | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2323-1201A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376698 | ||||||
| chr7:7376720
|
C | T | 39 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(36): Show | 39 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.2323-1223G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376720 | ||||||
| chr7:7376727
|
A | AATACT | 182 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2323-1231_2323-123 others(9): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376727 | ||||||
| chr7:7376746
|
T | C | 6 | a0002c0002t0002g0004a0012c0016t0002g0016a0012c0035t0002g0072others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2323-1249A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376746 | ||||||
| chr7:7376890
|
C | G | 39 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(36): Show | 39 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.2323-1393G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376890 | ||||||
| chr7:7376912
|
G | A | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2323-1415C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376912 | ||||||
| chr7:7376981
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2323-1484A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7376981 | ||||||
| chr7:7377018
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2323-1521C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377018 | ||||||
| chr7:7377109
|
T | C | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2323-1612A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377109 | ||||||
| chr7:7377136
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2323-1639A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377136 | ||||||
| chr7:7377159
|
T | C | 31 | a0001c0005t0001g0099a0001c0007t0003g0102a0001c0007t0003g0148others(28): Show | 31 | HG00099.hp1 HG01106.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.2323-1662A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377159 | ||||||
| chr7:7377186
|
A | C | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2323-1689T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377186 | ||||||
| chr7:7377411
|
G | A | 5 | a0012c0016t0002g0016a0012c0035t0002g0072a0020c0022t0002g0163others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2323-1914C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377411 | ||||||
| chr7:7377511
|
C | T | 39 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(36): Show | 39 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.2323-2014G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377511 | ||||||
| chr7:7377516
|
A | G | 43 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(40): Show | 43 | HG01106.hp2 HG01255.hp2 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2323-2019T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377516 | ||||||
| chr7:7377559
|
A | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2323-2062T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377559 | ||||||
| chr7:7377790
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2323-2293A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377790 | ||||||
| chr7:7377807
|
C | CA | 56 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0047others(53): Show | 56 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.2323-2311dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377807 | ||||||
| chr7:7377807
|
C | CAA | 85 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0049others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.2323-2312_2323-231 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377807 | ||||||
| chr7:7377807
|
C | CAAA | 6 | a0001c0001t0001g0018a0001c0001t0001g0168a0001c0001t0002g0051others(3): Show | 6 | HG01106.hp1 HG01433.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2323-2313_2323-231 others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377807 | ||||||
| chr7:7377807
|
CA | C | 26 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(23): Show | 26 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.2323-2311delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377807 | ||||||
| chr7:7377818
|
A | AC | 6 | a0002c0002t0002g0004a0012c0016t0002g0016a0012c0035t0002g0072others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2323-2322_2323-232 others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377818 | ||||||
| chr7:7377916
|
C | G | 13 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2323-2419G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377916 | ||||||
| chr7:7377927
|
G | T | 1 | a0001c0007t0003g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2323-2430C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377927 | ||||||
| chr7:7377953
|
G | A | 2 | a0001c0001t0009g0131a0001c0001t0009g0136 | 2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2323-2456C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377953 | ||||||
| chr7:7377967
|
T | G | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2323-2470A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7377967 | ||||||
| chr7:7378063
|
C | T | 29 | a0001c0007t0003g0102a0001c0007t0003g0148a0001c0007t0003g0175others(26): Show | 29 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2323-2566G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378063 | ||||||
| chr7:7378199
|
G | A | 29 | a0001c0007t0003g0102a0001c0007t0003g0148a0001c0007t0003g0175others(26): Show | 29 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2322+2461C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378199 | ||||||
| chr7:7378240
|
C | T | 29 | a0001c0007t0003g0102a0001c0007t0003g0148a0001c0007t0003g0175others(26): Show | 29 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2322+2420G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378240 | ||||||
| chr7:7378251
|
T | C | 29 | a0001c0007t0003g0102a0001c0007t0003g0148a0001c0007t0003g0175others(26): Show | 29 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2322+2409A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378251 | ||||||
| chr7:7378273
|
A | G | 13 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2322+2387T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378273 | ||||||
| chr7:7378459
|
G | A | 5 | a0012c0016t0002g0016a0012c0035t0002g0072a0020c0022t0002g0163others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2322+2201C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378459 | ||||||
| chr7:7378481
|
T | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2322+2179A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378481 | ||||||
| chr7:7378507
|
G | A | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2322+2153C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378507 | ||||||
| chr7:7378594
|
C | T | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2322+2066G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378594 | ||||||
| chr7:7378603
|
A | G | 2 | a0002c0004t0003g0041a0010c0028t0003g0020 | 2 | HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2322+2057T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378603 | ||||||
| chr7:7378651
|
T | C | 74 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0048others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.2322+2009A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378651 | ||||||
| chr7:7378736
|
T | C | 20 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(17): Show | 20 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.2322+1924A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378736 | ||||||
| chr7:7378745
|
A | C | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2322+1915T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378745 | ||||||
| chr7:7378904
|
T | C | 1 | a0003c0003t0001g0081 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2322+1756A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7378904 | ||||||
| chr7:7379052
|
G | A | 1 | a0003c0003t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2322+1608C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379052 | ||||||
| chr7:7379098
|
T | C | 4 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2322+1562A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379098 | ||||||
| chr7:7379103
|
A | C | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2322+1557T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379103 | ||||||
| chr7:7379144
|
C | T | 52 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(49): Show | 52 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.2322+1516G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379144 | ||||||
| chr7:7379174
|
C | T | 52 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0102others(49): Show | 52 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.2322+1486G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379174 | ||||||
| chr7:7379254
|
T | C | 1 | a0001c0005t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2322+1406A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379254 | ||||||
| chr7:7379306
|
G | A | 1 | a0002c0002t0001g0126 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2322+1354C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379306 | ||||||
| chr7:7379335
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2322+1325C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379335 | ||||||
| chr7:7379481
|
T | C | 13 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2322+1179A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379481 | ||||||
| chr7:7379563
|
G | A | 10 | a0012c0016t0002g0016a0012c0016t0002g0123a0012c0035t0002g0072others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2322+1097C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379563 | ||||||
| chr7:7379605
|
G | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2322+1055C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379605 | ||||||
| chr7:7379618
|
A | G | 1 | a0003c0003t0001g0080 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2322+1042T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379618 | ||||||
| chr7:7379674
|
T | C | 13 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2322+986A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379674 | ||||||
| chr7:7379707
|
C | T | 13 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(10): Show | 13 | HG01255.hp2 HG01361.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.2322+953G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379707 | ||||||
| chr7:7379744
|
C | T | 26 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(23): Show | 26 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.2322+916G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379744 | ||||||
| chr7:7379898
|
T | G | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2322+762A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379898 | ||||||
| chr7:7379958
|
C | T | 10 | a0012c0016t0002g0016a0012c0016t0002g0123a0012c0035t0002g0072others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2322+702G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379958 | ||||||
| chr7:7379978
|
C | T | 1 | a0003c0003t0001g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2322+682G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7379978 | ||||||
| chr7:7380464
|
G | A | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2322+196C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7380464 | ||||||
| chr7:7380478
|
C | T | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2322+182G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7380478 | ||||||
| chr7:7380573
|
A | C | 10 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2322+87T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7380573 | ||||||
| chr7:7380601
|
T | A | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2322+59A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 30/34 | chr7 | 7380601 | ||||||
| chr7:7380698
|
A | G | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
splice_region_variant&intron_variant | LOW | c.2287-3T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 29/34 | chr7 | 7380698 | ||||||
| chr7:7380767
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2286+15A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 29/34 | chr7 | 7380767 | ||||||
| chr7:7380888
|
G | A | 1 | a0003c0003t0004g0195 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2206-26C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7380888 | ||||||
| chr7:7380937
|
G | GT | 11 | a0002c0002t0002g0004a0002c0004t0003g0032a0002c0004t0003g0068others(8): Show | 11 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2206-76dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7380937 | ||||||
| chr7:7380982
|
T | C | 103 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.2206-120A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7380982 | ||||||
| chr7:7381014
|
T | C | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2206-152A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7381014 | ||||||
| chr7:7381021
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2206-159A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7381021 | ||||||
| chr7:7381156
|
T | C | 2 | a0012c0016t0002g0123a0018c0023t0003g0165 | 2 | HG01081.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2206-294A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7381156 | ||||||
| chr7:7381356
|
C | T | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2205+188G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7381356 | ||||||
| chr7:7381382
|
G | A | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2205+162C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7381382 | ||||||
| chr7:7381388
|
C | A | 182 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2205+156G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 28/34 | chr7 | 7381388 | ||||||
| chr7:7381679
|
A | G | 92 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2137-67T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7381679 | ||||||
| chr7:7381692
|
C | T | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-80G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7381692 | ||||||
| chr7:7381734
|
AAT | A | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2137-124_2137-123d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7381734 | ||||||
| chr7:7381863
|
A | G | 1 | a0001c0005t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2137-251T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7381863 | ||||||
| chr7:7382016
|
A | C | 1 | a0028c0036t0010g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2137-404T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382016 | ||||||
| chr7:7382037
|
C | T | 1 | a0003c0003t0002g0159 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2137-425G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382037 | ||||||
| chr7:7382101
|
T | C | 182 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2137-489A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382101 | ||||||
| chr7:7382102
|
G | A | 29 | a0001c0007t0003g0102a0001c0007t0003g0148a0001c0007t0003g0175others(26): Show | 29 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2137-490C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382102 | ||||||
| chr7:7382263
|
T | C | 13 | a0002c0004t0003g0030a0002c0004t0003g0032a0002c0004t0003g0068others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2137-651A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382263 | ||||||
| chr7:7382310
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2137-698G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382310 | ||||||
| chr7:7382347
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG00280.hp1 HG01169.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2137-735G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382347 | ||||||
| chr7:7382348
|
G | A | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2137-736C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382348 | ||||||
| chr7:7382852
|
C | T | 2 | a0001c0001t0009g0131a0001c0001t0009g0136 | 2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2137-1240G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7382852 | ||||||
| chr7:7383186
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2137-1574A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383186 | ||||||
| chr7:7383250
|
T | TTG | 18 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0054others(15): Show | 18 | HG00438.hp2 HG00741.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-1640_2137-163 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383250 | ||||||
| chr7:7383250
|
TTG | T | 8 | a0001c0001t0002g0178a0001c0001t0005g0011a0001c0005t0002g0069others(5): Show | 8 | HG01256.hp1 HG01346.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2137-1640_2137-163 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383250 | ||||||
| chr7:7383250
|
TTGTG | T | 2 | a0002c0002t0002g0182a0002c0031t0001g0115 | 2 | HG02486.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2137-1642_2137-163 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383250 | ||||||
| chr7:7383250
|
TTGTGTG | T | 11 | a0001c0007t0003g0148a0002c0004t0003g0030a0007c0008t0006g0003others(8): Show | 11 | HG01081.hp1 HG01106.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2137-1644_2137-163 others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383250 | ||||||
| chr7:7383250
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2137-1650_2137-163 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383250 | ||||||
| chr7:7383280
|
GTGTGTGT others(3): Show |
G | 4 | a0002c0002t0002g0004a0002c0004t0003g0032a0002c0004t0003g0068others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-1678_2137-166 others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383280 | ||||||
| chr7:7383282
|
GTGTGTGT others(1): Show |
G | 24 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0056others(21): Show | 24 | HG01361.hp1 HG02083.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.2137-1678_2137-167 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383282 | ||||||
| chr7:7383284
|
GTGTGTT | G | 14 | a0001c0001t0001g0055a0001c0007t0003g0102a0002c0004t0003g0027others(11): Show | 14 | HG01109.hp1 HG01255.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2137-1678_2137-167 others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383284 | ||||||
| chr7:7383286
|
GTGTT | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0169a0001c0001t0003g0173 | 3 | HG02451.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2137-1678_2137-167 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383286 | ||||||
| chr7:7383288
|
G | T | 21 | a0001c0001t0002g0051a0001c0001t0002g0103a0001c0001t0002g0149others(18): Show | 21 | HG00140.hp2 HG00438.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.2137-1676C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383288 | ||||||
| chr7:7383288
|
GTT | G | 15 | a0001c0001t0001g0018a0001c0001t0001g0153a0001c0001t0002g0171others(12): Show | 15 | HG00741.hp1 HG01167.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.2137-1678_2137-167 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383288 | ||||||
| chr7:7383289
|
T | TG | 3 | a0002c0002t0002g0117a0003c0003t0001g0081a0004c0006t0002g0006 | 3 | HG02559.hp2 NA18960.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2137-1678_2137-167 others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383289 | ||||||
| chr7:7383290
|
T | G | 73 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0047others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.2137-1678A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383290 | ||||||
| chr7:7383291
|
T | G | 2 | a0002c0002t0002g0117a0003c0003t0001g0081 | 2 | NA18960.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2137-1679A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383291 | ||||||
| chr7:7383292
|
T | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0145a0001c0001t0002g0127others(1): Show | 4 | HG00423.hp2 HG02056.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-1680A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383292 | ||||||
| chr7:7383325
|
T | C | 195 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2137-1713A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383325 | ||||||
| chr7:7383340
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2137-1728C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383340 | ||||||
| chr7:7383433
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2137-1821A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383433 | ||||||
| chr7:7383445
|
A | C | 1 | a0003c0003t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2137-1833T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383445 | ||||||
| chr7:7383455
|
T | C | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2137-1843A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383455 | ||||||
| chr7:7383476
|
A | G | 1 | a0002c0049t0003g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2137-1864T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383476 | ||||||
| chr7:7383533
|
C | A | 1 | a0028c0036t0010g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2137-1921G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383533 | ||||||
| chr7:7383666
|
T | TTG | 26 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.2137-2056_2137-205 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383666 | ||||||
| chr7:7383666
|
T | TTGTGTGT others(1): Show |
8 | a0002c0004t0003g0030a0012c0016t0002g0016a0012c0016t0002g0123others(5): Show | 8 | HG01081.hp1 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-2062_2137-205 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383666 | ||||||
| chr7:7383682
|
G | GTA | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0127others(1): Show | 4 | HG02004.hp1 HG02056.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-2072_2137-207 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTATA | 25 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0052others(22): Show | 25 | HG00423.hp2 HG01070.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2137-2074_2137-207 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTATATA | 33 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0056others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.2137-2076_2137-207 others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTATATAT others(1): Show |
19 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0050others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.2137-2078_2137-207 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTATATAT others(3): Show |
4 | a0001c0001t0001g0042a0001c0001t0001g0169a0001c0001t0002g0160others(1): Show | 4 | HG00741.hp2 HG02735.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-2080_2137-207 others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0104 | 2 | HG03579.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2137-2082_2137-207 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2137-2084_2137-207 others(18): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTATATAT others(9): Show |
1 | a0035c0041t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2137-2086_2137-207 others(20): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTGTATA | 3 | a0001c0001t0001g0143a0002c0004t0003g0032a0002c0004t0003g0070 | 3 | HG01256.hp2 HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2137-2071_2137-207 others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTGTGTGT others(3): Show |
1 | a0007c0008t0006g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2137-2071_2137-207 others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
G | GTGTGTGT others(5): Show |
1 | a0020c0022t0002g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2137-2071_2137-207 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383682
|
GTA | G | 15 | a0001c0001t0002g0178a0001c0001t0005g0011a0001c0001t0005g0059others(12): Show | 15 | HG01256.hp1 HG01346.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2137-2072_2137-207 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383682 | ||||||
| chr7:7383684
|
A | G | 51 | a0001c0001t0002g0171a0001c0001t0003g0173a0001c0005t0002g0067others(48): Show | 51 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.2137-2072T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383684 | ||||||
| chr7:7383686
|
A | G | 18 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(15): Show | 18 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.2137-2074T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383686 | ||||||
| chr7:7383688
|
A | G | 1 | a0031c0033t0003g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2137-2076T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383688 | ||||||
| chr7:7383694
|
ATATATAT others(3): Show |
A | 23 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(20): Show | 23 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.2137-2092_2137-208 others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383694 | ||||||
| chr7:7383697
|
T | A | 5 | a0001c0001t0002g0171a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2137-2085A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383697 | ||||||
| chr7:7383700
|
ATATG | A | 13 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0148others(10): Show | 13 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2137-2092_2137-208 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383700 | ||||||
| chr7:7383702
|
ATG | A | 2 | a0002c0002t0002g0182a0015c0052t0003g0191 | 2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2137-2092_2137-209 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383702 | ||||||
| chr7:7383704
|
G | A | 103 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.2137-2092C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383704 | ||||||
| chr7:7383766
|
A | T | 89 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2137-2154T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383766 | ||||||
| chr7:7383903
|
G | A | 5 | a0001c0001t0002g0171a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2137-2291C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383903 | ||||||
| chr7:7383913
|
T | C | 1 | a0013c0011t0002g0035 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2137-2301A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7383913 | ||||||
| chr7:7384008
|
C | T | 27 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.2137-2396G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384008 | ||||||
| chr7:7384148
|
G | T | 23 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(20): Show | 23 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.2137-2536C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384148 | ||||||
| chr7:7384266
|
G | A | 3 | a0002c0004t0003g0030a0007c0008t0006g0003a0032c0034t0003g0038 | 3 | HG02630.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2137-2654C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384266 | ||||||
| chr7:7384266
|
G | C | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2137-2654C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384266 | ||||||
| chr7:7384347
|
T | C | 10 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2137-2735A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384347 | ||||||
| chr7:7384376
|
A | G | 2 | a0012c0016t0002g0123a0018c0023t0003g0165 | 2 | HG01081.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2137-2764T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384376 | ||||||
| chr7:7384393
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2137-2781G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384393 | ||||||
| chr7:7384396
|
C | G | 2 | a0012c0016t0002g0123a0018c0023t0003g0165 | 2 | HG01081.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2137-2784G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384396 | ||||||
| chr7:7384524
|
T | C | 13 | a0002c0004t0003g0030a0002c0004t0003g0032a0002c0004t0003g0068others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2137-2912A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384524 | ||||||
| chr7:7384702
|
G | T | 8 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(5): Show | 8 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-3090C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384702 | ||||||
| chr7:7384957
|
C | A | 154 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.2137-3345G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384957 | ||||||
| chr7:7384968
|
T | C | 172 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2137-3356A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7384968 | ||||||
| chr7:7385135
|
G | T | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2137-3523C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385135 | ||||||
| chr7:7385153
|
A | G | 11 | a0001c0001t0002g0178a0001c0005t0002g0069a0002c0002t0002g0037others(8): Show | 11 | HG01346.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2137-3541T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385153 | ||||||
| chr7:7385164
|
G | C | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-3552C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385164 | ||||||
| chr7:7385183
|
C | T | 2 | a0012c0016t0002g0123a0018c0023t0003g0165 | 2 | HG01081.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2137-3571G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385183 | ||||||
| chr7:7385376
|
C | T | 2 | a0012c0016t0002g0123a0018c0023t0003g0165 | 2 | HG01081.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2137-3764G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385376 | ||||||
| chr7:7385430
|
G | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-3818C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385430 | ||||||
| chr7:7385463
|
A | G | 38 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.2137-3851T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385463 | ||||||
| chr7:7385562
|
C | CCAGTAGC others(5): Show |
5 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-3951_2137-395 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385562 | ||||||
| chr7:7385749
|
G | A | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2137-4137C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385749 | ||||||
| chr7:7385823
|
C | T | 22 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(19): Show | 22 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2137-4211G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7385823 | ||||||
| chr7:7386033
|
A | G | 97 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2137-4421T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386033 | ||||||
| chr7:7386227
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2137-4615A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386227 | ||||||
| chr7:7386253
|
T | C | 9 | a0001c0007t0003g0102a0002c0004t0003g0027a0002c0004t0003g0186others(6): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-4641A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386253 | ||||||
| chr7:7386275
|
G | C | 121 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.2137-4663C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386275 | ||||||
| chr7:7386339
|
C | T | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2137-4727G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386339 | ||||||
| chr7:7386471
|
T | C | 97 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2137-4859A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386471 | ||||||
| chr7:7386487
|
T | C | 1 | a0003c0003t0001g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2137-4875A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386487 | ||||||
| chr7:7386569
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2137-4957A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386569 | ||||||
| chr7:7386696
|
G | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-5084C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386696 | ||||||
| chr7:7386766
|
C | T | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2137-5154G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386766 | ||||||
| chr7:7386801
|
G | T | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2137-5189C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386801 | ||||||
| chr7:7386931
|
A | C | 1 | a0001c0001t0005g0011 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2137-5319T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7386931 | ||||||
| chr7:7387042
|
G | A | 2 | a0009c0029t0003g0009a0011c0027t0003g0024 | 2 | HG01106.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2137-5430C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387042 | ||||||
| chr7:7387072
|
A | C | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2137-5460T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387072 | ||||||
| chr7:7387088
|
C | T | 9 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-5476G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387088 | ||||||
| chr7:7387157
|
C | G | 13 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(10): Show | 13 | HG01255.hp2 HG01361.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.2137-5545G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387157 | ||||||
| chr7:7387197
|
T | C | 51 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(48): Show | 51 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2137-5585A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387197 | ||||||
| chr7:7387218
|
T | C | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-5606A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387218 | ||||||
| chr7:7387273
|
G | A | 17 | a0001c0001t0002g0171a0001c0001t0003g0173a0001c0005t0002g0067others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2137-5661C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387273 | ||||||
| chr7:7387280
|
C | G | 1 | a0003c0003t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2137-5668G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387280 | ||||||
| chr7:7387284
|
C | T | 50 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(47): Show | 50 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.2137-5672G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387284 | ||||||
| chr7:7387308
|
T | C | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-5696A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387308 | ||||||
| chr7:7387316
|
A | T | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2137-5704T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387316 | ||||||
| chr7:7387437
|
T | C | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2137-5825A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387437 | ||||||
| chr7:7387566
|
C | T | 4 | a0001c0007t0003g0175a0001c0007t0003g0176a0002c0004t0003g0088others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-5954G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387566 | ||||||
| chr7:7387593
|
C | CAT | 11 | a0002c0004t0003g0030a0002c0004t0003g0032a0002c0004t0003g0068others(8): Show | 11 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2137-5983_2137-598 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387593 | ||||||
| chr7:7387752
|
T | C | 19 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(16): Show | 19 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2137-6140A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387752 | ||||||
| chr7:7387813
|
G | C | 76 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2137-6201C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387813 | ||||||
| chr7:7387904
|
G | A | 88 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2137-6292C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387904 | ||||||
| chr7:7387908
|
G | C | 1 | a0001c0001t0001g0134 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2137-6296C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7387908 | ||||||
| chr7:7388011
|
C | T | 76 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2137-6399G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388011 | ||||||
| chr7:7388170
|
A | G | 94 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2137-6558T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388170 | ||||||
| chr7:7388220
|
T | TTCATTTT others(5): Show |
1 | a0001c0005t0001g0098 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2137-6609_2137-660 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388220 | ||||||
| chr7:7388223
|
T | C | 1 | a0001c0005t0001g0098 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2137-6611A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388223 | ||||||
| chr7:7388226
|
T | G | 2 | a0001c0001t0001g0050a0001c0005t0001g0098 | 2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2137-6614A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388226 | ||||||
| chr7:7388289
|
T | C | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-6677A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388289 | ||||||
| chr7:7388361
|
C | T | 9 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-6749G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388361 | ||||||
| chr7:7388457
|
G | A | 5 | a0002c0002t0002g0170a0002c0002t0002g0182a0004c0006t0002g0008others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-6845C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388457 | ||||||
| chr7:7388515
|
A | T | 12 | a0002c0004t0003g0030a0002c0004t0003g0032a0002c0004t0003g0068others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2137-6903T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388515 | ||||||
| chr7:7388516
|
T | C | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2137-6904A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388516 | ||||||
| chr7:7388528
|
T | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-6916A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388528 | ||||||
| chr7:7388616
|
CCCA | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2137-7007_2137-700 others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388616 | ||||||
| chr7:7388718
|
A | G | 2 | a0002c0049t0003g0189a0015c0052t0003g0191 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2137-7106T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388718 | ||||||
| chr7:7388849
|
T | A | 5 | a0001c0001t0002g0171a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2137-7237A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7388849 | ||||||
| chr7:7389005
|
T | G | 5 | a0001c0001t0002g0171a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2137-7393A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389005 | ||||||
| chr7:7389032
|
G | A | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2137-7420C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389032 | ||||||
| chr7:7389053
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-7441C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389053 | ||||||
| chr7:7389081
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2137-7469G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389081 | ||||||
| chr7:7389120
|
T | G | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2137-7508A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389120 | ||||||
| chr7:7389147
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2137-7535A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389147 | ||||||
| chr7:7389238
|
A | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-7626T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389238 | ||||||
| chr7:7389321
|
A | G | 9 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-7709T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389321 | ||||||
| chr7:7389406
|
T | A | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2137-7794A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389406 | ||||||
| chr7:7389421
|
C | T | 4 | a0008c0009t0003g0180a0008c0009t0003g0181a0008c0009t0003g0183others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-7809G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389421 | ||||||
| chr7:7389433
|
T | C | 97 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2137-7821A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389433 | ||||||
| chr7:7389756
|
G | A | 83 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2137-8144C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389756 | ||||||
| chr7:7389757
|
C | T | 83 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2137-8145G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389757 | ||||||
| chr7:7389769
|
G | A | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-8157C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389769 | ||||||
| chr7:7389812
|
A | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-8200T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389812 | ||||||
| chr7:7389893
|
G | A | 84 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2137-8281C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389893 | ||||||
| chr7:7389925
|
A | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2137-8313T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389925 | ||||||
| chr7:7389929
|
C | T | 139 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.2137-8317G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389929 | ||||||
| chr7:7389988
|
T | C | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2137-8376A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7389988 | ||||||
| chr7:7390002
|
G | A | 3 | a0013c0011t0002g0035a0013c0011t0002g0036a0013c0011t0002g0064 | 3 | HG01070.hp1 HG02004.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2137-8390C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390002 | ||||||
| chr7:7390026
|
A | G | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2137-8414T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390026 | ||||||
| chr7:7390051
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2137-8439C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390051 | ||||||
| chr7:7390158
|
T | G | 9 | a0002c0002t0002g0004a0002c0004t0003g0030a0007c0008t0006g0003others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-8546A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390158 | ||||||
| chr7:7390198
|
T | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-8586A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390198 | ||||||
| chr7:7390246
|
C | T | 139 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.2137-8634G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390246 | ||||||
| chr7:7390254
|
T | C | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2137-8642A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390254 | ||||||
| chr7:7390298
|
T | G | 1 | a0024c0045t0001g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2137-8686A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390298 | ||||||
| chr7:7390343
|
A | G | 57 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(54): Show | 57 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.2137-8731T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390343 | ||||||
| chr7:7390381
|
G | C | 22 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(19): Show | 22 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2137-8769C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390381 | ||||||
| chr7:7390404
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2137-8792A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390404 | ||||||
| chr7:7390416
|
G | A | 1 | a0007c0008t0003g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2137-8804C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390416 | ||||||
| chr7:7390518
|
G | C | 5 | a0002c0002t0002g0170a0002c0002t0002g0182a0004c0006t0002g0008others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-8906C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390518 | ||||||
| chr7:7390536
|
T | C | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2137-8924A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390536 | ||||||
| chr7:7390568
|
T | A | 9 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-8956A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390568 | ||||||
| chr7:7390802
|
A | G | 94 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2137-9190T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390802 | ||||||
| chr7:7390840
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2137-9228G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390840 | ||||||
| chr7:7390929
|
T | C | 1 | a0001c0005t0001g0100 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2137-9317A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7390929 | ||||||
| chr7:7391015
|
T | A | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2137-9403A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391015 | ||||||
| chr7:7391031
|
G | C | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2137-9419C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391031 | ||||||
| chr7:7391072
|
G | T | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2137-9460C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391072 | ||||||
| chr7:7391077
|
G | A | 9 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-9465C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391077 | ||||||
| chr7:7391105
|
T | C | 2 | a0005c0010t0001g0092a0005c0010t0001g0105 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2137-9493A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391105 | ||||||
| chr7:7391112
|
T | C | 12 | a0002c0004t0003g0030a0002c0004t0003g0032a0002c0004t0003g0068others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2137-9500A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391112 | ||||||
| chr7:7391114
|
C | A | 106 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2137-9502G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391114 | ||||||
| chr7:7391226
|
C | T | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2137-9614G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391226 | ||||||
| chr7:7391227
|
G | C | 12 | a0002c0004t0003g0030a0002c0004t0003g0032a0002c0004t0003g0068others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2137-9615C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391227 | ||||||
| chr7:7391267
|
T | C | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2137-9655A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391267 | ||||||
| chr7:7391463
|
G | T | 2 | a0001c0001t0001g0106a0005c0010t0001g0043 | 2 | NA18968.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2137-9851C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391463 | ||||||
| chr7:7391467
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2137-9855C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391467 | ||||||
| chr7:7391497
|
C | T | 127 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.2137-9885G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391497 | ||||||
| chr7:7391614
|
G | A | 76 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2137-10002C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391614 | ||||||
| chr7:7391741
|
C | A | 11 | a0001c0001t0002g0178a0001c0005t0002g0069a0002c0002t0002g0037others(8): Show | 11 | HG01346.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2137-10129G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391741 | ||||||
| chr7:7391760
|
T | C | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-10148A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391760 | ||||||
| chr7:7391801
|
C | CT | 7 | a0001c0001t0001g0046a0001c0001t0001g0082a0001c0007t0003g0148others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2137-10190dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391801 | ||||||
| chr7:7391801
|
CT | C | 36 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.2137-10190delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391801 | ||||||
| chr7:7391801
|
CTT | C | 23 | a0001c0001t0001g0047a0001c0001t0001g0124a0001c0001t0001g0154others(20): Show | 23 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2137-10191_2137-10 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391801 | ||||||
| chr7:7391801
|
CTTT | C | 78 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2137-10192_2137-10 others(9): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391801 | ||||||
| chr7:7391878
|
C | T | 2 | a0004c0006t0002g0008a0010c0013t0002g0019 | 2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2137-10266G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391878 | ||||||
| chr7:7391906
|
A | G | 9 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-10294T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391906 | ||||||
| chr7:7391912
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2137-10300G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391912 | ||||||
| chr7:7391923
|
C | A | 2 | a0002c0049t0003g0189a0015c0052t0003g0191 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2137-10311G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7391923 | ||||||
| chr7:7392013
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2137-10401G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392013 | ||||||
| chr7:7392046
|
A | G | 142 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2137-10434T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392046 | ||||||
| chr7:7392108
|
G | C | 9 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0006g0002others(6): Show | 9 | HG01243.hp2 HG02717.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-10496C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392108 | ||||||
| chr7:7392109
|
C | A | 76 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2137-10497G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392109 | ||||||
| chr7:7392199
|
T | C | 106 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2137-10587A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392199 | ||||||
| chr7:7392254
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2137-10642A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392254 | ||||||
| chr7:7392482
|
G | T | 1 | a0002c0031t0001g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2137-10870C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392482 | ||||||
| chr7:7392486
|
T | C | 10 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(7): Show | 10 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2137-10874A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392486 | ||||||
| chr7:7392569
|
T | C | 27 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.2137-10957A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392569 | ||||||
| chr7:7392693
|
A | C | 11 | a0001c0001t0002g0178a0001c0005t0002g0069a0002c0002t0002g0037others(8): Show | 11 | HG01346.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2137-11081T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392693 | ||||||
| chr7:7392718
|
T | C | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2137-11106A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392718 | ||||||
| chr7:7392771
|
A | G | 7 | a0001c0001t0002g0171a0002c0049t0003g0189a0008c0009t0003g0180others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2137-11159T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392771 | ||||||
| chr7:7392845
|
C | T | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2137-11233G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392845 | ||||||
| chr7:7392894
|
C | A | 1 | a0009c0014t0003g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2137-11282G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7392894 | ||||||
| chr7:7393052
|
G | C | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2137-11440C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393052 | ||||||
| chr7:7393337
|
C | T | 77 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2137-11725G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393337 | ||||||
| chr7:7393407
|
T | A | 1 | a0013c0011t0002g0036 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2137-11795A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393407 | ||||||
| chr7:7393438
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2137-11826G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393438 | ||||||
| chr7:7393507
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2137-11895G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393507 | ||||||
| chr7:7393568
|
C | G | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2137-11956G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393568 | ||||||
| chr7:7393611
|
C | A | 11 | a0001c0001t0003g0173a0001c0005t0002g0067a0002c0002t0002g0015others(8): Show | 11 | HG01081.hp1 HG01243.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2137-11999G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393611 | ||||||
| chr7:7393618
|
T | TG | 195 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2137-12007dupC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393618 | ||||||
| chr7:7393642
|
T | C | 9 | a0002c0002t0002g0004a0002c0004t0003g0030a0007c0008t0006g0003others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-12030A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393642 | ||||||
| chr7:7393649
|
A | C | 106 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2137-12037T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393649 | ||||||
| chr7:7393734
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2137-12122C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393734 | ||||||
| chr7:7393786
|
A | G | 179 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2137-12174T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393786 | ||||||
| chr7:7393863
|
G | T | 2 | a0002c0049t0003g0189a0015c0052t0003g0191 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2137-12251C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393863 | ||||||
| chr7:7393868
|
G | A | 84 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2137-12256C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393868 | ||||||
| chr7:7393949
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2137-12337C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393949 | ||||||
| chr7:7393977
|
GA | G | 106 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2137-12366delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7393977 | ||||||
| chr7:7394291
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2137-12679C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7394291 | ||||||
| chr7:7394543
|
T | C | 33 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.2137-12931A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7394543 | ||||||
| chr7:7394560
|
G | A | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-12948C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7394560 | ||||||
| chr7:7394589
|
A | G | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2137-12977T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7394589 | ||||||
| chr7:7394933
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2137-13321A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7394933 | ||||||
| chr7:7395029
|
T | G | 1 | a0028c0036t0010g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2137-13417A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7395029 | ||||||
| chr7:7395113
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2137-13501C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7395113 | ||||||
| chr7:7395721
|
G | A | 32 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.2137-14109C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7395721 | ||||||
| chr7:7395736
|
G | C | 6 | a0002c0002t0002g0004a0012c0016t0002g0016a0012c0035t0002g0072others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2137-14124C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7395736 | ||||||
| chr7:7395842
|
C | G | 8 | a0002c0004t0003g0030a0007c0008t0006g0003a0012c0016t0002g0016others(5): Show | 8 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-14230G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7395842 | ||||||
| chr7:7396033
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2137-14421A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396033 | ||||||
| chr7:7396099
|
T | C | 172 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2137-14487A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396099 | ||||||
| chr7:7396117
|
A | G | 3 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0111 | 3 | HG01496.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2137-14505T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396117 | ||||||
| chr7:7396239
|
C | T | 1 | a0012c0016t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2137-14627G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396239 | ||||||
| chr7:7396284
|
T | C | 4 | a0001c0001t0001g0130a0001c0007t0003g0148a0009c0029t0003g0009others(1): Show | 4 | HG01106.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-14672A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396284 | ||||||
| chr7:7396305
|
A | T | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2137-14693T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396305 | ||||||
| chr7:7396335
|
T | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-14723A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396335 | ||||||
| chr7:7396588
|
C | A | 5 | a0002c0002t0002g0170a0002c0002t0002g0182a0004c0006t0002g0008others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-14976G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396588 | ||||||
| chr7:7396589
|
G | A | 34 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(31): Show | 34 | HG01255.hp2 HG01361.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.2137-14977C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396589 | ||||||
| chr7:7396597
|
G | A | 1 | a0001c0007t0003g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2137-14985C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396597 | ||||||
| chr7:7396858
|
T | C | 1 | a0003c0003t0001g0080 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2137-15246A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396858 | ||||||
| chr7:7396882
|
C | A | 42 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.2137-15270G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7396882 | ||||||
| chr7:7397038
|
T | C | 1 | a0013c0011t0002g0036 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2137-15426A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397038 | ||||||
| chr7:7397047
|
G | C | 1 | a0011c0012t0002g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2137-15435C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397047 | ||||||
| chr7:7397413
|
G | A | 26 | a0001c0007t0003g0102a0001c0007t0003g0175a0001c0007t0003g0176others(23): Show | 26 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.2137-15801C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397413 | ||||||
| chr7:7397468
|
T | C | 182 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2137-15856A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397468 | ||||||
| chr7:7397495
|
T | C | 92 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2137-15883A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397495 | ||||||
| chr7:7397648
|
C | A | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-16036G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397648 | ||||||
| chr7:7397662
|
C | T | 1 | a0003c0003t0004g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2137-16050G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397662 | ||||||
| chr7:7397689
|
T | A | 2 | a0002c0049t0003g0189a0015c0052t0003g0191 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2137-16077A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397689 | ||||||
| chr7:7397816
|
C | T | 2 | a0021c0025t0002g0162a0034c0040t0002g0040 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2137-16204G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397816 | ||||||
| chr7:7397831
|
C | A | 9 | a0001c0007t0003g0102a0002c0004t0003g0027a0002c0004t0003g0186others(6): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2137-16219G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397831 | ||||||
| chr7:7397883
|
C | G | 1 | a0009c0014t0001g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2137-16271G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397883 | ||||||
| chr7:7397955
|
T | G | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2137-16343A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397955 | ||||||
| chr7:7397975
|
T | C | 1 | a0001c0001t0009g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2137-16363A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7397975 | ||||||
| chr7:7398248
|
T | C | 2 | a0001c0001t0009g0131a0001c0001t0009g0136 | 2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2137-16636A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398248 | ||||||
| chr7:7398325
|
T | C | 3 | a0001c0007t0003g0148a0009c0029t0003g0009a0011c0027t0003g0024 | 3 | HG01106.hp2 HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2137-16713A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398325 | ||||||
| chr7:7398452
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2137-16840A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398452 | ||||||
| chr7:7398471
|
A | C | 32 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.2137-16859T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398471 | ||||||
| chr7:7398483
|
T | A | 6 | a0001c0007t0003g0175a0001c0007t0003g0176a0001c0007t0003g0177others(3): Show | 6 | HG02257.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2137-16871A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398483 | ||||||
| chr7:7398521
|
T | C | 3 | a0022c0026t0007g0164a0026c0043t0007g0029a0031c0033t0003g0031 | 3 | HG02922.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2137-16909A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398521 | ||||||
| chr7:7398785
|
A | T | 1 | a0007c0008t0003g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2137-17173T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398785 | ||||||
| chr7:7398898
|
C | T | 57 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.2137-17286G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398898 | ||||||
| chr7:7398908
|
G | A | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2137-17296C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7398908 | ||||||
| chr7:7399065
|
T | G | 84 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2137-17453A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399065 | ||||||
| chr7:7399137
|
T | C | 183 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2137-17525A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399137 | ||||||
| chr7:7399277
|
C | T | 56 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.2137-17665G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399277 | ||||||
| chr7:7399301
|
T | C | 2 | a0024c0045t0001g0087a0029c0037t0001g0113 | 2 | HG00423.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.2137-17689A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399301 | ||||||
| chr7:7399354
|
G | A | 3 | a0002c0004t0003g0032a0002c0004t0003g0068a0002c0004t0003g0070 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2137-17742C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399354 | ||||||
| chr7:7399403
|
T | C | 32 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.2137-17791A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399403 | ||||||
| chr7:7399426
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2137-17814T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399426 | ||||||
| chr7:7399636
|
G | A | 1 | a0002c0031t0001g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2137-18024C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399636 | ||||||
| chr7:7399653
|
A | AT | 82 | a0001c0001t0002g0051a0001c0001t0002g0063a0001c0001t0002g0103others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.2137-18042dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399653 | ||||||
| chr7:7399742
|
T | G | 1 | a0003c0003t0001g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2136+18117A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399742 | ||||||
| chr7:7399782
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0104others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+18077G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399782 | ||||||
| chr7:7399912
|
A | G | 15 | a0001c0007t0003g0102a0002c0004t0003g0026a0002c0004t0003g0027others(12): Show | 15 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2136+17947T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399912 | ||||||
| chr7:7399954
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2136+17905T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7399954 | ||||||
| chr7:7400114
|
A | G | 2 | a0009c0029t0003g0009a0011c0027t0003g0024 | 2 | HG01106.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2136+17745T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400114 | ||||||
| chr7:7400138
|
T | C | 6 | a0001c0001t0002g0171a0002c0002t0002g0004a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2136+17721A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400138 | ||||||
| chr7:7400244
|
G | T | 1 | a0012c0016t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2136+17615C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400244 | ||||||
| chr7:7400488
|
G | C | 80 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2136+17371C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400488 | ||||||
| chr7:7400497
|
G | A | 26 | a0001c0001t0002g0051a0001c0001t0002g0103a0001c0001t0002g0107others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.2136+17362C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400497 | ||||||
| chr7:7400523
|
T | C | 1 | a0004c0006t0002g0005 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2136+17336A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400523 | ||||||
| chr7:7400687
|
T | TA | 11 | a0002c0002t0002g0182a0002c0004t0003g0070a0008c0009t0003g0180others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2136+17171dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400687 | ||||||
| chr7:7400687
|
TA | T | 26 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0096others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.2136+17171delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400687 | ||||||
| chr7:7400687
|
TAA | T | 58 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0005t0002g0067others(55): Show | 58 | HG00741.hp2 HG01081.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2136+17170_2136+17 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400687 | ||||||
| chr7:7400733
|
A | C | 20 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(17): Show | 20 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.2136+17126T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400733 | ||||||
| chr7:7400800
|
T | C | 1 | a0005c0044t0003g0039 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2136+17059A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400800 | ||||||
| chr7:7400906
|
A | G | 8 | a0001c0001t0002g0178a0001c0005t0002g0069a0006c0030t0003g0065others(5): Show | 8 | HG01346.hp2 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2136+16953T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400906 | ||||||
| chr7:7400910
|
A | G | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2136+16949T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400910 | ||||||
| chr7:7400911
|
G | C | 4 | a0001c0001t0002g0171a0002c0004t0003g0030a0002c0004t0003g0068others(1): Show | 4 | HG02647.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2136+16948C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400911 | ||||||
| chr7:7400950
|
G | T | 190 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.2136+16909C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400950 | ||||||
| chr7:7400975
|
G | GGGGTGT | 4 | a0001c0001t0001g0062a0001c0001t0001g0091a0001c0001t0002g0178others(1): Show | 4 | HG00280.hp1 HG01517.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2136+16883_2136+16 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GGGGTGTG others(3): Show |
1 | a0001c0001t0001g0097 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2136+16883_2136+16 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GGT | 21 | a0001c0001t0001g0046a0001c0001t0001g0082a0001c0001t0001g0154others(18): Show | 21 | HG00099.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2136+16882_2136+16 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GGTGT | 28 | a0001c0001t0001g0042a0001c0001t0001g0060a0001c0001t0001g0090others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.2136+16880_2136+16 others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GGTGTGT | 13 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0145others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2136+16878_2136+16 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GGTGTGTG others(1): Show |
14 | a0001c0001t0001g0125a0001c0001t0001g0168a0001c0001t0002g0051others(11): Show | 14 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+16876_2136+16 others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GGTGTGTG others(3): Show |
7 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0003g0173others(4): Show | 7 | HG00438.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2136+16874_2136+16 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GGTGTGTG others(5): Show |
3 | a0001c0001t0001g0138a0002c0002t0001g0147a0013c0011t0002g0064 | 3 | HG02258.hp1 HG03017.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2136+16872_2136+16 others(18): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2136+16870_2136+16 others(20): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GTGTGTGT others(2): Show |
2 | a0001c0001t0001g0094a0023c0021t0002g0025 | 2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2136+16883_2136+16 others(15): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
G | GTGTGTGT others(4): Show |
1 | a0020c0022t0002g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2136+16883_2136+16 others(17): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGT | G | 22 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0121others(19): Show | 22 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2136+16882_2136+16 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGTGT | G | 30 | a0001c0001t0001g0056a0001c0001t0001g0122a0001c0001t0001g0169others(27): Show | 30 | HG00140.hp1 HG01070.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2136+16880_2136+16 others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGTGTGT | G | 11 | a0001c0001t0001g0085a0001c0001t0001g0120a0001c0001t0002g0103others(8): Show | 11 | HG01346.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2136+16878_2136+16 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGTGTGTG others(1): Show |
G | 4 | a0001c0001t0001g0034a0001c0007t0003g0176a0007c0032t0003g0014others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2136+16876_2136+16 others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGTGTGTG others(3): Show |
G | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2136+16874_2136+16 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGTGTGTG others(7): Show |
G | 1 | a0012c0016t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2136+16870_2136+16 others(20): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGTGTGTG others(9): Show |
G | 2 | a0001c0001t0001g0156a0006c0019t0002g0188 | 2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2136+16868_2136+16 others(22): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2136+16866_2136+16 others(24): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400975
|
GGTGTGTG others(15): Show |
G | 1 | a0001c0007t0003g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2136+16862_2136+16 others(28): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400975 | ||||||
| chr7:7400977
|
T | G | 5 | a0001c0001t0001g0048a0001c0005t0002g0069a0002c0002t0002g0117others(2): Show | 5 | HG01346.hp2 HG01361.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+16882A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400977 | ||||||
| chr7:7400979
|
T | G | 4 | a0002c0004t0003g0070a0010c0013t0002g0022a0022c0026t0007g0164others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2136+16880A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400979 | ||||||
| chr7:7400981
|
T | G | 10 | a0001c0001t0002g0171a0002c0002t0002g0108a0002c0002t0006g0002others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2136+16878A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400981 | ||||||
| chr7:7400983
|
T | G | 4 | a0004c0006t0002g0008a0005c0010t0002g0044a0010c0013t0002g0019others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+16876A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400983 | ||||||
| chr7:7400985
|
T | G | 2 | a0001c0001t0002g0171a0010c0028t0003g0020 | 2 | HG02257.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2136+16874A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400985 | ||||||
| chr7:7400987
|
T | G | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2136+16872A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400987 | ||||||
| chr7:7400991
|
T | G | 1 | a0012c0016t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2136+16868A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7400991 | ||||||
| chr7:7401390
|
A | C | 1 | a0001c0005t0002g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2136+16469T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7401390 | ||||||
| chr7:7401403
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2136+16456A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7401403 | ||||||
| chr7:7401409
|
C | T | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2136+16450G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7401409 | ||||||
| chr7:7401422
|
G | A | 75 | a0001c0001t0001g0048a0001c0001t0001g0145a0001c0001t0001g0157others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.2136+16437C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7401422 | ||||||
| chr7:7401521
|
G | A | 113 | a0001c0001t0001g0048a0001c0001t0001g0145a0001c0001t0001g0157others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.2136+16338C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7401521 | ||||||
| chr7:7401665
|
C | T | 1 | a0002c0049t0003g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2136+16194G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7401665 | ||||||
| chr7:7401853
|
C | T | 1 | a0003c0003t0001g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2136+16006G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7401853 | ||||||
| chr7:7401957
|
C | T | 1 | a0005c0010t0001g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2136+15902G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7401957 | ||||||
| chr7:7402065
|
C | T | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2136+15794G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7402065 | ||||||
| chr7:7402144
|
A | G | 24 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0158others(21): Show | 24 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.2136+15715T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7402144 | ||||||
| chr7:7402174
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2136+15685A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7402174 | ||||||
| chr7:7402347
|
G | A | 34 | a0001c0001t0001g0048a0001c0001t0002g0149a0001c0001t0002g0150others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2136+15512C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7402347 | ||||||
| chr7:7402538
|
A | C | 31 | a0001c0001t0001g0048a0001c0001t0002g0149a0001c0001t0002g0150others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.2136+15321T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7402538 | ||||||
| chr7:7402549
|
T | C | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2136+15310A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7402549 | ||||||
| chr7:7402551
|
C | G | 77 | a0001c0001t0001g0048a0001c0001t0001g0145a0001c0001t0001g0157others(74): Show | 77 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.2136+15308G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7402551 | ||||||
| chr7:7402863
|
T | G | 11 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2136+14996A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7402863 | ||||||
| chr7:7403080
|
T | A | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2136+14779A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403080 | ||||||
| chr7:7403108
|
A | G | 1 | a0004c0006t0002g0184 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2136+14751T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403108 | ||||||
| chr7:7403139
|
T | C | 51 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0158others(48): Show | 51 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2136+14720A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403139 | ||||||
| chr7:7403192
|
TC | T | 46 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0158others(43): Show | 46 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.2136+14666delG | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403192 | ||||||
| chr7:7403212
|
C | T | 1 | a0001c0007t0003g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2136+14647G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403212 | ||||||
| chr7:7403386
|
G | C | 108 | a0001c0001t0001g0048a0001c0001t0001g0145a0001c0001t0001g0157others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2136+14473C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403386 | ||||||
| chr7:7403413
|
T | C | 38 | a0001c0001t0001g0048a0001c0001t0002g0107a0001c0001t0002g0149others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.2136+14446A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403413 | ||||||
| chr7:7403682
|
T | A | 1 | a0030c0038t0002g0114 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2136+14177A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403682 | ||||||
| chr7:7403861
|
A | G | 1 | a0001c0001t0003g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2136+13998T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403861 | ||||||
| chr7:7403895
|
T | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+13964A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403895 | ||||||
| chr7:7403938
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2136+13921T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403938 | ||||||
| chr7:7403971
|
G | T | 25 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0158others(22): Show | 25 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.2136+13888C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7403971 | ||||||
| chr7:7404067
|
T | C | 4 | a0002c0002t0006g0002a0002c0004t0003g0027a0002c0004t0003g0186others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+13792A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7404067 | ||||||
| chr7:7404078
|
C | T | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2136+13781G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7404078 | ||||||
| chr7:7404176
|
A | C | 48 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0158others(45): Show | 48 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2136+13683T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7404176 | ||||||
| chr7:7404188
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2136+13671C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7404188 | ||||||
| chr7:7404618
|
G | A | 1 | a0003c0003t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2136+13241C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7404618 | ||||||
| chr7:7404875
|
C | T | 52 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0158others(49): Show | 52 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.2136+12984G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7404875 | ||||||
| chr7:7405117
|
G | A | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2136+12742C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7405117 | ||||||
| chr7:7405224
|
G | A | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+12635C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7405224 | ||||||
| chr7:7405275
|
C | T | 4 | a0003c0003t0001g0079a0003c0003t0001g0080a0003c0003t0001g0081others(1): Show | 4 | NA18612.hp1 NA18957.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+12584G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7405275 | ||||||
| chr7:7405363
|
C | G | 138 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(135): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2136+12496G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7405363 | ||||||
| chr7:7405666
|
C | T | 8 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2136+12193G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7405666 | ||||||
| chr7:7405869
|
T | C | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+11990A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7405869 | ||||||
| chr7:7405963
|
C | G | 1 | a0001c0001t0002g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2136+11896G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7405963 | ||||||
| chr7:7406311
|
G | C | 1 | a0005c0010t0002g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2136+11548C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7406311 | ||||||
| chr7:7406431
|
G | A | 1 | a0001c0005t0002g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2136+11428C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7406431 | ||||||
| chr7:7406543
|
C | T | 1 | a0001c0005t0002g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2136+11316G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7406543 | ||||||
| chr7:7406643
|
G | A | 1 | a0005c0010t0002g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2136+11216C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7406643 | ||||||
| chr7:7406688
|
C | T | 36 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.2136+11171G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7406688 | ||||||
| chr7:7406712
|
A | G | 35 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(32): Show | 35 | HG00280.hp1 HG00438.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2136+11147T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7406712 | ||||||
| chr7:7406867
|
T | G | 20 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(17): Show | 20 | HG00280.hp1 HG00438.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.2136+10992A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7406867 | ||||||
| chr7:7407049
|
A | C | 44 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0158others(41): Show | 44 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.2136+10810T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407049 | ||||||
| chr7:7407121
|
G | A | 3 | a0002c0004t0003g0070a0012c0016t0002g0016a0018c0023t0003g0165 | 3 | HG01081.hp1 HG01109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2136+10738C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407121 | ||||||
| chr7:7407172
|
A | T | 1 | a0001c0001t0002g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2136+10687T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407172 | ||||||
| chr7:7407215
|
A | G | 16 | a0002c0002t0002g0182a0002c0004t0003g0088a0005c0010t0001g0043others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+10644T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407215 | ||||||
| chr7:7407226
|
C | T | 1 | a0005c0010t0002g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2136+10633G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407226 | ||||||
| chr7:7407393
|
A | C | 10 | a0002c0002t0002g0170a0002c0002t0006g0002a0002c0004t0003g0026others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2136+10466T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407393 | ||||||
| chr7:7407543
|
C | A | 1 | a0002c0031t0001g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2136+10316G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407543 | ||||||
| chr7:7407693
|
C | T | 42 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0158others(39): Show | 42 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.2136+10166G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407693 | ||||||
| chr7:7407705
|
A | C | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+10154T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407705 | ||||||
| chr7:7407824
|
G | C | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2136+10035C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407824 | ||||||
| chr7:7407928
|
C | T | 16 | a0002c0002t0002g0182a0002c0004t0003g0088a0005c0010t0001g0043others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+9931G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7407928 | ||||||
| chr7:7408104
|
G | A | 5 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(2): Show | 5 | HG02109.hp2 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2136+9755C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408104 | ||||||
| chr7:7408161
|
G | A | 1 | a0001c0005t0001g0098 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2136+9698C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408161 | ||||||
| chr7:7408167
|
A | G | 16 | a0002c0002t0002g0182a0002c0004t0003g0088a0005c0010t0001g0043others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+9692T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408167 | ||||||
| chr7:7408185
|
A | G | 1 | a0007c0008t0003g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2136+9674T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408185 | ||||||
| chr7:7408246
|
C | T | 10 | a0002c0002t0002g0170a0002c0002t0006g0002a0002c0004t0003g0026others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2136+9613G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408246 | ||||||
| chr7:7408300
|
C | T | 10 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2136+9559G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408300 | ||||||
| chr7:7408305
|
T | C | 2 | a0006c0030t0003g0065a0017c0020t0001g0086 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2136+9554A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408305 | ||||||
| chr7:7408436
|
A | G | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.2136+9423T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408436 | ||||||
| chr7:7408468
|
A | C | 5 | a0001c0005t0002g0067a0006c0015t0002g0101a0006c0015t0002g0179others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+9391T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408468 | ||||||
| chr7:7408869
|
G | A | 23 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.2136+8990C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408869 | ||||||
| chr7:7408880
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2136+8979A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7408880 | ||||||
| chr7:7409026
|
C | G | 103 | a0001c0001t0001g0048a0001c0001t0001g0157a0001c0001t0001g0158others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2136+8833G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7409026 | ||||||
| chr7:7409244
|
A | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2136+8615T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7409244 | ||||||
| chr7:7409517
|
C | T | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2136+8342G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7409517 | ||||||
| chr7:7409650
|
T | C | 34 | a0001c0001t0001g0048a0001c0001t0002g0149a0001c0001t0002g0150others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.2136+8209A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7409650 | ||||||
| chr7:7409782
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2136+8077A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7409782 | ||||||
| chr7:7409820
|
A | G | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2136+8039T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7409820 | ||||||
| chr7:7409842
|
G | T | 6 | a0001c0001t0002g0171a0001c0001t0003g0173a0001c0007t0003g0175others(3): Show | 6 | HG02109.hp2 HG02622.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2136+8017C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7409842 | ||||||
| chr7:7410005
|
A | C | 43 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.2136+7854T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410005 | ||||||
| chr7:7410096
|
G | A | 41 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.2136+7763C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410096 | ||||||
| chr7:7410287
|
A | G | 9 | a0002c0002t0002g0170a0002c0002t0006g0002a0002c0004t0003g0026others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+7572T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410287 | ||||||
| chr7:7410345
|
G | A | 2 | a0011c0012t0002g0166a0015c0048t0002g0017 | 2 | HG01346.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2136+7514C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410345 | ||||||
| chr7:7410347
|
C | T | 7 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(4): Show | 7 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2136+7512G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410347 | ||||||
| chr7:7410417
|
TG | T | 2 | a0001c0001t0001g0145a0001c0001t0002g0127 | 2 | HG00423.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2136+7441delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410417 | ||||||
| chr7:7410509
|
G | C | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.2136+7350C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410509 | ||||||
| chr7:7410531
|
C | G | 1 | a0009c0029t0003g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2136+7328G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410531 | ||||||
| chr7:7410575
|
T | C | 5 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(2): Show | 5 | HG02109.hp2 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2136+7284A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410575 | ||||||
| chr7:7410623
|
C | T | 5 | a0001c0005t0002g0067a0006c0015t0002g0101a0006c0015t0002g0179others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+7236G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410623 | ||||||
| chr7:7410626
|
G | A | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+7233C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410626 | ||||||
| chr7:7410654
|
TA | T | 82 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2136+7204delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410654 | ||||||
| chr7:7410687
|
GA | G | 6 | a0001c0001t0002g0171a0001c0001t0003g0173a0001c0007t0003g0175others(3): Show | 6 | HG02109.hp2 HG02622.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2136+7171delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410687 | ||||||
| chr7:7410938
|
G | A | 2 | a0012c0016t0002g0016a0018c0023t0003g0165 | 2 | HG01081.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2136+6921C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410938 | ||||||
| chr7:7410957
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2136+6902C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7410957 | ||||||
| chr7:7411103
|
T | C | 1 | a0034c0040t0002g0040 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2136+6756A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411103 | ||||||
| chr7:7411232
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2136+6627G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411232 | ||||||
| chr7:7411483
|
C | T | 1 | a0001c0007t0003g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2136+6376G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411483 | ||||||
| chr7:7411521
|
C | G | 15 | a0001c0005t0002g0067a0002c0002t0006g0002a0002c0004t0003g0026others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2136+6338G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411521 | ||||||
| chr7:7411620
|
C | G | 1 | a0030c0038t0002g0114 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2136+6239G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411620 | ||||||
| chr7:7411767
|
T | C | 42 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.2136+6092A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411767 | ||||||
| chr7:7411871
|
C | A | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2136+5988G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411871 | ||||||
| chr7:7411883
|
G | C | 4 | a0001c0001t0001g0048a0001c0005t0001g0098a0001c0005t0001g0099others(1): Show | 4 | HG00099.hp1 HG01255.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+5976C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411883 | ||||||
| chr7:7411907
|
G | A | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+5952C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411907 | ||||||
| chr7:7411915
|
G | A | 1 | a0003c0003t0001g0081 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2136+5944C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411915 | ||||||
| chr7:7411916
|
GAGACCAC others(1369): Show |
G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+4567_2136+594 others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411916 | ||||||
| chr7:7411994
|
T | C | 4 | a0002c0002t0002g0116a0002c0002t0002g0118a0002c0002t0002g0119others(1): Show | 4 | HG00642.hp2 HG00733.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+5865A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7411994 | ||||||
| chr7:7412083
|
C | G | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2136+5776G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7412083 | ||||||
| chr7:7412339
|
T | C | 42 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.2136+5520A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7412339 | ||||||
| chr7:7412623
|
C | G | 52 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.2136+5236G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7412623 | ||||||
| chr7:7412810
|
T | A | 32 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.2136+5049A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7412810 | ||||||
| chr7:7412914
|
G | A | 10 | a0002c0002t0002g0015a0002c0002t0006g0002a0002c0004t0003g0026others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2136+4945C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7412914 | ||||||
| chr7:7412995
|
A | G | 121 | a0001c0001t0001g0048a0001c0001t0001g0157a0001c0001t0001g0158others(118): Show | 121 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.2136+4864T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7412995 | ||||||
| chr7:7413138
|
C | T | 5 | a0001c0005t0002g0067a0006c0015t0002g0101a0006c0015t0002g0179others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+4721G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7413138 | ||||||
| chr7:7413191
|
C | T | 41 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.2136+4668G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7413191 | ||||||
| chr7:7413258
|
C | A | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+4601G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7413258 | ||||||
| chr7:7413697
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2136+4162G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7413697 | ||||||
| chr7:7413711
|
C | T | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+4148G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7413711 | ||||||
| chr7:7414130
|
G | A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+3729C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414130 | ||||||
| chr7:7414192
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2136+3667G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414192 | ||||||
| chr7:7414246
|
A | G | 4 | a0001c0001t0002g0171a0002c0002t0002g0015a0002c0049t0003g0189others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+3613T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414246 | ||||||
| chr7:7414285
|
C | T | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+3574G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414285 | ||||||
| chr7:7414401
|
G | A | 3 | a0002c0002t0002g0015a0002c0049t0003g0189a0019c0024t0003g0167 | 3 | HG02451.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2136+3458C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414401 | ||||||
| chr7:7414420
|
A | C | 23 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(20): Show | 23 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.2136+3439T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414420 | ||||||
| chr7:7414434
|
G | T | 5 | a0001c0005t0002g0067a0006c0015t0002g0101a0006c0015t0002g0179others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+3425C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414434 | ||||||
| chr7:7414512
|
T | C | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2136+3347A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414512 | ||||||
| chr7:7414532
|
G | A | 41 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.2136+3327C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414532 | ||||||
| chr7:7414594
|
C | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+3265G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414594 | ||||||
| chr7:7414606
|
C | T | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2136+3253G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414606 | ||||||
| chr7:7414661
|
A | G | 64 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.2136+3198T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414661 | ||||||
| chr7:7414685
|
C | G | 53 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(50): Show | 53 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2136+3174G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414685 | ||||||
| chr7:7414716
|
C | T | 1 | a0002c0004t0003g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2136+3143G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414716 | ||||||
| chr7:7414743
|
G | C | 53 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(50): Show | 53 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2136+3116C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414743 | ||||||
| chr7:7414930
|
G | A | 11 | a0002c0002t0002g0170a0002c0002t0006g0002a0002c0004t0003g0026others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2136+2929C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7414930 | ||||||
| chr7:7415026
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2136+2833A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415026 | ||||||
| chr7:7415148
|
G | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+2711C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415148 | ||||||
| chr7:7415247
|
T | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2136+2612A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415247 | ||||||
| chr7:7415407
|
C | T | 2 | a0005c0010t0001g0092a0005c0010t0001g0105 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2136+2452G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415407 | ||||||
| chr7:7415416
|
A | G | 8 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2136+2443T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415416 | ||||||
| chr7:7415457
|
A | G | 3 | a0002c0002t0002g0170a0002c0004t0003g0070a0002c0004t0003g0088 | 3 | HG02615.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2136+2402T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415457 | ||||||
| chr7:7415486
|
A | G | 63 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.2136+2373T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415486 | ||||||
| chr7:7415597
|
G | A | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2136+2262C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415597 | ||||||
| chr7:7415627
|
G | T | 1 | a0007c0008t0003g0012 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2136+2232C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415627 | ||||||
| chr7:7415658
|
T | C | 36 | a0001c0001t0001g0048a0001c0001t0002g0149a0001c0001t0002g0150others(33): Show | 36 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2136+2201A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415658 | ||||||
| chr7:7415765
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2136+2094G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415765 | ||||||
| chr7:7415835
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2136+2024G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415835 | ||||||
| chr7:7415878
|
C | T | 21 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.2136+1981G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415878 | ||||||
| chr7:7415903
|
A | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+1956T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415903 | ||||||
| chr7:7415951
|
C | A | 1 | a0028c0036t0010g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2136+1908G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7415951 | ||||||
| chr7:7416101
|
C | T | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2136+1758G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416101 | ||||||
| chr7:7416211
|
G | T | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2136+1648C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416211 | ||||||
| chr7:7416236
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2136+1623G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416236 | ||||||
| chr7:7416286
|
C | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+1573G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416286 | ||||||
| chr7:7416289
|
A | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+1570T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416289 | ||||||
| chr7:7416341
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2136+1518C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416341 | ||||||
| chr7:7416366
|
A | G | 52 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.2136+1493T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416366 | ||||||
| chr7:7416374
|
A | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2136+1485T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416374 | ||||||
| chr7:7416704
|
A | T | 69 | a0001c0001t0001g0048a0001c0001t0002g0149a0001c0001t0002g0150others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.2136+1155T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416704 | ||||||
| chr7:7416786
|
T | C | 8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+1073A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416786 | ||||||
| chr7:7416882
|
T | G | 1 | a0002c0002t0002g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2136+977A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416882 | ||||||
| chr7:7416995
|
A | AAT | 14 | a0001c0005t0002g0067a0002c0002t0002g0004a0006c0015t0002g0101others(11): Show | 14 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2136+862_2136+863d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416995 | ||||||
| chr7:7416995
|
A | T | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2136+864T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7416995 | ||||||
| chr7:7417102
|
A | G | 23 | a0001c0001t0003g0173a0001c0005t0002g0067a0001c0007t0003g0175others(20): Show | 23 | HG01081.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2136+757T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417102 | ||||||
| chr7:7417140
|
A | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.2136+719T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417140 | ||||||
| chr7:7417217
|
G | A | 9 | a0002c0002t0002g0170a0002c0002t0006g0002a0002c0004t0003g0026others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+642C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417217 | ||||||
| chr7:7417225
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2136+634G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417225 | ||||||
| chr7:7417281
|
C | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+578G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417281 | ||||||
| chr7:7417372
|
G | A | 1 | a0028c0036t0010g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2136+487C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417372 | ||||||
| chr7:7417453
|
C | A | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+406G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417453 | ||||||
| chr7:7417507
|
G | GGAGGGAA others(112): Show |
1 | a0001c0007t0003g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2136+351_2136+352i others(121): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417507 | ||||||
| chr7:7417520
|
A | AG | 7 | a0001c0001t0001g0093a0001c0001t0001g0106a0001c0001t0001g0125others(4): Show | 7 | HG00642.hp1 HG01169.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2136+338dupC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417520 | ||||||
| chr7:7417523
|
GGGGA | G | 5 | a0006c0030t0003g0065a0007c0008t0006g0003a0014c0017t0003g0057others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+332_2136+335d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417523 | ||||||
| chr7:7417529
|
GGAGGGAG others(3): Show |
G | 12 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(9): Show | 12 | HG00741.hp1 HG00741.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.2136+320_2136+329d others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417529 | ||||||
| chr7:7417530
|
GAGGGAGG others(2): Show |
G | 11 | a0002c0002t0002g0139a0003c0003t0001g0073a0003c0003t0001g0074others(8): Show | 11 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.2136+320_2136+328d others(11): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417530 | ||||||
| chr7:7417532
|
G | A | 15 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(12): Show | 15 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2136+327C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417532 | ||||||
| chr7:7417533
|
GGAGGGA | G | 13 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2136+320_2136+325d others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417533 | ||||||
| chr7:7417534
|
GAGGGA | G | 5 | a0004c0006t0002g0008a0004c0039t0003g0071a0007c0008t0003g0012others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2136+320_2136+324d others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417534 | ||||||
| chr7:7417539
|
A | AG | 22 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049others(19): Show | 22 | HG00423.hp2 HG00438.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.2136+319dupC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417539 | ||||||
| chr7:7417539
|
A | G | 11 | a0002c0002t0002g0116a0002c0002t0002g0182a0003c0003t0004g0193others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.2136+320T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417539 | ||||||
| chr7:7417539
|
AG | A | 16 | a0001c0001t0001g0048a0001c0001t0001g0137a0001c0001t0002g0149others(13): Show | 16 | HG01346.hp2 HG01361.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2136+319delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417539 | ||||||
| chr7:7417541
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2136+318C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417541 | ||||||
| chr7:7417543
|
G | A | 1 | a0001c0007t0003g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2136+316C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417543 | ||||||
| chr7:7417543
|
G | T | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2136+316C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417543 | ||||||
| chr7:7417545
|
G | A | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+314C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417545 | ||||||
| chr7:7417546
|
G | A | 7 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(4): Show | 7 | HG01081.hp1 HG01167.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2136+313C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417546 | ||||||
| chr7:7417546
|
G | GAGAGAGG others(8): Show |
1 | a0001c0007t0003g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2136+312_2136+313i others(17): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417546 | ||||||
| chr7:7417547
|
G | GGGAAGGA others(148): Show |
1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2136+311_2136+312i others(157): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417547 | ||||||
| chr7:7417548
|
G | A | 66 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0009g0131others(63): Show | 66 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2136+311C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417548 | ||||||
| chr7:7417548
|
G | GA | 6 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(3): Show | 6 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.2136+310_2136+311i others(3): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417548 | ||||||
| chr7:7417548
|
G | GAAGGAGG others(117): Show |
8 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+310_2136+311i others(126): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417548 | ||||||
| chr7:7417548
|
G | GAAGGAGG others(118): Show |
1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2136+310_2136+311i others(127): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417548 | ||||||
| chr7:7417548
|
G | GGAAGGAG others(129): Show |
5 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(2): Show | 5 | HG01081.hp1 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+310_2136+311i others(138): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417548 | ||||||
| chr7:7417600
|
CAA | C | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG01081.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2136+257_2136+258d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417600 | ||||||
| chr7:7417783
|
T | G | 3 | a0002c0002t0002g0015a0002c0049t0003g0189a0019c0024t0003g0167 | 3 | HG02451.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2136+76A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417783 | ||||||
| chr7:7417786
|
G | A | 16 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(13): Show | 16 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+73C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417786 | ||||||
| chr7:7417805
|
C | T | 16 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(13): Show | 16 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+54G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417805 | ||||||
| chr7:7417812
|
A | C | 16 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(13): Show | 16 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+47T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417812 | ||||||
| chr7:7417813
|
C | G | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+46G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 27/34 | chr7 | 7417813 | ||||||
| chr7:7417940
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0169a0001c0001t0005g0011others(1): Show | 4 | HG01256.hp1 HG02451.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068-13C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7417940 | ||||||
| chr7:7417991
|
A | C | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068-64T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7417991 | ||||||
| chr7:7418129
|
T | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2068-202A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418129 | ||||||
| chr7:7418164
|
C | T | 17 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(14): Show | 17 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2068-237G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418164 | ||||||
| chr7:7418197
|
C | T | 10 | a0002c0002t0002g0170a0002c0002t0006g0002a0002c0004t0003g0026others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2068-270G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418197 | ||||||
| chr7:7418395
|
G | A | 16 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(13): Show | 16 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2068-468C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418395 | ||||||
| chr7:7418419
|
G | A | 65 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.2068-492C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418419 | ||||||
| chr7:7418485
|
T | C | 1 | a0001c0007t0003g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2068-558A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418485 | ||||||
| chr7:7418562
|
A | G | 4 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068-635T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418562 | ||||||
| chr7:7418609
|
C | T | 1 | a0002c0002t0001g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2068-682G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418609 | ||||||
| chr7:7418677
|
G | A | 1 | a0005c0010t0001g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2068-750C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418677 | ||||||
| chr7:7418721
|
A | G | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG01081.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2068-794T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418721 | ||||||
| chr7:7418856
|
T | G | 51 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.2068-929A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418856 | ||||||
| chr7:7418904
|
G | A | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG01081.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2068-977C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7418904 | ||||||
| chr7:7419067
|
G | C | 2 | a0001c0001t0005g0011a0001c0007t0003g0148 | 2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2067+818C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419067 | ||||||
| chr7:7419158
|
C | G | 73 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(70): Show | 73 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.2067+727G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419158 | ||||||
| chr7:7419186
|
C | G | 8 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+699G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419186 | ||||||
| chr7:7419246
|
G | T | 7 | a0002c0002t0002g0004a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02886.hp1 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2067+639C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419246 | ||||||
| chr7:7419303
|
T | C | 73 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(70): Show | 73 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.2067+582A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419303 | ||||||
| chr7:7419317
|
C | G | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2067+568G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419317 | ||||||
| chr7:7419478
|
G | A | 72 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.2067+407C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419478 | ||||||
| chr7:7419604
|
G | A | 29 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.2067+281C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419604 | ||||||
| chr7:7419609
|
C | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2067+276G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419609 | ||||||
| chr7:7419659
|
A | G | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2067+226T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419659 | ||||||
| chr7:7419776
|
GA | G | 7 | a0001c0005t0002g0067a0006c0015t0002g0101a0006c0015t0002g0179others(4): Show | 7 | HG01243.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2067+108delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419776 | ||||||
| chr7:7419874
|
T | A | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG01081.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2067+11A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 26/34 | chr7 | 7419874 | ||||||
| chr7:7419985
|
A | AT | 55 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1999-33dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7419985 | ||||||
| chr7:7419999
|
TTATG | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1999-50_1999-47del others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7419999 | ||||||
| chr7:7420012
|
A | AAT | 4 | a0003c0003t0001g0079a0003c0003t0001g0080a0003c0003t0001g0081others(1): Show | 4 | NA18612.hp1 NA18957.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1999-61_1999-60dup others(2): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420012 | ||||||
| chr7:7420102
|
T | A | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-149A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420102 | ||||||
| chr7:7420313
|
G | T | 1 | a0001c0001t0002g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1999-360C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420313 | ||||||
| chr7:7420353
|
T | C | 1 | a0003c0003t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1999-400A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420353 | ||||||
| chr7:7420417
|
T | C | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-464A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420417 | ||||||
| chr7:7420423
|
C | T | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG01081.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-470G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420423 | ||||||
| chr7:7420509
|
A | G | 26 | a0002c0002t0002g0182a0004c0006t0002g0005a0004c0006t0002g0006others(23): Show | 26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1999-556T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420509 | ||||||
| chr7:7420590
|
A | G | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG01081.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-637T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420590 | ||||||
| chr7:7420653
|
G | GT | 3 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0096 | 3 | HG01516.hp2 HG01517.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1999-701dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420653 | ||||||
| chr7:7420713
|
A | T | 87 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(84): Show | 87 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1999-760T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420713 | ||||||
| chr7:7420755
|
A | G | 19 | a0001c0001t0009g0131a0002c0002t0001g0147a0002c0002t0002g0108others(16): Show | 19 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1999-802T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420755 | ||||||
| chr7:7420861
|
TG | T | 26 | a0002c0002t0002g0182a0004c0006t0002g0005a0004c0006t0002g0006others(23): Show | 26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1999-909delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420861 | ||||||
| chr7:7420919
|
T | G | 55 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1999-966A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420919 | ||||||
| chr7:7420991
|
T | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-1038A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420991 | ||||||
| chr7:7420993
|
C | A | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-1040G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7420993 | ||||||
| chr7:7421134
|
A | T | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-1181T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7421134 | ||||||
| chr7:7421516
|
A | G | 7 | a0002c0002t0002g0004a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02886.hp1 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1999-1563T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7421516 | ||||||
| chr7:7421531
|
TA | T | 10 | a0002c0002t0002g0170a0002c0002t0006g0002a0002c0004t0003g0026others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1999-1579delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7421531 | ||||||
| chr7:7421609
|
T | G | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-1656A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7421609 | ||||||
| chr7:7421688
|
C | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1999-1735G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7421688 | ||||||
| chr7:7421784
|
G | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-1831C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7421784 | ||||||
| chr7:7421865
|
C | A | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1999-1912G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7421865 | ||||||
| chr7:7422018
|
C | T | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-2065G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422018 | ||||||
| chr7:7422053
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00140.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1999-2100C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422053 | ||||||
| chr7:7422085
|
A | G | 5 | a0001c0005t0002g0067a0006c0015t0002g0101a0006c0015t0002g0179others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-2132T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422085 | ||||||
| chr7:7422131
|
T | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-2178A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422131 | ||||||
| chr7:7422211
|
C | T | 88 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(85): Show | 88 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.1999-2258G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422211 | ||||||
| chr7:7422215
|
A | T | 88 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(85): Show | 88 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.1999-2262T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422215 | ||||||
| chr7:7422234
|
C | A | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1999-2281G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422234 | ||||||
| chr7:7422356
|
C | T | 1 | a0003c0003t0004g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1999-2403G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422356 | ||||||
| chr7:7422408
|
A | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-2455T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422408 | ||||||
| chr7:7422414
|
T | A | 88 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(85): Show | 88 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.1999-2461A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422414 | ||||||
| chr7:7422458
|
G | A | 27 | a0002c0002t0002g0182a0004c0006t0002g0005a0004c0006t0002g0006others(24): Show | 27 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1999-2505C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422458 | ||||||
| chr7:7422547
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1999-2594A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422547 | ||||||
| chr7:7422595
|
C | T | 7 | a0002c0002t0002g0004a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02886.hp1 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1999-2642G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422595 | ||||||
| chr7:7422636
|
G | GA | 6 | a0001c0001t0003g0173a0001c0007t0003g0175a0001c0007t0003g0176others(3): Show | 6 | HG01081.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-2684dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422636 | ||||||
| chr7:7422640
|
A | G | 27 | a0002c0002t0002g0182a0004c0006t0002g0005a0004c0006t0002g0006others(24): Show | 27 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1999-2687T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422640 | ||||||
| chr7:7422793
|
T | G | 10 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(7): Show | 10 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1999-2840A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422793 | ||||||
| chr7:7422800
|
G | A | 6 | a0010c0013t0002g0019a0010c0013t0002g0022a0010c0028t0003g0020others(3): Show | 6 | HG02257.hp1 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-2847C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422800 | ||||||
| chr7:7422829
|
C | T | 1 | a0002c0004t0003g0028 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1999-2876G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422829 | ||||||
| chr7:7422958
|
A | T | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-3005T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422958 | ||||||
| chr7:7422961
|
G | A | 2 | a0005c0010t0001g0092a0005c0010t0001g0105 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1999-3008C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422961 | ||||||
| chr7:7422983
|
T | C | 63 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1999-3030A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7422983 | ||||||
| chr7:7423017
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1999-3064G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423017 | ||||||
| chr7:7423083
|
T | A | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-3130A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423083 | ||||||
| chr7:7423200
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1999-3247C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423200 | ||||||
| chr7:7423205
|
T | C | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-3252A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423205 | ||||||
| chr7:7423212
|
A | G | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1999-3259T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423212 | ||||||
| chr7:7423341
|
T | C | 7 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1999-3388A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423341 | ||||||
| chr7:7423383
|
C | A | 8 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1999-3430G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423383 | ||||||
| chr7:7423397
|
G | A | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1999-3444C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423397 | ||||||
| chr7:7423558
|
AT | A | 118 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(115): Show | 118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1999-3606delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423558 | ||||||
| chr7:7423658
|
G | C | 1 | a0002c0049t0003g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1999-3705C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423658 | ||||||
| chr7:7423666
|
T | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-3713A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423666 | ||||||
| chr7:7423725
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1999-3772G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423725 | ||||||
| chr7:7423830
|
T | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1999-3877A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423830 | ||||||
| chr7:7423871
|
T | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-3918A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423871 | ||||||
| chr7:7423943
|
C | T | 1 | a0007c0008t0006g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1999-3990G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423943 | ||||||
| chr7:7423955
|
A | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-4002T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423955 | ||||||
| chr7:7423967
|
T | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-4014A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423967 | ||||||
| chr7:7423983
|
T | C | 3 | a0013c0011t0002g0035a0013c0011t0002g0036a0013c0011t0002g0064 | 3 | HG01070.hp1 HG02004.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1999-4030A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7423983 | ||||||
| chr7:7424049
|
A | G | 7 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1999-4096T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424049 | ||||||
| chr7:7424084
|
C | T | 8 | a0001c0001t0001g0125a0003c0047t0003g0045a0005c0010t0001g0043others(5): Show | 8 | HG00642.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1999-4131G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424084 | ||||||
| chr7:7424085
|
G | A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-4132C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424085 | ||||||
| chr7:7424089
|
AAAT | A | 54 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1999-4139_1999-413 others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424089 | ||||||
| chr7:7424325
|
G | A | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-4372C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424325 | ||||||
| chr7:7424335
|
G | A | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999-4382C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424335 | ||||||
| chr7:7424431
|
T | C | 2 | a0001c0005t0002g0067a0001c0005t0002g0069 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1999-4478A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424431 | ||||||
| chr7:7424465
|
T | C | 7 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1999-4512A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424465 | ||||||
| chr7:7424478
|
T | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1999-4525A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424478 | ||||||
| chr7:7424559
|
C | G | 1 | a0001c0001t0002g0051 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1999-4606G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424559 | ||||||
| chr7:7424605
|
G | C | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1999-4652C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424605 | ||||||
| chr7:7424668
|
T | G | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-4715A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424668 | ||||||
| chr7:7424818
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1999-4865G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424818 | ||||||
| chr7:7424868
|
T | C | 21 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1999-4915A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424868 | ||||||
| chr7:7424949
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1999-4996A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424949 | ||||||
| chr7:7424950
|
G | A | 35 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0002g0015others(32): Show | 35 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1999-4997C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7424950 | ||||||
| chr7:7425096
|
CTTA | C | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-5146_1999-514 others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425096 | ||||||
| chr7:7425104
|
G | C | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1999-5151C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425104 | ||||||
| chr7:7425186
|
A | G | 2 | a0001c0001t0005g0011a0001c0007t0003g0148 | 2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1999-5233T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425186 | ||||||
| chr7:7425196
|
C | A | 2 | a0002c0002t0002g0118a0002c0002t0002g0119 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1999-5243G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425196 | ||||||
| chr7:7425358
|
G | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1999-5405C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425358 | ||||||
| chr7:7425524
|
G | A | 28 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1999-5571C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425524 | ||||||
| chr7:7425587
|
A | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1999-5634T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425587 | ||||||
| chr7:7425635
|
T | A | 16 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0002g0015others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1999-5682A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425635 | ||||||
| chr7:7425679
|
T | C | 15 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0002g0015others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1999-5726A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425679 | ||||||
| chr7:7425684
|
G | T | 78 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(75): Show | 78 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1999-5731C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425684 | ||||||
| chr7:7425810
|
C | T | 74 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0005t0002g0067others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1999-5857G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425810 | ||||||
| chr7:7425822
|
G | T | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1999-5869C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425822 | ||||||
| chr7:7425852
|
A | C | 15 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0002g0015others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1999-5899T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425852 | ||||||
| chr7:7425854
|
G | A | 74 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0005t0002g0067others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1999-5901C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7425854 | ||||||
| chr7:7426030
|
C | T | 1 | a0012c0016t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1999-6077G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426030 | ||||||
| chr7:7426200
|
T | G | 1 | a0006c0015t0002g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1999-6247A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426200 | ||||||
| chr7:7426385
|
T | C | 8 | a0002c0002t0002g0004a0002c0002t0002g0182a0006c0030t0003g0065others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1998+6088A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426385 | ||||||
| chr7:7426411
|
G | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1998+6062C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426411 | ||||||
| chr7:7426421
|
C | G | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1998+6052G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426421 | ||||||
| chr7:7426518
|
TGAATAG | T | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1998+5949_1998+595 others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426518 | ||||||
| chr7:7426843
|
T | C | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1998+5630A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426843 | ||||||
| chr7:7426991
|
A | G | 28 | a0003c0047t0003g0045a0004c0006t0002g0005a0004c0006t0002g0006others(25): Show | 28 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1998+5482T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426991 | ||||||
| chr7:7426992
|
A | G | 4 | a0001c0007t0003g0175a0001c0007t0003g0176a0001c0007t0003g0177others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1998+5481T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7426992 | ||||||
| chr7:7427101
|
A | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1998+5372T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7427101 | ||||||
| chr7:7427165
|
A | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1998+5308T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7427165 | ||||||
| chr7:7427183
|
A | G | 20 | a0001c0001t0009g0131a0001c0007t0003g0175a0001c0007t0003g0176others(17): Show | 20 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1998+5290T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7427183 | ||||||
| chr7:7427289
|
T | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1998+5184A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7427289 | ||||||
| chr7:7427358
|
T | C | 20 | a0001c0001t0009g0131a0001c0007t0003g0175a0001c0007t0003g0176others(17): Show | 20 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1998+5115A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7427358 | ||||||
| chr7:7427846
|
CAA | C | 7 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1998+4625_1998+462 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7427846 | ||||||
| chr7:7428054
|
A | G | 21 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1998+4419T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7428054 | ||||||
| chr7:7428169
|
C | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1998+4304G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7428169 | ||||||
| chr7:7428339
|
A | G | 61 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0005t0002g0067others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1998+4134T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7428339 | ||||||
| chr7:7428613
|
C | CA | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1998+3859_1998+386 others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7428613 | ||||||
| chr7:7428642
|
G | T | 1 | a0025c0046t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1998+3831C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7428642 | ||||||
| chr7:7428658
|
C | T | 61 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0005t0002g0067others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1998+3815G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7428658 | ||||||
| chr7:7428709
|
G | T | 46 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1998+3764C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7428709 | ||||||
| chr7:7428894
|
A | G | 1 | a0003c0003t0001g0079 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1998+3579T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7428894 | ||||||
| chr7:7429143
|
C | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1998+3330G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429143 | ||||||
| chr7:7429157
|
C | T | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1998+3316G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429157 | ||||||
| chr7:7429176
|
T | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1998+3297A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429176 | ||||||
| chr7:7429177
|
G | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1998+3296C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429177 | ||||||
| chr7:7429209
|
AC | A | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1998+3263delG | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429209 | ||||||
| chr7:7429221
|
T | C | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1998+3252A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429221 | ||||||
| chr7:7429223
|
T | C | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1998+3250A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429223 | ||||||
| chr7:7429227
|
C | A | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1998+3246G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429227 | ||||||
| chr7:7429228
|
AGT | A | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1998+3243_1998+324 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429228 | ||||||
| chr7:7429231
|
T | A | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1998+3242A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429231 | ||||||
| chr7:7429250
|
A | G | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1998+3223T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429250 | ||||||
| chr7:7429291
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1998+3182G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429291 | ||||||
| chr7:7429422
|
TCTCTCAC others(11): Show |
T | 12 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1998+3033_1998+305 others(22): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429422 | ||||||
| chr7:7429423
|
CTCTCACA others(17): Show |
C | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1998+3026_1998+304 others(28): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429423 | ||||||
| chr7:7429425
|
CTCACATA others(15): Show |
C | 26 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(23): Show | 26 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1998+3026_1998+304 others(26): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429425 | ||||||
| chr7:7429426
|
T | TCTCTCTC others(1): Show |
8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG01081.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1998+3046_1998+304 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429426 | ||||||
| chr7:7429427
|
CACATACA others(13): Show |
C | 23 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0006g0002others(20): Show | 23 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1998+3026_1998+304 others(24): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429427 | ||||||
| chr7:7429431
|
T | C | 8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG01081.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1998+3042A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429431 | ||||||
| chr7:7429440
|
A | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1998+3033T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429440 | ||||||
| chr7:7429447
|
T | C | 20 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(17): Show | 20 | HG01081.hp1 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1998+3026A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429447 | ||||||
| chr7:7429460
|
C | T | 3 | a0006c0015t0002g0179a0006c0019t0002g0187a0006c0019t0002g0188 | 3 | HG01243.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1998+3013G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429460 | ||||||
| chr7:7429460
|
CTG | C | 11 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0006g0002others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1998+3011_1998+301 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429460 | ||||||
| chr7:7429471
|
T | G | 3 | a0002c0002t0002g0015a0002c0049t0003g0189a0012c0016t0002g0123 | 3 | HG02451.hp1 HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1998+3002A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429471 | ||||||
| chr7:7429471
|
T | TG | 6 | a0001c0001t0001g0048a0002c0002t0002g0108a0002c0002t0002g0111others(3): Show | 6 | HG01361.hp2 HG01515.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1998+3001dupC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429471 | ||||||
| chr7:7429472
|
GT | G | 36 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0005t0001g0098others(33): Show | 36 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1998+3000delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429472 | ||||||
| chr7:7429473
|
T | G | 45 | a0001c0001t0001g0048a0001c0001t0002g0171a0001c0001t0009g0131others(42): Show | 45 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1998+3000A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429473 | ||||||
| chr7:7429473
|
TGG | T | 13 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(10): Show | 13 | HG01081.hp1 HG02257.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1998+2998_1998+299 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429473 | ||||||
| chr7:7429475
|
G | T | 36 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1998+2998C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429475 | ||||||
| chr7:7429536
|
G | T | 21 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1998+2937C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429536 | ||||||
| chr7:7429805
|
A | G | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1998+2668T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429805 | ||||||
| chr7:7429817
|
C | T | 21 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1998+2656G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429817 | ||||||
| chr7:7429820
|
G | C | 3 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100 | 3 | HG00099.hp1 HG01255.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1998+2653C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429820 | ||||||
| chr7:7429912
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1998+2561A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7429912 | ||||||
| chr7:7430112
|
A | G | 8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG01081.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1998+2361T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430112 | ||||||
| chr7:7430189
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1998+2284G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430189 | ||||||
| chr7:7430208
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1998+2265G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430208 | ||||||
| chr7:7430212
|
C | T | 1 | a0001c0007t0003g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1998+2261G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430212 | ||||||
| chr7:7430244
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0002g0107 | 2 | HG00099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1998+2229C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430244 | ||||||
| chr7:7430262
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1998+2211C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430262 | ||||||
| chr7:7430274
|
C | G | 70 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0005t0002g0067others(67): Show | 70 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.1998+2199G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430274 | ||||||
| chr7:7430308
|
G | C | 14 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0002g0015others(11): Show | 14 | HG01081.hp1 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1998+2165C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430308 | ||||||
| chr7:7430341
|
G | A | 17 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1998+2132C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430341 | ||||||
| chr7:7430461
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1998+2012G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430461 | ||||||
| chr7:7430498
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1998+1975G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430498 | ||||||
| chr7:7430505
|
G | A | 5 | a0003c0003t0004g0193a0003c0003t0004g0194a0003c0003t0004g0195others(2): Show | 5 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998+1968C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430505 | ||||||
| chr7:7430572
|
T | C | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1998+1901A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430572 | ||||||
| chr7:7430592
|
T | C | 4 | a0002c0002t0002g0015a0002c0002t0002g0170a0002c0004t0003g0088others(1): Show | 4 | HG02451.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998+1881A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430592 | ||||||
| chr7:7430611
|
G | C | 1 | a0003c0003t0004g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1998+1862C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430611 | ||||||
| chr7:7430927
|
G | A | 60 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1998+1546C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7430927 | ||||||
| chr7:7431120
|
G | C | 72 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1998+1353C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431120 | ||||||
| chr7:7431140
|
G | A | 38 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0172others(35): Show | 38 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1998+1333C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431140 | ||||||
| chr7:7431156
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1998+1317G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431156 | ||||||
| chr7:7431263
|
A | G | 72 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1998+1210T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431263 | ||||||
| chr7:7431455
|
T | C | 8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1998+1018A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431455 | ||||||
| chr7:7431667
|
G | T | 1 | a0004c0006t0002g0005 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1998+806C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431667 | ||||||
| chr7:7431764
|
G | C | 1 | a0003c0003t0004g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1998+709C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431764 | ||||||
| chr7:7431769
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1998+704T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431769 | ||||||
| chr7:7431771
|
G | A | 1 | a0002c0004t0003g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1998+702C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431771 | ||||||
| chr7:7431776
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1998+697C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431776 | ||||||
| chr7:7431815
|
C | T | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1998+658G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431815 | ||||||
| chr7:7431844
|
C | G | 21 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1998+629G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431844 | ||||||
| chr7:7431867
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1998+606C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431867 | ||||||
| chr7:7431962
|
A | G | 76 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.1998+511T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431962 | ||||||
| chr7:7431982
|
G | A | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1998+491C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7431982 | ||||||
| chr7:7432063
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1998+410C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7432063 | ||||||
| chr7:7432334
|
T | C | 13 | a0002c0002t0002g0015a0002c0002t0006g0002a0002c0004t0003g0026others(10): Show | 13 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1998+139A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7432334 | ||||||
| chr7:7432409
|
C | A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1998+64G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7432409 | ||||||
| chr7:7432410
|
C | A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1998+63G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7432410 | ||||||
| chr7:7432445
|
T | C | 18 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(15): Show | 18 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1998+28A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 25/34 | chr7 | 7432445 | ||||||
| chr7:7432587
|
C | G | 8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG01081.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1929+45G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 24/34 | chr7 | 7432587 | ||||||
| chr7:7432833
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1861-133C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7432833 | ||||||
| chr7:7432861
|
T | G | 1 | a0002c0002t0002g0110 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1861-161A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7432861 | ||||||
| chr7:7432966
|
T | TAC | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1861-267_1861-266i others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7432966 | ||||||
| chr7:7433020
|
T | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1861-320A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433020 | ||||||
| chr7:7433302
|
C | T | 1 | a0003c0003t0001g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1861-602G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433302 | ||||||
| chr7:7433303
|
G | A | 1 | a0025c0046t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1861-603C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433303 | ||||||
| chr7:7433392
|
T | A | 3 | a0001c0001t0008g0174a0001c0051t0008g0192a0009c0014t0003g0021 | 3 | HG03139.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1861-692A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433392 | ||||||
| chr7:7433411
|
G | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1861-711C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433411 | ||||||
| chr7:7433452
|
G | A | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1861-752C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433452 | ||||||
| chr7:7433590
|
C | T | 1 | a0026c0043t0007g0029 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1861-890G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433590 | ||||||
| chr7:7433613
|
G | A | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1861-913C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433613 | ||||||
| chr7:7433637
|
T | TA | 28 | a0001c0001t0001g0060a0001c0001t0002g0178a0001c0001t0003g0173others(25): Show | 28 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1861-938dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433637 | ||||||
| chr7:7433637
|
TA | T | 79 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0157others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1861-938delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433637 | ||||||
| chr7:7433670
|
T | TC | 25 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1861-971dupG | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433670 | ||||||
| chr7:7433676
|
A | G | 4 | a0003c0003t0001g0075a0003c0003t0001g0076a0003c0003t0001g0077others(1): Show | 4 | HG00733.hp2 HG00741.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1861-976T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433676 | ||||||
| chr7:7433679
|
C | T | 3 | a0013c0011t0002g0035a0013c0011t0002g0036a0013c0011t0002g0064 | 3 | HG01070.hp1 HG02004.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1861-979G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433679 | ||||||
| chr7:7433932
|
A | G | 72 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1861-1232T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7433932 | ||||||
| chr7:7434025
|
G | A | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1861-1325C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7434025 | ||||||
| chr7:7434420
|
T | G | 8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG01081.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-1720A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7434420 | ||||||
| chr7:7434516
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1861-1816A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7434516 | ||||||
| chr7:7434801
|
T | A | 25 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1860+1594A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7434801 | ||||||
| chr7:7435167
|
C | A | 6 | a0002c0002t0002g0004a0002c0002t0002g0182a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1860+1228G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435167 | ||||||
| chr7:7435332
|
C | T | 2 | a0002c0002t0002g0117a0029c0037t0001g0113 | 2 | HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1860+1063G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435332 | ||||||
| chr7:7435347
|
G | A | 5 | a0010c0013t0002g0019a0010c0013t0002g0022a0010c0028t0003g0020others(2): Show | 5 | HG02257.hp1 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1860+1048C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435347 | ||||||
| chr7:7435528
|
C | G | 17 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1860+867G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435528 | ||||||
| chr7:7435578
|
T | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1860+817A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435578 | ||||||
| chr7:7435875
|
G | A | 108 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1860+520C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435875 | ||||||
| chr7:7435892
|
T | G | 44 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1860+503A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435892 | ||||||
| chr7:7435900
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1860+495C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435900 | ||||||
| chr7:7435924
|
C | T | 2 | a0003c0003t0001g0080a0003c0003t0001g0081 | 2 | NA18957.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1860+471G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435924 | ||||||
| chr7:7435972
|
A | C | 50 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1860+423T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7435972 | ||||||
| chr7:7436029
|
C | A | 1 | a0003c0003t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1860+366G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7436029 | ||||||
| chr7:7436051
|
C | T | 21 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1860+344G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7436051 | ||||||
| chr7:7436123
|
T | A | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1860+272A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7436123 | ||||||
| chr7:7436254
|
T | A | 1 | a0001c0005t0001g0100 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1860+141A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7436254 | ||||||
| chr7:7436314
|
T | G | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1860+81A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 23/34 | chr7 | 7436314 | ||||||
| chr7:7436467
|
T | C | 14 | a0002c0002t0002g0015a0002c0002t0006g0002a0002c0004t0003g0026others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1792-4A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7436467 | ||||||
| chr7:7436504
|
G | A | 2 | a0002c0002t0006g0002a0028c0036t0010g0001 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1792-41C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7436504 | ||||||
| chr7:7436583
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1792-120C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7436583 | ||||||
| chr7:7436665
|
T | C | 21 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1792-202A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7436665 | ||||||
| chr7:7436705
|
C | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1792-242G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7436705 | ||||||
| chr7:7436934
|
T | C | 21 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1791+460A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7436934 | ||||||
| chr7:7436945
|
A | G | 150 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(147): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1791+449T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7436945 | ||||||
| chr7:7437061
|
G | A | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1791+333C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7437061 | ||||||
| chr7:7437103
|
G | A | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1791+291C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 22/34 | chr7 | 7437103 | ||||||
| chr7:7437546
|
G | A | 14 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1723-84C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437546 | ||||||
| chr7:7437556
|
A | C | 2 | a0001c0001t0001g0060a0001c0001t0002g0107 | 2 | HG00099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1723-94T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437556 | ||||||
| chr7:7437619
|
T | TA | 111 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1723-158dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437619 | ||||||
| chr7:7437625
|
C | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1723-163G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437625 | ||||||
| chr7:7437670
|
T | G | 47 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1723-208A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437670 | ||||||
| chr7:7437887
|
C | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0003c0003t0001g0073others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1723-425G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437887 | ||||||
| chr7:7437940
|
T | A | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1723-478A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437940 | ||||||
| chr7:7437952
|
G | A | 25 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1723-490C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437952 | ||||||
| chr7:7437970
|
C | T | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1723-508G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437970 | ||||||
| chr7:7437987
|
C | CA | 64 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1723-526_1723-525i others(3): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7437987 | ||||||
| chr7:7438080
|
C | CA | 5 | a0001c0001t0001g0124a0002c0002t0002g0015a0002c0049t0003g0189others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1723-619dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438080 | ||||||
| chr7:7438080
|
C | CAA | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723-620_1723-619d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438080 | ||||||
| chr7:7438134
|
C | A | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1723-672G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438134 | ||||||
| chr7:7438181
|
C | CGCA | 4 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723-722_1723-720d others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438181 | ||||||
| chr7:7438320
|
GGA | G | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1723-860_1723-859d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438320 | ||||||
| chr7:7438356
|
C | G | 6 | a0002c0002t0002g0004a0002c0002t0002g0182a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1723-894G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438356 | ||||||
| chr7:7438388
|
G | A | 1 | a0007c0008t0003g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1723-926C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438388 | ||||||
| chr7:7438418
|
A | AG | 119 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(116): Show | 119 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1723-957_1723-956i others(3): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438418 | ||||||
| chr7:7438450
|
G | C | 47 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1723-988C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438450 | ||||||
| chr7:7438517
|
C | T | 47 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1723-1055G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438517 | ||||||
| chr7:7438675
|
TCATAA | T | 64 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1723-1218_1723-121 others(9): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438675 | ||||||
| chr7:7438688
|
G | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1723-1226C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438688 | ||||||
| chr7:7438707
|
G | A | 1 | a0017c0020t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1723-1245C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438707 | ||||||
| chr7:7438717
|
T | C | 22 | a0002c0002t0002g0170a0004c0006t0002g0005a0004c0006t0002g0006others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1723-1255A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438717 | ||||||
| chr7:7438802
|
G | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1723-1340C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438802 | ||||||
| chr7:7438851
|
C | T | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1723-1389G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438851 | ||||||
| chr7:7438937
|
A | G | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1723-1475T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7438937 | ||||||
| chr7:7439013
|
A | T | 44 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1723-1551T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439013 | ||||||
| chr7:7439369
|
C | A | 1 | a0005c0010t0001g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1722+1421G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439369 | ||||||
| chr7:7439406
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1722+1384G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439406 | ||||||
| chr7:7439478
|
C | G | 47 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1722+1312G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439478 | ||||||
| chr7:7439556
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1722+1234T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439556 | ||||||
| chr7:7439739
|
C | T | 116 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1722+1051G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439739 | ||||||
| chr7:7439798
|
C | G | 25 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1722+992G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439798 | ||||||
| chr7:7439881
|
G | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1722+909C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439881 | ||||||
| chr7:7439950
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1722+840A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7439950 | ||||||
| chr7:7440041
|
C | G | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1722+749G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440041 | ||||||
| chr7:7440064
|
C | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1722+726G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440064 | ||||||
| chr7:7440163
|
G | T | 13 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(10): Show | 13 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1722+627C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440163 | ||||||
| chr7:7440191
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1722+599G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440191 | ||||||
| chr7:7440332
|
G | A | 44 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1722+458C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440332 | ||||||
| chr7:7440368
|
A | G | 14 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1722+422T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440368 | ||||||
| chr7:7440546
|
G | A | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1722+244C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440546 | ||||||
| chr7:7440565
|
G | A | 108 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1722+225C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440565 | ||||||
| chr7:7440745
|
C | CA | 55 | a0001c0001t0001g0060a0001c0001t0001g0091a0001c0001t0001g0093others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.1722+44dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440745 | ||||||
| chr7:7440751
|
A | G | 63 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1722+39T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 21/34 | chr7 | 7440751 | ||||||
| chr7:7440942
|
C | T | 6 | a0002c0002t0002g0004a0002c0002t0002g0182a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1651-81G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7440942 | ||||||
| chr7:7441155
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1651-294G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441155 | ||||||
| chr7:7441198
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1651-337C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441198 | ||||||
| chr7:7441260
|
T | C | 18 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(15): Show | 18 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1651-399A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441260 | ||||||
| chr7:7441331
|
C | G | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-470G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441331 | ||||||
| chr7:7441457
|
A | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1651-596T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441457 | ||||||
| chr7:7441524
|
G | GA | 37 | a0001c0001t0001g0018a0001c0001t0001g0061a0001c0001t0001g0062others(34): Show | 37 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.1651-664dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441524 | ||||||
| chr7:7441524
|
GA | G | 5 | a0001c0001t0009g0131a0002c0002t0001g0126a0002c0004t0003g0026others(2): Show | 5 | HG01081.hp1 HG01433.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-664delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441524 | ||||||
| chr7:7441524
|
GAA | G | 37 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(34): Show | 37 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1651-665_1651-664d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441524 | ||||||
| chr7:7441524
|
GAAA | G | 22 | a0002c0002t0002g0170a0004c0006t0002g0005a0004c0006t0002g0006others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1651-666_1651-664d others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441524 | ||||||
| chr7:7441546
|
C | T | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1651-685G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441546 | ||||||
| chr7:7441766
|
T | G | 1 | a0003c0003t0001g0080 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1651-905A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441766 | ||||||
| chr7:7441784
|
T | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1651-923A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441784 | ||||||
| chr7:7441857
|
T | C | 1 | a0006c0015t0002g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1651-996A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441857 | ||||||
| chr7:7441861
|
C | G | 4 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | NA19007.hp1 NA19011.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-1000G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441861 | ||||||
| chr7:7441898
|
A | C | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-1037T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441898 | ||||||
| chr7:7441943
|
T | C | 8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG01081.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1651-1082A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7441943 | ||||||
| chr7:7442045
|
T | C | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1651-1184A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442045 | ||||||
| chr7:7442078
|
G | T | 4 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | NA19007.hp1 NA19011.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-1217C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442078 | ||||||
| chr7:7442179
|
A | G | 57 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(54): Show | 57 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1651-1318T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442179 | ||||||
| chr7:7442510
|
C | T | 72 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1650+1075G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442510 | ||||||
| chr7:7442627
|
A | G | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1650+958T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442627 | ||||||
| chr7:7442762
|
C | A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1650+823G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442762 | ||||||
| chr7:7442862
|
CCATCTCT others(10): Show |
C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650+706_1650+722d others(19): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442862 | ||||||
| chr7:7442959
|
C | T | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | NA18612.hp2 NA19007.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1650+626G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442959 | ||||||
| chr7:7442990
|
G | T | 65 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0149others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.1650+595C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7442990 | ||||||
| chr7:7443007
|
C | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1650+578G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443007 | ||||||
| chr7:7443011
|
T | G | 1 | a0003c0003t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1650+574A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443011 | ||||||
| chr7:7443034
|
C | CA | 64 | a0001c0001t0001g0104a0001c0001t0001g0157a0001c0001t0001g0158others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1650+550dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443034 | ||||||
| chr7:7443034
|
CA | C | 6 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(3): Show | 6 | HG02004.hp2 NA18612.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.1650+550delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443034 | ||||||
| chr7:7443054
|
C | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650+531G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443054 | ||||||
| chr7:7443238
|
T | A | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1650+347A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443238 | ||||||
| chr7:7443239
|
T | C | 5 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1650+346A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443239 | ||||||
| chr7:7443405
|
AT | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650+179delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443405 | ||||||
| chr7:7443432
|
TCTTCCAA others(3): Show |
T | 2 | a0006c0030t0003g0065a0017c0020t0001g0086 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1650+143_1650+152d others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443432 | ||||||
| chr7:7443452
|
C | T | 110 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1650+133G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443452 | ||||||
| chr7:7443478
|
T | C | 3 | a0003c0047t0003g0045a0005c0010t0002g0044a0005c0044t0003g0039 | 3 | HG02486.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1650+107A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 20/34 | chr7 | 7443478 | ||||||
| chr7:7443771
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1582-118T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443771 | ||||||
| chr7:7443772
|
T | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1582-119A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443772 | ||||||
| chr7:7443816
|
T | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1582-163A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443816 | ||||||
| chr7:7443899
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1582-246C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443899 | ||||||
| chr7:7443949
|
T | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1582-296A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443949 | ||||||
| chr7:7443963
|
G | C | 2 | a0001c0005t0002g0067a0001c0005t0002g0069 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1582-310C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443963 | ||||||
| chr7:7443986
|
G | GT | 56 | a0001c0001t0001g0048a0001c0001t0001g0060a0001c0001t0001g0091others(53): Show | 56 | HG01070.hp1 HG01070.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1582-334dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443986 | ||||||
| chr7:7443986
|
G | GTT | 14 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.1582-335_1582-334d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443986 | ||||||
| chr7:7443986
|
G | GTTT | 20 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(17): Show | 20 | HG00438.hp1 HG00733.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1582-336_1582-334d others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443986 | ||||||
| chr7:7443986
|
G | GTTTT | 11 | a0002c0004t0003g0088a0003c0003t0001g0076a0003c0003t0004g0193others(8): Show | 11 | HG00423.hp1 HG00735.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1582-337_1582-334d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443986 | ||||||
| chr7:7443986
|
GT | G | 11 | a0001c0001t0001g0050a0001c0001t0001g0090a0001c0001t0002g0149others(8): Show | 11 | HG01167.hp2 HG01515.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1582-334delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7443986 | ||||||
| chr7:7444010
|
T | A | 19 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0001t0009g0131others(16): Show | 19 | HG00140.hp2 HG00733.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1582-357A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7444010 | ||||||
| chr7:7444046
|
A | T | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1581+372T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7444046 | ||||||
| chr7:7444088
|
T | A | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1581+330A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7444088 | ||||||
| chr7:7444090
|
T | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1581+328A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7444090 | ||||||
| chr7:7444104
|
T | C | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1581+314A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 19/34 | chr7 | 7444104 | ||||||
| chr7:7444653
|
C | A | 1 | a0002c0002t0002g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1510-164G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7444653 | ||||||
| chr7:7444966
|
T | A | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1510-477A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7444966 | ||||||
| chr7:7445178
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1510-689A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445178 | ||||||
| chr7:7445231
|
G | A | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510-742C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445231 | ||||||
| chr7:7445319
|
G | A | 6 | a0006c0015t0002g0101a0006c0015t0002g0179a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1510-830C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445319 | ||||||
| chr7:7445369
|
G | A | 20 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1510-880C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445369 | ||||||
| chr7:7445392
|
C | T | 1 | a0002c0002t0002g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1510-903G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445392 | ||||||
| chr7:7445485
|
C | T | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1510-996G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445485 | ||||||
| chr7:7445499
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1510-1010A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445499 | ||||||
| chr7:7445513
|
A | G | 2 | a0002c0002t0001g0126a0003c0003t0002g0159 | 2 | NA19058.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1510-1024T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445513 | ||||||
| chr7:7445593
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1510-1104T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445593 | ||||||
| chr7:7445687
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1510-1198C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445687 | ||||||
| chr7:7445821
|
A | T | 20 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1510-1332T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445821 | ||||||
| chr7:7445863
|
C | CT | 42 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1510-1375dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445863 | ||||||
| chr7:7445918
|
G | A | 20 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1510-1429C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7445918 | ||||||
| chr7:7446050
|
C | G | 65 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.1510-1561G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446050 | ||||||
| chr7:7446390
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1510-1901A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446390 | ||||||
| chr7:7446567
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1510-2078G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446567 | ||||||
| chr7:7446591
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1510-2102C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446591 | ||||||
| chr7:7446620
|
A | G | 1 | a0001c0005t0002g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1510-2131T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446620 | ||||||
| chr7:7446636
|
C | A | 67 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1510-2147G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446636 | ||||||
| chr7:7446926
|
C | T | 67 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1510-2437G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446926 | ||||||
| chr7:7446933
|
T | C | 67 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1510-2444A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446933 | ||||||
| chr7:7446948
|
G | A | 2 | a0003c0003t0004g0195a0003c0003t0004g0196 | 2 | HG00741.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1510-2459C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7446948 | ||||||
| chr7:7447122
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1510-2633G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447122 | ||||||
| chr7:7447319
|
C | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1510-2830G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447319 | ||||||
| chr7:7447365
|
G | T | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1510-2876C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447365 | ||||||
| chr7:7447464
|
G | A | 61 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1510-2975C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447464 | ||||||
| chr7:7447525
|
T | C | 67 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1510-3036A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447525 | ||||||
| chr7:7447677
|
A | G | 12 | a0002c0002t0002g0004a0002c0002t0002g0182a0006c0015t0002g0101others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1510-3188T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447677 | ||||||
| chr7:7447778
|
A | G | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1510-3289T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447778 | ||||||
| chr7:7447824
|
A | C | 6 | a0002c0002t0002g0004a0002c0002t0002g0182a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-3335T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447824 | ||||||
| chr7:7447884
|
T | A | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1510-3395A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447884 | ||||||
| chr7:7447940
|
G | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1510-3451C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7447940 | ||||||
| chr7:7448173
|
C | G | 3 | a0006c0015t0002g0179a0006c0019t0002g0187a0006c0019t0002g0188 | 3 | HG01243.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1510-3684G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448173 | ||||||
| chr7:7448209
|
C | T | 6 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1510-3720G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448209 | ||||||
| chr7:7448318
|
T | C | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1510-3829A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448318 | ||||||
| chr7:7448320
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1510-3831A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448320 | ||||||
| chr7:7448436
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1509+3883T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448436 | ||||||
| chr7:7448449
|
C | T | 58 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1509+3870G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448449 | ||||||
| chr7:7448470
|
A | AT | 20 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1509+3848dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448470 | ||||||
| chr7:7448473
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1509+3846A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448473 | ||||||
| chr7:7448712
|
C | G | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+3607G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448712 | ||||||
| chr7:7448880
|
A | G | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+3439T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448880 | ||||||
| chr7:7448957
|
C | A | 67 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1509+3362G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448957 | ||||||
| chr7:7448970
|
T | C | 59 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(56): Show | 59 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.1509+3349A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448970 | ||||||
| chr7:7448975
|
G | T | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1509+3344C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7448975 | ||||||
| chr7:7449001
|
A | G | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1509+3318T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449001 | ||||||
| chr7:7449089
|
T | G | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1509+3230A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449089 | ||||||
| chr7:7449189
|
T | G | 8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1509+3130A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449189 | ||||||
| chr7:7449280
|
G | A | 20 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1509+3039C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449280 | ||||||
| chr7:7449354
|
T | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+2965A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449354 | ||||||
| chr7:7449535
|
T | TA | 22 | a0001c0001t0001g0153a0004c0006t0002g0005a0004c0006t0002g0006others(19): Show | 22 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1509+2783dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449535 | ||||||
| chr7:7449535
|
T | TAA | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+2782_1509+278 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449535 | ||||||
| chr7:7449536
|
A | T | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1509+2783T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449536 | ||||||
| chr7:7449572
|
C | T | 67 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1509+2747G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449572 | ||||||
| chr7:7449695
|
A | C | 20 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(17): Show | 20 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1509+2624T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449695 | ||||||
| chr7:7449704
|
A | C | 1 | a0005c0010t0001g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1509+2615T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449704 | ||||||
| chr7:7449753
|
T | A | 2 | a0001c0001t0005g0011a0001c0007t0003g0148 | 2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1509+2566A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449753 | ||||||
| chr7:7449815
|
C | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1509+2504G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449815 | ||||||
| chr7:7449983
|
A | G | 3 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100 | 3 | HG00099.hp1 HG01255.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1509+2336T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7449983 | ||||||
| chr7:7450527
|
A | G | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0003c0003t0001g0073others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+1792T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7450527 | ||||||
| chr7:7450549
|
G | C | 1 | a0003c0003t0001g0074 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1509+1770C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7450549 | ||||||
| chr7:7450673
|
A | G | 6 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+1646T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7450673 | ||||||
| chr7:7450705
|
C | T | 1 | a0002c0004t0003g0032 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1509+1614G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7450705 | ||||||
| chr7:7450787
|
T | C | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1509+1532A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7450787 | ||||||
| chr7:7450789
|
A | AT | 2 | a0018c0023t0003g0165a0027c0042t0002g0089 | 2 | HG01081.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1509+1529dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7450789 | ||||||
| chr7:7450843
|
G | A | 2 | a0001c0001t0001g0124a0018c0023t0003g0165 | 2 | HG01081.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1509+1476C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7450843 | ||||||
| chr7:7450844
|
C | T | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509+1475G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7450844 | ||||||
| chr7:7451083
|
G | T | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+1236C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451083 | ||||||
| chr7:7451263
|
G | A | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1509+1056C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451263 | ||||||
| chr7:7451318
|
T | C | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1509+1001A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451318 | ||||||
| chr7:7451338
|
G | A | 2 | a0005c0010t0001g0092a0005c0010t0001g0105 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1509+981C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451338 | ||||||
| chr7:7451410
|
G | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1509+909C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451410 | ||||||
| chr7:7451431
|
G | T | 1 | a0002c0002t0001g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1509+888C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451431 | ||||||
| chr7:7451671
|
T | TATAC | 2 | a0002c0002t0002g0170a0012c0016t0002g0016 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1509+644_1509+647d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451671 | ||||||
| chr7:7451754
|
G | A | 2 | a0001c0005t0001g0098a0001c0005t0001g0099 | 2 | HG00099.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1509+565C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451754 | ||||||
| chr7:7451862
|
T | C | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1509+457A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451862 | ||||||
| chr7:7451867
|
T | G | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1509+452A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451867 | ||||||
| chr7:7451887
|
C | T | 61 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1509+432G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451887 | ||||||
| chr7:7451888
|
G | T | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+431C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451888 | ||||||
| chr7:7451929
|
C | T | 6 | a0002c0002t0002g0004a0002c0002t0002g0182a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1509+390G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451929 | ||||||
| chr7:7451972
|
T | A | 2 | a0018c0023t0003g0165a0027c0042t0002g0089 | 2 | HG01081.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1509+347A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7451972 | ||||||
| chr7:7452157
|
T | C | 7 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+162A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452157 | ||||||
| chr7:7452159
|
T | C | 1 | a0006c0019t0002g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1509+160A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452159 | ||||||
| chr7:7452185
|
C | G | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+134G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452185 | ||||||
| chr7:7452211
|
G | A | 20 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1509+108C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452211 | ||||||
| chr7:7452229
|
C | T | 13 | a0002c0002t0002g0015a0002c0002t0006g0002a0002c0004t0003g0026others(10): Show | 13 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1509+90G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452229 | ||||||
| chr7:7452230
|
A | G | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1509+89T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452230 | ||||||
| chr7:7452234
|
A | G | 68 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1509+85T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452234 | ||||||
| chr7:7452235
|
G | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1509+84C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452235 | ||||||
| chr7:7452242
|
A | C | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1509+77T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452242 | ||||||
| chr7:7452243
|
G | T | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1509+76C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452243 | ||||||
| chr7:7452277
|
T | G | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1509+42A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 18/34 | chr7 | 7452277 | ||||||
| chr7:7452510
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1441-123A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7452510 | ||||||
| chr7:7452544
|
A | G | 5 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0128others(2): Show | 5 | HG00642.hp1 HG03490.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-157T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7452544 | ||||||
| chr7:7452586
|
T | C | 39 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0126others(36): Show | 39 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1441-199A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7452586 | ||||||
| chr7:7452657
|
G | C | 53 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1441-270C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7452657 | ||||||
| chr7:7452659
|
G | A | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1441-272C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7452659 | ||||||
| chr7:7452771
|
C | T | 114 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(111): Show | 114 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1441-384G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7452771 | ||||||
| chr7:7452953
|
A | G | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1440+487T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7452953 | ||||||
| chr7:7453184
|
G | C | 114 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0171others(111): Show | 114 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1440+256C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7453184 | ||||||
| chr7:7453233
|
A | T | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1440+207T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7453233 | ||||||
| chr7:7453364
|
C | T | 20 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(17): Show | 20 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1440+76G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 17/34 | chr7 | 7453364 | ||||||
| chr7:7453604
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1372-96A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7453604 | ||||||
| chr7:7453613
|
A | G | 6 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(3): Show | 6 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1372-105T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7453613 | ||||||
| chr7:7453708
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1372-200C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7453708 | ||||||
| chr7:7453796
|
GGAATGAA others(35): Show |
G | 20 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1372-330_1372-289d others(44): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7453796 | ||||||
| chr7:7453907
|
G | A | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1372-399C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7453907 | ||||||
| chr7:7453909
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1372-401A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7453909 | ||||||
| chr7:7454027
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1372-519T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454027 | ||||||
| chr7:7454054
|
A | T | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1372-546T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454054 | ||||||
| chr7:7454207
|
T | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1372-699A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454207 | ||||||
| chr7:7454230
|
G | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1372-722C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454230 | ||||||
| chr7:7454273
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1372-765C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454273 | ||||||
| chr7:7454325
|
A | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1372-817T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454325 | ||||||
| chr7:7454490
|
A | AT | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1372-983dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454490 | ||||||
| chr7:7454492
|
T | G | 1 | a0003c0003t0001g0081 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1372-984A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454492 | ||||||
| chr7:7454513
|
A | G | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1372-1005T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454513 | ||||||
| chr7:7454614
|
G | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1372-1106C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454614 | ||||||
| chr7:7454655
|
T | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1372-1147A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454655 | ||||||
| chr7:7454712
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1372-1204T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454712 | ||||||
| chr7:7454790
|
A | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1371+1254T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454790 | ||||||
| chr7:7454793
|
A | G | 1 | a0011c0012t0002g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1371+1251T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454793 | ||||||
| chr7:7454799
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1371+1245T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454799 | ||||||
| chr7:7454816
|
G | A | 3 | a0002c0002t0002g0015a0002c0049t0003g0189a0004c0006t0002g0007 | 3 | HG02451.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1371+1228C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454816 | ||||||
| chr7:7454817
|
G | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG01361.hp1 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1371+1227C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454817 | ||||||
| chr7:7454833
|
G | C | 82 | a0001c0001t0001g0157a0001c0001t0001g0158a0002c0002t0001g0066others(79): Show | 82 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1371+1211C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454833 | ||||||
| chr7:7454922
|
G | A | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1371+1122C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7454922 | ||||||
| chr7:7455083
|
C | T | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1371+961G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455083 | ||||||
| chr7:7455257
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1371+787T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455257 | ||||||
| chr7:7455287
|
G | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1371+757C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455287 | ||||||
| chr7:7455380
|
T | C | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1371+664A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455380 | ||||||
| chr7:7455523
|
T | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+521A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455523 | ||||||
| chr7:7455528
|
T | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+516A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455528 | ||||||
| chr7:7455529
|
G | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+515C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455529 | ||||||
| chr7:7455535
|
A | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+509T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455535 | ||||||
| chr7:7455536
|
T | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+508A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455536 | ||||||
| chr7:7455537
|
T | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+507A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455537 | ||||||
| chr7:7455538
|
C | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+506G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455538 | ||||||
| chr7:7455539
|
C | T | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+505G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455539 | ||||||
| chr7:7455553
|
T | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+491A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455553 | ||||||
| chr7:7455554
|
T | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+490A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455554 | ||||||
| chr7:7455559
|
T | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1371+485A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455559 | ||||||
| chr7:7455617
|
G | A | 1 | a0003c0003t0001g0074 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1371+427C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455617 | ||||||
| chr7:7455654
|
C | T | 3 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100 | 3 | HG00099.hp1 HG01255.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1371+390G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455654 | ||||||
| chr7:7455923
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1371+121A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 16/34 | chr7 | 7455923 | ||||||
| chr7:7456205
|
A | G | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1303-93T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456205 | ||||||
| chr7:7456232
|
A | G | 6 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(3): Show | 6 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-120T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456232 | ||||||
| chr7:7456265
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-153T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456265 | ||||||
| chr7:7456346
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0002g0135 | 2 | NA19084.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1303-234A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456346 | ||||||
| chr7:7456419
|
G | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-307C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456419 | ||||||
| chr7:7456442
|
G | A | 5 | a0011c0012t0002g0166a0015c0048t0002g0017a0021c0025t0002g0162others(2): Show | 5 | HG01346.hp2 HG02145.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-330C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456442 | ||||||
| chr7:7456480
|
G | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303-368C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456480 | ||||||
| chr7:7456511
|
C | G | 26 | a0002c0002t0002g0015a0002c0002t0006g0002a0002c0004t0003g0026others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1303-399G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456511 | ||||||
| chr7:7456551
|
T | C | 6 | a0001c0001t0001g0172a0011c0012t0002g0166a0015c0048t0002g0017others(3): Show | 6 | HG01346.hp2 HG01496.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-439A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456551 | ||||||
| chr7:7456687
|
G | A | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1303-575C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456687 | ||||||
| chr7:7456937
|
C | T | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1303-825G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7456937 | ||||||
| chr7:7457025
|
A | T | 1 | a0001c0007t0003g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1303-913T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457025 | ||||||
| chr7:7457039
|
G | C | 6 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-927C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457039 | ||||||
| chr7:7457074
|
C | T | 3 | a0001c0001t0001g0049a0016c0018t0001g0129a0016c0018t0001g0144 | 3 | HG01070.hp2 HG01433.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1303-962G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457074 | ||||||
| chr7:7457406
|
G | C | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1303-1294C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457406 | ||||||
| chr7:7457420
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-1308A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457420 | ||||||
| chr7:7457634
|
A | G | 2 | a0006c0030t0003g0065a0017c0020t0001g0086 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1303-1522T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457634 | ||||||
| chr7:7457754
|
G | T | 5 | a0011c0012t0002g0166a0015c0048t0002g0017a0021c0025t0002g0162others(2): Show | 5 | HG01346.hp2 HG02145.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-1642C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457754 | ||||||
| chr7:7457830
|
G | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303-1718C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457830 | ||||||
| chr7:7457832
|
C | G | 3 | a0001c0001t0009g0136a0016c0018t0001g0129a0016c0018t0001g0144 | 3 | HG01070.hp2 HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1303-1720G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457832 | ||||||
| chr7:7457834
|
G | A | 3 | a0007c0008t0006g0003a0020c0022t0002g0163a0032c0034t0003g0038 | 3 | HG01884.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1303-1722C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457834 | ||||||
| chr7:7457874
|
C | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1303-1762G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457874 | ||||||
| chr7:7457888
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-1776G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457888 | ||||||
| chr7:7457892
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-1780T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457892 | ||||||
| chr7:7457950
|
T | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-1838A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457950 | ||||||
| chr7:7457964
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-1852C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7457964 | ||||||
| chr7:7458045
|
C | T | 21 | a0001c0001t0001g0018a0001c0001t0001g0085a0001c0001t0001g0130others(18): Show | 21 | HG00423.hp2 HG01070.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1303-1933G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458045 | ||||||
| chr7:7458105
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1303-1993T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458105 | ||||||
| chr7:7458154
|
C | T | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1303-2042G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458154 | ||||||
| chr7:7458192
|
G | A | 4 | a0006c0015t0002g0101a0006c0015t0002g0179a0006c0019t0002g0187others(1): Show | 4 | HG01243.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303-2080C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458192 | ||||||
| chr7:7458233
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1303-2121T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458233 | ||||||
| chr7:7458250
|
C | G | 1 | a0002c0004t0003g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1303-2138G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458250 | ||||||
| chr7:7458338
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-2226G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458338 | ||||||
| chr7:7458340
|
G | A | 1 | a0004c0039t0003g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1303-2228C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458340 | ||||||
| chr7:7458390
|
T | C | 17 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(14): Show | 17 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1303-2278A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458390 | ||||||
| chr7:7458403
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-2291A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458403 | ||||||
| chr7:7458411
|
T | C | 6 | a0002c0002t0002g0004a0002c0002t0002g0182a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-2299A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458411 | ||||||
| chr7:7458456
|
C | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-2344G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458456 | ||||||
| chr7:7458679
|
T | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-2567A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458679 | ||||||
| chr7:7458717
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1303-2605G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458717 | ||||||
| chr7:7458774
|
C | T | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-2662G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458774 | ||||||
| chr7:7458819
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-2707G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458819 | ||||||
| chr7:7458820
|
C | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-2708G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458820 | ||||||
| chr7:7458898
|
G | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1303-2786C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458898 | ||||||
| chr7:7458956
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-2844T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7458956 | ||||||
| chr7:7459040
|
G | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1303-2928C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459040 | ||||||
| chr7:7459134
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3022C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459134 | ||||||
| chr7:7459159
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3047T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459159 | ||||||
| chr7:7459183
|
T | C | 1 | a0007c0008t0006g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1303-3071A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459183 | ||||||
| chr7:7459190
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3078T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459190 | ||||||
| chr7:7459218
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3106A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459218 | ||||||
| chr7:7459262
|
A | C | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1303-3150T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459262 | ||||||
| chr7:7459268
|
A | C | 6 | a0006c0015t0002g0101a0006c0015t0002g0179a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-3156T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459268 | ||||||
| chr7:7459276
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3164T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459276 | ||||||
| chr7:7459362
|
C | A | 74 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1303-3250G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459362 | ||||||
| chr7:7459445
|
G | C | 2 | a0001c0005t0002g0067a0001c0005t0002g0069 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1303-3333C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459445 | ||||||
| chr7:7459460
|
C | T | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-3348G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459460 | ||||||
| chr7:7459490
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3378G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459490 | ||||||
| chr7:7459507
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3395A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459507 | ||||||
| chr7:7459513
|
T | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3401A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459513 | ||||||
| chr7:7459522
|
A | C | 7 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-3410T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459522 | ||||||
| chr7:7459613
|
C | T | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-3501G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459613 | ||||||
| chr7:7459650
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-3538G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459650 | ||||||
| chr7:7459698
|
G | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303-3586C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7459698 | ||||||
| chr7:7460012
|
A | G | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1303-3900T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460012 | ||||||
| chr7:7460040
|
A | T | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-3928T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460040 | ||||||
| chr7:7460130
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4018A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460130 | ||||||
| chr7:7460199
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4087A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460199 | ||||||
| chr7:7460218
|
C | T | 7 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-4106G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460218 | ||||||
| chr7:7460222
|
C | A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1303-4110G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460222 | ||||||
| chr7:7460222
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4110G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460222 | ||||||
| chr7:7460321
|
T | G | 1 | a0001c0001t0002g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1303-4209A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460321 | ||||||
| chr7:7460339
|
G | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4227C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460339 | ||||||
| chr7:7460450
|
T | G | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1303-4338A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460450 | ||||||
| chr7:7460517
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4405C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460517 | ||||||
| chr7:7460528
|
C | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4416G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460528 | ||||||
| chr7:7460529
|
G | A | 6 | a0009c0014t0003g0021a0010c0013t0002g0019a0010c0013t0002g0022others(3): Show | 6 | HG02257.hp1 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-4417C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460529 | ||||||
| chr7:7460540
|
C | T | 1 | a0006c0015t0002g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1303-4428G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460540 | ||||||
| chr7:7460573
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4461T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460573 | ||||||
| chr7:7460584
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4472C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460584 | ||||||
| chr7:7460625
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4513C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460625 | ||||||
| chr7:7460724
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1303-4612A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460724 | ||||||
| chr7:7460731
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4619G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460731 | ||||||
| chr7:7460737
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4625A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460737 | ||||||
| chr7:7460804
|
C | G | 5 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-4692G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460804 | ||||||
| chr7:7460895
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4783C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460895 | ||||||
| chr7:7460931
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4819G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460931 | ||||||
| chr7:7460959
|
A | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-4847T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7460959 | ||||||
| chr7:7461079
|
T | C | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-4967A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461079 | ||||||
| chr7:7461115
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-5003A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461115 | ||||||
| chr7:7461120
|
C | T | 1 | a0031c0033t0003g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1303-5008G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461120 | ||||||
| chr7:7461197
|
G | A | 10 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1303-5085C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461197 | ||||||
| chr7:7461327
|
G | T | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1303-5215C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461327 | ||||||
| chr7:7461352
|
C | A | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-5240G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461352 | ||||||
| chr7:7461352
|
C | T | 2 | a0018c0023t0003g0165a0027c0042t0002g0089 | 2 | HG01081.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1303-5240G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461352 | ||||||
| chr7:7461373
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1303-5261C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461373 | ||||||
| chr7:7461486
|
G | C | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1303-5374C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461486 | ||||||
| chr7:7461512
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-5400G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461512 | ||||||
| chr7:7461581
|
A | C | 1 | a0011c0027t0003g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1303-5469T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461581 | ||||||
| chr7:7461582
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-5470G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461582 | ||||||
| chr7:7461601
|
A | G | 107 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1303-5489T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461601 | ||||||
| chr7:7461695
|
A | T | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1303-5583T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461695 | ||||||
| chr7:7461717
|
C | T | 2 | a0001c0005t0002g0067a0001c0005t0002g0069 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1303-5605G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461717 | ||||||
| chr7:7461782
|
C | T | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-5670G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461782 | ||||||
| chr7:7461838
|
A | G | 30 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1303-5726T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461838 | ||||||
| chr7:7461868
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-5756C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461868 | ||||||
| chr7:7461868
|
G | C | 13 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(10): Show | 13 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1303-5756C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461868 | ||||||
| chr7:7461874
|
T | A | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-5762A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461874 | ||||||
| chr7:7461907
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-5795T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461907 | ||||||
| chr7:7461933
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-5821G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461933 | ||||||
| chr7:7461935
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1303-5823C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461935 | ||||||
| chr7:7461962
|
A | T | 1 | a0005c0010t0001g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1303-5850T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7461962 | ||||||
| chr7:7462060
|
G | A | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-5948C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462060 | ||||||
| chr7:7462065
|
C | T | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1303-5953G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462065 | ||||||
| chr7:7462105
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-5993T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462105 | ||||||
| chr7:7462196
|
G | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1303-6084C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462196 | ||||||
| chr7:7462200
|
C | T | 1 | a0006c0019t0002g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1303-6088G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462200 | ||||||
| chr7:7462309
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-6197G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462309 | ||||||
| chr7:7462322
|
T | C | 5 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-6210A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462322 | ||||||
| chr7:7462324
|
T | C | 2 | a0001c0001t0005g0011a0001c0007t0003g0148 | 2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1303-6212A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462324 | ||||||
| chr7:7462407
|
G | C | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-6295C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462407 | ||||||
| chr7:7462415
|
G | C | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1303-6303C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462415 | ||||||
| chr7:7462498
|
A | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-6386T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462498 | ||||||
| chr7:7462513
|
AATAG | A | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1303-6405_1303-640 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462513 | ||||||
| chr7:7462657
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-6545T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462657 | ||||||
| chr7:7462687
|
C | G | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-6575G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462687 | ||||||
| chr7:7462784
|
G | A | 16 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(13): Show | 16 | HG02486.hp1 HG02559.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1303-6672C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462784 | ||||||
| chr7:7462794
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-6682T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462794 | ||||||
| chr7:7462817
|
C | T | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1303-6705G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462817 | ||||||
| chr7:7462861
|
CA | C | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-6750delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462861 | ||||||
| chr7:7462861
|
CAA | C | 55 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1303-6751_1303-675 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462861 | ||||||
| chr7:7462871
|
AAAAAGAA others(5): Show |
A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-6771_1303-676 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462871 | ||||||
| chr7:7462908
|
G | A | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-6796C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7462908 | ||||||
| chr7:7463008
|
C | A | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-6896G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463008 | ||||||
| chr7:7463060
|
T | C | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1303-6948A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463060 | ||||||
| chr7:7463157
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-7045A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463157 | ||||||
| chr7:7463208
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1303-7096C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463208 | ||||||
| chr7:7463248
|
TAAG | T | 3 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100 | 3 | HG00099.hp1 HG01255.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1303-7139_1303-713 others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463248 | ||||||
| chr7:7463253
|
A | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-7141T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463253 | ||||||
| chr7:7463393
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-7281T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463393 | ||||||
| chr7:7463419
|
T | C | 27 | a0002c0002t0002g0015a0002c0002t0006g0002a0002c0004t0003g0026others(24): Show | 27 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1303-7307A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463419 | ||||||
| chr7:7463624
|
G | C | 5 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0110others(2): Show | 5 | HG00140.hp2 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-7512C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463624 | ||||||
| chr7:7463653
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1303-7541G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463653 | ||||||
| chr7:7463695
|
G | A | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-7583C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463695 | ||||||
| chr7:7463741
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1303-7629T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463741 | ||||||
| chr7:7463767
|
A | C | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-7655T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463767 | ||||||
| chr7:7463768
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-7656T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463768 | ||||||
| chr7:7463775
|
T | C | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1303-7663A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463775 | ||||||
| chr7:7463778
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-7666C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463778 | ||||||
| chr7:7463793
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-7681C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7463793 | ||||||
| chr7:7464011
|
T | C | 6 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(3): Show | 6 | HG02109.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-7899A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464011 | ||||||
| chr7:7464143
|
G | C | 22 | a0002c0002t0002g0015a0002c0049t0003g0189a0004c0006t0002g0005others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1303-8031C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464143 | ||||||
| chr7:7464173
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-8061A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464173 | ||||||
| chr7:7464205
|
A | G | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1303-8093T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464205 | ||||||
| chr7:7464217
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1303-8105G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464217 | ||||||
| chr7:7464229
|
G | T | 1 | a0001c0001t0002g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1303-8117C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464229 | ||||||
| chr7:7464248
|
G | T | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-8136C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464248 | ||||||
| chr7:7464255
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-8143C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464255 | ||||||
| chr7:7464308
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-8196G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464308 | ||||||
| chr7:7464380
|
G | A | 5 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-8268C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464380 | ||||||
| chr7:7464384
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-8272G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464384 | ||||||
| chr7:7464444
|
T | C | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1303-8332A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464444 | ||||||
| chr7:7464445
|
G | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1303-8333C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464445 | ||||||
| chr7:7464467
|
C | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-8355G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464467 | ||||||
| chr7:7464519
|
C | A | 4 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | NA19007.hp1 NA19011.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-8407G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464519 | ||||||
| chr7:7464698
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-8586T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464698 | ||||||
| chr7:7464864
|
T | C | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1303-8752A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464864 | ||||||
| chr7:7464865
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1303-8753A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464865 | ||||||
| chr7:7464890
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-8778G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464890 | ||||||
| chr7:7464968
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-8856G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7464968 | ||||||
| chr7:7465040
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1303-8928C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465040 | ||||||
| chr7:7465059
|
G | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-8947C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465059 | ||||||
| chr7:7465078
|
TGAAAAGA others(6059): Show |
T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+3457_1303-896 others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465078 | ||||||
| chr7:7465155
|
C | T | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1303-9043G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465155 | ||||||
| chr7:7465231
|
G | A | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1303-9119C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465231 | ||||||
| chr7:7465234
|
G | A | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-9122C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465234 | ||||||
| chr7:7465248
|
C | T | 33 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(30): Show | 33 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1303-9136G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465248 | ||||||
| chr7:7465259
|
C | T | 1 | a0003c0003t0001g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1303-9147G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465259 | ||||||
| chr7:7465274
|
C | T | 6 | a0009c0014t0003g0021a0010c0013t0002g0019a0010c0013t0002g0022others(3): Show | 6 | HG02257.hp1 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-9162G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465274 | ||||||
| chr7:7465275
|
G | A | 7 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-9163C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465275 | ||||||
| chr7:7465276
|
A | AG | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1303-9165dupC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465276 | ||||||
| chr7:7465343
|
C | T | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1303-9231G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465343 | ||||||
| chr7:7465369
|
T | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+9232A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465369 | ||||||
| chr7:7465433
|
C | A | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+9168G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465433 | ||||||
| chr7:7465443
|
C | G | 4 | a0007c0008t0003g0012a0007c0008t0003g0013a0014c0017t0003g0057others(1): Show | 4 | HG02257.hp2 HG02572.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+9158G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465443 | ||||||
| chr7:7465462
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1302+9139C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465462 | ||||||
| chr7:7465465
|
A | G | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+9136T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465465 | ||||||
| chr7:7465469
|
C | T | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1302+9132G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465469 | ||||||
| chr7:7465497
|
T | A | 1 | a0001c0005t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1302+9104A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465497 | ||||||
| chr7:7465515
|
A | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1302+9086T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465515 | ||||||
| chr7:7465574
|
C | T | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+9027G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465574 | ||||||
| chr7:7465575
|
G | A | 1 | a0005c0010t0001g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1302+9026C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465575 | ||||||
| chr7:7465576
|
A | G | 21 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(18): Show | 21 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+9025T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465576 | ||||||
| chr7:7465941
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+8660C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7465941 | ||||||
| chr7:7466111
|
C | T | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+8490G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466111 | ||||||
| chr7:7466117
|
A | C | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+8484T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466117 | ||||||
| chr7:7466163
|
C | T | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1302+8438G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466163 | ||||||
| chr7:7466289
|
C | T | 1 | a0001c0001t0009g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1302+8312G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466289 | ||||||
| chr7:7466298
|
C | T | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+8303G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466298 | ||||||
| chr7:7466386
|
A | C | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+8215T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466386 | ||||||
| chr7:7466465
|
C | A | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+8136G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466465 | ||||||
| chr7:7466482
|
G | T | 1 | a0001c0001t0002g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1302+8119C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466482 | ||||||
| chr7:7466516
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1302+8085T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466516 | ||||||
| chr7:7466517
|
C | G | 112 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1302+8084G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466517 | ||||||
| chr7:7466581
|
G | A | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+8020C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466581 | ||||||
| chr7:7466601
|
C | G | 106 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(103): Show | 106 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1302+8000G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466601 | ||||||
| chr7:7466615
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1302+7986C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466615 | ||||||
| chr7:7466750
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+7851G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466750 | ||||||
| chr7:7466760
|
G | A | 4 | a0002c0004t0003g0027a0007c0008t0006g0003a0020c0022t0002g0163others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+7841C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466760 | ||||||
| chr7:7466836
|
A | G | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1302+7765T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466836 | ||||||
| chr7:7466891
|
T | C | 2 | a0001c0005t0002g0067a0001c0005t0002g0069 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1302+7710A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466891 | ||||||
| chr7:7466912
|
A | C | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1302+7689T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466912 | ||||||
| chr7:7466957
|
C | T | 1 | a0020c0022t0002g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1302+7644G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466957 | ||||||
| chr7:7466980
|
C | T | 7 | a0004c0006t0002g0008a0009c0014t0003g0021a0010c0013t0002g0019others(4): Show | 7 | HG02257.hp1 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+7621G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466980 | ||||||
| chr7:7466990
|
C | T | 1 | a0007c0008t0003g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1302+7611G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7466990 | ||||||
| chr7:7467023
|
C | T | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+7578G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467023 | ||||||
| chr7:7467091
|
A | T | 1 | a0002c0002t0002g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1302+7510T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467091 | ||||||
| chr7:7467170
|
T | A | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+7431A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467170 | ||||||
| chr7:7467187
|
T | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+7414A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467187 | ||||||
| chr7:7467207
|
A | G | 6 | a0006c0015t0002g0101a0006c0015t0002g0179a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+7394T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467207 | ||||||
| chr7:7467219
|
G | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+7382C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467219 | ||||||
| chr7:7467220
|
T | C | 3 | a0003c0047t0003g0045a0005c0010t0002g0044a0005c0044t0003g0039 | 3 | HG02486.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1302+7381A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467220 | ||||||
| chr7:7467465
|
C | G | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+7136G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467465 | ||||||
| chr7:7467497
|
C | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1302+7104G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467497 | ||||||
| chr7:7467541
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1302+7060T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467541 | ||||||
| chr7:7467594
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1302+7007C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467594 | ||||||
| chr7:7467603
|
G | A | 112 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1302+6998C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467603 | ||||||
| chr7:7467700
|
C | G | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+6901G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467700 | ||||||
| chr7:7467848
|
G | T | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+6753C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467848 | ||||||
| chr7:7467870
|
C | T | 5 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+6731G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7467870 | ||||||
| chr7:7468069
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1302+6532G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468069 | ||||||
| chr7:7468122
|
G | A | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+6479C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468122 | ||||||
| chr7:7468378
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1302+6223C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468378 | ||||||
| chr7:7468430
|
G | C | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+6171C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468430 | ||||||
| chr7:7468526
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1302+6075C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468526 | ||||||
| chr7:7468690
|
A | C | 1 | a0001c0007t0003g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1302+5911T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468690 | ||||||
| chr7:7468711
|
A | G | 2 | a0011c0012t0002g0166a0015c0048t0002g0017 | 2 | HG01346.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1302+5890T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468711 | ||||||
| chr7:7468741
|
A | C | 33 | a0002c0002t0001g0147a0002c0002t0002g0015a0002c0002t0002g0108others(30): Show | 33 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+5860T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468741 | ||||||
| chr7:7468747
|
A | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+5854T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468747 | ||||||
| chr7:7468772
|
A | G | 79 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(76): Show | 79 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.1302+5829T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468772 | ||||||
| chr7:7468843
|
G | A | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+5758C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468843 | ||||||
| chr7:7468865
|
T | C | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+5736A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468865 | ||||||
| chr7:7468910
|
C | A | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1302+5691G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468910 | ||||||
| chr7:7468936
|
T | A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1302+5665A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468936 | ||||||
| chr7:7468953
|
G | A | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+5648C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7468953 | ||||||
| chr7:7469145
|
A | T | 2 | a0001c0005t0002g0067a0001c0005t0002g0069 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1302+5456T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469145 | ||||||
| chr7:7469155
|
G | T | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+5446C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469155 | ||||||
| chr7:7469184
|
C | T | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+5417G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469184 | ||||||
| chr7:7469214
|
C | T | 15 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+5387G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469214 | ||||||
| chr7:7469341
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1302+5260C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469341 | ||||||
| chr7:7469382
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+5219G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469382 | ||||||
| chr7:7469535
|
G | C | 10 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0001g0066others(7): Show | 10 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+5066C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469535 | ||||||
| chr7:7469581
|
A | C | 1 | a0001c0007t0003g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1302+5020T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469581 | ||||||
| chr7:7469646
|
T | C | 6 | a0002c0002t0002g0004a0002c0002t0002g0182a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+4955A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469646 | ||||||
| chr7:7469660
|
C | T | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+4941G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469660 | ||||||
| chr7:7469779
|
A | G | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+4822T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469779 | ||||||
| chr7:7469830
|
G | A | 6 | a0002c0002t0002g0004a0002c0002t0002g0182a0008c0009t0003g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+4771C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7469830 | ||||||
| chr7:7470003
|
A | T | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+4598T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470003 | ||||||
| chr7:7470005
|
C | A | 1 | a0032c0034t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1302+4596G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470005 | ||||||
| chr7:7470007
|
C | G | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1302+4594G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470007 | ||||||
| chr7:7470112
|
A | G | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+4489T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470112 | ||||||
| chr7:7470126
|
A | G | 33 | a0002c0002t0001g0147a0002c0002t0002g0015a0002c0002t0002g0108others(30): Show | 33 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+4475T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470126 | ||||||
| chr7:7470199
|
A | G | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+4402T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470199 | ||||||
| chr7:7470438
|
A | G | 3 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0002g0170 | 3 | HG02818.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1302+4163T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470438 | ||||||
| chr7:7470468
|
C | T | 8 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(5): Show | 8 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+4133G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470468 | ||||||
| chr7:7470565
|
G | A | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+4036C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470565 | ||||||
| chr7:7470661
|
C | T | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+3940G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470661 | ||||||
| chr7:7470735
|
T | G | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+3866A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470735 | ||||||
| chr7:7470804
|
CT | C | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+3796delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470804 | ||||||
| chr7:7470839
|
T | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+3762A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470839 | ||||||
| chr7:7470856
|
T | C | 73 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(70): Show | 73 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.1302+3745A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470856 | ||||||
| chr7:7470868
|
AC | A | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+3732delG | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470868 | ||||||
| chr7:7470903
|
T | A | 1 | a0005c0010t0001g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1302+3698A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470903 | ||||||
| chr7:7470920
|
G | A | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+3681C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470920 | ||||||
| chr7:7470990
|
C | T | 29 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1302+3611G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7470990 | ||||||
| chr7:7471017
|
C | T | 18 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+3584G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471017 | ||||||
| chr7:7471071
|
C | G | 21 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(18): Show | 21 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+3530G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471071 | ||||||
| chr7:7471125
|
T | TA | 16 | a0001c0001t0001g0172a0002c0002t0002g0170a0002c0004t0003g0026others(13): Show | 16 | HG01243.hp1 HG01496.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+3475dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471125 | ||||||
| chr7:7471125
|
T | TAAAA | 20 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(17): Show | 20 | HG00423.hp1 HG00438.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1302+3472_1302+347 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471125 | ||||||
| chr7:7471125
|
T | TAAAAA | 6 | a0002c0002t0002g0182a0003c0003t0001g0084a0008c0009t0003g0180others(3): Show | 6 | HG00733.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+3471_1302+347 others(9): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471125 | ||||||
| chr7:7471125
|
TA | T | 28 | a0001c0001t0001g0055a0001c0001t0001g0097a0001c0001t0001g0120others(25): Show | 28 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+3475delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471125 | ||||||
| chr7:7471126
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1302+3475T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471126 | ||||||
| chr7:7471141
|
A | G | 22 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(19): Show | 22 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1302+3460T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471141 | ||||||
| chr7:7471143
|
A | AG | 5 | a0011c0012t0002g0166a0015c0048t0002g0017a0021c0025t0002g0162others(2): Show | 5 | HG01346.hp2 HG02145.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+3457_1302+345 others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471143 | ||||||
| chr7:7471215
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+3386T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471215 | ||||||
| chr7:7471306
|
A | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+3295T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471306 | ||||||
| chr7:7471345
|
G | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+3256C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471345 | ||||||
| chr7:7471383
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+3218A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471383 | ||||||
| chr7:7471443
|
T | C | 27 | a0002c0002t0002g0015a0002c0002t0006g0002a0002c0004t0003g0026others(24): Show | 27 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3158A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471443 | ||||||
| chr7:7471503
|
T | G | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+3098A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471503 | ||||||
| chr7:7471570
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+3031C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471570 | ||||||
| chr7:7471689
|
G | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+2912C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471689 | ||||||
| chr7:7471692
|
T | C | 95 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0001g0147others(92): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1302+2909A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471692 | ||||||
| chr7:7471706
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+2895A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471706 | ||||||
| chr7:7471732
|
T | C | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+2869A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471732 | ||||||
| chr7:7471738
|
C | T | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+2863G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471738 | ||||||
| chr7:7471763
|
C | T | 9 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0002g0159others(6): Show | 9 | HG00423.hp1 HG00438.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+2838G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471763 | ||||||
| chr7:7471896
|
A | G | 33 | a0002c0002t0001g0147a0002c0002t0002g0015a0002c0002t0002g0108others(30): Show | 33 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+2705T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471896 | ||||||
| chr7:7471910
|
G | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+2691C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471910 | ||||||
| chr7:7471913
|
A | G | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1302+2688T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471913 | ||||||
| chr7:7471973
|
C | A | 1 | a0002c0004t0003g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1302+2628G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471973 | ||||||
| chr7:7471999
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1302+2602T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7471999 | ||||||
| chr7:7472035
|
A | G | 95 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0001g0147others(92): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1302+2566T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472035 | ||||||
| chr7:7472128
|
C | T | 1 | a0002c0004t0003g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1302+2473G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472128 | ||||||
| chr7:7472215
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1302+2386T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472215 | ||||||
| chr7:7472218
|
T | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+2383A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472218 | ||||||
| chr7:7472230
|
G | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+2371C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472230 | ||||||
| chr7:7472233
|
C | G | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+2368G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472233 | ||||||
| chr7:7472329
|
A | T | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+2272T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472329 | ||||||
| chr7:7472342
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+2259T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472342 | ||||||
| chr7:7472342
|
A | T | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1302+2259T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472342 | ||||||
| chr7:7472387
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+2214C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472387 | ||||||
| chr7:7472427
|
C | CA | 8 | a0001c0001t0001g0034a0001c0001t0001g0104a0001c0001t0002g0107others(5): Show | 8 | HG00099.hp2 HG01346.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+2173dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472427 | ||||||
| chr7:7472439
|
T | A | 7 | a0002c0004t0003g0186a0006c0015t0002g0101a0006c0015t0002g0179others(4): Show | 7 | HG01243.hp2 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+2162A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472439 | ||||||
| chr7:7472472
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+2129G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472472 | ||||||
| chr7:7472485
|
C | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1302+2116G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472485 | ||||||
| chr7:7472619
|
T | A | 30 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1302+1982A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472619 | ||||||
| chr7:7472676
|
C | G | 6 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(3): Show | 6 | HG02647.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+1925G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472676 | ||||||
| chr7:7472808
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+1793T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472808 | ||||||
| chr7:7472844
|
A | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+1757T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472844 | ||||||
| chr7:7472890
|
T | G | 37 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(34): Show | 37 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1302+1711A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7472890 | ||||||
| chr7:7473110
|
G | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+1491C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473110 | ||||||
| chr7:7473279
|
C | T | 3 | a0002c0002t0002g0116a0002c0002t0002g0118a0002c0002t0002g0119 | 3 | HG00642.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1302+1322G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473279 | ||||||
| chr7:7473293
|
G | C | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+1308C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473293 | ||||||
| chr7:7473343
|
G | GA | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+1257dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473343 | ||||||
| chr7:7473368
|
A | C | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+1233T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473368 | ||||||
| chr7:7473401
|
A | C | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1302+1200T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473401 | ||||||
| chr7:7473434
|
A | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0054 | 3 | HG00438.hp2 HG02080.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1302+1167T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473434 | ||||||
| chr7:7473549
|
C | T | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1302+1052G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473549 | ||||||
| chr7:7473837
|
C | T | 107 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1302+764G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473837 | ||||||
| chr7:7473838
|
AGTGT | A | 9 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+759_1302+762d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473838 | ||||||
| chr7:7473909
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+692A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473909 | ||||||
| chr7:7473920
|
A | C | 1 | a0005c0010t0001g0105 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1302+681T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473920 | ||||||
| chr7:7473976
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+625T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7473976 | ||||||
| chr7:7474049
|
A | G | 34 | a0002c0002t0001g0147a0002c0002t0002g0015a0002c0002t0002g0108others(31): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+552T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474049 | ||||||
| chr7:7474056
|
C | CTCTCTAT others(12): Show |
2 | a0002c0002t0002g0037a0002c0004t0003g0041 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1302+544_1302+545i others(21): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474056 | ||||||
| chr7:7474058
|
A | C | 9 | a0001c0005t0002g0067a0002c0002t0001g0066a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+543T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474058 | ||||||
| chr7:7474070
|
A | AAT | 60 | a0002c0002t0001g0126a0002c0002t0001g0147a0002c0002t0002g0015others(57): Show | 60 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1302+529_1302+530d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474070 | ||||||
| chr7:7474070
|
A | AATAT | 2 | a0003c0003t0001g0077a0012c0016t0002g0016 | 2 | HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1302+527_1302+530d others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474070 | ||||||
| chr7:7474070
|
A | AATATATA others(14): Show |
8 | a0002c0002t0001g0066a0002c0002t0002g0004a0002c0004t0003g0030others(5): Show | 8 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+530_1302+531i others(23): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474070 | ||||||
| chr7:7474070
|
A | AATATATA others(16): Show |
5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+530_1302+531i others(25): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474070 | ||||||
| chr7:7474070
|
A | AATATATA others(399): Show |
1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+530_1302+531i others(408): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474070 | ||||||
| chr7:7474136
|
T | C | 95 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0001g0147others(92): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1302+465A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474136 | ||||||
| chr7:7474141
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1302+460A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474141 | ||||||
| chr7:7474166
|
C | T | 56 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1302+435G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474166 | ||||||
| chr7:7474211
|
G | C | 33 | a0002c0002t0001g0147a0002c0002t0002g0015a0002c0002t0002g0108others(30): Show | 33 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+390C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474211 | ||||||
| chr7:7474237
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1302+364A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474237 | ||||||
| chr7:7474397
|
T | G | 37 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(34): Show | 37 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1302+204A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 15/34 | chr7 | 7474397 | ||||||
| chr7:7474691
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0096 | 3 | HG01516.hp2 HG01517.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1234-22T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7474691 | ||||||
| chr7:7474700
|
C | T | 37 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(34): Show | 37 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1234-31G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7474700 | ||||||
| chr7:7474811
|
A | G | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1234-142T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7474811 | ||||||
| chr7:7475006
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1234-337A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475006 | ||||||
| chr7:7475067
|
A | G | 5 | a0002c0002t0002g0139a0003c0003t0004g0193a0003c0003t0004g0194others(2): Show | 5 | HG00438.hp1 HG00735.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-398T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475067 | ||||||
| chr7:7475163
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1234-494T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475163 | ||||||
| chr7:7475202
|
A | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1234-533T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475202 | ||||||
| chr7:7475224
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1234-555T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475224 | ||||||
| chr7:7475484
|
C | T | 1 | a0002c0049t0003g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1234-815G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475484 | ||||||
| chr7:7475585
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1234-916A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475585 | ||||||
| chr7:7475764
|
A | G | 6 | a0006c0015t0002g0101a0006c0015t0002g0179a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-1095T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475764 | ||||||
| chr7:7475833
|
G | C | 3 | a0007c0008t0006g0003a0020c0022t0002g0163a0032c0034t0003g0038 | 3 | HG01884.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1234-1164C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475833 | ||||||
| chr7:7475941
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1233+1171T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7475941 | ||||||
| chr7:7476019
|
G | A | 1 | a0002c0002t0001g0126 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1233+1093C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476019 | ||||||
| chr7:7476128
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1233+984C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476128 | ||||||
| chr7:7476324
|
C | CA | 7 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+787dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476324 | ||||||
| chr7:7476359
|
A | G | 6 | a0006c0015t0002g0101a0006c0015t0002g0179a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+753T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476359 | ||||||
| chr7:7476461
|
T | C | 1 | a0001c0001t0002g0152 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1233+651A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476461 | ||||||
| chr7:7476493
|
T | A | 86 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(83): Show | 86 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.1233+619A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476493 | ||||||
| chr7:7476624
|
G | C | 43 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1233+488C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476624 | ||||||
| chr7:7476756
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1233+356G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476756 | ||||||
| chr7:7476796
|
G | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1233+316C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476796 | ||||||
| chr7:7476887
|
G | A | 2 | a0002c0002t0002g0117a0029c0037t0001g0113 | 2 | HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1233+225C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476887 | ||||||
| chr7:7476987
|
A | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1233+125T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7476987 | ||||||
| chr7:7477052
|
T | C | 24 | a0002c0002t0001g0147a0002c0002t0002g0108a0002c0002t0002g0109others(21): Show | 24 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1233+60A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7477052 | ||||||
| chr7:7477064
|
G | A | 3 | a0007c0008t0006g0003a0020c0022t0002g0163a0032c0034t0003g0038 | 3 | HG01884.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1233+48C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7477064 | ||||||
| chr7:7477087
|
T | C | 1 | a0003c0003t0001g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1233+25A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 14/34 | chr7 | 7477087 | ||||||
| chr7:7477218
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1165-38C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477218 | ||||||
| chr7:7477273
|
T | A | 28 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1165-93A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477273 | ||||||
| chr7:7477278
|
T | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-98A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477278 | ||||||
| chr7:7477292
|
C | CA | 13 | a0002c0002t0002g0004a0002c0002t0002g0182a0003c0047t0003g0045others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1165-113dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477292 | ||||||
| chr7:7477327
|
T | C | 44 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(41): Show | 44 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1165-147A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477327 | ||||||
| chr7:7477425
|
G | A | 2 | a0005c0010t0001g0092a0005c0010t0001g0105 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1165-245C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477425 | ||||||
| chr7:7477643
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1165-463A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477643 | ||||||
| chr7:7477677
|
G | C | 1 | a0003c0003t0004g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1165-497C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477677 | ||||||
| chr7:7477735
|
C | T | 147 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(144): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1165-555G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477735 | ||||||
| chr7:7477766
|
G | T | 6 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-586C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477766 | ||||||
| chr7:7477908
|
C | T | 10 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165-728G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477908 | ||||||
| chr7:7477923
|
C | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG00140.hp1 HG00735.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1165-743G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477923 | ||||||
| chr7:7477992
|
T | C | 1 | a0032c0034t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1165-812A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7477992 | ||||||
| chr7:7478002
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1165-822G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478002 | ||||||
| chr7:7478003
|
G | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1165-823C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478003 | ||||||
| chr7:7478088
|
G | C | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1165-908C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478088 | ||||||
| chr7:7478092
|
AT | A | 7 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165-913delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478092 | ||||||
| chr7:7478161
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1165-981C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478161 | ||||||
| chr7:7478196
|
AGTGCTGA others(153): Show |
A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1165-1176_1165-101 others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478196 | ||||||
| chr7:7478221
|
C | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1165-1041G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478221 | ||||||
| chr7:7478262
|
C | T | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1165-1082G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478262 | ||||||
| chr7:7478505
|
C | T | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1165-1325G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478505 | ||||||
| chr7:7478534
|
C | T | 1 | a0025c0046t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1165-1354G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478534 | ||||||
| chr7:7478573
|
C | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-1393G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478573 | ||||||
| chr7:7478581
|
G | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1165-1401C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478581 | ||||||
| chr7:7478668
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1165-1488C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478668 | ||||||
| chr7:7478760
|
G | T | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1165-1580C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478760 | ||||||
| chr7:7478771
|
G | A | 17 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1165-1591C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478771 | ||||||
| chr7:7478783
|
G | A | 2 | a0012c0016t0002g0016a0027c0042t0002g0089 | 2 | HG01109.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1165-1603C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478783 | ||||||
| chr7:7478812
|
C | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(25): Show | 28 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1165-1632G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478812 | ||||||
| chr7:7478824
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-1644A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478824 | ||||||
| chr7:7478826
|
G | A | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1165-1646C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478826 | ||||||
| chr7:7478833
|
C | T | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1165-1653G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478833 | ||||||
| chr7:7478857
|
A | G | 17 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1165-1677T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478857 | ||||||
| chr7:7478871
|
T | C | 34 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(31): Show | 34 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1165-1691A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478871 | ||||||
| chr7:7478893
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-1713T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478893 | ||||||
| chr7:7478898
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1165-1718C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478898 | ||||||
| chr7:7478902
|
T | C | 40 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(37): Show | 40 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1165-1722A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478902 | ||||||
| chr7:7478937
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-1757C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478937 | ||||||
| chr7:7478952
|
C | T | 1 | a0002c0031t0001g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1165-1772G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478952 | ||||||
| chr7:7478953
|
G | A | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1165-1773C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7478953 | ||||||
| chr7:7479020
|
G | T | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1165-1840C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7479020 | ||||||
| chr7:7479053
|
C | T | 10 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165-1873G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7479053 | ||||||
| chr7:7479066
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-1886A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7479066 | ||||||
| chr7:7479229
|
T | C | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1165-2049A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7479229 | ||||||
| chr7:7479285
|
C | T | 107 | a0001c0001t0002g0171a0001c0001t0002g0178a0001c0001t0003g0173others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1165-2105G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7479285 | ||||||
| chr7:7479953
|
C | T | 113 | a0001c0001t0001g0172a0001c0001t0002g0171a0001c0001t0002g0178others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1165-2773G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7479953 | ||||||
| chr7:7479972
|
A | G | 113 | a0001c0001t0001g0172a0001c0001t0002g0171a0001c0001t0002g0178others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1165-2792T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7479972 | ||||||
| chr7:7480035
|
T | C | 113 | a0001c0001t0001g0172a0001c0001t0002g0171a0001c0001t0002g0178others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1165-2855A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7480035 | ||||||
| chr7:7480205
|
C | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-3025G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7480205 | ||||||
| chr7:7480415
|
G | A | 5 | a0009c0014t0003g0021a0010c0013t0002g0019a0010c0013t0002g0022others(2): Show | 5 | HG02257.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-3235C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7480415 | ||||||
| chr7:7480419
|
G | A | 2 | a0002c0002t0002g0117a0029c0037t0001g0113 | 2 | HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1165-3239C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7480419 | ||||||
| chr7:7480545
|
T | G | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1165-3365A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7480545 | ||||||
| chr7:7480719
|
C | A | 25 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1165-3539G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7480719 | ||||||
| chr7:7480835
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-3655G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7480835 | ||||||
| chr7:7481074
|
G | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1165-3894C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481074 | ||||||
| chr7:7481140
|
T | C | 23 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1165-3960A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481140 | ||||||
| chr7:7481301
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1165-4121G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481301 | ||||||
| chr7:7481340
|
G | A | 25 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1165-4160C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481340 | ||||||
| chr7:7481399
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-4219C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481399 | ||||||
| chr7:7481557
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-4377G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481557 | ||||||
| chr7:7481685
|
C | T | 17 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1165-4505G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481685 | ||||||
| chr7:7481762
|
T | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1165-4582A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481762 | ||||||
| chr7:7481873
|
T | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1165-4693A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481873 | ||||||
| chr7:7481934
|
T | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-4754A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7481934 | ||||||
| chr7:7482086
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1165-4906T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482086 | ||||||
| chr7:7482124
|
C | T | 4 | a0003c0003t0004g0193a0003c0003t0004g0194a0003c0003t0004g0195others(1): Show | 4 | HG00735.hp1 HG00741.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-4944G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482124 | ||||||
| chr7:7482175
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1165-4995A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482175 | ||||||
| chr7:7482448
|
C | T | 39 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(36): Show | 39 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1165-5268G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482448 | ||||||
| chr7:7482449
|
C | T | 5 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165-5269G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482449 | ||||||
| chr7:7482527
|
G | GA | 42 | a0001c0001t0001g0172a0001c0005t0002g0067a0002c0002t0001g0066others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1165-5348dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482527 | ||||||
| chr7:7482552
|
A | G | 40 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(37): Show | 40 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1165-5372T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482552 | ||||||
| chr7:7482589
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-5409A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482589 | ||||||
| chr7:7482606
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-5426T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482606 | ||||||
| chr7:7482697
|
G | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-5517C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482697 | ||||||
| chr7:7482712
|
T | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1165-5532A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482712 | ||||||
| chr7:7482910
|
T | C | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1165-5730A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7482910 | ||||||
| chr7:7483045
|
C | G | 25 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1165-5865G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483045 | ||||||
| chr7:7483175
|
C | T | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1165-5995G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483175 | ||||||
| chr7:7483306
|
C | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1164+6083G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483306 | ||||||
| chr7:7483500
|
T | C | 7 | a0007c0008t0003g0012a0007c0008t0003g0013a0007c0008t0003g0161others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1164+5889A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483500 | ||||||
| chr7:7483630
|
G | C | 17 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1164+5759C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483630 | ||||||
| chr7:7483704
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164+5685A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483704 | ||||||
| chr7:7483713
|
G | A | 1 | a0009c0014t0001g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1164+5676C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483713 | ||||||
| chr7:7483718
|
C | T | 10 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1164+5671G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483718 | ||||||
| chr7:7483831
|
A | T | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1164+5558T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7483831 | ||||||
| chr7:7484142
|
A | G | 4 | a0003c0003t0004g0193a0003c0003t0004g0194a0003c0003t0004g0195others(1): Show | 4 | HG00735.hp1 HG00741.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+5247T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484142 | ||||||
| chr7:7484166
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1164+5223T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484166 | ||||||
| chr7:7484231
|
G | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1164+5158C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484231 | ||||||
| chr7:7484257
|
G | C | 8 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(5): Show | 8 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164+5132C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484257 | ||||||
| chr7:7484273
|
T | G | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1164+5116A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484273 | ||||||
| chr7:7484543
|
AAAT | A | 4 | a0006c0015t0002g0101a0006c0015t0002g0179a0006c0019t0002g0187others(1): Show | 4 | HG01243.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+4843_1164+484 others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484543 | ||||||
| chr7:7484595
|
T | A | 13 | a0002c0002t0002g0182a0003c0047t0003g0045a0005c0010t0001g0043others(10): Show | 13 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164+4794A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484595 | ||||||
| chr7:7484637
|
AG | A | 3 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100 | 3 | HG00099.hp1 HG01255.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1164+4751delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484637 | ||||||
| chr7:7484760
|
G | C | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1164+4629C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484760 | ||||||
| chr7:7484853
|
G | C | 39 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(36): Show | 39 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1164+4536C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484853 | ||||||
| chr7:7484936
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1164+4453C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7484936 | ||||||
| chr7:7485012
|
T | G | 10 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1164+4377A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485012 | ||||||
| chr7:7485033
|
C | A | 88 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0001g0147others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1164+4356G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485033 | ||||||
| chr7:7485258
|
T | C | 32 | a0002c0002t0001g0147a0002c0002t0002g0015a0002c0002t0002g0108others(29): Show | 32 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1164+4131A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485258 | ||||||
| chr7:7485378
|
T | C | 7 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+4011A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485378 | ||||||
| chr7:7485577
|
A | G | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164+3812T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485577 | ||||||
| chr7:7485658
|
T | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164+3731A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485658 | ||||||
| chr7:7485665
|
T | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164+3724A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485665 | ||||||
| chr7:7485698
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164+3691C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485698 | ||||||
| chr7:7485774
|
G | C | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1164+3615C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485774 | ||||||
| chr7:7485776
|
C | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1164+3613G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485776 | ||||||
| chr7:7485882
|
A | G | 1 | a0002c0002t0001g0126 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1164+3507T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7485882 | ||||||
| chr7:7486137
|
T | C | 17 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1164+3252A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486137 | ||||||
| chr7:7486252
|
T | C | 51 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1164+3137A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486252 | ||||||
| chr7:7486275
|
T | G | 1 | a0009c0029t0003g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1164+3114A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486275 | ||||||
| chr7:7486280
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1164+3109T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486280 | ||||||
| chr7:7486302
|
C | G | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164+3087G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486302 | ||||||
| chr7:7486363
|
T | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1164+3026A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486363 | ||||||
| chr7:7486378
|
C | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164+3011G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486378 | ||||||
| chr7:7486415
|
T | C | 17 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1164+2974A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486415 | ||||||
| chr7:7486474
|
T | C | 3 | a0001c0001t0009g0136a0016c0018t0001g0129a0016c0018t0001g0144 | 3 | HG01070.hp2 HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1164+2915A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486474 | ||||||
| chr7:7486643
|
C | T | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+2746G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486643 | ||||||
| chr7:7486669
|
A | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1164+2720T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486669 | ||||||
| chr7:7486777
|
C | G | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164+2612G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486777 | ||||||
| chr7:7486972
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1164+2417C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486972 | ||||||
| chr7:7486993
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1164+2396A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7486993 | ||||||
| chr7:7487072
|
T | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1164+2317A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487072 | ||||||
| chr7:7487097
|
G | A | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1164+2292C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487097 | ||||||
| chr7:7487125
|
T | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1164+2264A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487125 | ||||||
| chr7:7487154
|
TA | T | 33 | a0002c0002t0001g0066a0002c0002t0001g0126a0002c0002t0002g0004others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.1164+2234delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487154 | ||||||
| chr7:7487180
|
A | G | 24 | a0001c0001t0001g0172a0002c0002t0001g0126a0002c0002t0002g0004others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1164+2209T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487180 | ||||||
| chr7:7487193
|
A | C | 6 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(3): Show | 6 | HG02647.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+2196T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487193 | ||||||
| chr7:7487196
|
CATTCTT | C | 17 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1164+2187_1164+219 others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487196 | ||||||
| chr7:7487221
|
G | C | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+2168C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487221 | ||||||
| chr7:7487259
|
A | T | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164+2130T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487259 | ||||||
| chr7:7487288
|
A | T | 25 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(22): Show | 25 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1164+2101T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487288 | ||||||
| chr7:7487296
|
C | T | 122 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1164+2093G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487296 | ||||||
| chr7:7487297
|
G | A | 2 | a0002c0002t0002g0015a0002c0049t0003g0189 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1164+2092C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487297 | ||||||
| chr7:7487375
|
C | T | 1 | a0003c0003t0001g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1164+2014G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487375 | ||||||
| chr7:7487404
|
C | T | 9 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(6): Show | 9 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+1985G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487404 | ||||||
| chr7:7487409
|
C | A | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164+1980G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487409 | ||||||
| chr7:7487423
|
C | T | 2 | a0018c0023t0003g0165a0027c0042t0002g0089 | 2 | HG01081.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1164+1966G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487423 | ||||||
| chr7:7487433
|
C | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1164+1956G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487433 | ||||||
| chr7:7487460
|
C | A | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+1929G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487460 | ||||||
| chr7:7487470
|
C | T | 1 | a0003c0003t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1164+1919G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487470 | ||||||
| chr7:7487556
|
C | T | 130 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1164+1833G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487556 | ||||||
| chr7:7487893
|
A | G | 16 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0002g0037others(13): Show | 16 | HG01346.hp2 HG01496.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1164+1496T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7487893 | ||||||
| chr7:7488048
|
C | G | 1 | a0002c0004t0003g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1164+1341G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488048 | ||||||
| chr7:7488101
|
G | A | 41 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1164+1288C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488101 | ||||||
| chr7:7488101
|
G | T | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1164+1288C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488101 | ||||||
| chr7:7488134
|
C | T | 6 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+1255G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488134 | ||||||
| chr7:7488183
|
T | C | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1164+1206A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488183 | ||||||
| chr7:7488288
|
C | T | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164+1101G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488288 | ||||||
| chr7:7488321
|
G | T | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1164+1068C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488321 | ||||||
| chr7:7488517
|
T | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1164+872A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488517 | ||||||
| chr7:7488540
|
T | C | 58 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1164+849A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488540 | ||||||
| chr7:7488659
|
G | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1164+730C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488659 | ||||||
| chr7:7488746
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1164+643A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488746 | ||||||
| chr7:7488754
|
A | G | 42 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1164+635T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488754 | ||||||
| chr7:7488777
|
A | G | 1 | a0001c0001t0009g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1164+612T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488777 | ||||||
| chr7:7488804
|
G | C | 23 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164+585C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488804 | ||||||
| chr7:7488823
|
A | G | 41 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1164+566T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488823 | ||||||
| chr7:7488861
|
C | A | 31 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(28): Show | 31 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.1164+528G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488861 | ||||||
| chr7:7488902
|
A | G | 32 | a0002c0002t0001g0147a0002c0002t0002g0015a0002c0002t0002g0108others(29): Show | 32 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1164+487T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488902 | ||||||
| chr7:7488981
|
C | T | 41 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1164+408G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7488981 | ||||||
| chr7:7489110
|
A | G | 6 | a0001c0001t0001g0172a0011c0012t0002g0166a0015c0048t0002g0017others(3): Show | 6 | HG01346.hp2 HG01496.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+279T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7489110 | ||||||
| chr7:7489120
|
C | A | 25 | a0002c0002t0001g0126a0002c0002t0002g0004a0002c0002t0002g0139others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1164+269G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7489120 | ||||||
| chr7:7489152
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0096 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1164+237A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7489152 | ||||||
| chr7:7489247
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1164+142C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7489247 | ||||||
| chr7:7489249
|
G | A | 75 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.1164+140C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7489249 | ||||||
| chr7:7489278
|
A | G | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164+111T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7489278 | ||||||
| chr7:7489320
|
C | T | 189 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1164+69G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 13/34 | chr7 | 7489320 | ||||||
| chr7:7489578
|
A | G | 2 | a0006c0030t0003g0065a0017c0020t0001g0086 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1096-121T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7489578 | ||||||
| chr7:7489583
|
G | A | 2 | a0018c0023t0003g0165a0027c0042t0002g0089 | 2 | HG01081.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1096-126C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7489583 | ||||||
| chr7:7489614
|
C | T | 3 | a0013c0011t0002g0035a0013c0011t0002g0036a0013c0011t0002g0064 | 3 | HG01070.hp1 HG02004.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1096-157G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7489614 | ||||||
| chr7:7489898
|
ACT | A | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1096-443_1096-442d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7489898 | ||||||
| chr7:7490025
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1095+553A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7490025 | ||||||
| chr7:7490058
|
C | G | 1 | a0002c0002t0002g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1095+520G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7490058 | ||||||
| chr7:7490135
|
T | C | 9 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(6): Show | 9 | HG01346.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1095+443A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7490135 | ||||||
| chr7:7490189
|
T | C | 6 | a0001c0001t0001g0172a0002c0002t0002g0170a0011c0012t0002g0166others(3): Show | 6 | HG01496.hp2 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+389A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7490189 | ||||||
| chr7:7490412
|
G | T | 1 | a0005c0010t0002g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1095+166C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 12/34 | chr7 | 7490412 | ||||||
| chr7:7490874
|
C | T | 40 | a0001c0001t0001g0172a0002c0002t0001g0066a0002c0002t0001g0126others(37): Show | 40 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1027-228G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7490874 | ||||||
| chr7:7490975
|
A | T | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1027-329T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7490975 | ||||||
| chr7:7490987
|
G | T | 164 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1027-341C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7490987 | ||||||
| chr7:7491046
|
G | A | 8 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(5): Show | 8 | HG02559.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-400C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491046 | ||||||
| chr7:7491113
|
C | T | 3 | a0002c0002t0001g0147a0002c0002t0002g0141a0023c0021t0002g0025 | 3 | HG01346.hp1 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1027-467G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491113 | ||||||
| chr7:7491128
|
A | G | 4 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1027-482T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491128 | ||||||
| chr7:7491237
|
T | A | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1027-591A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491237 | ||||||
| chr7:7491278
|
T | C | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1027-632A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491278 | ||||||
| chr7:7491326
|
G | C | 7 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-680C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491326 | ||||||
| chr7:7491375
|
G | A | 76 | a0001c0001t0002g0171a0001c0005t0002g0067a0001c0005t0002g0069others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.1027-729C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491375 | ||||||
| chr7:7491446
|
C | G | 2 | a0001c0007t0003g0175a0001c0007t0003g0176 | 2 | HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1027-800G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491446 | ||||||
| chr7:7491491
|
T | C | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1027-845A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491491 | ||||||
| chr7:7491518
|
C | T | 30 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1027-872G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491518 | ||||||
| chr7:7491593
|
T | C | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1027-947A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491593 | ||||||
| chr7:7491637
|
T | C | 99 | a0001c0001t0001g0172a0001c0001t0002g0171a0001c0005t0001g0098others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1027-991A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491637 | ||||||
| chr7:7491771
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1027-1125G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491771 | ||||||
| chr7:7491811
|
C | T | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1027-1165G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491811 | ||||||
| chr7:7491988
|
G | A | 189 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1027-1342C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7491988 | ||||||
| chr7:7492174
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1027-1528A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492174 | ||||||
| chr7:7492188
|
G | A | 105 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.1027-1542C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492188 | ||||||
| chr7:7492279
|
T | A | 1 | a0006c0019t0002g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1027-1633A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492279 | ||||||
| chr7:7492478
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG00280.hp1 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-1832C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492478 | ||||||
| chr7:7492609
|
AAAG | A | 14 | a0001c0001t0001g0018a0001c0001t0001g0154a0001c0001t0001g0156others(11): Show | 14 | HG01243.hp1 HG01515.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1027-1966_1027-196 others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492609 | ||||||
| chr7:7492610
|
AAG | A | 74 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0085others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1027-1966_1027-196 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492610 | ||||||
| chr7:7492611
|
AG | A | 66 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1027-1966delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492611 | ||||||
| chr7:7492612
|
G | A | 33 | a0002c0002t0001g0126a0002c0002t0002g0110a0002c0002t0002g0139others(30): Show | 33 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1027-1966C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492612 | ||||||
| chr7:7492630
|
A | G | 9 | a0001c0001t0001g0172a0006c0030t0003g0065a0011c0012t0002g0166others(6): Show | 9 | HG01081.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1027-1984T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492630 | ||||||
| chr7:7492743
|
T | G | 5 | a0001c0001t0001g0172a0011c0012t0002g0166a0018c0023t0003g0165others(2): Show | 5 | HG01081.hp1 HG01496.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-2097A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492743 | ||||||
| chr7:7492766
|
A | C | 5 | a0001c0001t0001g0172a0011c0012t0002g0166a0018c0023t0003g0165others(2): Show | 5 | HG01081.hp1 HG01496.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-2120T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492766 | ||||||
| chr7:7492783
|
A | G | 7 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-2137T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492783 | ||||||
| chr7:7492833
|
A | C | 23 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1027-2187T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492833 | ||||||
| chr7:7492912
|
A | G | 30 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1027-2266T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492912 | ||||||
| chr7:7492969
|
T | C | 32 | a0001c0001t0001g0018a0001c0001t0001g0085a0001c0001t0001g0090others(29): Show | 32 | HG00423.hp2 HG00642.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1027-2323A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7492969 | ||||||
| chr7:7493057
|
A | AAT | 5 | a0009c0014t0003g0021a0010c0013t0002g0019a0010c0013t0002g0022others(2): Show | 5 | HG02257.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-2413_1027-241 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493057 | ||||||
| chr7:7493057
|
AAT | A | 25 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0001g0126others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1027-2413_1027-241 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493057 | ||||||
| chr7:7493085
|
CAAT | C | 10 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-2442_1027-244 others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493085 | ||||||
| chr7:7493169
|
C | G | 1 | a0002c0002t0001g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1027-2523G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493169 | ||||||
| chr7:7493237
|
A | G | 1 | a0002c0002t0001g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1027-2591T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493237 | ||||||
| chr7:7493473
|
T | C | 1 | a0001c0005t0002g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1027-2827A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493473 | ||||||
| chr7:7493599
|
G | C | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1027-2953C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493599 | ||||||
| chr7:7493642
|
T | C | 7 | a0002c0002t0001g0066a0002c0002t0002g0037a0002c0004t0003g0030others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-2996A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493642 | ||||||
| chr7:7493664
|
C | A | 31 | a0001c0007t0003g0102a0002c0002t0001g0126a0002c0002t0002g0139others(28): Show | 31 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.1027-3018G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493664 | ||||||
| chr7:7493668
|
T | C | 2 | a0006c0030t0003g0065a0017c0020t0001g0086 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1027-3022A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493668 | ||||||
| chr7:7493684
|
T | C | 36 | a0001c0001t0001g0140a0001c0001t0002g0178a0002c0002t0001g0147others(33): Show | 36 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1027-3038A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493684 | ||||||
| chr7:7493788
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1027-3142C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493788 | ||||||
| chr7:7493792
|
T | C | 31 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(28): Show | 31 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.1027-3146A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493792 | ||||||
| chr7:7493848
|
C | CGA | 5 | a0002c0002t0002g0015a0007c0008t0003g0012a0007c0008t0003g0161others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-3203_1027-320 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493848 | ||||||
| chr7:7493849
|
A | AAC | 34 | a0001c0001t0001g0140a0002c0002t0001g0066a0002c0002t0001g0147others(31): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1027-3205_1027-320 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493849 | ||||||
| chr7:7493849
|
A | C | 5 | a0002c0002t0002g0015a0007c0008t0003g0012a0007c0008t0003g0161others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-3203T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493849 | ||||||
| chr7:7493849
|
AAC | A | 40 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.1027-3205_1027-320 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7493849 | ||||||
| chr7:7494101
|
C | T | 1 | a0012c0016t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1027-3455G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494101 | ||||||
| chr7:7494233
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1027-3587A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494233 | ||||||
| chr7:7494277
|
G | A | 30 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1027-3631C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494277 | ||||||
| chr7:7494441
|
T | G | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1027-3795A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494441 | ||||||
| chr7:7494629
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1027-3983C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494629 | ||||||
| chr7:7494680
|
C | T | 3 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0084 | 3 | HG00733.hp2 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1027-4034G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494680 | ||||||
| chr7:7494734
|
C | A | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1027-4088G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494734 | ||||||
| chr7:7494918
|
A | G | 6 | a0001c0001t0001g0172a0011c0012t0002g0166a0018c0023t0003g0165others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027-4272T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494918 | ||||||
| chr7:7494926
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1027-4280T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494926 | ||||||
| chr7:7494950
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1027-4304T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494950 | ||||||
| chr7:7494984
|
C | T | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1027-4338G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7494984 | ||||||
| chr7:7495121
|
A | T | 36 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1027-4475T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495121 | ||||||
| chr7:7495127
|
A | G | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1027-4481T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495127 | ||||||
| chr7:7495326
|
T | C | 8 | a0002c0002t0002g0170a0003c0047t0003g0045a0005c0010t0001g0043others(5): Show | 8 | HG01346.hp2 HG02486.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-4680A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495326 | ||||||
| chr7:7495337
|
T | C | 8 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(5): Show | 8 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-4691A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495337 | ||||||
| chr7:7495348
|
G | A | 76 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0085others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.1027-4702C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495348 | ||||||
| chr7:7495405
|
A | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1027-4759T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495405 | ||||||
| chr7:7495546
|
C | T | 1 | a0002c0049t0003g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1027-4900G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495546 | ||||||
| chr7:7495750
|
A | G | 75 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0085others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(72): Show |
intron_variant | MODIFIER | c.1027-5104T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495750 | ||||||
| chr7:7495989
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1027-5343G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7495989 | ||||||
| chr7:7496281
|
G | T | 12 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1027-5635C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7496281 | ||||||
| chr7:7496290
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1027-5644T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7496290 | ||||||
| chr7:7496531
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1027-5885A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7496531 | ||||||
| chr7:7496551
|
CT | C | 32 | a0002c0002t0001g0126a0002c0002t0002g0139a0002c0002t0002g0170others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1027-5906delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7496551 | ||||||
| chr7:7496678
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1027-6032T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7496678 | ||||||
| chr7:7496875
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0009g0136a0016c0018t0001g0129others(1): Show | 4 | HG01070.hp2 HG01433.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1027-6229G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7496875 | ||||||
| chr7:7497058
|
G | A | 23 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1027-6412C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497058 | ||||||
| chr7:7497061
|
AGAAGGAA others(5): Show |
A | 5 | a0002c0002t0002g0015a0007c0008t0003g0013a0007c0008t0003g0161others(2): Show | 5 | HG01109.hp1 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-6427_1027-641 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497061 | ||||||
| chr7:7497082
|
A | AAAGG | 16 | a0002c0002t0001g0126a0002c0002t0002g0037a0002c0004t0003g0026others(13): Show | 16 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1027-6440_1027-643 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497082 | ||||||
| chr7:7497082
|
A | AAAGGAAG others(1): Show |
6 | a0001c0001t0001g0134a0001c0001t0002g0135a0003c0003t0001g0076others(3): Show | 6 | HG01167.hp1 HG02056.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027-6444_1027-643 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497082 | ||||||
| chr7:7497082
|
A | AAAGGAAG others(5): Show |
1 | a0003c0003t0002g0159 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1027-6437_1027-643 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497082 | ||||||
| chr7:7497082
|
AAAGGAAG others(9): Show |
A | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1027-6452_1027-643 others(20): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497082 | ||||||
| chr7:7497082
|
AAAGGAAG others(17): Show |
A | 6 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-6460_1027-643 others(28): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497082 | ||||||
| chr7:7497082
|
AAAGGAAG others(21): Show |
A | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1027-6464_1027-643 others(32): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497082 | ||||||
| chr7:7497086
|
GAAGGAAG others(1): Show |
G | 8 | a0002c0002t0002g0170a0002c0004t0003g0088a0003c0003t0001g0083others(5): Show | 8 | HG01346.hp2 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-6448_1027-644 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497086 | ||||||
| chr7:7497090
|
GAAGA | G | 12 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0004t0003g0027others(9): Show | 12 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1027-6448_1027-644 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497090 | ||||||
| chr7:7497094
|
A | AAAGG | 15 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0001g0094others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1027-6452_1027-644 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497094 | ||||||
| chr7:7497094
|
A | AAAGGAAG others(5): Show |
1 | a0001c0001t0001g0132 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1027-6449_1027-644 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497094 | ||||||
| chr7:7497094
|
A | AAAGGAAG others(1): Show |
24 | a0001c0001t0001g0018a0001c0001t0001g0085a0001c0001t0001g0093others(21): Show | 24 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1027-6456_1027-644 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497094 | ||||||
| chr7:7497094
|
A | AAAGGAAG others(5): Show |
4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0002g0107others(1): Show | 4 | HG00099.hp2 HG03017.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1027-6460_1027-644 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497094 | ||||||
| chr7:7497094
|
A | AAAGGAAG others(9): Show |
1 | a0001c0001t0001g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1027-6464_1027-644 others(20): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497094 | ||||||
| chr7:7497094
|
A | G | 41 | a0001c0001t0001g0134a0001c0001t0002g0135a0002c0002t0001g0066others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1027-6448T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497094 | ||||||
| chr7:7497094
|
AAAGG | A | 13 | a0001c0001t0001g0169a0001c0001t0001g0172a0002c0002t0002g0004others(10): Show | 13 | HG01496.hp2 HG01515.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1027-6452_1027-644 others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497094 | ||||||
| chr7:7497094
|
AAAGGAAG others(5): Show |
A | 4 | a0006c0030t0003g0065a0017c0020t0001g0086a0019c0024t0003g0167others(1): Show | 4 | HG02886.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1027-6460_1027-644 others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497094 | ||||||
| chr7:7497102
|
G | GAAGGAAG others(1): Show |
2 | a0003c0003t0001g0073a0003c0003t0001g0074 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1027-6457_1027-645 others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497102 | ||||||
| chr7:7497287
|
G | A | 144 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1027-6641C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497287 | ||||||
| chr7:7497404
|
T | C | 76 | a0001c0001t0002g0171a0001c0005t0002g0067a0001c0005t0002g0069others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.1027-6758A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497404 | ||||||
| chr7:7497407
|
C | A | 23 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1027-6761G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497407 | ||||||
| chr7:7497475
|
T | C | 36 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1027-6829A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497475 | ||||||
| chr7:7497565
|
AC | A | 2 | a0006c0030t0003g0065a0017c0020t0001g0086 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1027-6920delG | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497565 | ||||||
| chr7:7497713
|
A | G | 4 | a0001c0001t0001g0140a0002c0002t0001g0147a0002c0002t0002g0141others(1): Show | 4 | HG01081.hp2 HG01346.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-7067T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497713 | ||||||
| chr7:7497987
|
A | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1027-7341T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7497987 | ||||||
| chr7:7498015
|
T | C | 1 | a0003c0003t0004g0194 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1027-7369A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498015 | ||||||
| chr7:7498059
|
T | C | 22 | a0002c0002t0002g0015a0002c0002t0006g0002a0002c0004t0003g0026others(19): Show | 22 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1027-7413A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498059 | ||||||
| chr7:7498152
|
C | T | 8 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(5): Show | 8 | HG01243.hp2 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-7506G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498152 | ||||||
| chr7:7498218
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1027-7572C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498218 | ||||||
| chr7:7498223
|
A | T | 10 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0001g0066others(7): Show | 10 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-7577T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498223 | ||||||
| chr7:7498339
|
G | A | 1 | a0011c0027t0003g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1026+7675C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498339 | ||||||
| chr7:7498455
|
G | T | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1026+7559C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498455 | ||||||
| chr7:7498677
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1026+7337G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498677 | ||||||
| chr7:7498883
|
CT | C | 8 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(5): Show | 8 | HG01243.hp2 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026+7130delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498883 | ||||||
| chr7:7498910
|
G | GCA | 2 | a0019c0024t0003g0167a0027c0042t0002g0089 | 2 | HG03098.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1026+7102_1026+710 others(6): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498910 | ||||||
| chr7:7498912
|
A | G | 10 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026+7102T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498912 | ||||||
| chr7:7498916
|
A | T | 1 | a0003c0003t0001g0079 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1026+7098T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498916 | ||||||
| chr7:7498926
|
A | T | 23 | a0001c0001t0001g0018a0001c0001t0001g0085a0001c0001t0001g0090others(20): Show | 23 | HG00423.hp2 HG01070.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1026+7088T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498926 | ||||||
| chr7:7498930
|
A | G | 31 | a0002c0002t0001g0126a0002c0002t0002g0139a0002c0002t0002g0170others(28): Show | 31 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.1026+7084T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498930 | ||||||
| chr7:7498977
|
G | C | 16 | a0001c0001t0001g0172a0004c0006t0002g0005a0004c0006t0002g0006others(13): Show | 16 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1026+7037C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7498977 | ||||||
| chr7:7499032
|
C | T | 22 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1026+6982G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7499032 | ||||||
| chr7:7499268
|
A | G | 9 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(6): Show | 9 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026+6746T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7499268 | ||||||
| chr7:7499602
|
G | A | 36 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026+6412C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7499602 | ||||||
| chr7:7499829
|
C | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0104a0006c0015t0002g0101 | 3 | HG02258.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1026+6185G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7499829 | ||||||
| chr7:7500106
|
T | C | 1 | a0001c0007t0003g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1026+5908A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500106 | ||||||
| chr7:7500325
|
T | G | 1 | a0002c0004t0003g0032 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1026+5689A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500325 | ||||||
| chr7:7500347
|
T | C | 193 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1026+5667A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500347 | ||||||
| chr7:7500601
|
A | G | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1026+5413T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500601 | ||||||
| chr7:7500690
|
T | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1026+5324A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500690 | ||||||
| chr7:7500696
|
A | T | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1026+5318T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500696 | ||||||
| chr7:7500847
|
G | A | 32 | a0002c0002t0001g0126a0002c0002t0002g0139a0002c0002t0002g0170others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1026+5167C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500847 | ||||||
| chr7:7500928
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1026+5086G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500928 | ||||||
| chr7:7500938
|
G | A | 2 | a0002c0002t0006g0002a0028c0036t0010g0001 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1026+5076C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7500938 | ||||||
| chr7:7501146
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1026+4868C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7501146 | ||||||
| chr7:7501161
|
C | A | 21 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0001g0073others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1026+4853G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7501161 | ||||||
| chr7:7501406
|
T | A | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1026+4608A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7501406 | ||||||
| chr7:7501447
|
G | C | 6 | a0001c0001t0001g0172a0011c0012t0002g0166a0018c0023t0003g0165others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+4567C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7501447 | ||||||
| chr7:7501651
|
G | A | 8 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(5): Show | 8 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026+4363C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7501651 | ||||||
| chr7:7501677
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1026+4337A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7501677 | ||||||
| chr7:7501685
|
A | G | 10 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026+4329T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7501685 | ||||||
| chr7:7501951
|
A | G | 111 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(108): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1026+4063T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7501951 | ||||||
| chr7:7502039
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1026+3975G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502039 | ||||||
| chr7:7502083
|
C | T | 62 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(59): Show | 62 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1026+3931G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502083 | ||||||
| chr7:7502084
|
G | A | 1 | a0003c0003t0002g0159 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1026+3930C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502084 | ||||||
| chr7:7502161
|
A | T | 2 | a0001c0001t0008g0174a0001c0051t0008g0192 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1026+3853T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502161 | ||||||
| chr7:7502179
|
C | T | 1 | a0003c0003t0001g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1026+3835G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502179 | ||||||
| chr7:7502416
|
A | C | 9 | a0002c0002t0001g0126a0002c0002t0002g0139a0003c0003t0002g0159others(6): Show | 9 | HG00423.hp1 HG00438.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026+3598T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502416 | ||||||
| chr7:7502506
|
C | T | 113 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(110): Show | 113 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1026+3508G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502506 | ||||||
| chr7:7502528
|
T | G | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1026+3486A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502528 | ||||||
| chr7:7502550
|
A | G | 3 | a0005c0010t0001g0092a0005c0010t0001g0105a0015c0048t0002g0017 | 3 | HG01346.hp2 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1026+3464T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502550 | ||||||
| chr7:7502583
|
C | T | 12 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026+3431G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502583 | ||||||
| chr7:7502595
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1026+3419C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502595 | ||||||
| chr7:7502634
|
G | A | 113 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(110): Show | 113 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1026+3380C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502634 | ||||||
| chr7:7502678
|
AGATATTC others(293): Show |
A | 143 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(140): Show | 143 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1026+3036_1026+333 others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7502678 | ||||||
| chr7:7503131
|
G | C | 25 | a0001c0001t0001g0140a0001c0001t0002g0178a0001c0001t0003g0173others(22): Show | 25 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1026+2883C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7503131 | ||||||
| chr7:7503457
|
T | C | 1 | a0005c0010t0001g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1026+2557A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7503457 | ||||||
| chr7:7503513
|
C | A | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1026+2501G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7503513 | ||||||
| chr7:7503688
|
A | G | 1 | a0002c0004t0003g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1026+2326T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7503688 | ||||||
| chr7:7503948
|
C | A | 2 | a0006c0030t0003g0065a0017c0020t0001g0086 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1026+2066G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7503948 | ||||||
| chr7:7504005
|
C | T | 1 | a0005c0010t0001g0105 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1026+2009G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504005 | ||||||
| chr7:7504053
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1026+1961C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504053 | ||||||
| chr7:7504153
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1026+1861G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504153 | ||||||
| chr7:7504221
|
G | T | 25 | a0001c0001t0001g0140a0001c0001t0002g0178a0001c0001t0003g0173others(22): Show | 25 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1026+1793C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504221 | ||||||
| chr7:7504320
|
G | T | 1 | a0035c0041t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1026+1694C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504320 | ||||||
| chr7:7504461
|
C | G | 9 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(6): Show | 9 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026+1553G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504461 | ||||||
| chr7:7504481
|
C | G | 1 | a0001c0005t0001g0098 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1026+1533G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504481 | ||||||
| chr7:7504509
|
G | A | 36 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026+1505C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504509 | ||||||
| chr7:7504545
|
C | T | 2 | a0006c0030t0003g0065a0017c0020t0001g0086 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1026+1469G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504545 | ||||||
| chr7:7504691
|
C | A | 12 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026+1323G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504691 | ||||||
| chr7:7504783
|
C | G | 6 | a0001c0001t0001g0172a0011c0012t0002g0166a0018c0023t0003g0165others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+1231G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504783 | ||||||
| chr7:7504895
|
G | C | 10 | a0002c0002t0006g0002a0002c0004t0003g0026a0002c0004t0003g0027others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026+1119C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504895 | ||||||
| chr7:7504903
|
A | G | 12 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026+1111T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504903 | ||||||
| chr7:7504913
|
T | A | 76 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1026+1101A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7504913 | ||||||
| chr7:7505056
|
C | G | 6 | a0001c0001t0001g0172a0011c0012t0002g0166a0018c0023t0003g0165others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+958G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7505056 | ||||||
| chr7:7505111
|
G | A | 20 | a0002c0002t0001g0126a0003c0003t0001g0073a0003c0003t0001g0074others(17): Show | 20 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1026+903C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7505111 | ||||||
| chr7:7505157
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1026+857G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7505157 | ||||||
| chr7:7505198
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1026+816G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7505198 | ||||||
| chr7:7505225
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+789A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7505225 | ||||||
| chr7:7505444
|
C | G | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1026+570G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7505444 | ||||||
| chr7:7505487
|
G | A | 2 | a0009c0014t0003g0021a0026c0043t0007g0029 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1026+527C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7505487 | ||||||
| chr7:7505940
|
T | C | 36 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026+74A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 11/34 | chr7 | 7505940 | ||||||
| chr7:7506181
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.973-114C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 10/34 | chr7 | 7506181 | ||||||
| chr7:7506206
|
C | T | 11 | a0001c0005t0002g0067a0001c0005t0002g0069a0002c0002t0001g0066others(8): Show | 11 | HG01243.hp1 HG02559.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.973-139G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 10/34 | chr7 | 7506206 | ||||||
| chr7:7506336
|
G | A | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.973-269C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 10/34 | chr7 | 7506336 | ||||||
| chr7:7506552
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.973-485A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 10/34 | chr7 | 7506552 | ||||||
| chr7:7506667
|
A | C | 1 | a0015c0048t0002g0017 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.972+450T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 10/34 | chr7 | 7506667 | ||||||
| chr7:7507249
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18957.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.928-88G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7507249 | ||||||
| chr7:7507250
|
G | A | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.928-89C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7507250 | ||||||
| chr7:7507480
|
T | C | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.928-319A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7507480 | ||||||
| chr7:7507616
|
T | C | 19 | a0001c0001t0001g0140a0002c0002t0002g0108a0002c0002t0002g0109others(16): Show | 19 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.928-455A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7507616 | ||||||
| chr7:7507865
|
T | C | 19 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(16): Show | 19 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.928-704A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7507865 | ||||||
| chr7:7507931
|
T | A | 37 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(34): Show | 37 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.928-770A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7507931 | ||||||
| chr7:7508229
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.928-1068G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7508229 | ||||||
| chr7:7508231
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.928-1070G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7508231 | ||||||
| chr7:7508422
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.928-1261C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7508422 | ||||||
| chr7:7508723
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.928-1562G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7508723 | ||||||
| chr7:7508959
|
G | A | 1 | a0001c0001t0002g0152 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.928-1798C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7508959 | ||||||
| chr7:7509126
|
G | A | 5 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+1965C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509126 | ||||||
| chr7:7509144
|
T | C | 6 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+1947A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509144 | ||||||
| chr7:7509182
|
G | C | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.927+1909C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509182 | ||||||
| chr7:7509185
|
G | C | 117 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.927+1906C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509185 | ||||||
| chr7:7509274
|
G | A | 25 | a0001c0001t0001g0140a0002c0002t0002g0108a0002c0002t0002g0109others(22): Show | 25 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.927+1817C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509274 | ||||||
| chr7:7509276
|
A | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.927+1815T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509276 | ||||||
| chr7:7509309
|
G | A | 11 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.927+1782C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509309 | ||||||
| chr7:7509317
|
C | T | 7 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1774G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509317 | ||||||
| chr7:7509328
|
G | A | 6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG00280.hp1 HG01106.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+1763C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509328 | ||||||
| chr7:7509644
|
TG | T | 27 | a0001c0001t0002g0171a0003c0003t0001g0073a0003c0003t0001g0074others(24): Show | 27 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.927+1446delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509644 | ||||||
| chr7:7509645
|
G | T | 50 | a0001c0001t0001g0140a0001c0005t0002g0067a0001c0005t0002g0069others(47): Show | 50 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.927+1446C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509645 | ||||||
| chr7:7509648
|
G | T | 7 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(4): Show | 7 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1443C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509648 | ||||||
| chr7:7509785
|
A | G | 2 | a0007c0008t0003g0012a0007c0008t0003g0013 | 2 | HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.927+1306T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509785 | ||||||
| chr7:7509887
|
C | T | 7 | a0002c0002t0002g0015a0002c0049t0003g0189a0007c0008t0003g0012others(4): Show | 7 | HG01109.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+1204G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509887 | ||||||
| chr7:7509894
|
A | G | 11 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.927+1197T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7509894 | ||||||
| chr7:7510025
|
C | T | 28 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(25): Show | 28 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.927+1066G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510025 | ||||||
| chr7:7510037
|
C | T | 4 | a0003c0003t0001g0079a0003c0003t0001g0080a0003c0003t0001g0081others(1): Show | 4 | NA18612.hp1 NA18957.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+1054G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510037 | ||||||
| chr7:7510242
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.927+849T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510242 | ||||||
| chr7:7510274
|
T | TATTG | 12 | a0002c0004t0003g0088a0004c0006t0002g0005a0004c0006t0002g0006others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.927+813_927+816dup others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510274 | ||||||
| chr7:7510303
|
T | C | 2 | a0001c0001t0002g0146a0027c0042t0002g0089 | 2 | HG03654.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.927+788A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510303 | ||||||
| chr7:7510402
|
AG | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0104 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.927+688delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510402 | ||||||
| chr7:7510466
|
G | A | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.927+625C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510466 | ||||||
| chr7:7510743
|
T | G | 5 | a0002c0002t0002g0182a0008c0009t0003g0180a0008c0009t0003g0181others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+348A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510743 | ||||||
| chr7:7510818
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+273G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510818 | ||||||
| chr7:7510873
|
G | C | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.927+218C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510873 | ||||||
| chr7:7510916
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.927+175T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7510916 | ||||||
| chr7:7511001
|
T | G | 28 | a0001c0001t0001g0140a0002c0002t0001g0147a0002c0002t0002g0108others(25): Show | 28 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.927+90A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7511001 | ||||||
| chr7:7511028
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.927+63G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 9/34 | chr7 | 7511028 | ||||||
| chr7:7511177
|
G | A | 2 | a0021c0025t0002g0162a0022c0026t0007g0164 | 2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.883-42C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511177 | ||||||
| chr7:7511194
|
A | ATGTT | 8 | a0003c0047t0003g0045a0005c0010t0001g0043a0005c0010t0001g0092others(5): Show | 8 | HG01346.hp2 HG02486.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-63_883-60dupAA others(2): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511194 | ||||||
| chr7:7511281
|
T | G | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.883-146A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511281 | ||||||
| chr7:7511355
|
G | GAATAAAT others(3): Show |
1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.883-221_883-220ins others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511355 | ||||||
| chr7:7511358
|
C | A | 1 | a0002c0004t0003g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.883-223G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511358 | ||||||
| chr7:7511477
|
T | C | 194 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.883-342A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511477 | ||||||
| chr7:7511483
|
G | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG00280.hp1 HG01106.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-348C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511483 | ||||||
| chr7:7511657
|
C | T | 25 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(22): Show | 25 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.883-522G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511657 | ||||||
| chr7:7511812
|
A | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.883-677T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511812 | ||||||
| chr7:7511930
|
C | A | 25 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(22): Show | 25 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.883-795G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511930 | ||||||
| chr7:7511975
|
G | A | 5 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-840C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7511975 | ||||||
| chr7:7512231
|
G | T | 6 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-1096C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7512231 | ||||||
| chr7:7512394
|
T | C | 5 | a0009c0014t0003g0021a0010c0013t0002g0019a0010c0013t0002g0022others(2): Show | 5 | HG02257.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-1259A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7512394 | ||||||
| chr7:7512639
|
T | C | 131 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(128): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.883-1504A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7512639 | ||||||
| chr7:7512647
|
G | C | 25 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(22): Show | 25 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.883-1512C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7512647 | ||||||
| chr7:7512652
|
A | C | 5 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0007t0003g0175others(2): Show | 5 | HG02622.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-1517T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7512652 | ||||||
| chr7:7512803
|
G | T | 5 | a0009c0014t0003g0021a0010c0013t0002g0019a0010c0013t0002g0022others(2): Show | 5 | HG02257.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-1668C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7512803 | ||||||
| chr7:7512865
|
T | G | 1 | a0004c0039t0003g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-1730A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7512865 | ||||||
| chr7:7512982
|
A | C | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.883-1847T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7512982 | ||||||
| chr7:7513022
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.883-1887A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7513022 | ||||||
| chr7:7513436
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.883-2301C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7513436 | ||||||
| chr7:7513519
|
T | C | 1 | a0029c0037t0001g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.882+2295A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7513519 | ||||||
| chr7:7513684
|
A | G | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.882+2130T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7513684 | ||||||
| chr7:7513694
|
G | T | 7 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+2120C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7513694 | ||||||
| chr7:7513909
|
G | A | 32 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(29): Show | 32 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.882+1905C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7513909 | ||||||
| chr7:7514102
|
T | G | 161 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0046others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.882+1712A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514102 | ||||||
| chr7:7514177
|
AG | A | 28 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(25): Show | 28 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+1636delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514177 | ||||||
| chr7:7514208
|
C | T | 1 | a0027c0042t0002g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.882+1606G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514208 | ||||||
| chr7:7514265
|
T | C | 6 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+1549A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514265 | ||||||
| chr7:7514292
|
T | C | 1 | a0009c0014t0001g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.882+1522A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514292 | ||||||
| chr7:7514457
|
G | T | 25 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(22): Show | 25 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+1357C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514457 | ||||||
| chr7:7514583
|
G | A | 8 | a0006c0015t0002g0179a0006c0019t0002g0187a0006c0019t0002g0188others(5): Show | 8 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+1231C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514583 | ||||||
| chr7:7514583
|
G | C | 1 | a0002c0031t0001g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.882+1231C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514583 | ||||||
| chr7:7514672
|
C | T | 1 | a0001c0001t0009g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.882+1142G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514672 | ||||||
| chr7:7514679
|
G | A | 25 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(22): Show | 25 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+1135C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514679 | ||||||
| chr7:7514802
|
G | A | 24 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(21): Show | 24 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.882+1012C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514802 | ||||||
| chr7:7514814
|
C | T | 1 | a0002c0004t0003g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+1000G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514814 | ||||||
| chr7:7514874
|
G | A | 25 | a0003c0003t0001g0073a0003c0003t0001g0074a0003c0003t0001g0075others(22): Show | 25 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+940C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7514874 | ||||||
| chr7:7515012
|
G | A | 6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG00280.hp1 HG01106.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+802C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7515012 | ||||||
| chr7:7515134
|
T | G | 1 | a0002c0049t0003g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.882+680A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7515134 | ||||||
| chr7:7515275
|
C | T | 1 | a0006c0019t0002g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.882+539G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7515275 | ||||||
| chr7:7515318
|
T | G | 7 | a0002c0002t0002g0004a0002c0004t0003g0088a0004c0006t0002g0005others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+496A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7515318 | ||||||
| chr7:7515414
|
T | C | 143 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.882+400A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7515414 | ||||||
| chr7:7515802
|
T | A | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.882+12A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 8/34 | chr7 | 7515802 | ||||||
| chr7:7515924
|
G | C | 8 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-84C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7515924 | ||||||
| chr7:7515943
|
A | G | 1 | a0031c0033t0003g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.856-103T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7515943 | ||||||
| chr7:7515983
|
C | T | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-143G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7515983 | ||||||
| chr7:7516040
|
T | C | 1 | a0008c0009t0003g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.856-200A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516040 | ||||||
| chr7:7516082
|
C | T | 172 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.856-242G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516082 | ||||||
| chr7:7516104
|
T | C | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.856-264A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516104 | ||||||
| chr7:7516194
|
T | C | 77 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0090others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.856-354A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516194 | ||||||
| chr7:7516229
|
T | C | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-389A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516229 | ||||||
| chr7:7516328
|
C | T | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.856-488G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516328 | ||||||
| chr7:7516336
|
G | A | 7 | a0002c0002t0006g0002a0004c0006t0002g0005a0004c0006t0002g0006others(4): Show | 7 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-496C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516336 | ||||||
| chr7:7516472
|
C | A | 1 | a0001c0001t0001g0106 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.856-632G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516472 | ||||||
| chr7:7516675
|
T | G | 57 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(54): Show | 57 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.856-835A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516675 | ||||||
| chr7:7516716
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18957.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.856-876T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516716 | ||||||
| chr7:7516723
|
GTTCTATG others(9): Show |
G | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-899_856-884del others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516723 | ||||||
| chr7:7516757
|
C | CTATT | 11 | a0002c0002t0002g0004a0002c0002t0006g0002a0002c0049t0003g0189others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.856-921_856-918dup others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516757 | ||||||
| chr7:7516920
|
A | G | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.855+876T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516920 | ||||||
| chr7:7516926
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG00140.hp1 HG00735.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.855+870C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516926 | ||||||
| chr7:7516973
|
G | A | 1 | a0001c0005t0002g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.855+823C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516973 | ||||||
| chr7:7516981
|
C | G | 95 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(92): Show | 95 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.855+815G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7516981 | ||||||
| chr7:7517001
|
C | G | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.855+795G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517001 | ||||||
| chr7:7517019
|
A | G | 11 | a0002c0002t0002g0004a0002c0002t0006g0002a0002c0049t0003g0189others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.855+777T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517019 | ||||||
| chr7:7517072
|
C | A | 70 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(67): Show | 70 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.855+724G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517072 | ||||||
| chr7:7517124
|
A | T | 4 | a0009c0014t0003g0021a0010c0013t0002g0019a0010c0013t0002g0022others(1): Show | 4 | HG02257.hp1 HG03209.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+672T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517124 | ||||||
| chr7:7517218
|
G | T | 3 | a0002c0049t0003g0189a0006c0019t0002g0187a0006c0019t0002g0188 | 3 | HG01243.hp2 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.855+578C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517218 | ||||||
| chr7:7517271
|
T | A | 3 | a0002c0049t0003g0189a0006c0019t0002g0187a0006c0019t0002g0188 | 3 | HG01243.hp2 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.855+525A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517271 | ||||||
| chr7:7517358
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.855+438T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517358 | ||||||
| chr7:7517372
|
G | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.855+424C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517372 | ||||||
| chr7:7517419
|
T | C | 2 | a0006c0019t0002g0187a0006c0019t0002g0188 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.855+377A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517419 | ||||||
| chr7:7517465
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.855+331A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517465 | ||||||
| chr7:7517651
|
T | C | 3 | a0002c0002t0006g0002a0007c0008t0006g0003a0028c0036t0010g0001 | 3 | HG01243.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.855+145A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517651 | ||||||
| chr7:7517666
|
T | C | 183 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.855+130A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 7/34 | chr7 | 7517666 | ||||||
| chr7:7517839
|
T | A | 1 | a0018c0023t0003g0165 | 1 | HG01081.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.814-2A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7517839 | ||||||
| chr7:7517987
|
CA | C | 105 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0085others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.814-151delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7517987 | ||||||
| chr7:7518051
|
G | T | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.814-214C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7518051 | ||||||
| chr7:7518331
|
A | G | 3 | a0002c0049t0003g0189a0006c0019t0002g0187a0006c0019t0002g0188 | 3 | HG01243.hp2 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.814-494T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7518331 | ||||||
| chr7:7518585
|
C | T | 4 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(1): Show | 4 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-748G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7518585 | ||||||
| chr7:7518634
|
T | C | 189 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.814-797A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7518634 | ||||||
| chr7:7518641
|
A | C | 1 | a0003c0003t0004g0194 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.814-804T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7518641 | ||||||
| chr7:7518688
|
G | A | 55 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(52): Show | 55 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.814-851C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7518688 | ||||||
| chr7:7519236
|
C | T | 2 | a0002c0004t0003g0041a0032c0034t0003g0038 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.813+826G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519236 | ||||||
| chr7:7519271
|
A | G | 70 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(67): Show | 70 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.813+791T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519271 | ||||||
| chr7:7519276
|
C | T | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.813+786G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519276 | ||||||
| chr7:7519301
|
G | A | 9 | a0001c0001t0001g0042a0002c0004t0003g0041a0003c0047t0003g0045others(6): Show | 9 | HG02486.hp1 HG02630.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.813+761C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519301 | ||||||
| chr7:7519344
|
A | C | 1 | a0009c0029t0003g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.813+718T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519344 | ||||||
| chr7:7519407
|
C | T | 1 | a0034c0040t0002g0040 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.813+655G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519407 | ||||||
| chr7:7519535
|
C | A | 5 | a0002c0002t0002g0004a0004c0006t0002g0005a0004c0006t0002g0006others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+527G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519535 | ||||||
| chr7:7519895
|
A | G | 6 | a0001c0051t0008g0192a0002c0049t0003g0189a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+167T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519895 | ||||||
| chr7:7519910
|
A | C | 70 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(67): Show | 70 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.813+152T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519910 | ||||||
| chr7:7519994
|
T | C | 5 | a0002c0002t0002g0015a0007c0008t0003g0012a0007c0008t0003g0013others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.813+68A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7519994 | ||||||
| chr7:7520003
|
T | TA | 15 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0001t0008g0174others(12): Show | 15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.813+58dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7520003 | ||||||
| chr7:7520009
|
A | G | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+53T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 6/34 | chr7 | 7520009 | ||||||
| chr7:7520217
|
AT | A | 5 | a0002c0002t0002g0182a0004c0006t0002g0184a0008c0009t0003g0180others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-103delA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520217 | ||||||
| chr7:7520363
|
C | T | 1 | a0002c0049t0003g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-248G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520363 | ||||||
| chr7:7520372
|
C | T | 79 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(76): Show | 79 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.760-257G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520372 | ||||||
| chr7:7520407
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.760-292T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520407 | ||||||
| chr7:7520408
|
T | G | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.760-293A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520408 | ||||||
| chr7:7520561
|
T | C | 1 | a0012c0035t0002g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.760-446A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520561 | ||||||
| chr7:7520568
|
G | A | 1 | a0001c0051t0008g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.760-453C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520568 | ||||||
| chr7:7520611
|
C | T | 3 | a0002c0004t0003g0041a0032c0034t0003g0038a0034c0040t0002g0040 | 3 | HG02630.hp1 HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.760-496G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520611 | ||||||
| chr7:7520612
|
C | G | 6 | a0001c0051t0008g0192a0002c0049t0003g0189a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-497G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520612 | ||||||
| chr7:7520653
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.760-538C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520653 | ||||||
| chr7:7520667
|
G | C | 73 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(70): Show | 73 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.760-552C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520667 | ||||||
| chr7:7520713
|
G | A | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.760-598C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520713 | ||||||
| chr7:7520746
|
A | G | 9 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-631T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520746 | ||||||
| chr7:7520752
|
A | T | 1 | a0029c0037t0001g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.760-637T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520752 | ||||||
| chr7:7520869
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.760-754C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7520869 | ||||||
| chr7:7521068
|
A | G | 81 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(78): Show | 81 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.759+837T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7521068 | ||||||
| chr7:7521195
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.759+710G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7521195 | ||||||
| chr7:7521202
|
G | A | 74 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0090others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.759+703C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7521202 | ||||||
| chr7:7521443
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18957.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.759+462C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7521443 | ||||||
| chr7:7521482
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.759+423C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7521482 | ||||||
| chr7:7521780
|
T | C | 9 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+125A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 5/34 | chr7 | 7521780 | ||||||
| chr7:7522021
|
T | G | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.703-60A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522021 | ||||||
| chr7:7522099
|
TA | T | 5 | a0002c0002t0002g0004a0004c0006t0002g0005a0004c0006t0002g0006others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-139delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522099 | ||||||
| chr7:7522189
|
C | A | 5 | a0011c0012t0002g0166a0018c0023t0003g0165a0020c0022t0002g0163others(2): Show | 5 | HG01081.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-228G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522189 | ||||||
| chr7:7522419
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.703-458A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522419 | ||||||
| chr7:7522513
|
G | T | 1 | a0003c0003t0001g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703-552C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522513 | ||||||
| chr7:7522654
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.703-693C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522654 | ||||||
| chr7:7522741
|
T | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.703-780A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522741 | ||||||
| chr7:7522806
|
C | CA | 5 | a0001c0001t0001g0168a0010c0013t0002g0022a0011c0012t0002g0166others(2): Show | 5 | HG02145.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-846dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAA | 9 | a0001c0005t0002g0067a0002c0002t0002g0037a0002c0004t0003g0026others(6): Show | 9 | HG02055.hp1 HG02647.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.703-849_703-846dup others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAA | 6 | a0001c0005t0002g0069a0002c0002t0001g0066a0002c0004t0003g0032others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-850_703-846dup others(5): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAAAA | 6 | a0001c0001t0001g0050a0001c0001t0002g0051a0002c0004t0003g0186others(3): Show | 6 | HG01070.hp1 HG02004.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-852_703-846dup others(7): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAAAA others(1): Show |
16 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(13): Show | 16 | HG00438.hp2 HG00741.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.703-853_703-846dup others(8): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0060others(10): Show | 13 | HG00280.hp1 HG00733.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-854_703-846dup others(9): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAAAA others(3): Show |
8 | a0001c0001t0001g0049a0001c0001t0001g0082a0001c0001t0002g0063others(5): Show | 8 | HG01106.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-855_703-846dup others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAAAA others(4): Show |
3 | a0003c0003t0001g0083a0014c0017t0003g0057a0015c0052t0003g0191 | 3 | HG02109.hp2 NA18906.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.703-856_703-846dup others(11): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0172a0014c0017t0003g0058 | 2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.703-857_703-846dup others(12): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAAAA others(6): Show |
1 | a0004c0039t0003g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.703-858_703-846dup others(13): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CAAAAAAA others(9): Show |
1 | a0009c0014t0001g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.703-861_703-846dup others(16): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
C | CCAAAAAA others(3): Show |
3 | a0003c0047t0003g0045a0005c0010t0002g0044a0005c0044t0003g0039 | 3 | HG02486.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.703-846_703-845ins others(10): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
CA | C | 8 | a0002c0002t0002g0116a0002c0031t0001g0115a0012c0016t0002g0123others(5): Show | 8 | HG00642.hp2 HG00733.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-846delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
CAA | C | 17 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0001t0008g0174others(14): Show | 17 | HG00140.hp2 HG01496.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.703-847_703-846del others(2): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
CAAAAAAA others(4): Show |
C | 1 | a0004c0006t0002g0008 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.703-856_703-846del others(11): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
CAAAAAAA others(6): Show |
C | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.703-858_703-846del others(13): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
CAAAAAAA others(7): Show |
C | 79 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0090others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.703-859_703-846del others(14): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522806
|
CAAAAAAA others(8): Show |
C | 1 | a0016c0018t0001g0129 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.703-860_703-846del others(15): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522806 | ||||||
| chr7:7522837
|
G | A | 1 | a0033c0050t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.703-876C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522837 | ||||||
| chr7:7522860
|
G | C | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.703-899C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522860 | ||||||
| chr7:7522963
|
A | C | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.703-1002T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7522963 | ||||||
| chr7:7523023
|
T | C | 1 | a0007c0008t0003g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.703-1062A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523023 | ||||||
| chr7:7523047
|
A | T | 13 | a0001c0001t0002g0178a0001c0001t0003g0173a0001c0001t0008g0174others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-1086T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523047 | ||||||
| chr7:7523085
|
G | A | 8 | a0001c0001t0002g0171a0001c0051t0008g0192a0002c0002t0002g0170others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-1124C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523085 | ||||||
| chr7:7523179
|
A | T | 2 | a0003c0003t0001g0073a0003c0003t0001g0074 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.702+1050T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523179 | ||||||
| chr7:7523182
|
C | A | 2 | a0003c0003t0001g0073a0003c0003t0001g0074 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.702+1047G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523182 | ||||||
| chr7:7523182
|
CG | C | 189 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.702+1046delC | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523182 | ||||||
| chr7:7523183
|
G | C | 2 | a0003c0003t0001g0073a0003c0003t0001g0074 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.702+1046C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523183 | ||||||
| chr7:7523218
|
A | G | 182 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.702+1011T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523218 | ||||||
| chr7:7523385
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.702+844G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523385 | ||||||
| chr7:7523458
|
G | GT | 17 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0085others(14): Show | 17 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.702+770dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523458 | ||||||
| chr7:7523592
|
G | A | 3 | a0001c0051t0008g0192a0015c0052t0003g0191a0033c0050t0002g0190 | 3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.702+637C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523592 | ||||||
| chr7:7523718
|
T | C | 45 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.702+511A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523718 | ||||||
| chr7:7523780
|
A | G | 55 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(52): Show | 55 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.702+449T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7523780 | ||||||
| chr7:7524069
|
A | G | 3 | a0002c0002t0006g0002a0007c0008t0006g0003a0028c0036t0010g0001 | 3 | HG01243.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.702+160T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 4/34 | chr7 | 7524069 | ||||||
| chr7:7524265
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.682-16C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7524265 | ||||||
| chr7:7524310
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.682-61A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7524310 | ||||||
| chr7:7524578
|
C | G | 193 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.682-329G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7524578 | ||||||
| chr7:7524733
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.682-484C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7524733 | ||||||
| chr7:7524767
|
A | G | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.682-518T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7524767 | ||||||
| chr7:7525025
|
C | A | 4 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | NA19007.hp1 NA19011.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-776G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525025 | ||||||
| chr7:7525049
|
G | A | 86 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(83): Show | 86 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.682-800C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525049 | ||||||
| chr7:7525098
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.682-849A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525098 | ||||||
| chr7:7525132
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.682-883A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525132 | ||||||
| chr7:7525422
|
C | T | 11 | a0001c0051t0008g0192a0002c0002t0002g0004a0002c0049t0003g0189others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.682-1173G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525422 | ||||||
| chr7:7525683
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.682-1434C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525683 | ||||||
| chr7:7525738
|
G | C | 1 | a0012c0035t0002g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.682-1489C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525738 | ||||||
| chr7:7525764
|
T | C | 8 | a0001c0001t0001g0042a0002c0004t0003g0041a0003c0047t0003g0045others(5): Show | 8 | HG02486.hp1 HG02630.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.682-1515A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525764 | ||||||
| chr7:7525783
|
C | G | 23 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(20): Show | 23 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.682-1534G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525783 | ||||||
| chr7:7525823
|
T | C | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.682-1574A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525823 | ||||||
| chr7:7525865
|
G | C | 1 | a0001c0007t0003g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.682-1616C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7525865 | ||||||
| chr7:7526113
|
T | C | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.682-1864A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7526113 | ||||||
| chr7:7526337
|
T | C | 1 | a0002c0002t0001g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.682-2088A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7526337 | ||||||
| chr7:7526395
|
G | A | 18 | a0001c0001t0001g0085a0002c0002t0002g0108a0002c0002t0002g0109others(15): Show | 18 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.682-2146C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7526395 | ||||||
| chr7:7526438
|
C | T | 83 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(80): Show | 83 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.682-2189G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7526438 | ||||||
| chr7:7526837
|
G | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG00280.hp1 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-2588C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7526837 | ||||||
| chr7:7526925
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.682-2676C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7526925 | ||||||
| chr7:7526966
|
T | A | 5 | a0002c0002t0002g0015a0007c0008t0003g0012a0007c0008t0003g0013others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-2717A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7526966 | ||||||
| chr7:7527067
|
A | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.682-2818T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527067 | ||||||
| chr7:7527313
|
G | A | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.682-3064C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527313 | ||||||
| chr7:7527340
|
T | A | 1 | a0001c0007t0003g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.682-3091A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527340 | ||||||
| chr7:7527500
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG00140.hp1 HG00735.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.682-3251C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527500 | ||||||
| chr7:7527532
|
G | A | 80 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(77): Show | 80 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.682-3283C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527532 | ||||||
| chr7:7527550
|
C | T | 2 | a0006c0019t0002g0187a0006c0019t0002g0188 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.682-3301G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527550 | ||||||
| chr7:7527559
|
G | C | 9 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-3310C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527559 | ||||||
| chr7:7527730
|
T | C | 1 | a0019c0024t0003g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.682-3481A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527730 | ||||||
| chr7:7527781
|
T | C | 1 | a0002c0004t0003g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.682-3532A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7527781 | ||||||
| chr7:7528052
|
C | A | 2 | a0002c0004t0003g0186a0008c0009t0003g0185 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.681+3296G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528052 | ||||||
| chr7:7528129
|
T | A | 4 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(1): Show | 4 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+3219A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528129 | ||||||
| chr7:7528516
|
T | G | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.681+2832A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528516 | ||||||
| chr7:7528602
|
G | A | 4 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | NA19007.hp1 NA19011.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+2746C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528602 | ||||||
| chr7:7528626
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.681+2722G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528626 | ||||||
| chr7:7528797
|
T | C | 1 | a0002c0002t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.681+2551A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528797 | ||||||
| chr7:7528822
|
T | A | 1 | a0001c0001t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.681+2526A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528822 | ||||||
| chr7:7528824
|
C | G | 2 | a0001c0001t0001g0125a0002c0002t0001g0126 | 2 | HG00642.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.681+2524G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528824 | ||||||
| chr7:7528844
|
A | G | 1 | a0013c0011t0002g0035 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.681+2504T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7528844 | ||||||
| chr7:7529028
|
G | A | 5 | a0002c0002t0002g0015a0007c0008t0003g0012a0007c0008t0003g0013others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+2320C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529028 | ||||||
| chr7:7529030
|
G | A | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.681+2318C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529030 | ||||||
| chr7:7529076
|
C | A | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.681+2272G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529076 | ||||||
| chr7:7529171
|
G | C | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.681+2177C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529171 | ||||||
| chr7:7529213
|
C | A | 52 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(49): Show | 52 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.681+2135G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529213 | ||||||
| chr7:7529289
|
C | CA | 39 | a0001c0001t0001g0034a0001c0001t0001g0085a0001c0001t0001g0091others(36): Show | 39 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(36): Show |
intron_variant | MODIFIER | c.681+2058dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529289 | ||||||
| chr7:7529289
|
C | CAA | 41 | a0001c0001t0001g0018a0001c0001t0001g0125a0001c0001t0001g0128others(38): Show | 41 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.681+2057_681+2058d others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529289 | ||||||
| chr7:7529289
|
CA | C | 78 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(75): Show | 78 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.681+2058delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529289 | ||||||
| chr7:7529393
|
G | A | 2 | a0002c0004t0003g0186a0008c0009t0003g0185 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.681+1955C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529393 | ||||||
| chr7:7529615
|
G | A | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0003c0003t0002g0159 | 3 | NA18957.hp2 NA19063.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.681+1733C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529615 | ||||||
| chr7:7529672
|
T | C | 12 | a0001c0001t0001g0082a0003c0003t0001g0073a0003c0003t0001g0074others(9): Show | 12 | HG00733.hp2 HG00741.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.681+1676A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529672 | ||||||
| chr7:7529793
|
C | G | 1 | a0007c0008t0003g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.681+1555G>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529793 | ||||||
| chr7:7529793
|
C | T | 1 | a0002c0004t0003g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.681+1555G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7529793 | ||||||
| chr7:7530006
|
GA | G | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.681+1341delT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530006 | ||||||
| chr7:7530026
|
T | C | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+1322A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530026 | ||||||
| chr7:7530273
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01515.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.681+1075A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530273 | ||||||
| chr7:7530367
|
A | G | 1 | a0002c0002t0001g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.681+981T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530367 | ||||||
| chr7:7530387
|
C | A | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+961G>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530387 | ||||||
| chr7:7530422
|
A | T | 1 | a0024c0045t0001g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.681+926T>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530422 | ||||||
| chr7:7530431
|
C | T | 9 | a0001c0001t0001g0042a0002c0004t0003g0041a0003c0047t0003g0045others(6): Show | 9 | HG02486.hp1 HG02630.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+917G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530431 | ||||||
| chr7:7530467
|
T | C | 2 | a0002c0004t0003g0186a0008c0009t0003g0185 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.681+881A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530467 | ||||||
| chr7:7530473
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.681+875C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530473 | ||||||
| chr7:7530493
|
C | T | 1 | a0001c0051t0008g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.681+855G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530493 | ||||||
| chr7:7530590
|
T | C | 9 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.681+758A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530590 | ||||||
| chr7:7530597
|
G | C | 9 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.681+751C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530597 | ||||||
| chr7:7530685
|
CAACA | C | 6 | a0001c0051t0008g0192a0002c0049t0003g0189a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+659_681+662del others(4): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530685 | ||||||
| chr7:7530692
|
C | CA | 8 | a0002c0002t0002g0004a0002c0002t0006g0002a0004c0006t0002g0005others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+655dupT | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530692 | ||||||
| chr7:7530696
|
G | C | 1 | a0003c0003t0002g0159 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.681+652C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530696 | ||||||
| chr7:7530831
|
T | A | 2 | a0002c0004t0003g0186a0008c0009t0003g0185 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.681+517A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530831 | ||||||
| chr7:7530869
|
A | G | 6 | a0001c0051t0008g0192a0002c0049t0003g0189a0006c0019t0002g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+479T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530869 | ||||||
| chr7:7530977
|
G | A | 181 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.681+371C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7530977 | ||||||
| chr7:7531078
|
T | C | 9 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.681+270A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7531078 | ||||||
| chr7:7531081
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.681+267C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7531081 | ||||||
| chr7:7531130
|
A | G | 187 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.681+218T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7531130 | ||||||
| chr7:7531328
|
T | G | 84 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.681+20A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 3/34 | chr7 | 7531328 | ||||||
| chr7:7532254
|
T | C | 3 | a0001c0051t0008g0192a0015c0052t0003g0191a0033c0050t0002g0190 | 3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.125-350A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532254 | ||||||
| chr7:7532259
|
C | T | 14 | a0001c0051t0008g0192a0002c0002t0002g0004a0002c0002t0006g0002others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-355G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532259 | ||||||
| chr7:7532298
|
T | G | 31 | a0001c0001t0001g0082a0001c0005t0002g0067a0001c0005t0002g0069others(28): Show | 31 | HG00733.hp2 HG00741.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.125-394A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532298 | ||||||
| chr7:7532390
|
T | G | 86 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(83): Show | 86 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.124+362A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532390 | ||||||
| chr7:7532443
|
G | A | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.124+309C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532443 | ||||||
| chr7:7532478
|
T | A | 1 | a0015c0052t0003g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124+274A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532478 | ||||||
| chr7:7532486
|
A | C | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.124+266T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532486 | ||||||
| chr7:7532563
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.124+189C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532563 | ||||||
| chr7:7532582
|
A | C | 2 | a0013c0011t0002g0035a0013c0011t0002g0036 | 2 | HG01070.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.124+170T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532582 | ||||||
| chr7:7532584
|
G | A | 87 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0085others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.124+168C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532584 | ||||||
| chr7:7532736
|
A | AT | 23 | a0001c0001t0001g0172a0001c0001t0002g0171a0001c0001t0002g0178others(20): Show | 23 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.124+15dupA | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 2/34 | chr7 | 7532736 | ||||||
| chr7:7532974
|
T | G | 1 | a0012c0016t0002g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-37-62A>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7532974 | ||||||
| chr7:7533053
|
T | A | 1 | a0002c0004t0003g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-37-141A>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7533053 | ||||||
| chr7:7533178
|
G | T | 3 | a0002c0049t0003g0189a0006c0019t0002g0187a0006c0019t0002g0188 | 3 | HG01243.hp2 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-37-266C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7533178 | ||||||
| chr7:7533343
|
T | C | 1 | a0007c0008t0003g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-37-431A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7533343 | ||||||
| chr7:7533774
|
G | C | 172 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-37-862C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7533774 | ||||||
| chr7:7533810
|
C | T | 140 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-37-898G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7533810 | ||||||
| chr7:7533865
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-37-953A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7533865 | ||||||
| chr7:7533873
|
G | C | 1 | a0001c0051t0008g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-37-961C>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7533873 | ||||||
| chr7:7533986
|
G | T | 2 | a0001c0001t0002g0171a0002c0002t0002g0170 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-37-1074C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7533986 | ||||||
| chr7:7534223
|
G | A | 4 | a0004c0006t0002g0005a0004c0006t0002g0006a0004c0006t0002g0007others(1): Show | 4 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-1311C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7534223 | ||||||
| chr7:7534305
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-37-1393T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7534305 | ||||||
| chr7:7534516
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-38+1234G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7534516 | ||||||
| chr7:7534658
|
T | C | 11 | a0001c0051t0008g0192a0002c0002t0002g0004a0002c0049t0003g0189others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+1092A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7534658 | ||||||
| chr7:7534807
|
G | A | 178 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0042others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-38+943C>T | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7534807 | ||||||
| chr7:7534903
|
G | T | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-38+847C>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7534903 | ||||||
| chr7:7535087
|
C | T | 1 | a0015c0048t0002g0017 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-38+663G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535087 | ||||||
| chr7:7535213
|
C | T | 5 | a0002c0002t0002g0015a0007c0008t0003g0012a0007c0008t0003g0013others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+537G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535213 | ||||||
| chr7:7535330
|
C | T | 1 | a0003c0003t0004g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-38+420G>A | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535330 | ||||||
| chr7:7535346
|
A | C | 1 | a0001c0001t0005g0011 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-38+404T>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535346 | ||||||
| chr7:7535371
|
A | G | 2 | a0009c0014t0001g0010a0009c0029t0003g0009 | 2 | HG02109.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-38+379T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535371 | ||||||
| chr7:7535392
|
A | G | 17 | a0001c0001t0001g0172a0001c0001t0002g0171a0001c0001t0002g0178others(14): Show | 17 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-38+358T>C | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535392 | ||||||
| chr7:7535555
|
T | C | 28 | a0001c0001t0001g0172a0001c0001t0002g0171a0001c0001t0002g0178others(25): Show | 28 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.-38+195A>G | COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535555 | ||||||
| chr7:7535558
|
TAA | T | 5 | a0002c0002t0002g0004a0004c0006t0002g0005a0004c0006t0002g0006others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+190_-38+191del others(2): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535558 | ||||||
| chr7:7535656
|
CTAA | C | 5 | a0002c0002t0002g0004a0004c0006t0002g0005a0004c0006t0002g0006others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+91_-38+93delTT others(1): Show |
COL28A1 | ENSG00000215018.10 | transcript | ENST00000399429.8 | protein_coding | 1/34 | chr7 | 7535656 |