Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1306 |
|---|---|
| ensemblid | ENSG00000204291.12 |
| hgncid | 2192 |
| symbol | COL15A1 |
| name | collagen type XV alpha 1 chain |
| refseq_nuc | NM_001855.5 |
| refseq_prot | NP_001846.3 |
| ensembl_nuc | ENST00000375001.8 |
| ensembl_prot | ENSP00000364140.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 98943907 |
| end | 99070787 |
| strand | + |
| ver | v1.2 |
| region | chr9:98943907-99070787 |
| region5000 | chr9:98938907-99075787 |
| regionname0 | COL15A1_chr9_98943907_99070787 |
| regionname5000 | COL15A1_chr9_98938907_99075787 |
| 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 | 1/1 | 1388 | 53 | 10 | 12 | 15 | 2 | 12 | 13 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002 | 0/0 | 1388 | 52 | 13 | 5 | 29 | 1 | 4 | 25 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003 | 0/0 | 1388 | 30 | 0 | 3 | 20 | 2 | 5 | 16 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0004 | 0/0 | 1388 | 15 | 2 | 5 | 6 | 0 | 2 | 5 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005 | 0/0 | 1388 | 13 | 0 | 5 | 5 | 0 | 3 | 3 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0006 | 0/0 | 1388 | 13 | 6 | 2 | 4 | 0 | 1 | 4 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0007 | 0/0 | 1388 | 12 | 5 | 4 | 0 | 2 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0008 | 0/0 | 1388 | 11 | 0 | 6 | 4 | 0 | 1 | 3 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0009 | 0/0 | 1388 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0010 | 0/0 | 1388 | 8 | 5 | 2 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0011 | 0/0 | 1388 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0012 | 0/0 | 1388 | 6 | 3 | 0 | 0 | 2 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0013 | 0/0 | 1388 | 6 | 1 | 1 | 4 | 0 | 0 | 4 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0014 | 0/0 | 1388 | 6 | 0 | 2 | 4 | 0 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0015 | 0/0 | 1388 | 6 | 0 | 0 | 5 | 0 | 1 | 3 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0016 | 0/0 | 1388 | 5 | 0 | 2 | 3 | 0 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0017 | 0/0 | 1388 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0018 | 0/0 | 1388 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0019 | 0/0 | 1388 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0020 | 0/0 | 1388 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0021 | 0/0 | 1388 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0022 | 0/0 | 1388 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0023 | 0/0 | 1388 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0024 | 0/0 | 1388 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0025 | 0/0 | 1388 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0026 | 0/0 | 1388 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0027 | 0/0 | 1388 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0028 | 0/0 | 1388 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0029 | 0/0 | 1388 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0030 | 0/0 | 1388 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0031 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0032 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0033 | 0/0 | 1388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0034 | 0/0 | 1388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0035 | 0/0 | 1388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0036 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0037 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0038 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0039 | 0/0 | 1388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0040 | 0/0 | 1388 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0041 | 0/0 | 1388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0042 | 0/0 | 1388 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0043 | 0/0 | 1388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0044 | 0/0 | 402 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0045 | 0/0 | 1388 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0046 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0047 | 0/0 | 1388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0048 | 0/0 | 1388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0049 | 0/0 | 1388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0050 | 0/0 | 1388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0051 | 0/0 | 1388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0052 | 0/0 | 1388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0053 | 0/0 | 1388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0054 | 0/0 | 1388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0055 | 0/0 | 1388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0056 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0057 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| 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 | 1/1 | 4167 | 45 | 10 | 12 | 10 | 2 | 9 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0002 | 0/0 | 4167 | 24 | 1 | 1 | 19 | 1 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0003 | 0/0 | 4167 | 16 | 9 | 4 | 1 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0004 | 0/0 | 4167 | 15 | 0 | 3 | 8 | 2 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0005 | 0/0 | 4167 | 15 | 2 | 5 | 6 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0006 | 0/0 | 4167 | 14 | 0 | 0 | 11 | 0 | 3 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0007 | 0/0 | 4167 | 12 | 5 | 2 | 4 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0008 | 0/0 | 4167 | 11 | 5 | 4 | 0 | 2 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0009 | 0/0 | 4167 | 9 | 0 | 6 | 2 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0010 | 0/0 | 4167 | 9 | 1 | 0 | 8 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0011 | 0/0 | 4167 | 8 | 0 | 0 | 8 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0012 | 0/0 | 4167 | 7 | 4 | 2 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0013 | 0/0 | 4167 | 6 | 0 | 0 | 4 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0014 | 0/0 | 4167 | 6 | 3 | 0 | 0 | 2 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0015 | 0/0 | 4167 | 6 | 0 | 4 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0016 | 0/0 | 4167 | 5 | 4 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0017 | 0/0 | 4167 | 5 | 1 | 0 | 4 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0018 | 0/0 | 4167 | 5 | 0 | 0 | 4 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0019 | 0/0 | 4167 | 5 | 0 | 0 | 3 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0020 | 0/0 | 4167 | 4 | 0 | 2 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0021 | 0/0 | 4167 | 4 | 4 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0022 | 0/0 | 4167 | 4 | 0 | 2 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0023 | 0/0 | 4167 | 3 | 0 | 0 | 3 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0024 | 0/0 | 4167 | 3 | 3 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0025 | 0/0 | 4167 | 2 | 0 | 0 | 1 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0026 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0027 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0028 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0029 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0030 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0031 | 0/0 | 4167 | 2 | 0 | 0 | 1 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0032 | 0/0 | 4167 | 2 | 0 | 2 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0033 | 0/0 | 4167 | 2 | 0 | 0 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0034 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0035 | 0/0 | 4167 | 2 | 0 | 0 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0036 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0037 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0038 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0039 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0040 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0041 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0042 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0043 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0044 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0045 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0046 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0047 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0048 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0049 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0050 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0051 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0052 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0053 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0054 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0055 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0056 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0057 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0058 | 0/0 | 4220 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0059 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0060 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0061 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0062 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0063 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0064 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0065 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0066 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0067 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0068 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0069 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0070 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0071 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0072 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0073 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0074 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0075 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0076 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0077 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0078 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0079 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0080 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0081 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| c0082 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| 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 | 1059 | 144 | 23 | 19 | 82 | 1 | 19 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0002 | 0/1 | 1058 | 125 | 35 | 37 | 32 | 8 | 12 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0003 | 0/0 | 1059 | 17 | 3 | 0 | 9 | 0 | 5 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0004 | 0/0 | 1059 | 5 | 5 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0005 | 0/0 | 1060 | 4 | 3 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0006 | 0/0 | 1058 | 4 | 4 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0007 | 0/0 | 1058 | 3 | 3 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0008 | 1/0 | 1057 | 2 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0009 | 0/0 | 1058 | 2 | 1 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0010 | 0/0 | 1058 | 2 | 0 | 0 | 1 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0011 | 0/0 | 1059 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| t0012 | 0/0 | 1057 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| 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 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| 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 | 1/1 | 4167 | 45 | 10 | 12 | 10 | 2 | 9 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0001c0013 | 0/0 | 4167 | 6 | 0 | 0 | 4 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0001c0031 | 0/0 | 4167 | 2 | 0 | 0 | 1 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0002 | 0/0 | 4167 | 24 | 1 | 1 | 19 | 1 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0003 | 0/0 | 4167 | 16 | 9 | 4 | 1 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0010 | 0/0 | 4167 | 9 | 1 | 0 | 8 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0067 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0069 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0077 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003c0004 | 0/0 | 4167 | 15 | 0 | 3 | 8 | 2 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003c0006 | 0/0 | 4167 | 14 | 0 | 0 | 11 | 0 | 3 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003c0036 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0004c0005 | 0/0 | 4167 | 15 | 2 | 5 | 6 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005c0015 | 0/0 | 4167 | 6 | 0 | 4 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005c0019 | 0/0 | 4167 | 5 | 0 | 0 | 3 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005c0059 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005c0061 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0006c0007 | 0/0 | 4167 | 12 | 5 | 2 | 4 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0006c0078 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0007c0008 | 0/0 | 4167 | 11 | 5 | 4 | 0 | 2 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0007c0037 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0008c0009 | 0/0 | 4167 | 9 | 0 | 6 | 2 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0008c0033 | 0/0 | 4167 | 2 | 0 | 0 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0009c0011 | 0/0 | 4167 | 8 | 0 | 0 | 8 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0010c0012 | 0/0 | 4167 | 7 | 4 | 2 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0010c0075 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0011c0016 | 0/0 | 4167 | 5 | 4 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0011c0039 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0012c0014 | 0/0 | 4167 | 6 | 3 | 0 | 0 | 2 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0013c0017 | 0/0 | 4167 | 5 | 1 | 0 | 4 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0013c0047 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0014c0020 | 0/0 | 4167 | 4 | 0 | 2 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0014c0048 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0014c0049 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0015c0018 | 0/0 | 4167 | 5 | 0 | 0 | 4 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0015c0060 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0016c0022 | 0/0 | 4167 | 4 | 0 | 2 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0016c0064 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0017c0021 | 0/0 | 4167 | 4 | 4 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0018c0023 | 0/0 | 4167 | 3 | 0 | 0 | 3 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0019c0024 | 0/0 | 4167 | 3 | 3 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0020c0029 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0020c0046 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0021c0025 | 0/0 | 4167 | 2 | 0 | 0 | 1 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0022c0026 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0023c0027 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0024c0028 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0025c0032 | 0/0 | 4167 | 2 | 0 | 2 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0026c0053 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0026c0054 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0027c0035 | 0/0 | 4167 | 2 | 0 | 0 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0028c0034 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0029c0072 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0029c0073 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0030c0030 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0031c0041 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0032c0040 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0033c0038 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0034c0042 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0035c0043 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0036c0045 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0037c0044 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0038c0057 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0039c0050 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0040c0056 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0041c0055 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0042c0051 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0043c0052 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0044c0058 | 0/0 | 4220 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0045c0062 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0046c0079 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0047c0070 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0048c0068 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0049c0071 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0050c0066 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0051c0074 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0052c0076 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0053c0065 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0054c0063 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0055c0082 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0056c0081 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0057c0080 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0001c0001t0002 | 0/1 | 5224 | 42 | 10 | 12 | 9 | 2 | 8 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0001c0001t0003 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0001c0001t0008 | 1/0 | 5223 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0001c0013t0001 | 0/0 | 5225 | 6 | 0 | 0 | 4 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0001c0031t0001 | 0/0 | 5225 | 2 | 0 | 0 | 1 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0002t0001 | 0/0 | 5225 | 24 | 1 | 1 | 19 | 1 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0003t0002 | 0/0 | 5224 | 12 | 6 | 4 | 1 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0003t0003 | 0/0 | 5225 | 2 | 1 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0003t0007 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0003t0008 | 0/0 | 5223 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0010t0001 | 0/0 | 5225 | 8 | 0 | 0 | 8 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0010t0009 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0067t0002 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0069t0010 | 0/0 | 5224 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0002c0077t0002 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003c0004t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003c0004t0002 | 0/0 | 5224 | 13 | 0 | 3 | 7 | 2 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003c0004t0003 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003c0006t0001 | 0/0 | 5225 | 14 | 0 | 0 | 11 | 0 | 3 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0003c0036t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0004c0005t0001 | 0/0 | 5225 | 15 | 2 | 5 | 6 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005c0015t0001 | 0/0 | 5225 | 6 | 0 | 4 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005c0019t0003 | 0/0 | 5225 | 5 | 0 | 0 | 3 | 0 | 2 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005c0059t0001 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0005c0061t0001 | 0/0 | 5225 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0006c0007t0001 | 0/0 | 5225 | 12 | 5 | 2 | 4 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0006c0078t0001 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0007c0008t0002 | 0/0 | 5224 | 11 | 5 | 4 | 0 | 2 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0007c0037t0001 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0008c0009t0001 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0008c0009t0002 | 0/0 | 5224 | 8 | 0 | 6 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0008c0033t0001 | 0/0 | 5225 | 2 | 0 | 0 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0009c0011t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0009c0011t0002 | 0/0 | 5224 | 6 | 0 | 0 | 6 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0009c0011t0003 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0010c0012t0002 | 0/0 | 5224 | 5 | 3 | 1 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0010c0012t0005 | 0/0 | 5226 | 2 | 1 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0010c0075t0007 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0011c0016t0001 | 0/0 | 5225 | 5 | 4 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0011c0039t0001 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0012c0014t0002 | 0/0 | 5224 | 5 | 3 | 0 | 0 | 1 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0012c0014t0012 | 0/0 | 5223 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0013c0017t0001 | 0/0 | 5225 | 5 | 1 | 0 | 4 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0013c0047t0001 | 0/0 | 5225 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0014c0020t0001 | 0/0 | 5225 | 4 | 0 | 2 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0014c0048t0003 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0014c0049t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0015c0018t0001 | 0/0 | 5225 | 5 | 0 | 0 | 4 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0015c0060t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0016c0022t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0016c0022t0002 | 0/0 | 5224 | 3 | 0 | 2 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0016c0064t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0017c0021t0001 | 0/0 | 5225 | 4 | 4 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0018c0023t0002 | 0/0 | 5224 | 3 | 0 | 0 | 3 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0019c0024t0006 | 0/0 | 5224 | 3 | 3 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0020c0029t0002 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0020c0029t0004 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0020c0046t0007 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0021c0025t0003 | 0/0 | 5225 | 2 | 0 | 0 | 1 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0022c0026t0004 | 0/0 | 5225 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0023c0027t0002 | 0/0 | 5224 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0024c0028t0002 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0024c0028t0004 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0025c0032t0002 | 0/0 | 5224 | 2 | 0 | 2 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0026c0053t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0026c0054t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0027c0035t0003 | 0/0 | 5225 | 2 | 0 | 0 | 2 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0028c0034t0001 | 0/0 | 5225 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0029c0072t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0029c0073t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0030c0030t0005 | 0/0 | 5226 | 2 | 2 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0031c0041t0001 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0032c0040t0002 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0033c0038t0001 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0034c0042t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0035c0043t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0036c0045t0003 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0037c0044t0003 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0038c0057t0006 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0039c0050t0001 | 0/0 | 5225 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0040c0056t0002 | 0/0 | 5224 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0041c0055t0002 | 0/0 | 5224 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0042c0051t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0043c0052t0002 | 0/0 | 5224 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0044c0058t0002 | 0/0 | 5277 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0045c0062t0001 | 0/0 | 5225 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0046c0079t0004 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0047c0070t0011 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0048c0068t0002 | 0/0 | 5224 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0049c0071t0001 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0050c0066t0010 | 0/0 | 5224 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0051c0074t0002 | 0/0 | 5224 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0052c0076t0002 | 0/0 | 5224 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0053c0065t0001 | 0/0 | 5225 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0054c0063t0001 | 0/0 | 5225 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0055c0082t0009 | 0/0 | 5224 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0056c0081t0001 | 0/0 | 5225 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| a0057c0080t0002 | 0/0 | 5224 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | copy fasta | chr9 | 98938907 | 99075787 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0001t0008g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0013t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0013t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0013t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0013t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0013t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0013t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0031t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0001c0031t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0003t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0010t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0067t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0069t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0002c0077t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0006t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0003c0036t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0004c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0015t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0015t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0015t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0015t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0015t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0015t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0019t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0019t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0019t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0019t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0019t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0059t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0005c0061t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0007t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0006c0078t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0008t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0007c0037t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0009t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0033t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0008c0033t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0009c0011t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0009c0011t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0009c0011t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0009c0011t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0009c0011t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0009c0011t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0009c0011t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0009c0011t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0010c0012t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0010c0012t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0010c0012t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0010c0012t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0010c0012t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0010c0012t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0010c0012t0005g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0010c0075t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0011c0016t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0011c0016t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0011c0016t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0011c0016t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0011c0016t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0011c0039t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0012c0014t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0012c0014t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0012c0014t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0012c0014t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0012c0014t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0012c0014t0012g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0013c0017t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0013c0017t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0013c0017t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0013c0017t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0013c0017t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0013c0047t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0014c0020t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0014c0020t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0014c0020t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0014c0020t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0014c0048t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0014c0049t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0015c0018t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0015c0018t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0015c0018t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0015c0018t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0015c0018t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0015c0060t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0016c0022t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0016c0022t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0016c0022t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0016c0022t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0016c0064t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0017c0021t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0017c0021t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0017c0021t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0017c0021t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0018c0023t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0018c0023t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0018c0023t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0019c0024t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0019c0024t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0019c0024t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0020c0029t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0020c0029t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0020c0046t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0021c0025t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0021c0025t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0022c0026t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0022c0026t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0023c0027t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0023c0027t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0024c0028t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0024c0028t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0025c0032t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0025c0032t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0026c0053t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0026c0054t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0027c0035t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0027c0035t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0028c0034t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0028c0034t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0029c0072t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0029c0073t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0030c0030t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0030c0030t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0031c0041t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0032c0040t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0033c0038t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0034c0042t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0035c0043t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0036c0045t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0037c0044t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0038c0057t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0039c0050t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0040c0056t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0041c0055t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0042c0051t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0043c0052t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0044c0058t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0045c0062t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0046c0079t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0047c0070t0011g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0048c0068t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0049c0071t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0050c0066t0010g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0051c0074t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0052c0076t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0053c0065t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0054c0063t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0055c0082t0009g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0056c0081t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| a0057c0080t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0281 | EUR | FIN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00280 | hp2 | a0010 | c0012 | t0002 | g0087 | EUR | FIN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00408 | hp1 | a0003 | c0006 | t0001 | g0146 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00408 | hp2 | a0040 | c0056 | t0002 | g0009 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00423 | hp1 | a0003 | c0006 | t0001 | g0141 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00423 | hp2 | a0045 | c0062 | t0001 | g0020 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00438 | hp1 | a0004 | c0005 | t0001 | g0006 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00438 | hp2 | a0002 | c0010 | t0001 | g0164 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00544 | hp1 | a0009 | c0011 | t0002 | g0159 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00544 | hp2 | a0018 | c0023 | t0002 | g0248 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00558 | hp1 | a0014 | c0049 | t0001 | g0300 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00558 | hp2 | a0027 | c0035 | t0003 | g0296 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00597 | hp1 | a0015 | c0018 | t0001 | g0036 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00597 | hp2 | a0042 | c0051 | t0001 | g0149 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00621 | hp1 | a0002 | c0010 | t0001 | g0145 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00621 | hp2 | a0014 | c0020 | t0001 | g0058 | EAS | CHS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00642 | hp2 | a0003 | c0004 | t0002 | g0228 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00733 | hp2 | a0002 | c0003 | t0002 | g0236 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG00741 | hp2 | a0002 | c0003 | t0002 | g0130 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01069 | hp1 | a0008 | c0009 | t0002 | g0024 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01074 | hp1 | a0013 | c0047 | t0001 | g0093 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01074 | hp2 | a0008 | c0009 | t0002 | g0297 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01081 | hp1 | a0010 | c0012 | t0005 | g0304 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01081 | hp2 | a0002 | c0003 | t0002 | g0179 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01106 | hp1 | a0025 | c0032 | t0002 | g0243 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01106 | hp2 | a0004 | c0005 | t0001 | g0106 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01109 | hp1 | a0055 | c0082 | t0009 | g0005 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01168 | hp1 | a0043 | c0052 | t0002 | g0259 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01168 | hp2 | a0016 | c0022 | t0002 | g0227 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01169 | hp1 | a0007 | c0008 | t0002 | g0268 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01169 | hp2 | a0016 | c0022 | t0002 | g0226 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01175 | hp1 | a0039 | c0050 | t0001 | g0183 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01243 | hp1 | a0011 | c0016 | t0001 | g0086 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0214 | AMR | PUR | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01256 | hp1 | a0014 | c0020 | t0001 | g0131 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01256 | hp2 | a0003 | c0004 | t0002 | g0284 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01261 | hp1 | a0004 | c0005 | t0001 | g0101 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01261 | hp2 | a0008 | c0009 | t0002 | g0258 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01358 | hp2 | a0010 | c0012 | t0002 | g0277 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01433 | hp1 | a0003 | c0004 | t0002 | g0299 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01433 | hp2 | a0054 | c0063 | t0001 | g0023 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01496 | hp1 | a0005 | c0061 | t0001 | g0041 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01515 | hp1 | a0012 | c0014 | t0012 | g0210 | EUR | IBS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01515 | hp2 | a0007 | c0008 | t0002 | g0238 | EUR | IBS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01516 | hp1 | a0003 | c0004 | t0002 | g0189 | EUR | IBS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | IBS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01517 | hp1 | a0003 | c0004 | t0002 | g0188 | EUR | IBS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01517 | hp2 | a0007 | c0008 | t0002 | g0239 | EUR | IBS | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01884 | hp1 | a0002 | c0003 | t0002 | g0012 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01884 | hp2 | a0023 | c0027 | t0002 | g0233 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01928 | hp1 | a0005 | c0015 | t0001 | g0154 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01928 | hp2 | a0004 | c0005 | t0001 | g0045 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01934 | hp1 | a0007 | c0008 | t0002 | g0262 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01934 | hp2 | a0052 | c0076 | t0002 | g0027 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01952 | hp1 | a0006 | c0007 | t0001 | g0173 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01952 | hp2 | a0008 | c0009 | t0002 | g0001 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01975 | hp1 | a0025 | c0032 | t0002 | g0260 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01975 | hp2 | a0006 | c0007 | t0001 | g0160 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01978 | hp1 | a0008 | c0009 | t0002 | g0237 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01978 | hp2 | a0004 | c0005 | t0001 | g0042 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01981 | hp1 | a0004 | c0005 | t0001 | g0276 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01981 | hp2 | a0005 | c0015 | t0001 | g0029 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01993 | hp1 | a0008 | c0009 | t0002 | g0026 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01993 | hp2 | a0005 | c0015 | t0001 | g0040 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02004 | hp1 | a0005 | c0015 | t0001 | g0273 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02004 | hp2 | a0007 | c0008 | t0002 | g0247 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02027 | hp1 | a0005 | c0019 | t0003 | g0054 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02027 | hp2 | a0003 | c0004 | t0002 | g0256 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02040 | hp1 | a0001 | c0013 | t0001 | g0257 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02040 | hp2 | a0005 | c0019 | t0003 | g0062 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02071 | hp1 | a0009 | c0011 | t0001 | g0103 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02071 | hp2 | a0021 | c0025 | t0003 | g0135 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02074 | hp2 | a0018 | c0023 | t0002 | g0266 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02129 | hp1 | a0003 | c0004 | t0001 | g0030 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02129 | hp2 | a0016 | c0022 | t0001 | g0301 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02135 | hp1 | a0008 | c0009 | t0002 | g0285 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02135 | hp2 | a0015 | c0060 | t0001 | g0073 | EAS | KHV | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02145 | hp1 | a0007 | c0008 | t0002 | g0136 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02145 | hp2 | a0046 | c0079 | t0004 | g0283 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02155 | hp1 | a0026 | c0053 | t0001 | g0291 | EAS | CDX | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02155 | hp2 | a0001 | c0013 | t0001 | g0046 | EAS | CDX | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02257 | hp1 | a0028 | c0034 | t0001 | g0151 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02257 | hp2 | a0012 | c0014 | t0002 | g0181 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02258 | hp1 | a0002 | c0067 | t0002 | g0206 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02258 | hp2 | a0030 | c0030 | t0005 | g0127 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02273 | hp1 | a0014 | c0020 | t0001 | g0129 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02273 | hp2 | a0007 | c0008 | t0002 | g0240 | AMR | PEL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02280 | hp1 | a0011 | c0016 | t0001 | g0092 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02451 | hp1 | a0031 | c0041 | t0001 | g0292 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02451 | hp2 | a0006 | c0007 | t0001 | g0180 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02572 | hp1 | a0002 | c0003 | t0002 | g0223 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02572 | hp2 | a0004 | c0005 | t0001 | g0074 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02602 | hp1 | a0002 | c0003 | t0003 | g0147 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02602 | hp2 | a0047 | c0070 | t0011 | g0169 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02622 | hp1 | a0006 | c0007 | t0001 | g0225 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02647 | hp1 | a0010 | c0075 | t0007 | g0002 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02647 | hp2 | a0028 | c0034 | t0001 | g0152 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02683 | hp1 | a0053 | c0065 | t0001 | g0143 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02683 | hp2 | a0005 | c0019 | t0003 | g0140 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02717 | hp1 | a0036 | c0045 | t0003 | g0212 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02717 | hp2 | a0024 | c0028 | t0004 | g0165 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02723 | hp1 | a0019 | c0024 | t0006 | g0124 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02723 | hp2 | a0006 | c0007 | t0001 | g0217 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02735 | hp2 | a0050 | c0066 | t0010 | g0048 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02738 | hp2 | a0003 | c0004 | t0002 | g0303 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02809 | hp1 | a0024 | c0028 | t0002 | g0088 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02809 | hp2 | a0011 | c0039 | t0001 | g0218 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02818 | hp1 | a0006 | c0007 | t0001 | g0116 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02818 | hp2 | a0038 | c0057 | t0006 | g0126 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02895 | hp1 | a0002 | c0003 | t0007 | g0003 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02895 | hp2 | a0007 | c0008 | t0002 | g0306 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02922 | hp1 | a0020 | c0046 | t0007 | g0004 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02922 | hp2 | a0007 | c0008 | t0002 | g0117 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02965 | hp1 | a0002 | c0010 | t0009 | g0204 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02965 | hp2 | a0020 | c0029 | t0002 | g0049 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02970 | hp1 | a0002 | c0077 | t0002 | g0174 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03017 | hp1 | a0003 | c0006 | t0001 | g0279 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03041 | hp1 | a0056 | c0081 | t0001 | g0175 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03041 | hp2 | a0022 | c0026 | t0004 | g0201 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03098 | hp1 | a0002 | c0003 | t0002 | g0184 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03098 | hp2 | a0032 | c0040 | t0002 | g0137 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03130 | hp1 | a0010 | c0012 | t0002 | g0011 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03130 | hp2 | a0002 | c0003 | t0002 | g0118 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03139 | hp1 | a0057 | c0080 | t0002 | g0075 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03195 | hp2 | a0002 | c0003 | t0002 | g0224 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03209 | hp1 | a0020 | c0029 | t0004 | g0156 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03209 | hp2 | a0010 | c0012 | t0005 | g0215 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03225 | hp1 | a0010 | c0012 | t0002 | g0220 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03225 | hp2 | a0022 | c0026 | t0004 | g0139 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03239 | hp2 | a0007 | c0037 | t0001 | g0187 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03486 | hp2 | a0006 | c0007 | t0001 | g0216 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03491 | hp1 | a0051 | c0074 | t0002 | g0207 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03516 | hp1 | a0007 | c0008 | t0002 | g0244 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03516 | hp2 | a0012 | c0014 | t0002 | g0229 | AFR | ESN | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03540 | hp1 | a0004 | c0005 | t0001 | g0307 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03579 | hp1 | a0011 | c0016 | t0001 | g0309 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03579 | hp2 | a0019 | c0024 | t0006 | g0122 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0193 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03669 | hp2 | a0003 | c0006 | t0001 | g0298 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03688 | hp1 | a0004 | c0005 | t0001 | g0261 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03704 | hp1 | a0004 | c0005 | t0001 | g0121 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03704 | hp2 | a0012 | c0014 | t0002 | g0280 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03710 | hp1 | a0049 | c0071 | t0001 | g0278 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03710 | hp2 | a0001 | c0013 | t0001 | g0242 | SAS | PJL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03834 | hp1 | a0015 | c0018 | t0001 | g0282 | SAS | BEB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03834 | hp2 | a0001 | c0013 | t0001 | g0064 | SAS | BEB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03927 | hp1 | a0003 | c0006 | t0001 | g0264 | SAS | BEB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03927 | hp2 | a0005 | c0019 | t0003 | g0104 | SAS | BEB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03942 | hp1 | a0003 | c0004 | t0003 | g0263 | SAS | BEB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG04115 | hp1 | a0001 | c0031 | t0001 | g0205 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0245 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG04199 | hp2 | a0008 | c0009 | t0001 | g0208 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG04204 | hp2 | a0021 | c0025 | t0003 | g0255 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG04228 | hp1 | a0005 | c0059 | t0001 | g0112 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | CHB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18747 | hp2 | a0026 | c0054 | t0001 | g0013 | EAS | CHB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18906 | hp1 | a0010 | c0012 | t0002 | g0221 | AFR | YRI | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18906 | hp2 | a0011 | c0016 | t0001 | g0090 | AFR | YRI | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18939 | hp1 | a0003 | c0004 | t0002 | g0142 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18942 | hp1 | a0048 | c0068 | t0002 | g0079 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18942 | hp2 | a0003 | c0004 | t0002 | g0275 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18944 | hp1 | a0003 | c0004 | t0002 | g0270 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18944 | hp2 | a0029 | c0072 | t0001 | g0034 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18945 | hp1 | a0005 | c0015 | t0001 | g0163 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18946 | hp1 | a0003 | c0006 | t0001 | g0081 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18948 | hp1 | a0003 | c0006 | t0001 | g0097 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18948 | hp2 | a0027 | c0035 | t0003 | g0286 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18950 | hp1 | a0002 | c0003 | t0002 | g0241 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18950 | hp2 | a0003 | c0006 | t0001 | g0095 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18952 | hp2 | a0009 | c0011 | t0003 | g0246 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18960 | hp1 | a0002 | c0010 | t0001 | g0107 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18960 | hp2 | a0018 | c0023 | t0002 | g0267 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18964 | hp1 | a0035 | c0043 | t0001 | g0063 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18964 | hp2 | a0003 | c0006 | t0001 | g0080 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18966 | hp2 | a0006 | c0007 | t0001 | g0060 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18967 | hp1 | a0009 | c0011 | t0002 | g0031 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18967 | hp2 | a0014 | c0020 | t0001 | g0294 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18968 | hp1 | a0013 | c0017 | t0001 | g0071 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18968 | hp2 | a0015 | c0018 | t0001 | g0035 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18971 | hp1 | a0002 | c0069 | t0010 | g0047 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18971 | hp2 | a0009 | c0011 | t0002 | g0044 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18974 | hp1 | a0013 | c0017 | t0001 | g0114 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18979 | hp2 | a0003 | c0006 | t0001 | g0096 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18981 | hp1 | a0002 | c0010 | t0001 | g0161 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18981 | hp2 | a0003 | c0006 | t0001 | g0269 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18982 | hp1 | a0008 | c0033 | t0001 | g0134 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18982 | hp2 | a0004 | c0005 | t0001 | g0158 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18983 | hp2 | a0002 | c0010 | t0001 | g0170 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18984 | hp1 | a0001 | c0013 | t0001 | g0015 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18984 | hp2 | a0003 | c0006 | t0001 | g0098 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18985 | hp1 | a0013 | c0017 | t0001 | g0065 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18985 | hp2 | a0044 | c0058 | t0002 | g0144 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18986 | hp2 | a0003 | c0006 | t0001 | g0085 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18992 | hp1 | a0003 | c0036 | t0001 | g0274 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18992 | hp2 | a0013 | c0017 | t0001 | g0019 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18997 | hp2 | a0004 | c0005 | t0001 | g0010 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18998 | hp2 | a0004 | c0005 | t0001 | g0094 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19004 | hp1 | a0015 | c0018 | t0001 | g0252 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19004 | hp2 | a0009 | c0011 | t0002 | g0032 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19005 | hp2 | a0003 | c0004 | t0002 | g0271 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19009 | hp1 | a0008 | c0033 | t0001 | g0120 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19009 | hp2 | a0002 | c0010 | t0001 | g0021 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19010 | hp2 | a0005 | c0015 | t0001 | g0290 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19011 | hp1 | a0008 | c0009 | t0002 | g0056 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19030 | hp1 | a0017 | c0021 | t0001 | g0230 | AFR | LWK | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19030 | hp2 | a0002 | c0003 | t0003 | g0100 | AFR | LWK | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19057 | hp1 | a0009 | c0011 | t0002 | g0037 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19057 | hp2 | a0002 | c0010 | t0001 | g0008 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19063 | hp1 | a0003 | c0006 | t0001 | g0072 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19063 | hp2 | a0009 | c0011 | t0002 | g0055 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19064 | hp1 | a0003 | c0004 | t0002 | g0272 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19064 | hp2 | a0015 | c0018 | t0001 | g0033 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19066 | hp1 | a0004 | c0005 | t0001 | g0295 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19066 | hp2 | a0016 | c0064 | t0001 | g0077 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19067 | hp1 | a0006 | c0007 | t0001 | g0039 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19067 | hp2 | a0001 | c0031 | t0001 | g0157 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19074 | hp1 | a0029 | c0073 | t0001 | g0162 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19074 | hp2 | a0034 | c0042 | t0001 | g0133 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19078 | hp2 | a0005 | c0019 | t0003 | g0289 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19080 | hp1 | a0001 | c0013 | t0001 | g0068 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19080 | hp2 | a0016 | c0022 | t0002 | g0078 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19082 | hp2 | a0006 | c0007 | t0001 | g0038 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19084 | hp1 | a0004 | c0005 | t0001 | g0017 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19087 | hp2 | a0014 | c0048 | t0003 | g0115 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19091 | hp1 | a0003 | c0004 | t0002 | g0132 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19091 | hp2 | a0002 | c0010 | t0001 | g0125 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19240 | hp1 | a0002 | c0003 | t0002 | g0182 | AFR | YRI | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA19240 | hp2 | a0017 | c0021 | t0001 | g0232 | AFR | YRI | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA20129 | hp1 | a0037 | c0044 | t0003 | g0138 | AFR | ASW | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA20129 | hp2 | a0006 | c0078 | t0001 | g0231 | AFR | ASW | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0251 | EUR | TSI | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA20752 | hp2 | a0012 | c0014 | t0002 | g0250 | EUR | TSI | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA20905 | hp1 | a0006 | c0007 | t0001 | g0194 | SAS | GIH | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA20905 | hp2 | a0033 | c0038 | t0001 | g0028 | SAS | GIH | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01123 | hp1 | a0041 | c0055 | t0002 | g0025 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | CLM | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02109 | hp1 | a0017 | c0021 | t0001 | g0213 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02109 | hp2 | a0030 | c0030 | t0005 | g0128 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02486 | hp1 | a0017 | c0021 | t0001 | g0099 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02486 | hp2 | a0012 | c0014 | t0002 | g0203 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02559 | hp1 | a0002 | c0003 | t0008 | g0185 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG02559 | hp2 | a0013 | c0017 | t0001 | g0084 | AFR | ACB | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG03471 | hp2 | a0019 | c0024 | t0006 | g0166 | AFR | MSL | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG06807 | hp1 | a0023 | c0027 | t0002 | g0091 | AFR | USA | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | USA | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18955 | hp1 | a0006 | c0007 | t0001 | g0069 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA20300 | hp1 | a0011 | c0016 | t0001 | g0155 | AFR | USA | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| NA20300 | hp2 | a0007 | c0008 | t0002 | g0293 | AFR | USA | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0199 | REF | REF | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0008 | g0200 | REF | REF | COL15A1_chr9_98938907_99075787 | COL15A1 | chr9 | 98938907 | 99075787 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98985603
|
A | G | 3 | a0055a0056a0057 | 3 | HG01109.hp1 HG03041.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.139A>G | p.Ile47Val | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/42 | 294/5223 | 139/4167 | 47/1388 | chr9 | 98985603 | ||
| chr9:98985952
|
G | A | 15 | a0003a0004a0007others(12): Show | 79 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
missense_variant | MODERATE | c.488G>A | p.Arg163His | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/42 | 643/5223 | 488/4167 | 163/1388 | chr9 | 98985952 | ||
| chr9:98986030
|
G | A | 1 | a0035 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.566G>A | p.Arg189Gln | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/42 | 721/5223 | 566/4167 | 189/1388 | chr9 | 98986030 | ||
| chr9:98986035
|
T | C | 3 | a0024a0036a0037 | 4 | HG02717.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.571T>C | p.Ser191Pro | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/42 | 726/5223 | 571/4167 | 191/1388 | chr9 | 98986035 | ||
| chr9:98986062
|
G | A | 2 | a0020a0030 | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
missense_variant | MODERATE | c.598G>A | p.Ala200Thr | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/42 | 753/5223 | 598/4167 | 200/1388 | chr9 | 98986062 | ||
| chr9:98986074
|
A | G | 42 | a0002a0003a0004others(39): Show | 206 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
missense_variant | MODERATE | c.610A>G | p.Met204Val | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/42 | 765/5223 | 610/4167 | 204/1388 | chr9 | 98986074 | ||
| chr9:98987315
|
G | A | 3 | a0024a0036a0037 | 4 | HG02717.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.670G>A | p.Val224Met | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/42 | 825/5223 | 670/4167 | 224/1388 | chr9 | 98987315 | ||
| chr9:99003532
|
C | T | 1 | a0038 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1145C>T | p.Thr382Ile | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/42 | 1300/5223 | 1145/4167 | 382/1388 | chr9 | 99003532 | ||
| chr9:99003558
|
A | ACGGAGAA others(46): Show |
1 | a0044 | 1 | NA18985.hp2 | frameshift_variant&stop_gained | HIGH | c.1178_1179insACCCAG others(47): Show |
p.Asn393fs | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/42 | 1334/5223 | 1179/4167 | 393/1388 | INFO_REALIGN_3_PRIME | chr9 | 99003558 | |
| chr9:99003559
|
C | T | 2 | a0009a0027 | 10 | HG00544.hp1 HG00558.hp2 HG02071.hp1 others(7): Show |
missense_variant | MODERATE | c.1172C>T | p.Thr391Met | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/42 | 1327/5223 | 1172/4167 | 391/1388 | chr9 | 99003559 | ||
| chr9:99004963
|
G | A | 5 | a0005a0015a0018others(2): Show | 25 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(22): Show |
missense_variant | MODERATE | c.1266G>A | p.Met422Ile | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/42 | 1421/5223 | 1266/4167 | 422/1388 | chr9 | 99004963 | ||
| chr9:99005021
|
G | A | 4 | a0005a0015a0021others(1): Show | 22 | HG00597.hp1 HG01433.hp2 HG01496.hp1 others(19): Show |
missense_variant | MODERATE | c.1324G>A | p.Ala442Thr | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/42 | 1479/5223 | 1324/4167 | 442/1388 | chr9 | 99005021 | ||
| chr9:99005033
|
G | A | 9 | a0003a0004a0013others(6): Show | 68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
missense_variant | MODERATE | c.1336G>A | p.Gly446Arg | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/42 | 1491/5223 | 1336/4167 | 446/1388 | chr9 | 99005033 | ||
| chr9:99015983
|
G | T | 10 | a0008a0009a0026others(7): Show | 29 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(26): Show |
missense_variant | MODERATE | c.1511G>T | p.Gly504Val | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/42 | 1666/5223 | 1511/4167 | 504/1388 | chr9 | 99015983 | ||
| chr9:99015990
|
A | C | 8 | a0010a0019a0024others(5): Show | 20 | HG00280.hp2 HG01081.hp1 HG01358.hp2 others(17): Show |
missense_variant | MODERATE | c.1518A>C | p.Glu506Asp | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/42 | 1673/5223 | 1518/4167 | 506/1388 | chr9 | 99015990 | ||
| chr9:99016064
|
C | G | 4 | a0012a0037a0039others(1): Show | 9 | HG01175.hp1 HG01515.hp1 HG02257.hp2 others(6): Show |
missense_variant | MODERATE | c.1592C>G | p.Pro531Arg | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/42 | 1747/5223 | 1592/4167 | 531/1388 | chr9 | 99016064 | ||
| chr9:99024952
|
C | T | 1 | a0023 | 2 | HG01884.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.1933C>T | p.Pro645Ser | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 15/42 | 2088/5223 | 1933/4167 | 645/1388 | chr9 | 99024952 | ||
| chr9:99024976
|
C | A | 1 | a0050 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1957C>A | p.Pro653Thr | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 15/42 | 2112/5223 | 1957/4167 | 653/1388 | chr9 | 99024976 | ||
| chr9:99024998
|
C | T | 2 | a0034a0040 | 2 | HG00408.hp2 NA19074.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1979C>T | p.Pro660Leu | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 15/42 | 2134/5223 | 1979/4167 | 660/1388 | chr9 | 99024998 | ||
| chr9:99035048
|
C | T | 2 | a0025a0041 | 3 | HG01106.hp1 HG01123.hp1 HG01975.hp1 |
missense_variant | MODERATE | c.2114C>T | p.Pro705Leu | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 18/42 | 2269/5223 | 2114/4167 | 705/1388 | chr9 | 99035048 | ||
| chr9:99035074
|
C | T | 2 | a0024a0046 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.2140C>T | p.Pro714Ser | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 18/42 | 2295/5223 | 2140/4167 | 714/1388 | chr9 | 99035074 | ||
| chr9:99047989
|
G | A | 1 | a0042 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.2782G>A | p.Val928Ile | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/42 | 2937/5223 | 2782/4167 | 928/1388 | chr9 | 99047989 | ||
| chr9:99054576
|
G | A | 1 | a0029 | 2 | NA18944.hp2 NA19074.hp1 |
missense_variant&splice_region_variant | MODERATE | c.2951G>A | p.Gly984Asp | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 32/42 | 3106/5223 | 2951/4167 | 984/1388 | chr9 | 99054576 | ||
| chr9:99054591
|
A | G | 1 | a0022 | 2 | HG03041.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.2966A>G | p.Lys989Arg | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 32/42 | 3121/5223 | 2966/4167 | 989/1388 | chr9 | 99054591 | ||
| chr9:99054627
|
A | G | 2 | a0033a0049 | 2 | HG03710.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.3002A>G | p.Lys1001Arg | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 32/42 | 3157/5223 | 3002/4167 | 1001/1388 | chr9 | 99054627 | ||
| chr9:99055126
|
T | G | 1 | a0048 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.3056T>G | p.Leu1019Arg | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 33/42 | 3211/5223 | 3056/4167 | 1019/1388 | chr9 | 99055126 | ||
| chr9:99055323
|
G | A | 1 | a0039 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.3143G>A | p.Ser1048Asn | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/42 | 3298/5223 | 3143/4167 | 1048/1388 | chr9 | 99055323 | ||
| chr9:99055368
|
C | T | 2 | a0019a0038 | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
missense_variant | MODERATE | c.3188C>T | p.Pro1063Leu | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/42 | 3343/5223 | 3188/4167 | 1063/1388 | chr9 | 99055368 | ||
| chr9:99062272
|
G | A | 1 | a0043 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.3559G>A | p.Asp1187Asn | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 38/42 | 3714/5223 | 3559/4167 | 1187/1388 | chr9 | 99062272 | ||
| chr9:99063090
|
C | T | 1 | a0047 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.3632C>T | p.Ala1211Val | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/42 | 3787/5223 | 3632/4167 | 1211/1388 | chr9 | 99063090 | ||
| chr9:99068651
|
A | C | 1 | a0032 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.3934A>C | p.Ile1312Leu | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/42 | 4089/5223 | 3934/4167 | 1312/1388 | chr9 | 99068651 | ||
| chr9:99069713
|
G | A | 15 | a0004a0006a0011others(12): Show | 61 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
missense_variant | MODERATE | c.3994G>A | p.Val1332Ile | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 4149/5223 | 3994/4167 | 1332/1388 | chr9 | 99069713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98985902
|
C | T | 2 | a0006c0078a0046c0079 | 2 | HG02145.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.438C>T | p.Ser146Ser | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/42 | 593/5223 | 438/4167 | 146/1388 | chr9 | 98985902 | ||
| chr9:98996981
|
C | G | 2 | a0002c0077a0024c0028 | 3 | HG02717.hp2 HG02809.hp1 HG02970.hp1 |
synonymous_variant | LOW | c.852C>G | p.Ser284Ser | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/42 | 1007/5223 | 852/4167 | 284/1388 | chr9 | 98996981 | ||
| chr9:99005029
|
C | T | 1 | a0036c0045 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1332C>T | p.Ser444Ser | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/42 | 1487/5223 | 1332/4167 | 444/1388 | chr9 | 99005029 | ||
| chr9:99015449
|
T | C | 1 | a0005c0059 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1386T>C | p.Ala462Ala | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 10/42 | 1541/5223 | 1386/4167 | 462/1388 | chr9 | 99015449 | ||
| chr9:99025951
|
G | A | 1 | a0002c0067 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.2028G>A | p.Gly676Gly | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/42 | 2183/5223 | 2028/4167 | 676/1388 | chr9 | 99025951 | ||
| chr9:99036363
|
A | G | 1 | a0010c0075 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.2376A>G | p.Arg792Arg | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/42 | 2531/5223 | 2376/4167 | 792/1388 | chr9 | 99036363 | ||
| chr9:99042047
|
T | C | 17 | a0001c0013a0002c0002a0002c0069others(14): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
splice_region_variant&synonymous_variant | LOW | c.2514T>C | p.Gly838Gly | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/42 | 2669/5223 | 2514/4167 | 838/1388 | chr9 | 99042047 | ||
| chr9:99044585
|
G | A | 1 | a0029c0072 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.2592G>A | p.Pro864Pro | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 25/42 | 2747/5223 | 2592/4167 | 864/1388 | chr9 | 99044585 | ||
| chr9:99059911
|
T | C | 1 | a0031c0041 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.3360T>C | p.Pro1120Pro | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/42 | 3515/5223 | 3360/4167 | 1120/1388 | chr9 | 99059911 | ||
| chr9:99059938
|
C | T | 42 | a0001c0013a0001c0031a0002c0002others(39): Show | 140 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
synonymous_variant | LOW | c.3387C>T | p.Pro1129Pro | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/42 | 3542/5223 | 3387/4167 | 1129/1388 | chr9 | 99059938 | ||
| chr9:99069823
|
C | T | 1 | a0005c0061 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.4104C>T | p.Ser1368Ser | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 4259/5223 | 4104/4167 | 1368/1388 | chr9 | 99069823 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98943915
|
C | A | 3 | a0002c0003t0007a0010c0075t0007a0020c0046t0007 | 3 | HG02647.hp1 HG02895.hp1 HG02922.hp1 |
5_prime_UTR_variant | MODIFIER | c.-147C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 1/42 | 147 | chr9 | 98943915 | |||||
| chr9:98943970
|
C | G | 2 | a0002c0069t0010a0050c0066t0010 | 2 | HG02735.hp2 NA18971.hp1 |
5_prime_UTR_variant | MODIFIER | c.-92C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 1/42 | 92 | chr9 | 98943970 | |||||
| chr9:99069930
|
G | A | 1 | a0047c0070t0011 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*44G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 44 | chr9 | 99069930 | |||||
| chr9:99069981
|
G | GGT | 45 | a0001c0001t0001a0001c0013t0001a0001c0031t0001others(42): Show | 144 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*95_*96insGT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 96 | chr9 | 99069981 | |||||
| chr9:99069981
|
G | GGTT | 2 | a0010c0012t0005a0030c0030t0005 | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*95_*96insGTT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 96 | chr9 | 99069981 | |||||
| chr9:99069981
|
G | GT | 34 | a0001c0001t0002a0002c0003t0002a0002c0003t0007others(31): Show | 136 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*107dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 108 | INFO_REALIGN_3_PRIME | chr9 | 99069981 | ||||
| chr9:99069981
|
G | GTT | 15 | a0001c0001t0003a0002c0003t0003a0003c0004t0003others(12): Show | 23 | HG00558.hp2 HG02027.hp1 HG02040.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*106_*107dupTT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 108 | INFO_REALIGN_3_PRIME | chr9 | 99069981 | ||||
| chr9:99070009
|
C | T | 1 | a0012c0014t0012 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*123C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 123 | chr9 | 99070009 | |||||
| chr9:99070119
|
C | A | 2 | a0019c0024t0006a0038c0057t0006 | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*233C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 233 | chr9 | 99070119 | |||||
| chr9:99070160
|
G | A | 53 | a0001c0001t0001a0001c0013t0001a0001c0031t0001others(50): Show | 155 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*274G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 274 | chr9 | 99070160 | |||||
| chr9:99070773
|
C | T | 2 | a0019c0024t0006a0038c0057t0006 | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*887C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 42/42 | 887 | chr9 | 99070773 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98944134
|
C | T | 1 | a0002c0002t0001g0310 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.12-28C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 1/41 | chr9 | 98944134 | ||||||
| chr9:98944692
|
C | G | 81 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(78): Show | 81 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.100+442C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98944692 | ||||||
| chr9:98944693
|
T | G | 81 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(78): Show | 81 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.100+443T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98944693 | ||||||
| chr9:98944752
|
A | T | 1 | a0003c0004t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.100+502A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98944752 | ||||||
| chr9:98944892
|
T | C | 78 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(75): Show | 78 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.100+642T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98944892 | ||||||
| chr9:98945038
|
C | T | 1 | a0002c0002t0001g0305 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100+788C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945038 | ||||||
| chr9:98945108
|
T | G | 49 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(46): Show | 49 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.100+858T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945108 | ||||||
| chr9:98945156
|
C | T | 2 | a0001c0001t0002g0050a0020c0029t0002g0049 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+906C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945156 | ||||||
| chr9:98945525
|
G | A | 6 | a0001c0001t0002g0050a0002c0003t0007g0003a0010c0075t0007g0002others(3): Show | 6 | HG01109.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+1275G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945525 | ||||||
| chr9:98945528
|
CCAAAGGA | C | 82 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+1279_100+1285d others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945528 | ||||||
| chr9:98945538
|
C | A | 82 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+1288C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945538 | ||||||
| chr9:98945868
|
T | C | 129 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0057others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.100+1618T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945868 | ||||||
| chr9:98945951
|
C | A | 4 | a0002c0002t0001g0007a0002c0010t0001g0008a0004c0005t0001g0006others(1): Show | 4 | HG00408.hp2 HG00438.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+1701C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945951 | ||||||
| chr9:98945967
|
A | C | 31 | a0001c0001t0002g0022a0001c0013t0001g0046a0002c0002t0001g0018others(28): Show | 31 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.100+1717A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98945967 | ||||||
| chr9:98946003
|
G | A | 83 | a0001c0001t0002g0051a0001c0001t0002g0249a0001c0001t0002g0251others(80): Show | 83 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.100+1753G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946003 | ||||||
| chr9:98946062
|
C | T | 2 | a0016c0022t0002g0226a0016c0022t0002g0227 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.100+1812C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946062 | ||||||
| chr9:98946128
|
A | G | 82 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+1878A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946128 | ||||||
| chr9:98946200
|
C | G | 82 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+1950C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946200 | ||||||
| chr9:98946203
|
C | A | 82 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+1953C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946203 | ||||||
| chr9:98946568
|
C | T | 1 | a0011c0016t0001g0309 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.100+2318C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946568 | ||||||
| chr9:98946740
|
A | G | 1 | a0050c0066t0010g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.100+2490A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946740 | ||||||
| chr9:98946861
|
C | T | 1 | a0010c0012t0005g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.100+2611C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946861 | ||||||
| chr9:98946918
|
G | C | 3 | a0004c0005t0001g0307a0007c0008t0002g0306a0011c0016t0001g0309 | 3 | HG02895.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.100+2668G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946918 | ||||||
| chr9:98946961
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.100+2711G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98946961 | ||||||
| chr9:98947030
|
A | C | 274 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(271): Show | 274 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.100+2780A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947030 | ||||||
| chr9:98947075
|
G | T | 137 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(134): Show | 137 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.100+2825G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947075 | ||||||
| chr9:98947103
|
T | C | 2 | a0001c0001t0002g0050a0020c0029t0002g0049 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+2853T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947103 | ||||||
| chr9:98947196
|
T | A | 1 | a0002c0002t0001g0053 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.100+2946T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947196 | ||||||
| chr9:98947375
|
C | A | 5 | a0006c0078t0001g0231a0012c0014t0002g0229a0017c0021t0001g0230others(2): Show | 5 | HG01884.hp2 HG03516.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+3125C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947375 | ||||||
| chr9:98947401
|
G | A | 2 | a0001c0001t0002g0219a0010c0012t0002g0220 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.100+3151G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947401 | ||||||
| chr9:98947528
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100+3278A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947528 | ||||||
| chr9:98947759
|
T | C | 18 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0059others(15): Show | 18 | HG00621.hp2 HG02027.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+3509T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947759 | ||||||
| chr9:98947834
|
T | C | 1 | a0001c0001t0003g0234 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.100+3584T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947834 | ||||||
| chr9:98947872
|
A | C | 1 | a0002c0002t0001g0176 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.100+3622A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947872 | ||||||
| chr9:98947953
|
C | G | 6 | a0001c0001t0002g0050a0002c0003t0007g0003a0010c0075t0007g0002others(3): Show | 6 | HG01109.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+3703C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98947953 | ||||||
| chr9:98948029
|
A | G | 2 | a0002c0077t0002g0174a0056c0081t0001g0175 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.100+3779A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948029 | ||||||
| chr9:98948150
|
T | A | 1 | a0010c0012t0002g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+3900T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948150 | ||||||
| chr9:98948320
|
C | G | 1 | a0002c0002t0001g0176 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.100+4070C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948320 | ||||||
| chr9:98948419
|
A | G | 1 | a0002c0002t0001g0176 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.100+4169A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948419 | ||||||
| chr9:98948491
|
G | T | 5 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0002g0177others(2): Show | 5 | HG01358.hp1 HG01516.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+4241G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948491 | ||||||
| chr9:98948547
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100+4297A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948547 | ||||||
| chr9:98948554
|
C | T | 6 | a0001c0001t0002g0050a0002c0003t0007g0003a0010c0075t0007g0002others(3): Show | 6 | HG01109.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+4304C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948554 | ||||||
| chr9:98948582
|
G | A | 1 | a0013c0017t0001g0071 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.100+4332G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948582 | ||||||
| chr9:98948596
|
C | CA | 139 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0057others(136): Show | 139 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.100+4367dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98948596 | |||||
| chr9:98948596
|
C | CAA | 7 | a0001c0001t0002g0219a0001c0001t0002g0222a0002c0002t0001g0176others(4): Show | 7 | HG02027.hp1 HG02135.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+4366_100+4367d others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98948596 | |||||
| chr9:98948596
|
CA | C | 115 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(112): Show | 115 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.100+4367delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98948596 | |||||
| chr9:98948670
|
C | T | 1 | a0003c0004t0002g0303 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.100+4420C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948670 | ||||||
| chr9:98948695
|
A | T | 30 | a0001c0001t0002g0022a0001c0013t0001g0046a0002c0002t0001g0043others(27): Show | 30 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+4445A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948695 | ||||||
| chr9:98948950
|
T | C | 4 | a0001c0001t0002g0308a0004c0005t0001g0307a0007c0008t0002g0306others(1): Show | 4 | HG02280.hp2 HG02895.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+4700T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948950 | ||||||
| chr9:98948989
|
T | C | 1 | a0002c0003t0008g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100+4739T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98948989 | ||||||
| chr9:98949052
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.100+4802C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98949052 | ||||||
| chr9:98949150
|
TATTCTTT others(8): Show |
T | 1 | a0004c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+4910_100+4924d others(17): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98949150 | |||||
| chr9:98949253
|
T | C | 1 | a0057c0080t0002g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100+5003T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98949253 | ||||||
| chr9:98949707
|
G | T | 137 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(134): Show | 137 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.100+5457G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98949707 | ||||||
| chr9:98949756
|
A | G | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.100+5506A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98949756 | ||||||
| chr9:98949848
|
T | C | 131 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.100+5598T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98949848 | ||||||
| chr9:98950011
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+5761G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950011 | ||||||
| chr9:98950026
|
C | G | 10 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(7): Show | 10 | HG00408.hp2 HG00438.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+5776C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950026 | ||||||
| chr9:98950239
|
T | G | 1 | a0001c0001t0002g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+5989T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950239 | ||||||
| chr9:98950250
|
C | T | 6 | a0001c0001t0002g0050a0002c0003t0007g0003a0010c0075t0007g0002others(3): Show | 6 | HG01109.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+6000C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950250 | ||||||
| chr9:98950328
|
C | T | 1 | a0010c0012t0002g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+6078C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950328 | ||||||
| chr9:98950384
|
A | G | 1 | a0006c0007t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.100+6134A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950384 | ||||||
| chr9:98950449
|
T | TCCTTCCC others(6): Show |
1 | a0001c0001t0002g0186 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100+6209_100+6210i others(15): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950449 | |||||
| chr9:98950449
|
T | TCCTTCCC others(18): Show |
5 | a0001c0001t0002g0209a0002c0002t0001g0178a0003c0004t0002g0188others(2): Show | 5 | HG01516.hp1 HG01517.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+6231_100+6255d others(27): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950449 | |||||
| chr9:98950544
|
C | CCCCTT | 5 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(2): Show | 5 | NA18747.hp2 NA18983.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+6296_100+6297i others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950544 | |||||
| chr9:98950550
|
C | CCCTT | 24 | a0001c0001t0002g0089a0002c0002t0001g0053a0002c0002t0001g0076others(21): Show | 24 | HG00280.hp2 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.100+6340_100+6343d others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950550 | |||||
| chr9:98950550
|
C | CCCTTCCT others(1): Show |
44 | a0001c0001t0002g0052a0001c0001t0002g0102a0001c0001t0002g0113others(41): Show | 44 | HG01074.hp1 HG01106.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.100+6336_100+6343d others(10): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950550 | |||||
| chr9:98950550
|
C | CCCTTCCT others(5): Show |
40 | a0001c0001t0002g0051a0001c0001t0002g0057a0001c0001t0002g0059others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.100+6332_100+6343d others(14): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950550 | |||||
| chr9:98950550
|
C | CCCTTCCT others(9): Show |
24 | a0001c0001t0002g0067a0001c0001t0002g0070a0001c0013t0001g0064others(21): Show | 24 | HG00438.hp2 HG00544.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+6328_100+6343d others(18): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950550 | |||||
| chr9:98950550
|
C | CCCTTCCT others(13): Show |
4 | a0001c0001t0002g0167a0001c0013t0001g0068a0013c0017t0001g0071others(1): Show | 4 | HG03041.hp1 HG06807.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+6324_100+6343d others(22): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950550 | |||||
| chr9:98950550
|
C | CCCTTCCT others(17): Show |
1 | a0001c0001t0002g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+6320_100+6343d others(26): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950550 | |||||
| chr9:98950550
|
C | CTT | 7 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(4): Show | 7 | HG01109.hp1 NA18747.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+6300_100+6301i others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950550 | ||||||
| chr9:98950550
|
CCCTTCCT others(5): Show |
C | 1 | a0010c0012t0002g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+6332_100+6343d others(14): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950550 | |||||
| chr9:98950586
|
T | C | 7 | a0002c0002t0001g0235a0002c0003t0002g0241a0008c0009t0002g0024others(4): Show | 7 | HG01069.hp1 HG01123.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6336T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950586 | ||||||
| chr9:98950586
|
T | TCCTC | 64 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(61): Show | 64 | HG00280.hp1 HG00544.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.100+6339_100+6340i others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950586 | |||||
| chr9:98950590
|
T | C | 78 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0249others(75): Show | 78 | HG00280.hp1 HG00544.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.100+6340T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950590 | ||||||
| chr9:98950590
|
T | TCCTCCCT others(1): Show |
14 | a0002c0002t0001g0302a0002c0002t0001g0305a0003c0004t0002g0299others(11): Show | 14 | HG00558.hp1 HG00558.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.100+6349_100+6356d others(10): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(1): Show |
5 | a0002c0002t0001g0007a0002c0010t0001g0008a0002c0010t0001g0170others(2): Show | 5 | HG00408.hp2 HG00438.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+6343_100+6344i others(10): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(5): Show |
1 | a0033c0038t0001g0028 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+6343_100+6344i others(14): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(5): Show |
1 | a0001c0001t0002g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6343_100+6344i others(14): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(9): Show |
15 | a0003c0004t0001g0030a0004c0005t0001g0042a0005c0015t0001g0029others(12): Show | 15 | HG00423.hp2 HG00597.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+6343_100+6344i others(18): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(9): Show |
1 | a0002c0003t0002g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.100+6343_100+6344i others(18): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(13): Show |
6 | a0001c0013t0001g0046a0002c0002t0001g0043a0002c0010t0001g0021others(3): Show | 6 | HG01928.hp2 HG02155.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+6343_100+6344i others(22): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(13): Show |
4 | a0001c0001t0002g0219a0002c0003t0002g0224a0006c0007t0001g0225others(1): Show | 4 | HG02622.hp1 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+6343_100+6344i others(22): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(17): Show |
6 | a0001c0001t0002g0022a0002c0003t0007g0003a0002c0069t0010g0047others(3): Show | 6 | HG02895.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+6343_100+6344i others(26): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(21): Show |
1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.100+6343_100+6344i others(30): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(17): Show |
1 | a0011c0016t0001g0309 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.100+6343_100+6344i others(26): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(21): Show |
3 | a0001c0001t0002g0050a0001c0001t0002g0308a0002c0003t0002g0012 | 3 | HG01884.hp1 HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+6343_100+6344i others(30): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950590
|
T | TCCTTCCT others(21): Show |
2 | a0004c0005t0001g0307a0007c0008t0002g0306 | 2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.100+6343_100+6344i others(30): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98950590 | |||||
| chr9:98950655
|
C | T | 3 | a0002c0003t0007g0003a0010c0075t0007g0002a0020c0046t0007g0004 | 3 | HG02647.hp1 HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.100+6405C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950655 | ||||||
| chr9:98950700
|
C | T | 2 | a0001c0001t0002g0061a0008c0009t0002g0056 | 2 | NA19002.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.100+6450C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950700 | ||||||
| chr9:98950739
|
C | T | 1 | a0038c0057t0006g0126 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100+6489C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950739 | ||||||
| chr9:98950764
|
C | T | 1 | a0010c0012t0005g0215 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100+6514C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950764 | ||||||
| chr9:98950854
|
C | T | 84 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0057others(81): Show | 84 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.100+6604C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950854 | ||||||
| chr9:98950873
|
G | A | 1 | a0038c0057t0006g0126 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100+6623G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950873 | ||||||
| chr9:98950883
|
G | A | 2 | a0002c0003t0002g0179a0006c0007t0001g0180 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.100+6633G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98950883 | ||||||
| chr9:98951051
|
C | T | 30 | a0001c0001t0002g0022a0001c0013t0001g0046a0002c0002t0001g0043others(27): Show | 30 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+6801C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98951051 | ||||||
| chr9:98951283
|
C | G | 1 | a0002c0002t0001g0302 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.100+7033C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98951283 | ||||||
| chr9:98951513
|
T | G | 1 | a0002c0003t0002g0236 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.100+7263T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98951513 | ||||||
| chr9:98951569
|
C | T | 266 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(263): Show | 266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.100+7319C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98951569 | ||||||
| chr9:98951732
|
AT | A | 30 | a0001c0001t0002g0022a0001c0013t0001g0046a0002c0002t0001g0043others(27): Show | 30 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+7488delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98951732 | |||||
| chr9:98951889
|
A | T | 1 | a0011c0039t0001g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100+7639A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98951889 | ||||||
| chr9:98951960
|
A | G | 3 | a0005c0015t0001g0290a0005c0019t0003g0289a0026c0053t0001g0291 | 3 | HG02155.hp1 NA19010.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.100+7710A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98951960 | ||||||
| chr9:98952001
|
A | T | 255 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(252): Show | 255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.100+7751A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952001 | ||||||
| chr9:98952061
|
G | A | 2 | a0001c0001t0002g0050a0020c0029t0002g0049 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+7811G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952061 | ||||||
| chr9:98952124
|
G | T | 1 | a0001c0001t0002g0288 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.100+7874G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952124 | ||||||
| chr9:98952226
|
G | A | 1 | a0001c0031t0001g0157 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.100+7976G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952226 | ||||||
| chr9:98952504
|
A | T | 10 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(7): Show | 10 | HG00408.hp2 HG00438.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+8254A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952504 | ||||||
| chr9:98952693
|
G | A | 5 | a0002c0003t0002g0130a0005c0015t0001g0154a0013c0047t0001g0093others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+8443G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952693 | ||||||
| chr9:98952726
|
G | T | 2 | a0001c0001t0002g0067a0002c0002t0001g0066 | 2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.100+8476G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952726 | ||||||
| chr9:98952745
|
A | C | 2 | a0001c0001t0002g0050a0020c0029t0002g0049 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+8495A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952745 | ||||||
| chr9:98952984
|
C | A | 1 | a0056c0081t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.100+8734C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98952984 | ||||||
| chr9:98953058
|
G | T | 1 | a0002c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100+8808G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98953058 | ||||||
| chr9:98953316
|
G | A | 42 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(39): Show | 42 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.100+9066G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98953316 | ||||||
| chr9:98953611
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.100+9361T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98953611 | ||||||
| chr9:98953696
|
G | C | 1 | a0001c0013t0001g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.100+9446G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98953696 | ||||||
| chr9:98954019
|
T | A | 2 | a0001c0001t0002g0050a0020c0029t0002g0049 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+9769T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954019 | ||||||
| chr9:98954130
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.100+9880T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954130 | ||||||
| chr9:98954146
|
A | G | 3 | a0004c0005t0001g0307a0007c0008t0002g0306a0011c0016t0001g0309 | 3 | HG02895.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.100+9896A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954146 | ||||||
| chr9:98954169
|
G | A | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.100+9919G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954169 | ||||||
| chr9:98954178
|
G | C | 1 | a0051c0074t0002g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.100+9928G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954178 | ||||||
| chr9:98954213
|
AT | A | 127 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0022others(124): Show | 127 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.100+9970delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98954213 | |||||
| chr9:98954344
|
T | C | 1 | a0025c0032t0002g0243 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.100+10094T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954344 | ||||||
| chr9:98954422
|
A | G | 1 | a0010c0012t0002g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+10172A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954422 | ||||||
| chr9:98954601
|
T | C | 1 | a0001c0001t0002g0057 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.100+10351T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954601 | ||||||
| chr9:98954766
|
G | A | 5 | a0006c0078t0001g0231a0012c0014t0002g0229a0017c0021t0001g0230others(2): Show | 5 | HG01884.hp2 HG03516.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+10516G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954766 | ||||||
| chr9:98954786
|
C | T | 1 | a0004c0005t0001g0101 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.100+10536C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98954786 | ||||||
| chr9:98955131
|
G | T | 10 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(7): Show | 10 | HG00408.hp2 HG00438.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+10881G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98955131 | ||||||
| chr9:98955591
|
C | T | 78 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(75): Show | 78 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.100+11341C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98955591 | ||||||
| chr9:98955652
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.100+11402T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98955652 | ||||||
| chr9:98955719
|
C | T | 31 | a0001c0001t0002g0022a0001c0013t0001g0046a0002c0002t0001g0018others(28): Show | 31 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.100+11469C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98955719 | ||||||
| chr9:98955915
|
A | G | 1 | a0014c0020t0001g0131 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.100+11665A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98955915 | ||||||
| chr9:98956033
|
T | C | 107 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(104): Show | 107 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.100+11783T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956033 | ||||||
| chr9:98956178
|
C | T | 6 | a0001c0001t0002g0219a0001c0001t0002g0222a0002c0003t0002g0223others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+11928C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956178 | ||||||
| chr9:98956186
|
G | C | 129 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0057others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.100+11936G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956186 | ||||||
| chr9:98956262
|
T | C | 97 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(94): Show | 97 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.100+12012T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956262 | ||||||
| chr9:98956340
|
A | G | 1 | a0002c0002t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.100+12090A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956340 | ||||||
| chr9:98956492
|
T | C | 1 | a0005c0019t0003g0140 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.100+12242T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956492 | ||||||
| chr9:98956539
|
T | G | 95 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(92): Show | 95 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+12289T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956539 | ||||||
| chr9:98956845
|
A | G | 1 | a0001c0001t0002g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100+12595A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956845 | ||||||
| chr9:98956962
|
A | G | 1 | a0003c0006t0001g0085 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.100+12712A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98956962 | ||||||
| chr9:98957042
|
C | T | 1 | a0023c0027t0002g0233 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+12792C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98957042 | ||||||
| chr9:98957051
|
G | T | 3 | a0001c0001t0002g0050a0020c0029t0002g0049a0055c0082t0009g0005 | 3 | HG01109.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+12801G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98957051 | ||||||
| chr9:98957252
|
T | C | 3 | a0007c0008t0002g0244a0010c0012t0005g0304a0031c0041t0001g0292 | 3 | HG01081.hp1 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100+13002T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98957252 | ||||||
| chr9:98957256
|
C | T | 1 | a0010c0012t0002g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+13006C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98957256 | ||||||
| chr9:98957474
|
G | A | 1 | a0055c0082t0009g0005 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.100+13224G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98957474 | ||||||
| chr9:98958380
|
T | C | 1 | a0002c0002t0001g0076 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.100+14130T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98958380 | ||||||
| chr9:98958603
|
A | T | 2 | a0020c0029t0004g0156a0022c0026t0004g0139 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.100+14353A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98958603 | ||||||
| chr9:98958639
|
T | G | 101 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(98): Show | 101 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.100+14389T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98958639 | ||||||
| chr9:98958764
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+14514G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98958764 | ||||||
| chr9:98958782
|
G | A | 1 | a0017c0021t0001g0213 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100+14532G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98958782 | ||||||
| chr9:98958848
|
A | T | 106 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(103): Show | 106 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.100+14598A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98958848 | ||||||
| chr9:98958890
|
C | T | 2 | a0010c0075t0007g0002a0055c0082t0009g0005 | 2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.100+14640C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98958890 | ||||||
| chr9:98958924
|
T | C | 77 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(74): Show | 77 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.100+14674T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98958924 | ||||||
| chr9:98959118
|
T | C | 100 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(97): Show | 100 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.100+14868T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98959118 | ||||||
| chr9:98959227
|
C | CA | 25 | a0001c0001t0002g0057a0001c0001t0002g0172a0001c0001t0002g0192others(22): Show | 25 | HG01106.hp2 HG01192.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.100+14997dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98959227 | |||||
| chr9:98959227
|
C | CAA | 10 | a0001c0001t0002g0102a0002c0003t0002g0223a0003c0004t0002g0284others(7): Show | 10 | HG01109.hp1 HG01256.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+14996_100+1499 others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98959227 | |||||
| chr9:98959227
|
C | CAAA | 70 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.100+14995_100+1499 others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98959227 | |||||
| chr9:98959227
|
C | CAAAA | 21 | a0001c0001t0002g0249a0002c0002t0001g0007a0002c0002t0001g0245others(18): Show | 21 | HG00438.hp1 HG00544.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.100+14994_100+1499 others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98959227 | |||||
| chr9:98959505
|
T | G | 3 | a0004c0005t0001g0307a0007c0008t0002g0306a0011c0016t0001g0309 | 3 | HG02895.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.100+15255T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98959505 | ||||||
| chr9:98959508
|
C | T | 2 | a0001c0001t0002g0067a0002c0002t0001g0066 | 2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.100+15258C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98959508 | ||||||
| chr9:98959597
|
T | TA | 8 | a0001c0001t0002g0050a0001c0001t0002g0308a0004c0005t0001g0307others(5): Show | 8 | HG01109.hp1 HG02280.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+15360dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98959597 | |||||
| chr9:98959702
|
C | A | 98 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(95): Show | 98 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.100+15452C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98959702 | ||||||
| chr9:98959852
|
C | T | 1 | a0002c0010t0001g0125 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100+15602C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98959852 | ||||||
| chr9:98959998
|
C | T | 1 | a0019c0024t0006g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100+15748C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98959998 | ||||||
| chr9:98960061
|
A | T | 2 | a0001c0001t0002g0050a0020c0029t0002g0049 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+15811A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960061 | ||||||
| chr9:98960168
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+15918G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960168 | ||||||
| chr9:98960184
|
G | GA | 99 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(96): Show | 99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100+15935dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98960184 | |||||
| chr9:98960235
|
A | C | 99 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(96): Show | 99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100+15985A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960235 | ||||||
| chr9:98960347
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100+16097C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960347 | ||||||
| chr9:98960366
|
C | T | 90 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(87): Show | 90 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.100+16116C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960366 | ||||||
| chr9:98960483
|
A | C | 1 | a0025c0032t0002g0243 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.100+16233A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960483 | ||||||
| chr9:98960505
|
G | A | 30 | a0001c0001t0002g0168a0002c0002t0001g0076a0002c0002t0001g0082others(27): Show | 30 | HG00741.hp2 HG01074.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+16255G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960505 | ||||||
| chr9:98960714
|
G | A | 3 | a0001c0031t0001g0157a0002c0002t0001g0176a0003c0006t0001g0141 | 3 | HG00423.hp1 NA19067.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.100+16464G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960714 | ||||||
| chr9:98960825
|
T | C | 1 | a0010c0012t0005g0215 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100+16575T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960825 | ||||||
| chr9:98960998
|
A | C | 2 | a0010c0012t0002g0221a0010c0075t0007g0002 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.100+16748A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98960998 | ||||||
| chr9:98961109
|
C | T | 1 | a0011c0016t0001g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+16859C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961109 | ||||||
| chr9:98961249
|
C | T | 136 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0057others(133): Show | 136 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.100+16999C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961249 | ||||||
| chr9:98961264
|
G | T | 1 | a0013c0017t0001g0065 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.100+17014G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961264 | ||||||
| chr9:98961590
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.100+17340G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961590 | ||||||
| chr9:98961615
|
G | C | 38 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0265others(35): Show | 38 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.100+17365G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961615 | ||||||
| chr9:98961616
|
G | A | 155 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0050others(152): Show | 155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.100+17366G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961616 | ||||||
| chr9:98961653
|
G | A | 10 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(7): Show | 10 | HG00408.hp2 HG00438.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+17403G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961653 | ||||||
| chr9:98961714
|
C | T | 82 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0001t0002g0249others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+17464C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961714 | ||||||
| chr9:98961739
|
A | G | 137 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0057others(134): Show | 137 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.100+17489A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961739 | ||||||
| chr9:98961806
|
T | C | 6 | a0001c0001t0002g0219a0001c0001t0002g0222a0002c0003t0002g0223others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+17556T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98961806 | ||||||
| chr9:98962135
|
T | G | 1 | a0007c0008t0002g0268 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.100+17885T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962135 | ||||||
| chr9:98962307
|
G | T | 4 | a0002c0003t0002g0012a0002c0003t0007g0003a0010c0012t0002g0011others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+18057G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962307 | ||||||
| chr9:98962404
|
C | G | 226 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0052others(223): Show | 226 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.100+18154C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962404 | ||||||
| chr9:98962459
|
G | T | 10 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(7): Show | 10 | HG00408.hp2 HG00438.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+18209G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962459 | ||||||
| chr9:98962557
|
A | G | 78 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(75): Show | 78 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.100+18307A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962557 | ||||||
| chr9:98962659
|
T | A | 6 | a0001c0001t0002g0219a0001c0001t0002g0222a0002c0003t0002g0223others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+18409T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962659 | ||||||
| chr9:98962661
|
C | A | 1 | a0001c0001t0002g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+18411C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962661 | ||||||
| chr9:98962801
|
A | G | 8 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(5): Show | 8 | HG00408.hp2 HG00438.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+18551A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962801 | ||||||
| chr9:98962819
|
T | G | 119 | a0001c0001t0002g0022a0001c0001t0002g0051a0001c0001t0002g0067others(116): Show | 119 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.100+18569T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962819 | ||||||
| chr9:98962857
|
G | A | 8 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015others(5): Show | 8 | HG00408.hp2 HG00438.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+18607G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962857 | ||||||
| chr9:98962937
|
A | G | 10 | a0001c0001t0002g0089a0001c0001t0002g0123a0002c0003t0002g0012others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+18687A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962937 | ||||||
| chr9:98962993
|
A | G | 11 | a0001c0001t0002g0167a0002c0003t0002g0012a0002c0003t0007g0003others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+18743A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962993 | ||||||
| chr9:98962996
|
T | C | 55 | a0001c0001t0002g0014a0001c0001t0002g0022a0001c0013t0001g0015others(52): Show | 55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.100+18746T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98962996 | ||||||
| chr9:98963056
|
T | C | 1 | a0015c0018t0001g0252 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.100+18806T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963056 | ||||||
| chr9:98963171
|
T | C | 1 | a0004c0005t0001g0010 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.100+18921T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963171 | ||||||
| chr9:98963227
|
A | G | 84 | a0001c0001t0002g0050a0001c0001t0002g0059a0001c0001t0002g0061others(81): Show | 84 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.100+18977A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963227 | ||||||
| chr9:98963244
|
C | A | 4 | a0001c0001t0002g0051a0001c0013t0001g0046a0003c0006t0001g0141others(1): Show | 4 | HG00423.hp1 HG02155.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+18994C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963244 | ||||||
| chr9:98963244
|
C | T | 12 | a0001c0001t0002g0219a0001c0001t0002g0222a0002c0003t0002g0223others(9): Show | 12 | HG01952.hp1 HG02572.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.100+18994C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963244 | ||||||
| chr9:98963247
|
A | C | 52 | a0001c0001t0002g0022a0001c0001t0002g0051a0001c0001t0002g0102others(49): Show | 52 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.100+18997A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963247 | ||||||
| chr9:98963277
|
G | GC | 21 | a0002c0003t0002g0130a0003c0004t0002g0132a0003c0004t0002g0142others(18): Show | 21 | HG00423.hp2 HG00597.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+19027_100+1902 others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963277 | ||||||
| chr9:98963278
|
T | C | 21 | a0002c0003t0002g0130a0003c0004t0002g0132a0003c0004t0002g0142others(18): Show | 21 | HG00423.hp2 HG00597.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+19028T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963278 | ||||||
| chr9:98963278
|
T | TC | 137 | a0001c0001t0002g0014a0001c0001t0002g0050a0001c0001t0002g0057others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.100+19034dupC | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98963278 | |||||
| chr9:98963278
|
TC | T | 7 | a0002c0003t0002g0118a0007c0008t0002g0117a0010c0012t0002g0221others(4): Show | 7 | HG01109.hp1 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+19034delC | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98963278 | |||||
| chr9:98963280
|
C | CT | 6 | a0001c0001t0002g0168a0001c0001t0002g0219a0002c0003t0002g0223others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+19030_100+1903 others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963280 | ||||||
| chr9:98963317
|
A | C | 52 | a0001c0001t0002g0202a0001c0001t0002g0222a0002c0002t0001g0150others(49): Show | 52 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.100+19067A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963317 | ||||||
| chr9:98963453
|
A | G | 23 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0061others(20): Show | 23 | HG00438.hp2 HG01081.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.100+19203A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963453 | ||||||
| chr9:98963552
|
C | A | 2 | a0008c0009t0002g0258a0043c0052t0002g0259 | 2 | HG01168.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.100+19302C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963552 | ||||||
| chr9:98963637
|
G | A | 52 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0061others(49): Show | 52 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.100+19387G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963637 | ||||||
| chr9:98963653
|
T | A | 1 | a0002c0003t0003g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.100+19403T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963653 | ||||||
| chr9:98963812
|
G | A | 5 | a0004c0005t0001g0307a0007c0008t0002g0306a0011c0016t0001g0155others(2): Show | 5 | HG02717.hp2 HG02895.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+19562G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963812 | ||||||
| chr9:98963953
|
G | A | 37 | a0001c0001t0001g0196a0001c0001t0002g0172a0001c0001t0002g0186others(34): Show | 37 | HG00558.hp1 HG00741.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.100+19703G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963953 | ||||||
| chr9:98963956
|
A | G | 1 | a0004c0005t0001g0017 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.100+19706A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963956 | ||||||
| chr9:98963966
|
T | C | 1 | a0029c0072t0001g0034 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.100+19716T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963966 | ||||||
| chr9:98963985
|
T | C | 1 | a0025c0032t0002g0260 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.100+19735T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98963985 | ||||||
| chr9:98964038
|
G | C | 3 | a0001c0001t0002g0202a0001c0001t0002g0253a0001c0001t0002g0254 | 3 | HG01069.hp2 HG01071.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.100+19788G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964038 | ||||||
| chr9:98964137
|
C | T | 30 | a0001c0001t0002g0288a0003c0004t0002g0132a0003c0004t0002g0142others(27): Show | 30 | HG00423.hp2 HG00597.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+19887C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964137 | ||||||
| chr9:98964220
|
T | C | 236 | a0001c0001t0001g0196a0001c0001t0002g0014a0001c0001t0002g0016others(233): Show | 236 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.100+19970T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964220 | ||||||
| chr9:98964305
|
G | T | 55 | a0001c0001t0002g0211a0001c0001t0003g0234a0002c0002t0001g0007others(52): Show | 55 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.100+20055G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964305 | ||||||
| chr9:98964517
|
A | G | 1 | a0010c0012t0005g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.100+20267A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964517 | ||||||
| chr9:98964538
|
C | T | 8 | a0010c0012t0002g0011a0011c0016t0001g0086a0011c0016t0001g0090others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+20288C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964538 | ||||||
| chr9:98964699
|
C | T | 4 | a0002c0003t0002g0193a0002c0077t0002g0174a0006c0007t0001g0194others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+20449C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964699 | ||||||
| chr9:98964874
|
C | T | 1 | a0055c0082t0009g0005 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.100+20624C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964874 | ||||||
| chr9:98964903
|
G | A | 4 | a0008c0009t0002g0024a0008c0009t0002g0026a0008c0009t0002g0237others(1): Show | 4 | HG01069.hp1 HG01123.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+20653G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964903 | ||||||
| chr9:98964976
|
C | G | 3 | a0002c0003t0002g0012a0006c0007t0001g0180a0020c0046t0007g0004 | 3 | HG01884.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.101-20589C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98964976 | ||||||
| chr9:98965113
|
C | T | 4 | a0006c0078t0001g0231a0012c0014t0002g0280a0025c0032t0002g0243others(1): Show | 4 | HG01106.hp1 HG03041.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-20452C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965113 | ||||||
| chr9:98965333
|
G | A | 90 | a0001c0001t0001g0196a0001c0001t0002g0172a0001c0001t0002g0186others(87): Show | 90 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-20232G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965333 | ||||||
| chr9:98965450
|
T | G | 2 | a0036c0045t0003g0212a0037c0044t0003g0138 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.101-20115T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965450 | ||||||
| chr9:98965477
|
G | A | 1 | a0053c0065t0001g0143 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.101-20088G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965477 | ||||||
| chr9:98965541
|
A | G | 31 | a0001c0001t0002g0288a0002c0002t0001g0176a0003c0004t0002g0132others(28): Show | 31 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.101-20024A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965541 | ||||||
| chr9:98965626
|
T | G | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101-19939T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965626 | ||||||
| chr9:98965712
|
C | T | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101-19853C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965712 | ||||||
| chr9:98965751
|
G | A | 40 | a0001c0001t0002g0288a0002c0002t0001g0176a0002c0077t0002g0174others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.101-19814G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965751 | ||||||
| chr9:98965837
|
G | A | 33 | a0001c0001t0002g0288a0002c0002t0001g0176a0002c0003t0002g0193others(30): Show | 33 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.101-19728G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965837 | ||||||
| chr9:98965945
|
C | T | 2 | a0001c0001t0002g0014a0001c0013t0001g0015 | 2 | NA18983.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.101-19620C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965945 | ||||||
| chr9:98965960
|
G | A | 32 | a0001c0001t0001g0196a0001c0001t0002g0172a0001c0001t0002g0186others(29): Show | 32 | HG00558.hp1 HG00741.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.101-19605G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965960 | ||||||
| chr9:98965982
|
T | A | 227 | a0001c0001t0001g0196a0001c0001t0002g0014a0001c0001t0002g0016others(224): Show | 227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.101-19583T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98965982 | ||||||
| chr9:98966239
|
C | A | 75 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0191others(72): Show | 75 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.101-19326C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98966239 | ||||||
| chr9:98966398
|
G | A | 89 | a0001c0001t0002g0211a0001c0001t0002g0288a0001c0001t0003g0234others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.101-19167G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98966398 | ||||||
| chr9:98966582
|
C | A | 1 | a0021c0025t0003g0135 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.101-18983C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98966582 | ||||||
| chr9:98966648
|
G | A | 2 | a0012c0014t0002g0280a0025c0032t0002g0243 | 2 | HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.101-18917G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98966648 | ||||||
| chr9:98966821
|
G | A | 19 | a0001c0001t0001g0196a0001c0001t0002g0172a0001c0001t0002g0186others(16): Show | 19 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-18744G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98966821 | ||||||
| chr9:98966873
|
A | G | 3 | a0003c0004t0002g0142a0005c0015t0001g0163a0013c0017t0001g0071 | 3 | NA18939.hp1 NA18945.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.101-18692A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98966873 | ||||||
| chr9:98966892
|
A | T | 83 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0191others(80): Show | 83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.101-18673A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98966892 | ||||||
| chr9:98966957
|
A | T | 170 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0191others(167): Show | 170 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.101-18608A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98966957 | ||||||
| chr9:98967295
|
G | C | 2 | a0001c0001t0002g0067a0002c0002t0001g0066 | 2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.101-18270G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967295 | ||||||
| chr9:98967300
|
G | A | 2 | a0005c0019t0003g0140a0049c0071t0001g0278 | 2 | HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.101-18265G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967300 | ||||||
| chr9:98967314
|
C | A | 1 | a0039c0050t0001g0183 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.101-18251C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967314 | ||||||
| chr9:98967485
|
C | T | 74 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0191others(71): Show | 74 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.101-18080C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967485 | ||||||
| chr9:98967567
|
G | A | 1 | a0010c0012t0005g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-17998G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967567 | ||||||
| chr9:98967573
|
T | C | 8 | a0004c0005t0001g0307a0007c0008t0002g0306a0011c0016t0001g0155others(5): Show | 8 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-17992T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967573 | ||||||
| chr9:98967596
|
G | A | 31 | a0001c0001t0002g0288a0002c0002t0001g0176a0003c0004t0002g0132others(28): Show | 31 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.101-17969G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967596 | ||||||
| chr9:98967744
|
G | A | 1 | a0055c0082t0009g0005 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.101-17821G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967744 | ||||||
| chr9:98967839
|
G | A | 7 | a0001c0001t0002g0171a0001c0001t0002g0177a0007c0008t0002g0238others(4): Show | 7 | HG00280.hp2 HG01074.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-17726G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967839 | ||||||
| chr9:98967954
|
A | G | 25 | a0001c0001t0001g0196a0001c0001t0002g0089a0001c0001t0002g0123others(22): Show | 25 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.101-17611A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98967954 | ||||||
| chr9:98968044
|
C | A | 1 | a0015c0018t0001g0035 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.101-17521C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968044 | ||||||
| chr9:98968058
|
T | C | 1 | a0015c0018t0001g0035 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.101-17507T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968058 | ||||||
| chr9:98968111
|
G | A | 29 | a0001c0001t0002g0288a0002c0002t0001g0176a0003c0004t0002g0132others(26): Show | 29 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.101-17454G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968111 | ||||||
| chr9:98968176
|
C | A | 1 | a0048c0068t0002g0079 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.101-17389C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968176 | ||||||
| chr9:98968225
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101-17340A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968225 | ||||||
| chr9:98968282
|
A | C | 1 | a0020c0029t0002g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101-17283A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968282 | ||||||
| chr9:98968397
|
C | T | 5 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0007g0003others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-17168C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968397 | ||||||
| chr9:98968470
|
T | C | 1 | a0019c0024t0006g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101-17095T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968470 | ||||||
| chr9:98968750
|
G | A | 1 | a0010c0012t0005g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-16815G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968750 | ||||||
| chr9:98968771
|
G | C | 3 | a0019c0024t0006g0122a0028c0034t0001g0151a0028c0034t0001g0152 | 3 | HG02257.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.101-16794G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968771 | ||||||
| chr9:98968804
|
C | T | 1 | a0010c0012t0002g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.101-16761C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968804 | ||||||
| chr9:98968805
|
G | A | 47 | a0001c0001t0001g0196a0001c0001t0002g0052a0001c0001t0002g0057others(44): Show | 47 | HG00558.hp1 HG00741.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.101-16760G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98968805 | ||||||
| chr9:98969023
|
T | G | 1 | a0010c0012t0005g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-16542T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969023 | ||||||
| chr9:98969117
|
T | C | 72 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0191others(69): Show | 72 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.101-16448T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969117 | ||||||
| chr9:98969123
|
C | T | 3 | a0010c0012t0002g0011a0036c0045t0003g0212a0037c0044t0003g0138 | 3 | HG02717.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.101-16442C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969123 | ||||||
| chr9:98969139
|
A | T | 47 | a0001c0001t0001g0196a0001c0001t0002g0052a0001c0001t0002g0057others(44): Show | 47 | HG00558.hp1 HG00741.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.101-16426A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969139 | ||||||
| chr9:98969210
|
G | A | 7 | a0002c0003t0002g0118a0002c0003t0002g0182a0002c0003t0002g0214others(4): Show | 7 | HG01243.hp2 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-16355G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969210 | ||||||
| chr9:98969304
|
G | A | 2 | a0002c0002t0001g0281a0012c0014t0002g0250 | 2 | HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.101-16261G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969304 | ||||||
| chr9:98969344
|
C | T | 29 | a0001c0001t0002g0288a0002c0002t0001g0176a0003c0004t0002g0132others(26): Show | 29 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.101-16221C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969344 | ||||||
| chr9:98969351
|
T | C | 1 | a0002c0003t0003g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.101-16214T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969351 | ||||||
| chr9:98969377
|
G | A | 1 | a0015c0018t0001g0035 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.101-16188G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969377 | ||||||
| chr9:98969484
|
G | A | 52 | a0001c0001t0002g0211a0001c0001t0003g0234a0002c0002t0001g0007others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.101-16081G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969484 | ||||||
| chr9:98969527
|
C | T | 22 | a0002c0002t0001g0007a0002c0010t0001g0008a0002c0010t0001g0125others(19): Show | 22 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.101-16038C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969527 | ||||||
| chr9:98969947
|
A | C | 1 | a0011c0016t0001g0092 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.101-15618A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98969947 | ||||||
| chr9:98970043
|
T | TA | 8 | a0001c0001t0002g0222a0002c0003t0003g0100a0010c0012t0002g0221others(5): Show | 8 | HG01175.hp1 HG02965.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-15504dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98970043 | |||||
| chr9:98970043
|
TA | T | 151 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0051others(148): Show | 151 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.101-15504delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98970043 | |||||
| chr9:98970043
|
TAA | T | 6 | a0002c0003t0002g0118a0002c0077t0002g0174a0003c0006t0001g0098others(3): Show | 6 | HG02572.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-15505_101-1550 others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98970043 | |||||
| chr9:98970044
|
A | AAAAAAAA others(82): Show |
1 | a0010c0012t0002g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.101-15505_101-1550 others(93): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98970044 | |||||
| chr9:98970117
|
T | C | 1 | a0001c0001t0002g0199 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.101-15448T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98970117 | ||||||
| chr9:98970230
|
T | C | 2 | a0036c0045t0003g0212a0037c0044t0003g0138 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.101-15335T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98970230 | ||||||
| chr9:98970261
|
C | A | 1 | a0046c0079t0004g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.101-15304C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98970261 | ||||||
| chr9:98970306
|
A | G | 75 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0191others(72): Show | 75 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.101-15259A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98970306 | ||||||
| chr9:98970687
|
T | C | 3 | a0010c0012t0005g0215a0030c0030t0005g0127a0030c0030t0005g0128 | 3 | HG02109.hp2 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.101-14878T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98970687 | ||||||
| chr9:98970823
|
CG | C | 3 | a0002c0003t0002g0012a0006c0007t0001g0180a0020c0046t0007g0004 | 3 | HG01884.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.101-14739delG | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98970823 | |||||
| chr9:98970904
|
C | T | 1 | a0024c0028t0002g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.101-14661C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98970904 | ||||||
| chr9:98970905
|
G | A | 3 | a0002c0003t0002g0012a0006c0007t0001g0180a0020c0046t0007g0004 | 3 | HG01884.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.101-14660G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98970905 | ||||||
| chr9:98971018
|
C | T | 3 | a0010c0012t0005g0215a0030c0030t0005g0127a0030c0030t0005g0128 | 3 | HG02109.hp2 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.101-14547C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971018 | ||||||
| chr9:98971060
|
G | A | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-14505G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971060 | ||||||
| chr9:98971244
|
C | A | 1 | a0008c0009t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.101-14321C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971244 | ||||||
| chr9:98971258
|
A | G | 4 | a0008c0009t0002g0297a0010c0012t0002g0087a0010c0012t0002g0277others(1): Show | 4 | HG00280.hp2 HG01074.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-14307A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971258 | ||||||
| chr9:98971580
|
T | C | 281 | a0001c0001t0001g0196a0001c0001t0002g0050a0001c0001t0002g0052others(278): Show | 281 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.101-13985T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971580 | ||||||
| chr9:98971599
|
A | G | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101-13966A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971599 | ||||||
| chr9:98971738
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.101-13827G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971738 | ||||||
| chr9:98971790
|
T | C | 85 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.101-13775T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971790 | ||||||
| chr9:98971829
|
G | A | 1 | a0010c0012t0005g0215 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101-13736G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98971829 | ||||||
| chr9:98972183
|
C | T | 116 | a0001c0001t0002g0172a0001c0031t0001g0157a0002c0002t0001g0176others(113): Show | 116 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.101-13382C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98972183 | ||||||
| chr9:98972227
|
C | T | 1 | a0002c0003t0002g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.101-13338C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98972227 | ||||||
| chr9:98972321
|
C | G | 1 | a0004c0005t0001g0106 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.101-13244C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98972321 | ||||||
| chr9:98972858
|
G | GAGAGCCA others(14): Show |
1 | a0002c0002t0001g0235 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.101-12705_101-1268 others(25): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98972858 | |||||
| chr9:98972874
|
G | A | 21 | a0002c0002t0001g0176a0005c0015t0001g0029a0005c0015t0001g0040others(18): Show | 21 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.101-12691G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98972874 | ||||||
| chr9:98973032
|
C | T | 4 | a0002c0003t0002g0012a0006c0007t0001g0180a0006c0007t0001g0217others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12533C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973032 | ||||||
| chr9:98973095
|
T | G | 1 | a0052c0076t0002g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.101-12470T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973095 | ||||||
| chr9:98973128
|
C | T | 2 | a0005c0019t0003g0054a0005c0019t0003g0062 | 2 | HG02027.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.101-12437C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973128 | ||||||
| chr9:98973151
|
G | C | 1 | a0007c0008t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-12414G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973151 | ||||||
| chr9:98973206
|
G | A | 2 | a0002c0002t0001g0178a0047c0070t0011g0169 | 2 | HG02055.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.101-12359G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973206 | ||||||
| chr9:98973235
|
C | A | 3 | a0002c0003t0003g0100a0010c0012t0002g0220a0010c0012t0002g0221 | 3 | HG03225.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-12330C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973235 | ||||||
| chr9:98973255
|
G | GGA | 4 | a0002c0003t0002g0012a0006c0007t0001g0180a0006c0007t0001g0217others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12294_101-1229 others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98973255 | |||||
| chr9:98973389
|
T | C | 85 | a0001c0001t0002g0172a0002c0002t0001g0007a0002c0002t0001g0018others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.101-12176T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973389 | ||||||
| chr9:98973414
|
T | C | 3 | a0002c0003t0003g0100a0010c0012t0002g0220a0010c0012t0002g0221 | 3 | HG03225.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-12151T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973414 | ||||||
| chr9:98973474
|
T | G | 2 | a0001c0001t0002g0168a0013c0017t0001g0084 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.101-12091T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973474 | ||||||
| chr9:98973482
|
T | A | 1 | a0002c0002t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.101-12083T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973482 | ||||||
| chr9:98973500
|
A | T | 1 | a0002c0010t0001g0161 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.101-12065A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973500 | ||||||
| chr9:98973517
|
C | A | 1 | a0003c0004t0002g0270 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.101-12048C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973517 | ||||||
| chr9:98973686
|
G | A | 2 | a0002c0003t0002g0193a0006c0007t0001g0194 | 2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.101-11879G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973686 | ||||||
| chr9:98973823
|
G | A | 1 | a0002c0003t0008g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101-11742G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98973823 | ||||||
| chr9:98974124
|
G | A | 6 | a0002c0003t0002g0193a0006c0007t0001g0194a0024c0028t0002g0088others(3): Show | 6 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-11441G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98974124 | ||||||
| chr9:98974438
|
A | T | 3 | a0002c0003t0002g0012a0006c0007t0001g0180a0020c0046t0007g0004 | 3 | HG01884.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.101-11127A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98974438 | ||||||
| chr9:98974591
|
C | T | 1 | a0020c0029t0002g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101-10974C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98974591 | ||||||
| chr9:98974760
|
C | T | 1 | a0001c0001t0003g0234 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.101-10805C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98974760 | ||||||
| chr9:98974775
|
G | T | 2 | a0003c0004t0003g0263a0004c0005t0001g0121 | 2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.101-10790G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98974775 | ||||||
| chr9:98974823
|
T | C | 1 | a0040c0056t0002g0009 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.101-10742T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98974823 | ||||||
| chr9:98974989
|
A | ACAGACCT others(331): Show |
1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.101-10561_101-1056 others(342): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98974989 | |||||
| chr9:98975036
|
C | G | 1 | a0002c0002t0001g0076 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.101-10529C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975036 | ||||||
| chr9:98975156
|
T | A | 3 | a0002c0003t0003g0100a0010c0012t0002g0220a0010c0012t0002g0221 | 3 | HG03225.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-10409T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975156 | ||||||
| chr9:98975156
|
T | C | 1 | a0004c0005t0001g0106 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.101-10409T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975156 | ||||||
| chr9:98975175
|
T | C | 4 | a0002c0003t0002g0012a0006c0007t0001g0180a0006c0007t0001g0217others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-10390T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975175 | ||||||
| chr9:98975507
|
A | T | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.101-10058A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975507 | ||||||
| chr9:98975531
|
C | T | 4 | a0002c0003t0002g0193a0006c0007t0001g0194a0030c0030t0005g0127others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-10034C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975531 | ||||||
| chr9:98975772
|
C | T | 3 | a0002c0003t0003g0100a0010c0012t0002g0220a0010c0012t0002g0221 | 3 | HG03225.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-9793C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975772 | ||||||
| chr9:98975813
|
G | C | 10 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0003g0100others(7): Show | 10 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-9752G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975813 | ||||||
| chr9:98975861
|
C | T | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.101-9704C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975861 | ||||||
| chr9:98975905
|
TA | T | 17 | a0001c0001t0002g0167a0002c0003t0002g0223a0002c0003t0002g0224others(14): Show | 17 | HG01081.hp1 HG02257.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-9658delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98975905 | |||||
| chr9:98975906
|
A | G | 182 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(179): Show | 182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.101-9659A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975906 | ||||||
| chr9:98975907
|
A | G | 17 | a0001c0001t0002g0167a0002c0003t0002g0223a0002c0003t0002g0224others(14): Show | 17 | HG01081.hp1 HG02257.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-9658A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98975907 | ||||||
| chr9:98976151
|
C | CGG | 4 | a0002c0003t0002g0012a0006c0007t0001g0180a0006c0007t0001g0217others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-9414_101-9413i others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976151 | ||||||
| chr9:98976156
|
G | C | 1 | a0005c0015t0001g0040 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.101-9409G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976156 | ||||||
| chr9:98976188
|
A | C | 8 | a0002c0003t0002g0193a0006c0007t0001g0194a0006c0078t0001g0231others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-9377A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976188 | ||||||
| chr9:98976218
|
C | A | 8 | a0002c0003t0002g0193a0006c0007t0001g0194a0006c0078t0001g0231others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-9347C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976218 | ||||||
| chr9:98976289
|
A | G | 9 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0007g0003others(6): Show | 9 | HG01081.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-9276A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976289 | ||||||
| chr9:98976567
|
A | G | 3 | a0009c0011t0001g0103a0009c0011t0002g0037a0009c0011t0002g0159 | 3 | HG00544.hp1 HG02071.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.101-8998A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976567 | ||||||
| chr9:98976707
|
G | T | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.101-8858G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976707 | ||||||
| chr9:98976765
|
A | C | 3 | a0001c0001t0002g0050a0001c0001t0002g0167a0001c0001t0002g0308 | 3 | HG02280.hp2 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.101-8800A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976765 | ||||||
| chr9:98976852
|
G | A | 3 | a0002c0003t0002g0182a0002c0003t0002g0214a0006c0007t0001g0216 | 3 | HG01243.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.101-8713G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976852 | ||||||
| chr9:98976853
|
C | T | 1 | a0018c0023t0002g0266 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.101-8712C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976853 | ||||||
| chr9:98976900
|
G | T | 1 | a0001c0013t0001g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.101-8665G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98976900 | ||||||
| chr9:98977427
|
A | G | 202 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(199): Show | 202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.101-8138A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98977427 | ||||||
| chr9:98977520
|
G | A | 1 | a0007c0008t0002g0306 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.101-8045G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98977520 | ||||||
| chr9:98977553
|
T | G | 1 | a0036c0045t0003g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.101-8012T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98977553 | ||||||
| chr9:98977671
|
C | T | 2 | a0002c0003t0002g0179a0002c0003t0002g0184 | 2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.101-7894C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98977671 | ||||||
| chr9:98977724
|
T | G | 70 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(67): Show | 70 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.101-7841T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98977724 | ||||||
| chr9:98977998
|
C | T | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-7567C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98977998 | ||||||
| chr9:98978064
|
C | T | 1 | a0006c0078t0001g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101-7501C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978064 | ||||||
| chr9:98978065
|
C | G | 9 | a0002c0003t0002g0193a0002c0003t0003g0100a0006c0007t0001g0194others(6): Show | 9 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-7500C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978065 | ||||||
| chr9:98978115
|
G | A | 80 | a0001c0031t0001g0157a0003c0004t0001g0030a0003c0004t0002g0132others(77): Show | 80 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.101-7450G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978115 | ||||||
| chr9:98978130
|
A | G | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101-7435A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978130 | ||||||
| chr9:98978156
|
G | A | 1 | a0006c0078t0001g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101-7409G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978156 | ||||||
| chr9:98978222
|
G | T | 2 | a0001c0001t0002g0249a0001c0001t0002g0251 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.101-7343G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978222 | ||||||
| chr9:98978321
|
C | A | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.101-7244C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978321 | ||||||
| chr9:98978322
|
G | C | 171 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(168): Show | 171 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.101-7243G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978322 | ||||||
| chr9:98978450
|
C | G | 1 | a0002c0002t0001g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.101-7115C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978450 | ||||||
| chr9:98978577
|
G | A | 9 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(6): Show | 9 | HG01081.hp1 HG01081.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-6988G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978577 | ||||||
| chr9:98978597
|
C | G | 8 | a0002c0003t0002g0193a0002c0003t0003g0100a0006c0007t0001g0194others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-6968C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98978597 | ||||||
| chr9:98979231
|
C | A | 129 | a0001c0031t0001g0157a0002c0003t0002g0130a0002c0003t0002g0179others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.101-6334C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979231 | ||||||
| chr9:98979337
|
A | C | 1 | a0006c0078t0001g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101-6228A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979337 | ||||||
| chr9:98979384
|
G | A | 199 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(196): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.101-6181G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979384 | ||||||
| chr9:98979402
|
G | A | 1 | a0016c0022t0001g0301 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.101-6163G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979402 | ||||||
| chr9:98979459
|
G | A | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.101-6106G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979459 | ||||||
| chr9:98979516
|
C | G | 4 | a0020c0029t0002g0049a0020c0029t0004g0156a0030c0030t0005g0127others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6049C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979516 | ||||||
| chr9:98979647
|
T | TTTA | 202 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(199): Show | 202 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.101-5900_101-5898d others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98979647 | |||||
| chr9:98979687
|
A | T | 200 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(197): Show | 200 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.101-5878A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979687 | ||||||
| chr9:98979812
|
T | C | 4 | a0001c0031t0001g0157a0003c0006t0001g0141a0004c0005t0001g0017others(1): Show | 4 | HG00423.hp1 NA18982.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-5753T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979812 | ||||||
| chr9:98979815
|
C | T | 2 | a0002c0003t0008g0185a0051c0074t0002g0207 | 2 | HG02559.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.101-5750C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979815 | ||||||
| chr9:98979819
|
C | T | 4 | a0001c0001t0002g0171a0001c0001t0002g0177a0025c0032t0002g0243others(1): Show | 4 | HG01106.hp1 HG01358.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-5746C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979819 | ||||||
| chr9:98979866
|
G | T | 1 | a0026c0054t0001g0013 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.101-5699G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979866 | ||||||
| chr9:98979891
|
C | G | 5 | a0007c0008t0002g0117a0007c0008t0002g0136a0007c0008t0002g0244others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-5674C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979891 | ||||||
| chr9:98979954
|
C | T | 8 | a0002c0003t0002g0193a0003c0004t0002g0256a0006c0007t0001g0194others(5): Show | 8 | HG02027.hp2 HG02257.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-5611C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98979954 | ||||||
| chr9:98979963
|
C | CGTAGGCA others(28): Show |
1 | a0001c0001t0002g0016 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.101-5601_101-5567d others(37): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98979963 | |||||
| chr9:98980005
|
A | G | 1 | a0009c0011t0002g0055 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.101-5560A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980005 | ||||||
| chr9:98980047
|
A | T | 2 | a0006c0078t0001g0231a0046c0079t0004g0283 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-5518A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980047 | ||||||
| chr9:98980160
|
CA | C | 201 | a0001c0001t0002g0016a0001c0031t0001g0157a0002c0002t0001g0007others(198): Show | 201 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.101-5392delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98980160 | |||||
| chr9:98980321
|
C | T | 3 | a0020c0029t0004g0156a0030c0030t0005g0127a0030c0030t0005g0128 | 3 | HG02109.hp2 HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.101-5244C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980321 | ||||||
| chr9:98980370
|
G | T | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101-5195G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980370 | ||||||
| chr9:98980507
|
G | A | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-5058G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980507 | ||||||
| chr9:98980525
|
T | C | 204 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(201): Show | 204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.101-5040T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980525 | ||||||
| chr9:98980539
|
G | A | 2 | a0006c0078t0001g0231a0046c0079t0004g0283 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-5026G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980539 | ||||||
| chr9:98980702
|
G | A | 2 | a0001c0001t0002g0168a0013c0017t0001g0084 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.101-4863G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980702 | ||||||
| chr9:98980836
|
C | T | 4 | a0001c0031t0001g0157a0003c0006t0001g0141a0004c0005t0001g0017others(1): Show | 4 | HG00423.hp1 NA18982.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-4729C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980836 | ||||||
| chr9:98980848
|
C | A | 1 | a0010c0012t0002g0087 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.101-4717C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980848 | ||||||
| chr9:98980891
|
T | C | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.101-4674T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98980891 | ||||||
| chr9:98981035
|
G | A | 81 | a0001c0031t0001g0157a0002c0003t0002g0130a0003c0004t0001g0030others(78): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.101-4530G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98981035 | ||||||
| chr9:98981054
|
T | C | 153 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(150): Show | 153 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.101-4511T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98981054 | ||||||
| chr9:98981057
|
G | A | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-4508G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98981057 | ||||||
| chr9:98981167
|
G | A | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-4398G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98981167 | ||||||
| chr9:98981246
|
T | C | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-4319T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98981246 | ||||||
| chr9:98981432
|
G | C | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-4133G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98981432 | ||||||
| chr9:98981655
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.101-3910C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98981655 | ||||||
| chr9:98981717
|
A | G | 1 | a0014c0048t0003g0115 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.101-3848A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98981717 | ||||||
| chr9:98982060
|
T | A | 1 | a0005c0019t0003g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.101-3505T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98982060 | ||||||
| chr9:98982065
|
C | G | 1 | a0005c0019t0003g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.101-3500C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98982065 | ||||||
| chr9:98982078
|
G | T | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.101-3487G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98982078 | ||||||
| chr9:98982085
|
G | A | 1 | a0007c0008t0002g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.101-3480G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98982085 | ||||||
| chr9:98982131
|
T | G | 89 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0061others(86): Show | 89 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.101-3434T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98982131 | ||||||
| chr9:98982168
|
A | C | 2 | a0002c0003t0002g0193a0006c0007t0001g0194 | 2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.101-3397A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98982168 | ||||||
| chr9:98982372
|
A | G | 7 | a0002c0003t0002g0118a0002c0003t0002g0182a0002c0003t0002g0214others(4): Show | 7 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-3193A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98982372 | ||||||
| chr9:98982501
|
A | G | 81 | a0001c0031t0001g0157a0002c0003t0002g0130a0003c0004t0001g0030others(78): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.101-3064A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98982501 | ||||||
| chr9:98982617
|
C | CGAT | 176 | a0001c0031t0001g0157a0002c0002t0001g0007a0002c0002t0001g0018others(173): Show | 176 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.101-2931_101-2929d others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98982617 | |||||
| chr9:98983018
|
CTAAT | C | 7 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(4): Show | 7 | HG01081.hp1 HG01081.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-2544_101-2541d others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr9 | 98983018 | |||||
| chr9:98983324
|
C | A | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.101-2241C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98983324 | ||||||
| chr9:98983355
|
G | A | 81 | a0001c0031t0001g0157a0002c0003t0002g0130a0003c0004t0001g0030others(78): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.101-2210G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98983355 | ||||||
| chr9:98983377
|
C | T | 9 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-2188C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98983377 | ||||||
| chr9:98983402
|
A | G | 1 | a0009c0011t0002g0037 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.101-2163A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98983402 | ||||||
| chr9:98983420
|
A | G | 7 | a0002c0003t0002g0118a0002c0003t0002g0182a0002c0003t0002g0214others(4): Show | 7 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-2145A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98983420 | ||||||
| chr9:98983506
|
G | A | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101-2059G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98983506 | ||||||
| chr9:98983828
|
C | T | 7 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(4): Show | 7 | HG01081.hp1 HG01081.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-1737C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98983828 | ||||||
| chr9:98983850
|
G | A | 1 | a0016c0022t0001g0301 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.101-1715G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98983850 | ||||||
| chr9:98984549
|
C | G | 1 | a0015c0018t0001g0033 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.101-1016C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98984549 | ||||||
| chr9:98984659
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-906G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98984659 | ||||||
| chr9:98984661
|
C | T | 1 | a0003c0004t0002g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.101-904C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98984661 | ||||||
| chr9:98984843
|
G | A | 1 | a0039c0050t0001g0183 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.101-722G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98984843 | ||||||
| chr9:98985259
|
G | A | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-306G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98985259 | ||||||
| chr9:98985308
|
A | G | 7 | a0002c0003t0002g0193a0006c0007t0001g0194a0010c0012t0002g0011others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-257A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98985308 | ||||||
| chr9:98985365
|
C | T | 7 | a0002c0003t0002g0193a0006c0007t0001g0194a0010c0012t0002g0011others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-200C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98985365 | ||||||
| chr9:98985401
|
T | C | 16 | a0001c0001t0002g0050a0001c0001t0002g0308a0002c0003t0002g0118others(13): Show | 16 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.101-164T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 2/41 | chr9 | 98985401 | ||||||
| chr9:98986264
|
C | T | 2 | a0002c0003t0002g0179a0002c0003t0002g0184 | 2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.648+152C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98986264 | ||||||
| chr9:98986575
|
G | A | 7 | a0002c0003t0002g0193a0006c0007t0001g0194a0010c0012t0002g0011others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.648+463G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98986575 | ||||||
| chr9:98986625
|
AAAATGGG others(4): Show |
A | 1 | a0001c0001t0002g0016 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.648+514_648+524del others(11): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98986625 | ||||||
| chr9:98986697
|
G | A | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.648+585G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98986697 | ||||||
| chr9:98986698
|
T | C | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.648+586T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98986698 | ||||||
| chr9:98986714
|
G | A | 1 | a0002c0002t0001g0150 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.649-580G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98986714 | ||||||
| chr9:98986930
|
T | C | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.649-364T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98986930 | ||||||
| chr9:98987041
|
C | T | 27 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(24): Show | 27 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.649-253C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98987041 | ||||||
| chr9:98987047
|
T | G | 3 | a0002c0003t0002g0012a0006c0007t0001g0180a0006c0007t0001g0217 | 3 | HG01884.hp1 HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.649-247T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98987047 | ||||||
| chr9:98987190
|
C | T | 5 | a0002c0003t0002g0118a0002c0003t0002g0182a0002c0003t0002g0214others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-104C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98987190 | ||||||
| chr9:98987195
|
T | G | 1 | a0009c0011t0002g0037 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.649-99T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98987195 | ||||||
| chr9:98987216
|
C | A | 189 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.649-78C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98987216 | ||||||
| chr9:98987222
|
A | C | 27 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(24): Show | 27 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.649-72A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 3/41 | chr9 | 98987222 | ||||||
| chr9:98987573
|
T | C | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.723+205T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98987573 | ||||||
| chr9:98987603
|
C | T | 7 | a0002c0003t0002g0193a0006c0007t0001g0194a0010c0012t0002g0011others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.723+235C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98987603 | ||||||
| chr9:98987604
|
G | A | 1 | a0030c0030t0005g0127 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.723+236G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98987604 | ||||||
| chr9:98987623
|
G | A | 5 | a0007c0008t0002g0306a0011c0016t0001g0086a0011c0016t0001g0090others(2): Show | 5 | HG01243.hp1 HG02895.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.723+255G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98987623 | ||||||
| chr9:98987661
|
A | T | 156 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(153): Show | 156 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.723+293A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98987661 | ||||||
| chr9:98987743
|
C | T | 4 | a0024c0028t0002g0088a0024c0028t0004g0165a0036c0045t0003g0212others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+375C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98987743 | ||||||
| chr9:98987833
|
T | C | 2 | a0001c0001t0002g0168a0013c0017t0001g0084 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.723+465T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98987833 | ||||||
| chr9:98987975
|
GT | G | 264 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0057others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.723+609delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98987975 | |||||
| chr9:98988013
|
T | C | 7 | a0010c0012t0002g0220a0010c0012t0002g0221a0020c0029t0002g0049others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.723+645T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988013 | ||||||
| chr9:98988065
|
C | CCCAGGGA others(8): Show |
1 | a0003c0004t0002g0299 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.723+703_723+717dup others(15): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98988065 | |||||
| chr9:98988167
|
A | G | 1 | a0002c0003t0003g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.723+799A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988167 | ||||||
| chr9:98988223
|
G | A | 193 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(190): Show | 193 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.723+855G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988223 | ||||||
| chr9:98988321
|
G | A | 1 | a0004c0005t0001g0261 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.724-857G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988321 | ||||||
| chr9:98988355
|
A | C | 1 | a0007c0008t0002g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.724-823A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988355 | ||||||
| chr9:98988492
|
C | A | 79 | a0003c0004t0001g0030a0003c0004t0002g0132a0003c0004t0002g0142others(76): Show | 79 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.724-686C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988492 | ||||||
| chr9:98988780
|
C | T | 86 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(83): Show | 86 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.724-398C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988780 | ||||||
| chr9:98988790
|
G | T | 2 | a0010c0012t0005g0215a0010c0075t0007g0002 | 2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.724-388G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988790 | ||||||
| chr9:98988798
|
T | C | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-380T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988798 | ||||||
| chr9:98988825
|
C | A | 198 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(195): Show | 198 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.724-353C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988825 | ||||||
| chr9:98988878
|
G | A | 8 | a0002c0003t0002g0012a0002c0003t0002g0118a0002c0003t0002g0182others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.724-300G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988878 | ||||||
| chr9:98988938
|
A | T | 5 | a0002c0003t0002g0118a0002c0003t0002g0182a0002c0003t0002g0214others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-240A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98988938 | ||||||
| chr9:98989013
|
G | A | 2 | a0002c0003t0002g0012a0006c0007t0001g0180 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.724-165G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98989013 | ||||||
| chr9:98989023
|
G | GAC | 77 | a0001c0001t0002g0014a0001c0001t0002g0113a0001c0001t0002g0168others(74): Show | 77 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.724-114_724-113dup others(2): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989023
|
G | GACAC | 45 | a0001c0001t0001g0196a0001c0001t0002g0148a0001c0001t0002g0265others(42): Show | 45 | HG00280.hp2 HG00423.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.724-116_724-113dup others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989023
|
G | GACACAC | 42 | a0002c0002t0001g0076a0002c0002t0001g0178a0003c0004t0001g0030others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.724-118_724-113dup others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989023
|
G | GACACACA others(1): Show |
17 | a0003c0004t0002g0271a0003c0004t0002g0275a0003c0004t0002g0303others(14): Show | 17 | HG01081.hp1 HG01261.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.724-120_724-113dup others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989023
|
G | GACACACA others(3): Show |
9 | a0003c0004t0003g0263a0003c0006t0001g0096a0003c0006t0001g0098others(6): Show | 9 | HG01243.hp1 HG01981.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.724-122_724-113dup others(10): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989023
|
GAC | G | 28 | a0001c0001t0002g0050a0001c0001t0002g0167a0001c0001t0002g0172others(25): Show | 28 | HG00408.hp2 HG01069.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.724-114_724-113del others(2): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989023
|
GACAC | G | 12 | a0001c0001t0002g0070a0001c0001t0002g0089a0001c0001t0002g0123others(9): Show | 12 | HG02486.hp2 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.724-116_724-113del others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989023
|
GACACAC | G | 5 | a0012c0014t0012g0210a0014c0020t0001g0294a0014c0049t0001g0300others(2): Show | 5 | HG00558.hp1 HG01175.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-118_724-113del others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989023
|
GACACACA others(1): Show |
G | 5 | a0010c0012t0002g0011a0019c0024t0006g0122a0019c0024t0006g0166others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-120_724-113del others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | INFO_REALIGN_3_PRIME | chr9 | 98989023 | |||||
| chr9:98989097
|
T | G | 1 | a0020c0029t0002g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.724-81T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 4/41 | chr9 | 98989097 | ||||||
| chr9:98989325
|
G | A | 9 | a0002c0003t0002g0012a0002c0003t0002g0193a0006c0007t0001g0180others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.804+67G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989325 | ||||||
| chr9:98989334
|
G | A | 1 | a0025c0032t0002g0260 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.804+76G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989334 | ||||||
| chr9:98989416
|
T | C | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+158T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989416 | ||||||
| chr9:98989660
|
G | A | 1 | a0005c0015t0001g0290 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.804+402G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989660 | ||||||
| chr9:98989734
|
G | A | 46 | a0002c0003t0002g0012a0002c0003t0002g0118a0002c0003t0002g0179others(43): Show | 46 | HG00423.hp2 HG00597.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.804+476G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989734 | ||||||
| chr9:98989764
|
C | T | 1 | a0053c0065t0001g0143 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.804+506C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989764 | ||||||
| chr9:98989807
|
C | T | 81 | a0003c0004t0001g0030a0003c0004t0002g0132a0003c0004t0002g0142others(78): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.804+549C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989807 | ||||||
| chr9:98989915
|
G | T | 2 | a0010c0012t0005g0215a0010c0075t0007g0002 | 2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.804+657G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989915 | ||||||
| chr9:98989948
|
A | T | 1 | a0009c0011t0002g0037 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.804+690A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98989948 | ||||||
| chr9:98990009
|
A | G | 309 | a0001c0001t0001g0196a0001c0001t0002g0014a0001c0001t0002g0016others(306): Show | 309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.804+751A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990009 | ||||||
| chr9:98990147
|
G | C | 10 | a0003c0004t0002g0132a0003c0004t0002g0142a0003c0004t0002g0270others(7): Show | 10 | NA18939.hp1 NA18942.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.804+889G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990147 | ||||||
| chr9:98990179
|
T | G | 1 | a0006c0007t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.804+921T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990179 | ||||||
| chr9:98990202
|
G | A | 200 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(197): Show | 200 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.804+944G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990202 | ||||||
| chr9:98990254
|
A | G | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804+996A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990254 | ||||||
| chr9:98990280
|
C | T | 5 | a0002c0003t0002g0118a0002c0003t0002g0182a0002c0003t0002g0214others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+1022C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990280 | ||||||
| chr9:98990397
|
A | G | 1 | a0055c0082t0009g0005 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.804+1139A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990397 | ||||||
| chr9:98990673
|
C | T | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1415C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990673 | ||||||
| chr9:98990675
|
G | A | 42 | a0002c0003t0002g0118a0002c0003t0002g0179a0002c0003t0002g0182others(39): Show | 42 | HG00423.hp2 HG00597.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.804+1417G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990675 | ||||||
| chr9:98990683
|
A | G | 200 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(197): Show | 200 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.804+1425A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990683 | ||||||
| chr9:98990710
|
G | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0013t0001g0015 | 3 | NA18983.hp1 NA18984.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.804+1452G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990710 | ||||||
| chr9:98990806
|
G | C | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1548G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990806 | ||||||
| chr9:98990837
|
C | T | 83 | a0003c0004t0001g0030a0003c0004t0002g0132a0003c0004t0002g0142others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.804+1579C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990837 | ||||||
| chr9:98990868
|
G | A | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.804+1610G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990868 | ||||||
| chr9:98990880
|
A | C | 1 | a0010c0012t0005g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.804+1622A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990880 | ||||||
| chr9:98990967
|
C | T | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1709C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98990967 | ||||||
| chr9:98991001
|
G | C | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.804+1743G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991001 | ||||||
| chr9:98991119
|
C | T | 1 | a0014c0048t0003g0115 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.804+1861C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991119 | ||||||
| chr9:98991132
|
C | T | 1 | a0009c0011t0003g0246 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.804+1874C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991132 | ||||||
| chr9:98991133
|
G | A | 4 | a0001c0001t0002g0113a0001c0001t0002g0148a0010c0012t0002g0220others(1): Show | 4 | HG00642.hp1 HG01175.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+1875G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991133 | ||||||
| chr9:98991154
|
G | C | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1896G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991154 | ||||||
| chr9:98991226
|
C | G | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.804+1968C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991226 | ||||||
| chr9:98991227
|
A | G | 200 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(197): Show | 200 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.804+1969A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991227 | ||||||
| chr9:98991230
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.804+1972C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991230 | ||||||
| chr9:98991259
|
AC | A | 238 | a0001c0001t0001g0196a0001c0001t0002g0014a0001c0001t0002g0016others(235): Show | 238 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.804+2010delC | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | INFO_REALIGN_3_PRIME | chr9 | 98991259 | |||||
| chr9:98991269
|
A | G | 2 | a0002c0003t0002g0012a0006c0007t0001g0180 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.804+2011A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991269 | ||||||
| chr9:98991280
|
A | G | 1 | a0006c0007t0001g0160 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.804+2022A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991280 | ||||||
| chr9:98991333
|
T | C | 8 | a0001c0001t0002g0172a0001c0001t0002g0222a0002c0067t0002g0206others(5): Show | 8 | HG00558.hp1 HG01516.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+2075T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991333 | ||||||
| chr9:98991465
|
C | T | 1 | a0044c0058t0002g0144 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.804+2207C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991465 | ||||||
| chr9:98991741
|
C | T | 1 | a0021c0025t0003g0255 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.804+2483C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991741 | ||||||
| chr9:98991909
|
A | G | 1 | a0025c0032t0002g0243 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.804+2651A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991909 | ||||||
| chr9:98991918
|
G | A | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.804+2660G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991918 | ||||||
| chr9:98991920
|
T | A | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804+2662T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98991920 | ||||||
| chr9:98992038
|
G | C | 2 | a0002c0002t0001g0043a0002c0002t0001g0245 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.804+2780G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992038 | ||||||
| chr9:98992041
|
G | A | 8 | a0001c0001t0002g0172a0001c0001t0002g0222a0002c0067t0002g0206others(5): Show | 8 | HG00558.hp1 HG01516.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+2783G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992041 | ||||||
| chr9:98992075
|
G | A | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804+2817G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992075 | ||||||
| chr9:98992082
|
A | G | 1 | a0005c0015t0001g0029 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.804+2824A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992082 | ||||||
| chr9:98992100
|
G | A | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.804+2842G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992100 | ||||||
| chr9:98992100
|
G | T | 59 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(56): Show | 59 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.804+2842G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992100 | ||||||
| chr9:98992162
|
C | T | 83 | a0003c0004t0001g0030a0003c0004t0002g0132a0003c0004t0002g0142others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.804+2904C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992162 | ||||||
| chr9:98992210
|
G | A | 2 | a0001c0001t0002g0253a0001c0001t0002g0254 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.804+2952G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992210 | ||||||
| chr9:98992251
|
C | T | 6 | a0002c0003t0002g0236a0007c0008t0002g0306a0011c0016t0001g0086others(3): Show | 6 | HG00733.hp2 HG01243.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+2993C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992251 | ||||||
| chr9:98992261
|
G | T | 1 | a0001c0001t0002g0051 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.804+3003G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992261 | ||||||
| chr9:98992298
|
G | A | 4 | a0002c0003t0002g0118a0002c0003t0002g0182a0002c0003t0002g0214others(1): Show | 4 | HG01243.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+3040G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992298 | ||||||
| chr9:98992374
|
C | T | 7 | a0006c0078t0001g0231a0010c0012t0002g0087a0010c0012t0002g0277others(4): Show | 7 | HG00280.hp2 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+3116C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992374 | ||||||
| chr9:98992392
|
G | A | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+3134G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992392 | ||||||
| chr9:98992517
|
C | T | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.804+3259C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992517 | ||||||
| chr9:98992526
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.804+3268C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992526 | ||||||
| chr9:98992563
|
G | C | 7 | a0006c0078t0001g0231a0010c0012t0002g0087a0010c0012t0002g0277others(4): Show | 7 | HG00280.hp2 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+3305G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992563 | ||||||
| chr9:98992586
|
T | C | 200 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(197): Show | 200 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.804+3328T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992586 | ||||||
| chr9:98992601
|
C | T | 1 | a0009c0011t0003g0246 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.804+3343C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992601 | ||||||
| chr9:98992639
|
G | T | 3 | a0002c0077t0002g0174a0024c0028t0002g0088a0024c0028t0004g0165 | 3 | HG02717.hp2 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.804+3381G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992639 | ||||||
| chr9:98992781
|
G | A | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804+3523G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992781 | ||||||
| chr9:98992914
|
A | G | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.804+3656A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98992914 | ||||||
| chr9:98993067
|
G | A | 3 | a0001c0001t0002g0050a0001c0001t0002g0167a0001c0001t0002g0308 | 3 | HG02280.hp2 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.804+3809G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993067 | ||||||
| chr9:98993121
|
C | A | 1 | a0008c0009t0002g0024 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.805-3813C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993121 | ||||||
| chr9:98993208
|
C | A | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.805-3726C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993208 | ||||||
| chr9:98993443
|
C | T | 1 | a0002c0003t0002g0118 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.805-3491C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993443 | ||||||
| chr9:98993446
|
G | A | 1 | a0043c0052t0002g0259 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.805-3488G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993446 | ||||||
| chr9:98993532
|
A | T | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-3402A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993532 | ||||||
| chr9:98993534
|
G | A | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.805-3400G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993534 | ||||||
| chr9:98993618
|
A | G | 59 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(56): Show | 59 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.805-3316A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993618 | ||||||
| chr9:98993705
|
C | A | 5 | a0002c0003t0002g0118a0002c0003t0002g0182a0002c0003t0002g0214others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-3229C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98993705 | ||||||
| chr9:98994057
|
C | G | 1 | a0002c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.805-2877C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98994057 | ||||||
| chr9:98994117
|
G | T | 1 | a0008c0009t0002g0026 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.805-2817G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98994117 | ||||||
| chr9:98994148
|
T | G | 59 | a0002c0002t0001g0007a0002c0002t0001g0018a0002c0002t0001g0043others(56): Show | 59 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.805-2786T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98994148 | ||||||
| chr9:98994286
|
C | T | 1 | a0007c0008t0002g0240 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.805-2648C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98994286 | ||||||
| chr9:98994289
|
G | C | 4 | a0002c0003t0002g0182a0002c0003t0002g0214a0006c0007t0001g0216others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-2645G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98994289 | ||||||
| chr9:98994338
|
G | A | 80 | a0002c0003t0002g0130a0003c0004t0001g0030a0003c0004t0002g0132others(77): Show | 80 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.805-2596G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98994338 | ||||||
| chr9:98994381
|
G | A | 2 | a0007c0008t0002g0238a0007c0008t0002g0239 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.805-2553G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98994381 | ||||||
| chr9:98994492
|
C | G | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.805-2442C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98994492 | ||||||
| chr9:98995400
|
C | T | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.805-1534C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98995400 | ||||||
| chr9:98995478
|
G | T | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.805-1456G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98995478 | ||||||
| chr9:98995501
|
C | T | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1433C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98995501 | ||||||
| chr9:98995766
|
C | T | 1 | a0005c0059t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.805-1168C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98995766 | ||||||
| chr9:98996005
|
T | G | 38 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0193others(35): Show | 38 | HG00423.hp2 HG00597.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.805-929T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996005 | ||||||
| chr9:98996070
|
A | G | 64 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(61): Show | 64 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.805-864A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996070 | ||||||
| chr9:98996079
|
T | G | 6 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(3): Show | 6 | HG01081.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-855T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996079 | ||||||
| chr9:98996298
|
C | A | 1 | a0009c0011t0001g0103 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.805-636C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996298 | ||||||
| chr9:98996309
|
T | C | 1 | a0011c0016t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.805-625T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996309 | ||||||
| chr9:98996336
|
T | C | 1 | a0008c0009t0002g0001 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.805-598T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996336 | ||||||
| chr9:98996499
|
C | T | 4 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0007g0003others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-435C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996499 | ||||||
| chr9:98996656
|
G | C | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.805-278G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996656 | ||||||
| chr9:98996734
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.805-200C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 5/41 | chr9 | 98996734 | ||||||
| chr9:98997090
|
G | A | 22 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.952+9G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98997090 | ||||||
| chr9:98997105
|
C | T | 4 | a0002c0003t0002g0182a0002c0003t0002g0214a0006c0007t0001g0216others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+24C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98997105 | ||||||
| chr9:98997145
|
G | A | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.952+64G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98997145 | ||||||
| chr9:98997146
|
G | A | 85 | a0002c0003t0002g0130a0003c0004t0001g0030a0003c0004t0002g0132others(82): Show | 85 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.952+65G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98997146 | ||||||
| chr9:98997366
|
T | C | 1 | a0001c0001t0002g0067 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.952+285T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98997366 | ||||||
| chr9:98997714
|
G | T | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.952+633G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98997714 | ||||||
| chr9:98997744
|
T | C | 204 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(201): Show | 204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.952+663T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98997744 | ||||||
| chr9:98997894
|
T | C | 3 | a0014c0020t0001g0294a0014c0048t0003g0115a0014c0049t0001g0300 | 3 | HG00558.hp1 NA18967.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.952+813T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98997894 | ||||||
| chr9:98998275
|
A | G | 1 | a0008c0009t0002g0001 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.952+1194A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998275 | ||||||
| chr9:98998409
|
A | T | 1 | a0001c0013t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.952+1328A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998409 | ||||||
| chr9:98998415
|
T | C | 2 | a0036c0045t0003g0212a0037c0044t0003g0138 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.952+1334T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998415 | ||||||
| chr9:98998458
|
C | G | 1 | a0007c0037t0001g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.952+1377C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998458 | ||||||
| chr9:98998619
|
T | G | 1 | a0002c0010t0001g0107 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.952+1538T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998619 | ||||||
| chr9:98998623
|
C | G | 62 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(59): Show | 62 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.952+1542C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998623 | ||||||
| chr9:98998651
|
C | T | 1 | a0004c0005t0001g0006 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.952+1570C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998651 | ||||||
| chr9:98998717
|
G | A | 1 | a0016c0022t0002g0078 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.952+1636G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998717 | ||||||
| chr9:98998792
|
C | G | 2 | a0003c0004t0002g0188a0003c0004t0002g0189 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.952+1711C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998792 | ||||||
| chr9:98998843
|
T | C | 26 | a0002c0003t0002g0182a0002c0003t0002g0214a0005c0015t0001g0029others(23): Show | 26 | HG00423.hp2 HG00597.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.952+1762T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998843 | ||||||
| chr9:98998888
|
C | T | 1 | a0002c0003t0003g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.952+1807C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998888 | ||||||
| chr9:98998959
|
G | T | 204 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(201): Show | 204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.952+1878G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998959 | ||||||
| chr9:98998973
|
G | A | 1 | a0018c0023t0002g0248 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.953-1866G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998973 | ||||||
| chr9:98998978
|
A | T | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.953-1861A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98998978 | ||||||
| chr9:98999068
|
C | T | 2 | a0017c0021t0001g0099a0017c0021t0001g0230 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.953-1771C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98999068 | ||||||
| chr9:98999078
|
C | T | 4 | a0020c0029t0002g0049a0020c0029t0004g0156a0030c0030t0005g0127others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-1761C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98999078 | ||||||
| chr9:98999398
|
C | T | 5 | a0020c0029t0002g0049a0020c0029t0004g0156a0020c0046t0007g0004others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.953-1441C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98999398 | ||||||
| chr9:98999434
|
T | C | 204 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(201): Show | 204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.953-1405T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98999434 | ||||||
| chr9:98999527
|
C | CT | 50 | a0001c0031t0001g0205a0002c0002t0001g0066a0002c0003t0002g0179others(47): Show | 50 | HG00423.hp2 HG00597.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.953-1297dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | INFO_REALIGN_3_PRIME | chr9 | 98999527 | |||||
| chr9:98999685
|
T | A | 165 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(162): Show | 165 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.953-1154T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 98999685 | ||||||
| chr9:98999857
|
G | GT | 24 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0102others(21): Show | 24 | HG01175.hp1 HG01192.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.953-967dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | INFO_REALIGN_3_PRIME | chr9 | 98999857 | |||||
| chr9:98999857
|
GT | G | 86 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(83): Show | 86 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.953-967delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | INFO_REALIGN_3_PRIME | chr9 | 98999857 | |||||
| chr9:98999857
|
GTT | G | 62 | a0002c0003t0002g0130a0003c0004t0002g0132a0003c0004t0002g0142others(59): Show | 62 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.953-968_953-967del others(2): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | INFO_REALIGN_3_PRIME | chr9 | 98999857 | |||||
| chr9:99000016
|
A | G | 4 | a0002c0003t0002g0182a0002c0003t0002g0214a0006c0007t0001g0216others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-823A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000016 | ||||||
| chr9:99000073
|
G | T | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.953-766G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000073 | ||||||
| chr9:99000146
|
C | T | 1 | a0020c0029t0002g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.953-693C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000146 | ||||||
| chr9:99000246
|
C | T | 82 | a0002c0003t0002g0130a0003c0004t0001g0030a0003c0004t0002g0132others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.953-593C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000246 | ||||||
| chr9:99000300
|
A | C | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.953-539A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000300 | ||||||
| chr9:99000310
|
A | G | 38 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0193others(35): Show | 38 | HG00423.hp2 HG00597.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.953-529A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000310 | ||||||
| chr9:99000315
|
C | CATACAT | 7 | a0001c0001t0002g0059a0002c0003t0002g0182a0002c0003t0002g0214others(4): Show | 7 | HG01243.hp2 HG02723.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.953-502_953-497dup others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | INFO_REALIGN_3_PRIME | chr9 | 99000315 | |||||
| chr9:99000324
|
A | G | 85 | a0002c0003t0002g0130a0003c0004t0001g0030a0003c0004t0002g0132others(82): Show | 85 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.953-515A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000324 | ||||||
| chr9:99000332
|
A | G | 1 | a0007c0008t0002g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953-507A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000332 | ||||||
| chr9:99000347
|
T | C | 5 | a0001c0001t0002g0186a0001c0001t0002g0192a0001c0001t0002g0199others(2): Show | 5 | HG00741.hp1 HG01192.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.953-492T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000347 | ||||||
| chr9:99000611
|
G | A | 5 | a0002c0003t0002g0182a0002c0003t0002g0214a0006c0007t0001g0216others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.953-228G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000611 | ||||||
| chr9:99000633
|
G | A | 3 | a0002c0003t0002g0193a0002c0003t0008g0185a0006c0007t0001g0194 | 3 | HG02559.hp1 HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.953-206G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000633 | ||||||
| chr9:99000809
|
T | C | 41 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0193others(38): Show | 41 | HG00423.hp2 HG00597.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.953-30T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 6/41 | chr9 | 99000809 | ||||||
| chr9:99001012
|
C | CT | 79 | a0002c0003t0002g0130a0002c0003t0002g0214a0003c0004t0001g0030others(76): Show | 79 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1065+63dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | INFO_REALIGN_3_PRIME | chr9 | 99001012 | |||||
| chr9:99001195
|
T | C | 202 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(199): Show | 202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1065+244T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99001195 | ||||||
| chr9:99001224
|
A | C | 101 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(98): Show | 101 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1065+273A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99001224 | ||||||
| chr9:99001351
|
A | G | 111 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(108): Show | 111 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1065+400A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99001351 | ||||||
| chr9:99001595
|
C | T | 1 | a0002c0002t0001g0083 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1065+644C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99001595 | ||||||
| chr9:99001622
|
A | C | 21 | a0002c0003t0002g0182a0002c0003t0002g0193a0002c0003t0008g0185others(18): Show | 21 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1065+671A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99001622 | ||||||
| chr9:99001727
|
A | G | 36 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(33): Show | 36 | HG00423.hp2 HG00597.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1065+776A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99001727 | ||||||
| chr9:99001803
|
G | A | 2 | a0004c0005t0001g0017a0013c0017t0001g0065 | 2 | NA18985.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1065+852G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99001803 | ||||||
| chr9:99001930
|
G | A | 75 | a0002c0003t0002g0130a0002c0003t0002g0214a0003c0004t0001g0030others(72): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1065+979G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99001930 | ||||||
| chr9:99002078
|
T | A | 4 | a0001c0001t0002g0287a0017c0021t0001g0099a0017c0021t0001g0213others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065+1127T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002078 | ||||||
| chr9:99002141
|
TTCCTC | T | 156 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0001t0002g0113others(153): Show | 156 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1065+1209_1065+121 others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | INFO_REALIGN_3_PRIME | chr9 | 99002141 | |||||
| chr9:99002360
|
G | A | 4 | a0011c0039t0001g0218a0019c0024t0006g0124a0022c0026t0004g0139others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-1093G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002360 | ||||||
| chr9:99002666
|
T | C | 6 | a0002c0003t0002g0193a0002c0003t0008g0185a0006c0007t0001g0194others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066-787T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002666 | ||||||
| chr9:99002715
|
T | G | 1 | a0008c0009t0002g0001 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1066-738T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002715 | ||||||
| chr9:99002732
|
T | C | 1 | a0002c0010t0009g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1066-721T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002732 | ||||||
| chr9:99002768
|
A | G | 39 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(36): Show | 39 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1066-685A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002768 | ||||||
| chr9:99002819
|
A | G | 2 | a0001c0001t0002g0113a0001c0001t0002g0148 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1066-634A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002819 | ||||||
| chr9:99002866
|
G | A | 3 | a0012c0014t0002g0181a0012c0014t0002g0229a0031c0041t0001g0292 | 3 | HG02257.hp2 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1066-587G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002866 | ||||||
| chr9:99002905
|
T | C | 61 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(58): Show | 61 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1066-548T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002905 | ||||||
| chr9:99002955
|
T | G | 11 | a0002c0077t0002g0174a0006c0078t0001g0231a0010c0012t0005g0215others(8): Show | 11 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1066-498T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99002955 | ||||||
| chr9:99003186
|
C | A | 61 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(58): Show | 61 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1066-267C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99003186 | ||||||
| chr9:99003276
|
G | A | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1066-177G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99003276 | ||||||
| chr9:99003350
|
A | T | 5 | a0002c0077t0002g0174a0006c0078t0001g0231a0010c0012t0005g0215others(2): Show | 5 | HG01081.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1066-103A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 7/41 | chr9 | 99003350 | ||||||
| chr9:99003704
|
G | C | 1 | a0011c0039t0001g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1200+117G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99003704 | ||||||
| chr9:99003717
|
C | T | 1 | a0001c0031t0001g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1200+130C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99003717 | ||||||
| chr9:99003828
|
A | G | 12 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(9): Show | 12 | HG01081.hp2 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1200+241A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99003828 | ||||||
| chr9:99003846
|
G | A | 61 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(58): Show | 61 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1200+259G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99003846 | ||||||
| chr9:99004087
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1200+500C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99004087 | ||||||
| chr9:99004267
|
G | C | 1 | a0002c0002t0001g0310 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1201-631G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99004267 | ||||||
| chr9:99004326
|
G | A | 69 | a0002c0003t0002g0214a0003c0004t0001g0030a0003c0004t0002g0132others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1201-572G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99004326 | ||||||
| chr9:99004356
|
G | C | 1 | a0006c0007t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1201-542G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99004356 | ||||||
| chr9:99004426
|
A | G | 1 | a0005c0019t0003g0289 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1201-472A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99004426 | ||||||
| chr9:99004631
|
C | T | 4 | a0020c0029t0004g0156a0020c0046t0007g0004a0030c0030t0005g0127others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-267C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99004631 | ||||||
| chr9:99004659
|
T | A | 23 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1201-239T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99004659 | ||||||
| chr9:99004718
|
T | A | 1 | a0040c0056t0002g0009 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1201-180T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 8/41 | chr9 | 99004718 | ||||||
| chr9:99005100
|
C | T | 84 | a0002c0003t0002g0182a0002c0003t0002g0193a0002c0003t0003g0100others(81): Show | 84 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1353+50C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005100 | ||||||
| chr9:99005103
|
A | G | 195 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(192): Show | 195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1353+53A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005103 | ||||||
| chr9:99005346
|
G | A | 142 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(139): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1353+296G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005346 | ||||||
| chr9:99005628
|
C | T | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1353+578C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005628 | ||||||
| chr9:99005679
|
T | C | 197 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(194): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1353+629T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005679 | ||||||
| chr9:99005702
|
G | A | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1353+652G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005702 | ||||||
| chr9:99005737
|
G | A | 1 | a0004c0005t0001g0158 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1353+687G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005737 | ||||||
| chr9:99005754
|
A | G | 3 | a0010c0012t0002g0087a0010c0012t0002g0277a0020c0046t0007g0004 | 3 | HG00280.hp2 HG01358.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1353+704A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005754 | ||||||
| chr9:99005780
|
G | A | 1 | a0002c0010t0001g0021 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1353+730G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005780 | ||||||
| chr9:99005971
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1353+921C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99005971 | ||||||
| chr9:99006035
|
C | T | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1353+985C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006035 | ||||||
| chr9:99006165
|
A | G | 3 | a0010c0012t0002g0087a0010c0012t0002g0277a0020c0046t0007g0004 | 3 | HG00280.hp2 HG01358.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1353+1115A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006165 | ||||||
| chr9:99006212
|
A | G | 2 | a0001c0001t0002g0102a0001c0001t0002g0288 | 2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1353+1162A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006212 | ||||||
| chr9:99006293
|
T | C | 1 | a0002c0002t0001g0281 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1353+1243T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006293 | ||||||
| chr9:99006396
|
G | T | 1 | a0054c0063t0001g0023 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1353+1346G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006396 | ||||||
| chr9:99006422
|
C | T | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1353+1372C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006422 | ||||||
| chr9:99006464
|
T | G | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353+1414T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006464 | ||||||
| chr9:99006565
|
A | G | 157 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0242others(154): Show | 157 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1353+1515A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006565 | ||||||
| chr9:99006565
|
A | T | 2 | a0001c0013t0001g0064a0001c0013t0001g0068 | 2 | HG03834.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1353+1515A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006565 | ||||||
| chr9:99006623
|
CCTT | C | 3 | a0010c0012t0002g0087a0010c0012t0002g0277a0020c0046t0007g0004 | 3 | HG00280.hp2 HG01358.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1353+1581_1353+158 others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99006623 | |||||
| chr9:99006634
|
C | A | 44 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(41): Show | 44 | HG00423.hp2 HG00597.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.1353+1584C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006634 | ||||||
| chr9:99006663
|
CTCT | C | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1353+1620_1353+162 others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99006663 | |||||
| chr9:99006962
|
C | T | 7 | a0003c0004t0002g0132a0003c0004t0002g0142a0003c0004t0002g0270others(4): Show | 7 | NA18939.hp1 NA18942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1353+1912C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99006962 | ||||||
| chr9:99007062
|
A | G | 281 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0057others(278): Show | 281 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.1353+2012A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007062 | ||||||
| chr9:99007078
|
A | G | 4 | a0002c0003t0002g0193a0002c0003t0008g0185a0006c0007t0001g0194others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+2028A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007078 | ||||||
| chr9:99007130
|
CGCTTGCA others(4): Show |
C | 6 | a0002c0003t0003g0100a0002c0010t0009g0204a0006c0007t0001g0216others(3): Show | 6 | HG01109.hp1 HG02965.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1353+2081_1353+209 others(15): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007130 | ||||||
| chr9:99007211
|
G | A | 67 | a0001c0031t0001g0205a0003c0004t0001g0030a0003c0004t0002g0132others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1353+2161G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007211 | ||||||
| chr9:99007274
|
G | A | 1 | a0010c0012t0005g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1353+2224G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007274 | ||||||
| chr9:99007329
|
G | A | 1 | a0005c0015t0001g0273 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1353+2279G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007329 | ||||||
| chr9:99007385
|
G | A | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1353+2335G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007385 | ||||||
| chr9:99007590
|
C | A | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1353+2540C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007590 | ||||||
| chr9:99007590
|
C | T | 7 | a0010c0012t0005g0215a0010c0012t0005g0304a0013c0047t0001g0093others(4): Show | 7 | HG01074.hp1 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1353+2540C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007590 | ||||||
| chr9:99007596
|
G | A | 1 | a0001c0031t0001g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1353+2546G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007596 | ||||||
| chr9:99007604
|
A | C | 7 | a0006c0007t0001g0217a0006c0078t0001g0231a0007c0008t0002g0306others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1353+2554A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007604 | ||||||
| chr9:99007672
|
A | G | 6 | a0002c0003t0003g0100a0002c0010t0009g0204a0006c0007t0001g0216others(3): Show | 6 | HG01109.hp1 HG02965.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1353+2622A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007672 | ||||||
| chr9:99007740
|
G | A | 1 | a0004c0005t0001g0261 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1353+2690G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007740 | ||||||
| chr9:99007917
|
G | T | 1 | a0001c0013t0001g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1353+2867G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99007917 | ||||||
| chr9:99008121
|
T | G | 1 | a0001c0001t0002g0051 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1353+3071T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008121 | ||||||
| chr9:99008126
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0002g0197 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1353+3076T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008126 | ||||||
| chr9:99008199
|
A | G | 2 | a0004c0005t0001g0006a0053c0065t0001g0143 | 2 | HG00438.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1353+3149A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008199 | ||||||
| chr9:99008211
|
AC | A | 8 | a0002c0003t0003g0100a0002c0010t0009g0204a0006c0007t0001g0216others(5): Show | 8 | HG01109.hp1 HG02965.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1353+3163delC | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99008211 | |||||
| chr9:99008240
|
T | C | 14 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(11): Show | 14 | HG01081.hp2 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1353+3190T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008240 | ||||||
| chr9:99008485
|
A | T | 70 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(67): Show | 70 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1353+3435A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008485 | ||||||
| chr9:99008545
|
T | A | 1 | a0003c0004t0001g0030 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1353+3495T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008545 | ||||||
| chr9:99008568
|
T | A | 6 | a0002c0003t0003g0100a0002c0010t0009g0204a0006c0007t0001g0216others(3): Show | 6 | HG01109.hp1 HG02965.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1353+3518T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008568 | ||||||
| chr9:99008659
|
G | C | 1 | a0013c0017t0001g0114 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1353+3609G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008659 | ||||||
| chr9:99008692
|
C | G | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1353+3642C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008692 | ||||||
| chr9:99008773
|
C | T | 1 | a0017c0021t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1353+3723C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008773 | ||||||
| chr9:99008792
|
C | T | 309 | a0001c0001t0001g0196a0001c0001t0002g0014a0001c0001t0002g0016others(306): Show | 309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.1353+3742C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008792 | ||||||
| chr9:99008801
|
G | C | 1 | a0007c0037t0001g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1353+3751G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008801 | ||||||
| chr9:99008833
|
C | T | 16 | a0002c0002t0001g0007a0002c0002t0001g0082a0002c0010t0001g0008others(13): Show | 16 | HG00438.hp2 HG00621.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+3783C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008833 | ||||||
| chr9:99008844
|
A | T | 67 | a0001c0031t0001g0205a0003c0004t0001g0030a0003c0004t0002g0132others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1353+3794A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008844 | ||||||
| chr9:99008901
|
C | T | 69 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(66): Show | 69 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1353+3851C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008901 | ||||||
| chr9:99008961
|
C | T | 1 | a0003c0004t0002g0132 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1353+3911C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008961 | ||||||
| chr9:99008962
|
G | A | 23 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1353+3912G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99008962 | ||||||
| chr9:99009071
|
A | G | 1 | a0002c0069t0010g0047 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1353+4021A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009071 | ||||||
| chr9:99009167
|
T | C | 3 | a0010c0012t0002g0087a0010c0012t0002g0277a0020c0046t0007g0004 | 3 | HG00280.hp2 HG01358.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1353+4117T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009167 | ||||||
| chr9:99009179
|
AACC | A | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1353+4133_1353+413 others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99009179 | |||||
| chr9:99009221
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+4171A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009221 | ||||||
| chr9:99009236
|
C | G | 4 | a0003c0006t0001g0141a0004c0005t0001g0017a0004c0005t0001g0158others(1): Show | 4 | HG00423.hp1 NA18982.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+4186C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009236 | ||||||
| chr9:99009462
|
T | C | 3 | a0024c0028t0002g0088a0024c0028t0004g0165a0046c0079t0004g0283 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1353+4412T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009462 | ||||||
| chr9:99009463
|
C | T | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353+4413C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009463 | ||||||
| chr9:99009492
|
T | C | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1353+4442T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009492 | ||||||
| chr9:99009547
|
T | A | 2 | a0006c0007t0001g0116a0006c0007t0001g0173 | 2 | HG01952.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1353+4497T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009547 | ||||||
| chr9:99009919
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1353+4869A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99009919 | ||||||
| chr9:99010166
|
C | A | 1 | a0003c0004t0002g0275 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1353+5116C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010166 | ||||||
| chr9:99010256
|
A | C | 3 | a0024c0028t0002g0088a0024c0028t0004g0165a0046c0079t0004g0283 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1354-5161A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010256 | ||||||
| chr9:99010416
|
T | C | 14 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(11): Show | 14 | HG01081.hp2 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-5001T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010416 | ||||||
| chr9:99010567
|
G | A | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1354-4850G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010567 | ||||||
| chr9:99010620
|
G | A | 195 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(192): Show | 195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1354-4797G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010620 | ||||||
| chr9:99010683
|
T | C | 3 | a0024c0028t0002g0088a0024c0028t0004g0165a0046c0079t0004g0283 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1354-4734T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010683 | ||||||
| chr9:99010765
|
T | G | 22 | a0002c0003t0002g0179a0002c0003t0002g0182a0002c0003t0002g0184others(19): Show | 22 | HG01081.hp2 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1354-4652T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010765 | ||||||
| chr9:99010848
|
T | C | 1 | a0056c0081t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1354-4569T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010848 | ||||||
| chr9:99010868
|
T | C | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1354-4549T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99010868 | ||||||
| chr9:99010985
|
AT | A | 69 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(66): Show | 69 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1354-4425delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99010985 | |||||
| chr9:99011423
|
A | AAAAAAAA others(1): Show |
6 | a0003c0006t0001g0269a0004c0005t0001g0261a0010c0012t0002g0087others(3): Show | 6 | HG00280.hp2 HG01358.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-3993_1354-399 others(12): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99011423 | |||||
| chr9:99011423
|
A | AAAAAAAC | 33 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1354-3993_1354-399 others(11): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99011423 | |||||
| chr9:99011423
|
A | AAAAAAC | 48 | a0001c0031t0001g0205a0002c0003t0007g0003a0002c0003t0008g0185others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1354-3993_1354-399 others(10): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99011423 | |||||
| chr9:99011423
|
A | AAAAAC | 33 | a0002c0003t0002g0193a0002c0010t0009g0204a0003c0004t0002g0275others(30): Show | 33 | HG00423.hp2 HG00597.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1354-3993_1354-399 others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99011423 | |||||
| chr9:99011423
|
A | AAAAC | 6 | a0002c0077t0002g0174a0024c0028t0002g0088a0024c0028t0004g0165others(3): Show | 6 | HG02145.hp2 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1354-3993_1354-399 others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99011423 | |||||
| chr9:99011423
|
A | AAAC | 12 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0109others(9): Show | 12 | HG02647.hp1 HG03225.hp1 NA18906.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-3993_1354-399 others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99011423 | |||||
| chr9:99011423
|
A | AAC | 47 | a0001c0001t0002g0059a0001c0013t0001g0064a0001c0013t0001g0068others(44): Show | 47 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1354-3993_1354-399 others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99011423 | |||||
| chr9:99011493
|
C | G | 1 | a0015c0018t0001g0035 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1354-3924C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011493 | ||||||
| chr9:99011527
|
C | G | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1354-3890C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011527 | ||||||
| chr9:99011580
|
A | G | 68 | a0001c0031t0001g0205a0003c0004t0001g0030a0003c0004t0002g0132others(65): Show | 68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1354-3837A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011580 | ||||||
| chr9:99011629
|
A | G | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1354-3788A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011629 | ||||||
| chr9:99011705
|
A | G | 1 | a0004c0005t0001g0010 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1354-3712A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011705 | ||||||
| chr9:99011722
|
T | C | 1 | a0056c0081t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1354-3695T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011722 | ||||||
| chr9:99011730
|
A | G | 14 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(11): Show | 14 | HG01081.hp2 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-3687A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011730 | ||||||
| chr9:99011740
|
A | T | 3 | a0024c0028t0002g0088a0024c0028t0004g0165a0046c0079t0004g0283 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1354-3677A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011740 | ||||||
| chr9:99011868
|
G | A | 20 | a0003c0004t0001g0030a0003c0004t0002g0256a0003c0004t0002g0299others(17): Show | 20 | HG00423.hp1 HG00544.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1354-3549G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011868 | ||||||
| chr9:99011945
|
C | G | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1354-3472C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99011945 | ||||||
| chr9:99012107
|
G | A | 3 | a0002c0077t0002g0174a0020c0029t0004g0156a0036c0045t0003g0212 | 3 | HG02717.hp1 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1354-3310G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012107 | ||||||
| chr9:99012513
|
T | C | 7 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(4): Show | 7 | HG01081.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354-2904T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012513 | ||||||
| chr9:99012536
|
C | T | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1354-2881C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012536 | ||||||
| chr9:99012554
|
T | G | 23 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-2863T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012554 | ||||||
| chr9:99012621
|
A | T | 1 | a0001c0001t0002g0014 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1354-2796A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012621 | ||||||
| chr9:99012703
|
C | CT | 26 | a0001c0001t0002g0022a0001c0001t0002g0113a0001c0001t0002g0123others(23): Show | 26 | HG01175.hp1 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1354-2688dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99012703 | |||||
| chr9:99012703
|
CT | C | 132 | a0001c0001t0002g0059a0001c0001t0002g0067a0001c0001t0002g0070others(129): Show | 132 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1354-2688delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99012703 | |||||
| chr9:99012703
|
CTT | C | 30 | a0002c0002t0001g0305a0002c0077t0002g0174a0005c0015t0001g0029others(27): Show | 30 | HG00423.hp2 HG00597.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-2689_1354-268 others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99012703 | |||||
| chr9:99012703
|
CTTTTTTT others(9): Show |
C | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1354-2703_1354-268 others(20): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99012703 | |||||
| chr9:99012748
|
A | G | 1 | a0020c0029t0002g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1354-2669A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012748 | ||||||
| chr9:99012757
|
G | A | 1 | a0003c0004t0002g0275 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1354-2660G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012757 | ||||||
| chr9:99012764
|
T | A | 77 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(74): Show | 77 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1354-2653T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012764 | ||||||
| chr9:99012807
|
G | A | 1 | a0019c0024t0006g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1354-2610G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012807 | ||||||
| chr9:99012832
|
G | A | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-2585G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012832 | ||||||
| chr9:99012916
|
G | C | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1354-2501G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012916 | ||||||
| chr9:99012989
|
C | T | 1 | a0001c0001t0002g0061 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1354-2428C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99012989 | ||||||
| chr9:99013083
|
T | C | 1 | a0005c0015t0001g0163 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1354-2334T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013083 | ||||||
| chr9:99013087
|
G | A | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1354-2330G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013087 | ||||||
| chr9:99013144
|
G | A | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1354-2273G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013144 | ||||||
| chr9:99013288
|
G | C | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1354-2129G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013288 | ||||||
| chr9:99013545
|
T | G | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1354-1872T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013545 | ||||||
| chr9:99013550
|
G | GA | 90 | a0001c0031t0001g0205a0002c0003t0002g0193a0002c0003t0008g0185others(87): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1354-1852dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99013550 | |||||
| chr9:99013550
|
G | GAA | 6 | a0003c0006t0001g0095a0003c0006t0001g0096a0003c0006t0001g0097others(3): Show | 6 | HG00423.hp1 HG03927.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1853_1354-185 others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99013550 | |||||
| chr9:99013550
|
GA | G | 62 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(59): Show | 62 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1354-1852delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99013550 | |||||
| chr9:99013550
|
GAA | G | 7 | a0002c0002t0001g0105a0002c0002t0001g0109a0002c0002t0001g0110others(4): Show | 7 | HG02647.hp1 NA18946.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354-1853_1354-185 others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99013550 | |||||
| chr9:99013702
|
G | T | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-1715G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013702 | ||||||
| chr9:99013708
|
C | G | 1 | a0006c0007t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1354-1709C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013708 | ||||||
| chr9:99013728
|
T | A | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1354-1689T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013728 | ||||||
| chr9:99013815
|
C | A | 10 | a0010c0012t0002g0011a0019c0024t0006g0122a0019c0024t0006g0124others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1354-1602C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013815 | ||||||
| chr9:99013824
|
T | C | 58 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1354-1593T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013824 | ||||||
| chr9:99013843
|
G | A | 194 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1354-1574G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013843 | ||||||
| chr9:99013899
|
T | C | 6 | a0001c0001t0002g0191a0002c0003t0003g0100a0002c0010t0009g0204others(3): Show | 6 | HG00733.hp1 HG01109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1518T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013899 | ||||||
| chr9:99013974
|
G | GT | 57 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(54): Show | 57 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1354-1434dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr9 | 99013974 | |||||
| chr9:99013987
|
CT | C | 36 | a0002c0003t0002g0193a0002c0003t0008g0185a0002c0077t0002g0174others(33): Show | 36 | HG00423.hp2 HG00597.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1354-1429delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99013987 | ||||||
| chr9:99014205
|
T | C | 195 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(192): Show | 195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1354-1212T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99014205 | ||||||
| chr9:99014239
|
A | T | 78 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1354-1178A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99014239 | ||||||
| chr9:99014612
|
A | G | 2 | a0002c0003t0002g0118a0002c0067t0002g0206 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1354-805A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99014612 | ||||||
| chr9:99014679
|
A | G | 194 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1354-738A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99014679 | ||||||
| chr9:99014787
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1354-630A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99014787 | ||||||
| chr9:99014983
|
G | T | 1 | a0004c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-434G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99014983 | ||||||
| chr9:99014992
|
G | T | 23 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-425G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99014992 | ||||||
| chr9:99015199
|
G | A | 3 | a0024c0028t0002g0088a0024c0028t0004g0165a0046c0079t0004g0283 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1354-218G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99015199 | ||||||
| chr9:99015319
|
T | A | 27 | a0002c0077t0002g0174a0005c0015t0001g0029a0005c0015t0001g0040others(24): Show | 27 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1354-98T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99015319 | ||||||
| chr9:99015379
|
G | A | 1 | a0002c0003t0003g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1354-38G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 9/41 | chr9 | 99015379 | ||||||
| chr9:99015584
|
T | C | 1 | a0003c0004t0001g0030 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1503+18T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 10/41 | chr9 | 99015584 | ||||||
| chr9:99015624
|
C | T | 4 | a0002c0010t0009g0204a0006c0007t0001g0216a0017c0021t0001g0232others(1): Show | 4 | HG01109.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+58C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 10/41 | chr9 | 99015624 | ||||||
| chr9:99015874
|
G | A | 1 | a0023c0027t0002g0233 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1504-102G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 10/41 | chr9 | 99015874 | ||||||
| chr9:99015924
|
G | C | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1504-52G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 10/41 | chr9 | 99015924 | ||||||
| chr9:99015937
|
C | T | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1504-39C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 10/41 | chr9 | 99015937 | ||||||
| chr9:99015938
|
G | A | 2 | a0010c0012t0002g0087a0010c0012t0002g0277 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1504-38G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 10/41 | chr9 | 99015938 | ||||||
| chr9:99016217
|
A | C | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1647+98A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016217 | ||||||
| chr9:99016223
|
A | G | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1647+104A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016223 | ||||||
| chr9:99016323
|
G | A | 1 | a0002c0010t0001g0161 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1647+204G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016323 | ||||||
| chr9:99016380
|
C | T | 4 | a0006c0078t0001g0231a0011c0016t0001g0086a0011c0016t0001g0090others(1): Show | 4 | HG01243.hp1 NA18906.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647+261C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016380 | ||||||
| chr9:99016382
|
G | A | 92 | a0001c0031t0001g0205a0002c0077t0002g0174a0003c0004t0001g0030others(89): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1647+263G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016382 | ||||||
| chr9:99016541
|
C | T | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1647+422C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016541 | ||||||
| chr9:99016542
|
C | G | 17 | a0010c0012t0002g0011a0010c0012t0002g0220a0010c0012t0002g0221others(14): Show | 17 | HG01081.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1647+423C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016542 | ||||||
| chr9:99016559
|
C | G | 1 | a0002c0002t0001g0245 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1647+440C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016559 | ||||||
| chr9:99016565
|
T | C | 7 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(4): Show | 7 | HG01081.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1647+446T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016565 | ||||||
| chr9:99016638
|
G | A | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647+519G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016638 | ||||||
| chr9:99016780
|
A | G | 3 | a0013c0047t0001g0093a0014c0020t0001g0129a0014c0020t0001g0131 | 3 | HG01074.hp1 HG01256.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1647+661A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016780 | ||||||
| chr9:99016888
|
G | A | 92 | a0001c0031t0001g0205a0002c0077t0002g0174a0003c0004t0001g0030others(89): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1647+769G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99016888 | ||||||
| chr9:99017127
|
C | T | 3 | a0002c0003t0002g0193a0002c0003t0008g0185a0006c0007t0001g0194 | 3 | HG02559.hp1 HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1647+1008C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017127 | ||||||
| chr9:99017138
|
C | CA | 3 | a0002c0003t0002g0193a0002c0003t0008g0185a0006c0007t0001g0194 | 3 | HG02559.hp1 HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1647+1020dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | INFO_REALIGN_3_PRIME | chr9 | 99017138 | |||||
| chr9:99017157
|
G | A | 193 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(190): Show | 193 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1647+1038G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017157 | ||||||
| chr9:99017235
|
G | T | 11 | a0010c0012t0002g0011a0019c0024t0006g0122a0019c0024t0006g0124others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1647+1116G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017235 | ||||||
| chr9:99017312
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1647+1193G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017312 | ||||||
| chr9:99017387
|
A | T | 23 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1647+1268A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017387 | ||||||
| chr9:99017542
|
C | T | 92 | a0001c0031t0001g0205a0002c0077t0002g0174a0003c0004t0001g0030others(89): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1647+1423C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017542 | ||||||
| chr9:99017543
|
G | A | 6 | a0010c0012t0002g0220a0010c0012t0002g0221a0010c0012t0005g0215others(3): Show | 6 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+1424G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017543 | ||||||
| chr9:99017576
|
C | G | 6 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1647+1457C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017576 | ||||||
| chr9:99017679
|
C | T | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1647+1560C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017679 | ||||||
| chr9:99017758
|
A | T | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647+1639A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017758 | ||||||
| chr9:99017780
|
C | T | 100 | a0001c0031t0001g0205a0002c0003t0002g0182a0002c0003t0002g0214others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1647+1661C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017780 | ||||||
| chr9:99017819
|
T | C | 7 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(4): Show | 7 | HG01081.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1647+1700T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99017819 | ||||||
| chr9:99018065
|
A | G | 2 | a0033c0038t0001g0028a0049c0071t0001g0278 | 2 | HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1647+1946A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99018065 | ||||||
| chr9:99018084
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1647+1965G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99018084 | ||||||
| chr9:99018250
|
CGTCTCTT others(4): Show |
C | 6 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0061others(3): Show | 6 | HG01192.hp2 HG02155.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1648-2129_1648-211 others(15): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | INFO_REALIGN_3_PRIME | chr9 | 99018250 | |||||
| chr9:99018330
|
G | A | 66 | a0001c0031t0001g0205a0003c0004t0001g0030a0003c0004t0002g0132others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1648-2059G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99018330 | ||||||
| chr9:99018610
|
G | A | 7 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(4): Show | 7 | HG01081.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648-1779G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99018610 | ||||||
| chr9:99018640
|
TAATTG | T | 3 | a0018c0023t0002g0248a0018c0023t0002g0266a0018c0023t0002g0267 | 3 | HG00544.hp2 HG02074.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1648-1744_1648-174 others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | INFO_REALIGN_3_PRIME | chr9 | 99018640 | |||||
| chr9:99018717
|
T | C | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1648-1672T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99018717 | ||||||
| chr9:99018741
|
G | C | 1 | a0048c0068t0002g0079 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1648-1648G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99018741 | ||||||
| chr9:99018773
|
A | C | 1 | a0001c0001t0002g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1648-1616A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99018773 | ||||||
| chr9:99018973
|
A | AAG | 7 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(4): Show | 7 | HG01081.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648-1400_1648-139 others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | INFO_REALIGN_3_PRIME | chr9 | 99018973 | |||||
| chr9:99019019
|
G | A | 28 | a0008c0009t0001g0208a0008c0009t0002g0024a0008c0009t0002g0026others(25): Show | 28 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.1648-1370G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019019 | ||||||
| chr9:99019047
|
G | A | 4 | a0002c0002t0001g0176a0002c0002t0001g0235a0002c0003t0002g0241others(1): Show | 4 | NA18950.hp1 NA18960.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648-1342G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019047 | ||||||
| chr9:99019088
|
C | T | 1 | a0016c0022t0002g0078 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1648-1301C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019088 | ||||||
| chr9:99019192
|
G | A | 1 | a0002c0003t0002g0236 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1648-1197G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019192 | ||||||
| chr9:99019261
|
T | G | 7 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(4): Show | 7 | HG01081.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648-1128T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019261 | ||||||
| chr9:99019350
|
G | A | 1 | a0043c0052t0002g0259 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1648-1039G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019350 | ||||||
| chr9:99019463
|
C | T | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1648-926C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019463 | ||||||
| chr9:99019576
|
G | A | 105 | a0001c0031t0001g0205a0002c0077t0002g0174a0003c0004t0001g0030others(102): Show | 105 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1648-813G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019576 | ||||||
| chr9:99019817
|
T | C | 1 | a0055c0082t0009g0005 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1648-572T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019817 | ||||||
| chr9:99019836
|
G | T | 5 | a0004c0005t0001g0006a0014c0020t0001g0294a0014c0048t0003g0115others(2): Show | 5 | HG00438.hp1 HG00558.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1648-553G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99019836 | ||||||
| chr9:99020023
|
A | G | 1 | a0015c0018t0001g0035 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1648-366A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99020023 | ||||||
| chr9:99020096
|
T | C | 1 | a0008c0009t0002g0024 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1648-293T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99020096 | ||||||
| chr9:99020253
|
T | C | 66 | a0001c0031t0001g0205a0003c0004t0001g0030a0003c0004t0002g0132others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1648-136T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | chr9 | 99020253 | ||||||
| chr9:99020374
|
ATCT | A | 4 | a0003c0006t0001g0095a0003c0006t0001g0096a0003c0006t0001g0097others(1): Show | 4 | NA18948.hp1 NA18950.hp2 NA18979.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1648-7_1648-5delCT others(1): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 11/41 | INFO_REALIGN_3_PRIME | chr9 | 99020374 | |||||
| chr9:99020486
|
A | G | 9 | a0002c0003t0003g0100a0002c0010t0009g0204a0002c0077t0002g0174others(6): Show | 9 | HG01109.hp1 HG02717.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1701+44A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99020486 | ||||||
| chr9:99020554
|
A | C | 81 | a0001c0031t0001g0205a0002c0003t0002g0179a0002c0003t0002g0182others(78): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1701+112A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99020554 | ||||||
| chr9:99020772
|
C | T | 1 | a0002c0002t0001g0150 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1701+330C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99020772 | ||||||
| chr9:99020827
|
A | T | 1 | a0002c0002t0001g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1701+385A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99020827 | ||||||
| chr9:99020881
|
G | A | 5 | a0002c0003t0003g0100a0002c0010t0009g0204a0006c0007t0001g0216others(2): Show | 5 | HG01109.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1701+439G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99020881 | ||||||
| chr9:99021009
|
C | T | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1701+567C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021009 | ||||||
| chr9:99021097
|
T | C | 66 | a0001c0031t0001g0205a0003c0004t0001g0030a0003c0004t0002g0132others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1701+655T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021097 | ||||||
| chr9:99021279
|
G | A | 11 | a0010c0012t0002g0011a0019c0024t0006g0122a0019c0024t0006g0124others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1702-812G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021279 | ||||||
| chr9:99021355
|
G | GC | 196 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(193): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1702-736_1702-735i others(3): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021355 | ||||||
| chr9:99021356
|
G | C | 196 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(193): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1702-735G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021356 | ||||||
| chr9:99021359
|
C | T | 128 | a0001c0031t0001g0205a0002c0003t0002g0179a0002c0003t0002g0184others(125): Show | 128 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1702-732C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021359 | ||||||
| chr9:99021413
|
A | G | 3 | a0024c0028t0002g0088a0024c0028t0004g0165a0046c0079t0004g0283 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1702-678A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021413 | ||||||
| chr9:99021493
|
C | T | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1702-598C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021493 | ||||||
| chr9:99021726
|
G | T | 2 | a0001c0001t0002g0113a0001c0001t0002g0148 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1702-365G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021726 | ||||||
| chr9:99021791
|
A | G | 122 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(119): Show | 122 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1702-300A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021791 | ||||||
| chr9:99021814
|
A | G | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1702-277A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021814 | ||||||
| chr9:99021839
|
T | A | 189 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0001t0002g0190others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1702-252T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021839 | ||||||
| chr9:99021930
|
G | C | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1702-161G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021930 | ||||||
| chr9:99021941
|
G | A | 3 | a0002c0002t0001g0235a0002c0003t0002g0241a0002c0010t0001g0107 | 3 | NA18950.hp1 NA18960.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1702-150G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 12/41 | chr9 | 99021941 | ||||||
| chr9:99022156
|
A | G | 67 | a0001c0001t0002g0190a0001c0031t0001g0205a0003c0004t0001g0030others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
splice_region_variant&intron_variant | LOW | c.1761+6A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022156 | ||||||
| chr9:99022172
|
G | C | 3 | a0002c0003t0002g0193a0002c0003t0008g0185a0006c0007t0001g0194 | 3 | HG02559.hp1 HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1761+22G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022172 | ||||||
| chr9:99022482
|
T | C | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1761+332T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022482 | ||||||
| chr9:99022495
|
C | T | 60 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(57): Show | 60 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1761+345C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022495 | ||||||
| chr9:99022614
|
A | G | 35 | a0002c0003t0003g0100a0002c0010t0009g0204a0005c0015t0001g0029others(32): Show | 35 | HG00423.hp2 HG00597.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1761+464A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022614 | ||||||
| chr9:99022859
|
C | T | 44 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(41): Show | 44 | HG00423.hp2 HG00597.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.1762-498C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022859 | ||||||
| chr9:99022923
|
T | C | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-434T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022923 | ||||||
| chr9:99022925
|
G | A | 60 | a0001c0001t0002g0190a0001c0031t0001g0205a0003c0004t0001g0030others(57): Show | 60 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1762-432G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022925 | ||||||
| chr9:99022972
|
G | A | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1762-385G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99022972 | ||||||
| chr9:99023087
|
T | C | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1762-270T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99023087 | ||||||
| chr9:99023153
|
T | C | 64 | a0001c0001t0002g0190a0001c0031t0001g0205a0002c0003t0002g0193others(61): Show | 64 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1762-204T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99023153 | ||||||
| chr9:99023276
|
T | G | 73 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(70): Show | 73 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1762-81T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99023276 | ||||||
| chr9:99023316
|
G | T | 73 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(70): Show | 73 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1762-41G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99023316 | ||||||
| chr9:99023351
|
T | C | 77 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(74): Show | 77 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
splice_region_variant&intron_variant | LOW | c.1762-6T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 13/41 | chr9 | 99023351 | ||||||
| chr9:99023470
|
G | A | 1 | a0001c0001t0002g0014 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1854+21G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99023470 | ||||||
| chr9:99023561
|
T | G | 1 | a0027c0035t0003g0286 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1854+112T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99023561 | ||||||
| chr9:99023605
|
G | A | 2 | a0017c0021t0001g0099a0017c0021t0001g0230 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1854+156G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99023605 | ||||||
| chr9:99023613
|
A | G | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1854+164A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99023613 | ||||||
| chr9:99023616
|
T | C | 1 | a0005c0015t0001g0163 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1854+167T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99023616 | ||||||
| chr9:99023660
|
C | T | 66 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0061others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1854+211C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99023660 | ||||||
| chr9:99023824
|
C | T | 60 | a0001c0001t0002g0190a0001c0031t0001g0205a0003c0004t0001g0030others(57): Show | 60 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1854+375C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99023824 | ||||||
| chr9:99023984
|
C | T | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1854+535C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99023984 | ||||||
| chr9:99024095
|
G | T | 7 | a0010c0012t0002g0011a0019c0024t0006g0122a0019c0024t0006g0124others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854+646G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024095 | ||||||
| chr9:99024104
|
C | T | 1 | a0012c0014t0002g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1854+655C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024104 | ||||||
| chr9:99024268
|
G | GTTTT | 6 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1855-601_1855-598d others(6): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTT | 9 | a0002c0010t0001g0021a0002c0010t0001g0125a0002c0010t0001g0164others(6): Show | 9 | HG00438.hp2 HG01975.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1855-603_1855-598d others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT | 7 | a0002c0010t0001g0008a0002c0010t0001g0145a0002c0010t0001g0161others(4): Show | 7 | HG00597.hp2 HG00621.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1855-604_1855-598d others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(3): Show |
1 | a0006c0007t0001g0069 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1855-598_1855-597i others(12): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(9): Show |
1 | a0002c0003t0003g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1855-598_1855-597i others(18): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(11): Show |
2 | a0002c0002t0001g0082a0002c0002t0001g0109 | 2 | NA18946.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1855-598_1855-597i others(20): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(12): Show |
11 | a0001c0001t0002g0070a0001c0013t0001g0064a0001c0013t0001g0068others(8): Show | 11 | HG00280.hp1 HG02040.hp1 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.1855-598_1855-597i others(21): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(13): Show |
12 | a0001c0001t0002g0059a0001c0013t0001g0242a0002c0002t0001g0018others(9): Show | 12 | HG00733.hp2 HG01123.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1855-598_1855-597i others(22): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(14): Show |
8 | a0002c0002t0001g0043a0002c0002t0001g0066a0002c0002t0001g0076others(5): Show | 8 | HG04204.hp1 NA18944.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.1855-598_1855-597i others(23): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(15): Show |
1 | a0002c0002t0001g0310 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1855-598_1855-597i others(24): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(16): Show |
1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1855-598_1855-597i others(25): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(17): Show |
1 | a0002c0002t0001g0302 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1855-598_1855-597i others(26): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(18): Show |
1 | a0002c0002t0001g0245 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1855-598_1855-597i others(27): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(19): Show |
2 | a0002c0002t0001g0178a0007c0037t0001g0187 | 2 | HG02055.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1855-598_1855-597i others(28): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024268
|
G | GTTTTTTT others(20): Show |
1 | a0002c0010t0001g0170 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1855-598_1855-597i others(29): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024268 | |||||
| chr9:99024277
|
G | GT | 11 | a0001c0001t0002g0057a0002c0003t0002g0012a0007c0008t0002g0262others(8): Show | 11 | HG01081.hp1 HG01123.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1855-590dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | INFO_REALIGN_3_PRIME | chr9 | 99024277 | |||||
| chr9:99024277
|
G | T | 79 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(76): Show | 79 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1855-597G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024277 | ||||||
| chr9:99024282
|
T | G | 1 | a0023c0027t0002g0233 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1855-592T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024282 | ||||||
| chr9:99024283
|
T | G | 23 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1855-591T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024283 | ||||||
| chr9:99024285
|
G | T | 254 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0059others(251): Show | 254 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.1855-589G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024285 | ||||||
| chr9:99024286
|
T | G | 57 | a0001c0031t0001g0205a0003c0004t0001g0030a0003c0004t0002g0188others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1855-588T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024286 | ||||||
| chr9:99024289
|
T | G | 1 | a0005c0019t0003g0140 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1855-585T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024289 | ||||||
| chr9:99024319
|
C | T | 8 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1855-555C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024319 | ||||||
| chr9:99024327
|
C | T | 5 | a0002c0003t0003g0100a0002c0010t0009g0204a0006c0007t0001g0216others(2): Show | 5 | HG01109.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855-547C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024327 | ||||||
| chr9:99024735
|
T | G | 121 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0013t0001g0064others(118): Show | 121 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1855-139T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024735 | ||||||
| chr9:99024741
|
G | C | 6 | a0002c0003t0002g0182a0002c0003t0002g0214a0002c0003t0003g0100others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1855-133G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 14/41 | chr9 | 99024741 | ||||||
| chr9:99025546
|
T | A | 2 | a0002c0010t0009g0204a0055c0082t0009g0005 | 2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1981-358T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 15/41 | chr9 | 99025546 | ||||||
| chr9:99025548
|
T | C | 2 | a0004c0005t0001g0017a0013c0017t0001g0065 | 2 | NA18985.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1981-356T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 15/41 | chr9 | 99025548 | ||||||
| chr9:99025559
|
G | A | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1981-345G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 15/41 | chr9 | 99025559 | ||||||
| chr9:99026011
|
C | A | 3 | a0017c0021t0001g0099a0017c0021t0001g0213a0017c0021t0001g0230 | 3 | HG02109.hp1 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2043+45C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026011 | ||||||
| chr9:99026144
|
C | T | 7 | a0003c0004t0002g0132a0003c0004t0002g0142a0003c0004t0002g0270others(4): Show | 7 | NA18939.hp1 NA18942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043+178C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026144 | ||||||
| chr9:99026148
|
G | A | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2043+182G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026148 | ||||||
| chr9:99026182
|
T | C | 1 | a0002c0003t0002g0193 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2043+216T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026182 | ||||||
| chr9:99026239
|
C | G | 4 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043+273C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026239 | ||||||
| chr9:99026240
|
T | C | 59 | a0001c0001t0002g0191a0001c0031t0001g0205a0002c0003t0002g0012others(56): Show | 59 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2043+274T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026240 | ||||||
| chr9:99026345
|
C | A | 1 | a0006c0007t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2043+379C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026345 | ||||||
| chr9:99026357
|
G | A | 1 | a0012c0014t0002g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2043+391G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026357 | ||||||
| chr9:99026489
|
A | G | 1 | a0002c0003t0003g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2043+523A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026489 | ||||||
| chr9:99026892
|
G | C | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2043+926G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026892 | ||||||
| chr9:99026986
|
A | G | 1 | a0003c0004t0002g0303 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2043+1020A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99026986 | ||||||
| chr9:99027001
|
T | C | 2 | a0007c0008t0002g0136a0007c0008t0002g0244 | 2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2043+1035T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027001 | ||||||
| chr9:99027200
|
C | T | 2 | a0003c0004t0002g0188a0003c0004t0002g0189 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2043+1234C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027200 | ||||||
| chr9:99027226
|
A | G | 32 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(29): Show | 32 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.2043+1260A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027226 | ||||||
| chr9:99027398
|
G | A | 60 | a0001c0001t0002g0191a0001c0031t0001g0205a0002c0003t0002g0012others(57): Show | 60 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2043+1432G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027398 | ||||||
| chr9:99027401
|
G | T | 1 | a0002c0003t0003g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2043+1435G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027401 | ||||||
| chr9:99027516
|
T | C | 1 | a0002c0003t0007g0003 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2043+1550T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027516 | ||||||
| chr9:99027599
|
A | G | 4 | a0003c0004t0002g0188a0003c0004t0002g0189a0006c0007t0001g0116others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043+1633A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027599 | ||||||
| chr9:99027666
|
C | G | 14 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(11): Show | 14 | HG01081.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2043+1700C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027666 | ||||||
| chr9:99027759
|
C | T | 50 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(47): Show | 50 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.2043+1793C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027759 | ||||||
| chr9:99027764
|
G | A | 1 | a0002c0002t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2043+1798G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027764 | ||||||
| chr9:99027843
|
A | G | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2043+1877A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027843 | ||||||
| chr9:99027978
|
A | G | 1 | a0011c0016t0001g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2043+2012A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99027978 | ||||||
| chr9:99028019
|
C | T | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2043+2053C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028019 | ||||||
| chr9:99028039
|
C | T | 1 | a0002c0002t0001g0111 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2043+2073C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028039 | ||||||
| chr9:99028063
|
C | T | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2043+2097C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028063 | ||||||
| chr9:99028083
|
G | A | 8 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(5): Show | 8 | HG02145.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2043+2117G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028083 | ||||||
| chr9:99028100
|
A | G | 3 | a0010c0012t0002g0220a0010c0012t0002g0221a0010c0075t0007g0002 | 3 | HG02647.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2043+2134A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028100 | ||||||
| chr9:99028257
|
T | A | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2043+2291T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028257 | ||||||
| chr9:99028480
|
G | A | 1 | a0002c0010t0009g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2043+2514G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028480 | ||||||
| chr9:99028489
|
A | G | 1 | a0002c0002t0001g0076 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2043+2523A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028489 | ||||||
| chr9:99028596
|
A | G | 185 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0001t0002g0191others(182): Show | 185 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.2043+2630A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028596 | ||||||
| chr9:99028606
|
C | T | 1 | a0014c0020t0001g0294 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2043+2640C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028606 | ||||||
| chr9:99028645
|
G | A | 1 | a0034c0042t0001g0133 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2043+2679G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028645 | ||||||
| chr9:99028651
|
A | G | 72 | a0001c0001t0002g0191a0001c0031t0001g0205a0002c0002t0001g0245others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.2043+2685A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028651 | ||||||
| chr9:99028738
|
T | C | 31 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(28): Show | 31 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2043+2772T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028738 | ||||||
| chr9:99028858
|
AT | A | 4 | a0001c0013t0001g0015a0023c0027t0002g0091a0023c0027t0002g0233others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043+2898delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr9 | 99028858 | |||||
| chr9:99028905
|
A | G | 1 | a0003c0004t0003g0263 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2043+2939A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028905 | ||||||
| chr9:99028906
|
T | C | 6 | a0002c0067t0002g0206a0002c0077t0002g0174a0022c0026t0004g0139others(3): Show | 6 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2043+2940T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028906 | ||||||
| chr9:99028915
|
C | T | 40 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(37): Show | 40 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.2043+2949C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99028915 | ||||||
| chr9:99029039
|
A | T | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2043+3073A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99029039 | ||||||
| chr9:99029392
|
A | G | 3 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212 | 3 | HG02258.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2043+3426A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99029392 | ||||||
| chr9:99029414
|
C | A | 64 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0170others(61): Show | 64 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2043+3448C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99029414 | ||||||
| chr9:99029428
|
T | C | 5 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2043+3462T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99029428 | ||||||
| chr9:99029652
|
G | A | 173 | a0001c0013t0001g0015a0001c0013t0001g0064a0001c0013t0001g0068others(170): Show | 173 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2043+3686G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99029652 | ||||||
| chr9:99029656
|
G | T | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2043+3690G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99029656 | ||||||
| chr9:99029786
|
A | G | 173 | a0001c0013t0001g0015a0001c0013t0001g0064a0001c0013t0001g0068others(170): Show | 173 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2043+3820A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99029786 | ||||||
| chr9:99029833
|
G | A | 1 | a0009c0011t0001g0103 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2043+3867G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99029833 | ||||||
| chr9:99029925
|
CA | C | 72 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0003t0002g0179others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.2043+3975delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr9 | 99029925 | |||||
| chr9:99030364
|
T | G | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2044-4185T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99030364 | ||||||
| chr9:99030380
|
T | C | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2044-4169T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99030380 | ||||||
| chr9:99030434
|
G | A | 35 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0001t0002g0191others(32): Show | 35 | HG00408.hp2 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2044-4115G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99030434 | ||||||
| chr9:99030466
|
C | T | 3 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212 | 3 | HG02258.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2044-4083C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99030466 | ||||||
| chr9:99030510
|
A | T | 3 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212 | 3 | HG02258.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2044-4039A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99030510 | ||||||
| chr9:99030517
|
C | T | 3 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212 | 3 | HG02258.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2044-4032C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99030517 | ||||||
| chr9:99030578
|
C | T | 29 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(26): Show | 29 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.2044-3971C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99030578 | ||||||
| chr9:99030877
|
G | A | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2044-3672G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99030877 | ||||||
| chr9:99031007
|
G | T | 1 | a0002c0010t0001g0170 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2044-3542G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031007 | ||||||
| chr9:99031016
|
C | T | 166 | a0001c0013t0001g0015a0001c0013t0001g0064a0001c0013t0001g0068others(163): Show | 166 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.2044-3533C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031016 | ||||||
| chr9:99031176
|
C | T | 3 | a0017c0021t0001g0099a0017c0021t0001g0213a0017c0021t0001g0230 | 3 | HG02109.hp1 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2044-3373C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031176 | ||||||
| chr9:99031521
|
C | T | 5 | a0001c0001t0001g0196a0001c0001t0002g0197a0025c0032t0002g0243others(2): Show | 5 | HG01106.hp1 HG01123.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044-3028C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031521 | ||||||
| chr9:99031522
|
G | A | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2044-3027G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031522 | ||||||
| chr9:99031548
|
A | G | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2044-3001A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031548 | ||||||
| chr9:99031552
|
T | C | 48 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(45): Show | 48 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2044-2997T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031552 | ||||||
| chr9:99031572
|
C | T | 1 | a0004c0005t0001g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2044-2977C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031572 | ||||||
| chr9:99031610
|
A | T | 1 | a0003c0006t0001g0146 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2044-2939A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031610 | ||||||
| chr9:99031773
|
A | C | 65 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0170others(62): Show | 65 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2044-2776A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031773 | ||||||
| chr9:99031782
|
G | A | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2044-2767G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031782 | ||||||
| chr9:99031857
|
A | G | 1 | a0022c0026t0004g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2044-2692A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031857 | ||||||
| chr9:99031922
|
A | G | 48 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(45): Show | 48 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2044-2627A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031922 | ||||||
| chr9:99031928
|
T | A | 1 | a0002c0003t0007g0003 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2044-2621T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99031928 | ||||||
| chr9:99032083
|
A | G | 1 | a0002c0002t0001g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2044-2466A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99032083 | ||||||
| chr9:99032154
|
A | G | 7 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2044-2395A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99032154 | ||||||
| chr9:99032246
|
G | C | 1 | a0002c0002t0001g0195 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2044-2303G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99032246 | ||||||
| chr9:99032552
|
T | G | 3 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212 | 3 | HG02258.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2044-1997T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99032552 | ||||||
| chr9:99032641
|
T | C | 2 | a0006c0078t0001g0231a0011c0016t0001g0155 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2044-1908T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99032641 | ||||||
| chr9:99032982
|
C | G | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2044-1567C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99032982 | ||||||
| chr9:99033038
|
T | C | 4 | a0002c0002t0001g0195a0002c0002t0001g0281a0033c0038t0001g0028others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044-1511T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033038 | ||||||
| chr9:99033115
|
C | A | 14 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(11): Show | 14 | HG01081.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2044-1434C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033115 | ||||||
| chr9:99033391
|
G | T | 1 | a0001c0031t0001g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2044-1158G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033391 | ||||||
| chr9:99033472
|
G | A | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2044-1077G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033472 | ||||||
| chr9:99033482
|
T | C | 59 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0170others(56): Show | 59 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2044-1067T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033482 | ||||||
| chr9:99033564
|
TC | T | 3 | a0015c0018t0001g0036a0015c0018t0001g0252a0045c0062t0001g0020 | 3 | HG00423.hp2 HG00597.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2044-982delC | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr9 | 99033564 | |||||
| chr9:99033764
|
C | T | 1 | a0002c0003t0003g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2044-785C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033764 | ||||||
| chr9:99033772
|
T | A | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2044-777T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033772 | ||||||
| chr9:99033775
|
C | T | 2 | a0006c0007t0001g0116a0006c0007t0001g0173 | 2 | HG01952.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2044-774C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033775 | ||||||
| chr9:99033781
|
A | G | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2044-768A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033781 | ||||||
| chr9:99033800
|
G | T | 1 | a0001c0001t0002g0249 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2044-749G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99033800 | ||||||
| chr9:99034174
|
G | A | 5 | a0002c0067t0002g0206a0002c0077t0002g0174a0022c0026t0004g0139others(2): Show | 5 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044-375G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99034174 | ||||||
| chr9:99034176
|
T | G | 7 | a0002c0003t0002g0182a0002c0003t0002g0214a0007c0008t0002g0117others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2044-373T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 16/41 | chr9 | 99034176 | ||||||
| chr9:99034586
|
T | TA | 20 | a0001c0001t0002g0057a0001c0001t0002g0171a0001c0001t0002g0172others(17): Show | 20 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2079+30dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | INFO_REALIGN_3_PRIME | chr9 | 99034586 | |||||
| chr9:99034586
|
TA | T | 20 | a0001c0001t0002g0254a0002c0002t0001g0018a0002c0002t0001g0108others(17): Show | 20 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.2079+30delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | INFO_REALIGN_3_PRIME | chr9 | 99034586 | |||||
| chr9:99034586
|
TAA | T | 125 | a0001c0013t0001g0064a0001c0013t0001g0068a0001c0013t0001g0242others(122): Show | 125 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2079+29_2079+30del others(2): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | INFO_REALIGN_3_PRIME | chr9 | 99034586 | |||||
| chr9:99034586
|
TAAA | T | 31 | a0001c0013t0001g0015a0002c0002t0001g0083a0002c0002t0001g0235others(28): Show | 31 | HG01081.hp1 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2079+28_2079+30del others(3): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | INFO_REALIGN_3_PRIME | chr9 | 99034586 | |||||
| chr9:99034624
|
T | TCTCCCTC | 248 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0059others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.2079+46_2079+52dup others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | INFO_REALIGN_3_PRIME | chr9 | 99034624 | |||||
| chr9:99034635
|
C | T | 7 | a0004c0005t0001g0307a0006c0007t0001g0217a0006c0078t0001g0231others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.2079+51C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | chr9 | 99034635 | ||||||
| chr9:99034680
|
T | C | 1 | a0034c0042t0001g0133 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2079+96T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | chr9 | 99034680 | ||||||
| chr9:99034740
|
G | A | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2079+156G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | chr9 | 99034740 | ||||||
| chr9:99034761
|
G | A | 59 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0170others(56): Show | 59 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2079+177G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | chr9 | 99034761 | ||||||
| chr9:99034773
|
A | C | 173 | a0001c0013t0001g0015a0001c0013t0001g0064a0001c0013t0001g0068others(170): Show | 173 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2079+189A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | chr9 | 99034773 | ||||||
| chr9:99034997
|
T | G | 1 | a0021c0025t0003g0135 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2080-17T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | chr9 | 99034997 | ||||||
| chr9:99035009
|
T | C | 1 | a0014c0020t0001g0129 | 1 | HG02273.hp1 | splice_region_variant&intron_variant | LOW | c.2080-5T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 17/41 | chr9 | 99035009 | ||||||
| chr9:99035249
|
G | A | 1 | a0026c0054t0001g0013 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2220+95G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 18/41 | chr9 | 99035249 | ||||||
| chr9:99035543
|
C | G | 1 | a0015c0018t0001g0035 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2289+125C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 19/41 | chr9 | 99035543 | ||||||
| chr9:99035720
|
T | C | 74 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0008others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2289+302T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 19/41 | chr9 | 99035720 | ||||||
| chr9:99035852
|
G | A | 1 | a0002c0002t0001g0111 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2290-318G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 19/41 | chr9 | 99035852 | ||||||
| chr9:99035936
|
C | A | 44 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(41): Show | 44 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.2290-234C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 19/41 | chr9 | 99035936 | ||||||
| chr9:99036102
|
G | A | 3 | a0008c0009t0001g0208a0008c0009t0002g0285a0044c0058t0002g0144 | 3 | HG02135.hp1 HG04199.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2290-68G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 19/41 | chr9 | 99036102 | ||||||
| chr9:99036144
|
A | C | 1 | a0035c0043t0001g0063 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2290-26A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 19/41 | chr9 | 99036144 | ||||||
| chr9:99036227
|
G | A | 1 | a0050c0066t0010g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2325+22G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 20/41 | chr9 | 99036227 | ||||||
| chr9:99036485
|
G | T | 1 | a0001c0013t0001g0068 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2409+89G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99036485 | ||||||
| chr9:99036974
|
G | T | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2409+578G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99036974 | ||||||
| chr9:99037011
|
A | G | 74 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0008others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2409+615A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037011 | ||||||
| chr9:99037117
|
T | C | 175 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(172): Show | 175 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.2409+721T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037117 | ||||||
| chr9:99037190
|
C | A | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2409+794C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037190 | ||||||
| chr9:99037224
|
T | C | 5 | a0003c0006t0001g0269a0004c0005t0001g0006a0014c0020t0001g0294others(2): Show | 5 | HG00438.hp1 HG00558.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409+828T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037224 | ||||||
| chr9:99037237
|
C | T | 1 | a0004c0005t0001g0106 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2409+841C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037237 | ||||||
| chr9:99037255
|
T | C | 1 | a0011c0039t0001g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2409+859T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037255 | ||||||
| chr9:99037350
|
C | T | 7 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0265others(4): Show | 7 | HG00544.hp2 HG01192.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.2409+954C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037350 | ||||||
| chr9:99037473
|
C | T | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2409+1077C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037473 | ||||||
| chr9:99037824
|
A | G | 24 | a0001c0001t0002g0052a0001c0001t0002g0057a0001c0001t0002g0061others(21): Show | 24 | HG00280.hp2 HG00544.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2410-844A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99037824 | ||||||
| chr9:99038124
|
C | T | 3 | a0010c0012t0002g0220a0010c0012t0002g0221a0020c0046t0007g0004 | 3 | HG02922.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2410-544C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99038124 | ||||||
| chr9:99038147
|
G | GT | 74 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0008others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2410-520dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | INFO_REALIGN_3_PRIME | chr9 | 99038147 | |||||
| chr9:99038396
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2410-272C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99038396 | ||||||
| chr9:99038511
|
G | C | 1 | a0013c0017t0001g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2410-157G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99038511 | ||||||
| chr9:99038565
|
G | A | 2 | a0002c0003t0008g0185a0012c0014t0012g0210 | 2 | HG01515.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2410-103G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99038565 | ||||||
| chr9:99038570
|
C | T | 1 | a0010c0012t0002g0087 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2410-98C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99038570 | ||||||
| chr9:99038602
|
G | A | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2410-66G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 21/41 | chr9 | 99038602 | ||||||
| chr9:99038797
|
G | A | 3 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212 | 3 | HG02258.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2475+64G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99038797 | ||||||
| chr9:99038868
|
C | T | 1 | a0003c0004t0001g0030 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2475+135C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99038868 | ||||||
| chr9:99038896
|
C | T | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2475+163C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99038896 | ||||||
| chr9:99038943
|
C | G | 1 | a0012c0014t0002g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2475+210C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99038943 | ||||||
| chr9:99038957
|
C | T | 1 | a0002c0002t0001g0066 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2475+224C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99038957 | ||||||
| chr9:99038972
|
T | C | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2475+239T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99038972 | ||||||
| chr9:99039109
|
A | G | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2475+376A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039109 | ||||||
| chr9:99039217
|
C | G | 6 | a0010c0012t0002g0220a0010c0012t0002g0221a0010c0075t0007g0002others(3): Show | 6 | HG02647.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2475+484C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039217 | ||||||
| chr9:99039228
|
T | G | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2475+495T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039228 | ||||||
| chr9:99039338
|
G | A | 3 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212 | 3 | HG02258.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2475+605G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039338 | ||||||
| chr9:99039436
|
G | T | 36 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0001t0002g0191others(33): Show | 36 | HG00408.hp2 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2475+703G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039436 | ||||||
| chr9:99039505
|
T | C | 5 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2475+772T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039505 | ||||||
| chr9:99039583
|
C | T | 1 | a0008c0009t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2475+850C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039583 | ||||||
| chr9:99039700
|
G | A | 7 | a0001c0001t0002g0067a0010c0012t0002g0277a0012c0014t0002g0181others(4): Show | 7 | HG01358.hp2 HG02257.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.2476-821G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039700 | ||||||
| chr9:99039708
|
C | T | 3 | a0001c0001t0002g0168a0001c0001t0002g0222a0002c0003t0002g0118 | 3 | HG03130.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2476-813C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039708 | ||||||
| chr9:99039747
|
T | C | 21 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2476-774T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039747 | ||||||
| chr9:99039785
|
T | A | 30 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(27): Show | 30 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2476-736T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039785 | ||||||
| chr9:99039880
|
G | A | 42 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(39): Show | 42 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2476-641G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99039880 | ||||||
| chr9:99040085
|
C | A | 5 | a0010c0012t0002g0220a0010c0012t0002g0221a0020c0046t0007g0004others(2): Show | 5 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2476-436C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99040085 | ||||||
| chr9:99040229
|
G | A | 1 | a0012c0014t0002g0250 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2476-292G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99040229 | ||||||
| chr9:99040278
|
G | A | 3 | a0013c0047t0001g0093a0014c0020t0001g0129a0014c0020t0001g0131 | 3 | HG01074.hp1 HG01256.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2476-243G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99040278 | ||||||
| chr9:99040294
|
A | G | 6 | a0010c0012t0002g0220a0010c0012t0002g0221a0010c0075t0007g0002others(3): Show | 6 | HG02647.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2476-227A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 22/41 | chr9 | 99040294 | ||||||
| chr9:99040932
|
G | A | 1 | a0003c0004t0001g0030 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2511+376G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99040932 | ||||||
| chr9:99041216
|
A | T | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2511+660A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041216 | ||||||
| chr9:99041233
|
A | G | 3 | a0017c0021t0001g0099a0017c0021t0001g0213a0017c0021t0001g0230 | 3 | HG02109.hp1 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2511+677A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041233 | ||||||
| chr9:99041313
|
C | G | 44 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(41): Show | 44 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.2512-732C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041313 | ||||||
| chr9:99041334
|
G | A | 1 | a0001c0013t0001g0015 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2512-711G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041334 | ||||||
| chr9:99041506
|
G | C | 3 | a0025c0032t0002g0243a0025c0032t0002g0260a0041c0055t0002g0025 | 3 | HG01106.hp1 HG01123.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2512-539G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041506 | ||||||
| chr9:99041508
|
G | C | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2512-537G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041508 | ||||||
| chr9:99041561
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2512-484C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041561 | ||||||
| chr9:99041567
|
G | A | 1 | a0026c0054t0001g0013 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2512-478G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041567 | ||||||
| chr9:99041652
|
A | G | 1 | a0050c0066t0010g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2512-393A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041652 | ||||||
| chr9:99041828
|
A | C | 1 | a0054c0063t0001g0023 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2512-217A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041828 | ||||||
| chr9:99041876
|
A | G | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2512-169A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 23/41 | chr9 | 99041876 | ||||||
| chr9:99042134
|
A | G | 101 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(98): Show | 101 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.2574+27A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042134 | ||||||
| chr9:99042135
|
G | A | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2574+28G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042135 | ||||||
| chr9:99042205
|
G | T | 6 | a0001c0001t0002g0113a0001c0001t0002g0119a0001c0001t0002g0148others(3): Show | 6 | HG00642.hp1 HG01109.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2574+98G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042205 | ||||||
| chr9:99042221
|
C | T | 2 | a0006c0007t0001g0216a0017c0021t0001g0232 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2574+114C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042221 | ||||||
| chr9:99042273
|
TA | T | 6 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(3): Show | 6 | HG01081.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2574+168delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | INFO_REALIGN_3_PRIME | chr9 | 99042273 | |||||
| chr9:99042274
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2574+167A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042274 | ||||||
| chr9:99042276
|
G | T | 30 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(27): Show | 30 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2574+169G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042276 | ||||||
| chr9:99042280
|
G | T | 14 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(11): Show | 14 | HG01081.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2574+173G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042280 | ||||||
| chr9:99042413
|
C | T | 2 | a0006c0007t0001g0216a0017c0021t0001g0232 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2574+306C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042413 | ||||||
| chr9:99042441
|
C | G | 3 | a0023c0027t0002g0091a0023c0027t0002g0233a0031c0041t0001g0292 | 3 | HG01884.hp2 HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2574+334C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042441 | ||||||
| chr9:99042484
|
A | T | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2574+377A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042484 | ||||||
| chr9:99042508
|
ACCTGCT | A | 49 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2574+402_2574+407d others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042508 | ||||||
| chr9:99042515
|
G | A | 49 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2574+408G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042515 | ||||||
| chr9:99042516
|
G | A | 49 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2574+409G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042516 | ||||||
| chr9:99042618
|
A | G | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2574+511A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042618 | ||||||
| chr9:99042642
|
G | A | 45 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(42): Show | 45 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.2574+535G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042642 | ||||||
| chr9:99042664
|
A | G | 1 | a0011c0016t0001g0092 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2574+557A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042664 | ||||||
| chr9:99042726
|
G | A | 49 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2574+619G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042726 | ||||||
| chr9:99042778
|
T | C | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2574+671T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042778 | ||||||
| chr9:99042806
|
T | C | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2574+699T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042806 | ||||||
| chr9:99042886
|
T | C | 4 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574+779T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042886 | ||||||
| chr9:99042898
|
T | C | 3 | a0001c0001t0002g0171a0001c0001t0002g0186a0001c0001t0002g0249 | 3 | HG00741.hp1 HG01358.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2574+791T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042898 | ||||||
| chr9:99042924
|
G | A | 1 | a0004c0005t0001g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2574+817G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042924 | ||||||
| chr9:99042935
|
C | T | 2 | a0008c0009t0002g0285a0044c0058t0002g0144 | 2 | HG02135.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2574+828C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042935 | ||||||
| chr9:99042959
|
T | C | 5 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2574+852T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042959 | ||||||
| chr9:99042964
|
T | A | 1 | a0002c0002t0001g0305 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2574+857T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99042964 | ||||||
| chr9:99043050
|
G | A | 1 | a0002c0002t0001g0305 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2574+943G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043050 | ||||||
| chr9:99043240
|
C | T | 1 | a0006c0007t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2574+1133C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043240 | ||||||
| chr9:99043414
|
G | A | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2575-1154G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043414 | ||||||
| chr9:99043440
|
C | T | 1 | a0003c0004t0002g0275 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2575-1128C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043440 | ||||||
| chr9:99043451
|
T | C | 49 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2575-1117T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043451 | ||||||
| chr9:99043475
|
T | C | 76 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0008others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2575-1093T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043475 | ||||||
| chr9:99043609
|
T | C | 49 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2575-959T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043609 | ||||||
| chr9:99043655
|
T | A | 1 | a0001c0013t0001g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2575-913T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043655 | ||||||
| chr9:99043729
|
C | G | 1 | a0003c0004t0002g0303 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2575-839C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043729 | ||||||
| chr9:99043735
|
G | C | 1 | a0003c0004t0002g0303 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2575-833G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043735 | ||||||
| chr9:99043757
|
GC | G | 3 | a0002c0003t0003g0100a0002c0010t0009g0204a0055c0082t0009g0005 | 3 | HG01109.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2575-809delC | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | INFO_REALIGN_3_PRIME | chr9 | 99043757 | |||||
| chr9:99043764
|
T | C | 1 | a0002c0002t0001g0305 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2575-804T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043764 | ||||||
| chr9:99043776
|
G | A | 76 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0008others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2575-792G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043776 | ||||||
| chr9:99043777
|
C | T | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2575-791C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043777 | ||||||
| chr9:99043809
|
C | T | 2 | a0001c0001t0002g0057a0001c0031t0001g0157 | 2 | NA18991.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2575-759C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043809 | ||||||
| chr9:99043882
|
G | T | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2575-686G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99043882 | ||||||
| chr9:99044002
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2575-566G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99044002 | ||||||
| chr9:99044099
|
T | A | 1 | a0001c0001t0002g0265 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2575-469T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99044099 | ||||||
| chr9:99044129
|
G | C | 26 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(23): Show | 26 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.2575-439G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 24/41 | chr9 | 99044129 | ||||||
| chr9:99044830
|
T | C | 51 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(48): Show | 51 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.2679+60T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99044830 | ||||||
| chr9:99044899
|
A | G | 3 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212 | 3 | HG02258.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2679+129A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99044899 | ||||||
| chr9:99045008
|
C | T | 49 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2679+238C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045008 | ||||||
| chr9:99045013
|
C | T | 74 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0008others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2679+243C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045013 | ||||||
| chr9:99045122
|
A | T | 74 | a0001c0031t0001g0205a0002c0003t0002g0012a0002c0010t0001g0008others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2679+352A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045122 | ||||||
| chr9:99045181
|
C | T | 102 | a0001c0001t0002g0014a0001c0013t0001g0015a0001c0013t0001g0046others(99): Show | 102 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.2679+411C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045181 | ||||||
| chr9:99045243
|
A | G | 1 | a0005c0059t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2679+473A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045243 | ||||||
| chr9:99045284
|
G | A | 49 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2679+514G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045284 | ||||||
| chr9:99045327
|
A | G | 3 | a0024c0028t0002g0088a0024c0028t0004g0165a0046c0079t0004g0283 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2679+557A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045327 | ||||||
| chr9:99045445
|
T | C | 30 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(27): Show | 30 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2679+675T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045445 | ||||||
| chr9:99045538
|
C | G | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2679+768C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045538 | ||||||
| chr9:99045738
|
G | A | 2 | a0024c0028t0002g0088a0024c0028t0004g0165 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2679+968G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045738 | ||||||
| chr9:99045820
|
C | T | 3 | a0017c0021t0001g0099a0017c0021t0001g0213a0017c0021t0001g0230 | 3 | HG02109.hp1 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2679+1050C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045820 | ||||||
| chr9:99045829
|
C | T | 2 | a0003c0004t0002g0284a0004c0005t0001g0106 | 2 | HG01106.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2679+1059C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045829 | ||||||
| chr9:99045942
|
G | A | 1 | a0006c0007t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2679+1172G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99045942 | ||||||
| chr9:99046093
|
A | G | 1 | a0012c0014t0002g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2679+1323A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046093 | ||||||
| chr9:99046184
|
A | G | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2679+1414A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046184 | ||||||
| chr9:99046268
|
C | T | 2 | a0002c0010t0009g0204a0055c0082t0009g0005 | 2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2679+1498C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046268 | ||||||
| chr9:99046337
|
T | C | 1 | a0013c0017t0001g0114 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2680-1449T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046337 | ||||||
| chr9:99046424
|
C | T | 1 | a0001c0013t0001g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2680-1362C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046424 | ||||||
| chr9:99046482
|
C | A | 14 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(11): Show | 14 | HG01081.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2680-1304C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046482 | ||||||
| chr9:99046499
|
C | CA | 3 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0007g0003 | 3 | HG02572.hp1 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2680-1284dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | INFO_REALIGN_3_PRIME | chr9 | 99046499 | |||||
| chr9:99046503
|
G | A | 14 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(11): Show | 14 | HG01081.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2680-1283G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046503 | ||||||
| chr9:99046563
|
T | C | 4 | a0002c0067t0002g0206a0002c0077t0002g0174a0036c0045t0003g0212others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2680-1223T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046563 | ||||||
| chr9:99046745
|
G | A | 1 | a0014c0048t0003g0115 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2680-1041G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046745 | ||||||
| chr9:99046861
|
A | T | 2 | a0002c0010t0001g0170a0003c0006t0001g0141 | 2 | HG00423.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2680-925A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046861 | ||||||
| chr9:99046940
|
G | A | 176 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(173): Show | 176 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.2680-846G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046940 | ||||||
| chr9:99046948
|
T | C | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2680-838T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046948 | ||||||
| chr9:99046992
|
G | A | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2680-794G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99046992 | ||||||
| chr9:99047086
|
T | C | 176 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(173): Show | 176 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.2680-700T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99047086 | ||||||
| chr9:99047114
|
G | A | 1 | a0008c0009t0002g0001 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2680-672G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99047114 | ||||||
| chr9:99047232
|
A | G | 1 | a0056c0081t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2680-554A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99047232 | ||||||
| chr9:99047257
|
C | A | 7 | a0005c0015t0001g0029a0005c0015t0001g0040a0005c0015t0001g0154others(4): Show | 7 | HG01496.hp1 HG01928.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2680-529C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99047257 | ||||||
| chr9:99047270
|
G | T | 26 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(23): Show | 26 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.2680-516G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99047270 | ||||||
| chr9:99047282
|
G | A | 4 | a0001c0001t0002g0089a0001c0001t0002g0123a0001c0001t0002g0219others(1): Show | 4 | HG02622.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2680-504G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99047282 | ||||||
| chr9:99047393
|
G | C | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2680-393G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99047393 | ||||||
| chr9:99047466
|
C | A | 30 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(27): Show | 30 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2680-320C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 26/41 | chr9 | 99047466 | ||||||
| chr9:99047877
|
G | A | 30 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(27): Show | 30 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2733+38G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 27/41 | chr9 | 99047877 | ||||||
| chr9:99048057
|
T | C | 177 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(174): Show | 177 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.2793+57T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048057 | ||||||
| chr9:99048121
|
C | T | 1 | a0001c0001t0002g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2793+121C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048121 | ||||||
| chr9:99048189
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2793+189A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048189 | ||||||
| chr9:99048238
|
G | C | 7 | a0009c0011t0002g0031a0009c0011t0002g0032a0009c0011t0002g0037others(4): Show | 7 | HG00544.hp1 NA18952.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.2793+238G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048238 | ||||||
| chr9:99048306
|
A | G | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2793+306A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048306 | ||||||
| chr9:99048519
|
ATTTTG | A | 51 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(48): Show | 51 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.2793+544_2793+548d others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr9 | 99048519 | |||||
| chr9:99048588
|
A | G | 3 | a0024c0028t0002g0088a0024c0028t0004g0165a0046c0079t0004g0283 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2793+588A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048588 | ||||||
| chr9:99048662
|
A | G | 1 | a0003c0004t0002g0271 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2793+662A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048662 | ||||||
| chr9:99048664
|
G | A | 26 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0015t0001g0029others(23): Show | 26 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.2793+664G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048664 | ||||||
| chr9:99048746
|
T | C | 2 | a0002c0002t0001g0043a0002c0002t0001g0245 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2793+746T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048746 | ||||||
| chr9:99048802
|
T | G | 1 | a0003c0006t0001g0269 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2793+802T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048802 | ||||||
| chr9:99048804
|
T | G | 49 | a0001c0001t0002g0190a0001c0001t0002g0199a0001c0013t0001g0015others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.2793+804T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048804 | ||||||
| chr9:99048988
|
T | G | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2794-702T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99048988 | ||||||
| chr9:99049033
|
G | A | 1 | a0008c0033t0001g0120 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2794-657G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049033 | ||||||
| chr9:99049054
|
C | T | 4 | a0017c0021t0001g0099a0017c0021t0001g0213a0017c0021t0001g0230others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2794-636C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049054 | ||||||
| chr9:99049055
|
G | A | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2794-635G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049055 | ||||||
| chr9:99049119
|
G | A | 5 | a0002c0002t0001g0018a0013c0047t0001g0093a0014c0020t0001g0058others(2): Show | 5 | HG00621.hp2 HG01074.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.2794-571G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049119 | ||||||
| chr9:99049215
|
G | C | 35 | a0001c0001t0002g0059a0001c0001t0002g0070a0001c0001t0002g0191others(32): Show | 35 | HG00408.hp2 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2794-475G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049215 | ||||||
| chr9:99049229
|
G | C | 50 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(47): Show | 50 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.2794-461G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049229 | ||||||
| chr9:99049399
|
G | A | 2 | a0030c0030t0005g0127a0030c0030t0005g0128 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2794-291G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049399 | ||||||
| chr9:99049443
|
G | A | 1 | a0004c0005t0001g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2794-247G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049443 | ||||||
| chr9:99049501
|
A | G | 21 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2794-189A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049501 | ||||||
| chr9:99049615
|
G | C | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2794-75G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 28/41 | chr9 | 99049615 | ||||||
| chr9:99049771
|
G | A | 17 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2862+13G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 29/41 | chr9 | 99049771 | ||||||
| chr9:99049790
|
G | A | 50 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(47): Show | 50 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.2862+32G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 29/41 | chr9 | 99049790 | ||||||
| chr9:99049840
|
C | G | 16 | a0002c0003t0002g0179a0002c0003t0002g0223a0002c0003t0002g0224others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.2863-14C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 29/41 | chr9 | 99049840 | ||||||
| chr9:99049923
|
C | T | 1 | a0020c0046t0007g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2904+28C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99049923 | ||||||
| chr9:99050056
|
A | G | 1 | a0003c0006t0001g0097 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2904+161A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050056 | ||||||
| chr9:99050330
|
C | A | 1 | a0001c0001t0002g0265 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2904+435C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050330 | ||||||
| chr9:99050372
|
CTG | C | 47 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(44): Show | 47 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.2904+480_2904+481d others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | INFO_REALIGN_3_PRIME | chr9 | 99050372 | |||||
| chr9:99050516
|
A | G | 1 | a0005c0019t0003g0140 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2904+621A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050516 | ||||||
| chr9:99050547
|
A | G | 18 | a0002c0003t0002g0179a0002c0003t0002g0184a0002c0003t0002g0223others(15): Show | 18 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2904+652A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050547 | ||||||
| chr9:99050651
|
G | A | 165 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(162): Show | 165 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2904+756G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050651 | ||||||
| chr9:99050713
|
G | A | 6 | a0002c0003t0003g0100a0002c0010t0009g0204a0024c0028t0002g0088others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2904+818G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050713 | ||||||
| chr9:99050724
|
C | T | 1 | a0019c0024t0006g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2904+829C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050724 | ||||||
| chr9:99050751
|
T | C | 1 | a0006c0007t0001g0069 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2904+856T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050751 | ||||||
| chr9:99050814
|
T | G | 2 | a0003c0006t0001g0264a0003c0006t0001g0298 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2904+919T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050814 | ||||||
| chr9:99050920
|
G | A | 1 | a0002c0003t0003g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2904+1025G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050920 | ||||||
| chr9:99050939
|
G | C | 2 | a0003c0004t0002g0284a0004c0005t0001g0106 | 2 | HG01106.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2904+1044G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050939 | ||||||
| chr9:99050988
|
A | G | 2 | a0004c0005t0001g0006a0053c0065t0001g0143 | 2 | HG00438.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2904+1093A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99050988 | ||||||
| chr9:99051224
|
C | T | 6 | a0001c0001t0002g0067a0001c0001t0002g0168a0003c0004t0002g0299others(3): Show | 6 | HG01433.hp1 HG03139.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.2905-1164C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051224 | ||||||
| chr9:99051246
|
G | A | 3 | a0008c0009t0002g0024a0008c0009t0002g0026a0052c0076t0002g0027 | 3 | HG01069.hp1 HG01934.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2905-1142G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051246 | ||||||
| chr9:99051270
|
A | G | 55 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2905-1118A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051270 | ||||||
| chr9:99051420
|
G | A | 24 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0019t0003g0054others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.2905-968G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051420 | ||||||
| chr9:99051520
|
C | T | 24 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0019t0003g0054others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.2905-868C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051520 | ||||||
| chr9:99051568
|
T | G | 1 | a0001c0001t0002g0288 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2905-820T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051568 | ||||||
| chr9:99051695
|
G | A | 1 | a0002c0067t0002g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2905-693G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051695 | ||||||
| chr9:99051747
|
A | G | 3 | a0008c0009t0002g0024a0008c0009t0002g0026a0052c0076t0002g0027 | 3 | HG01069.hp1 HG01934.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2905-641A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051747 | ||||||
| chr9:99051799
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2905-589G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051799 | ||||||
| chr9:99051849
|
C | G | 4 | a0001c0013t0001g0015a0001c0013t0001g0064a0001c0013t0001g0068others(1): Show | 4 | HG02040.hp1 HG03834.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.2905-539C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051849 | ||||||
| chr9:99051858
|
C | A | 1 | a0001c0001t0002g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2905-530C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051858 | ||||||
| chr9:99051925
|
T | C | 1 | a0004c0005t0001g0261 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2905-463T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051925 | ||||||
| chr9:99051979
|
G | A | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2905-409G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051979 | ||||||
| chr9:99051991
|
G | A | 1 | a0007c0008t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2905-397G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99051991 | ||||||
| chr9:99052171
|
C | A | 2 | a0016c0022t0002g0226a0016c0022t0002g0227 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2905-217C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99052171 | ||||||
| chr9:99052344
|
C | G | 272 | a0001c0001t0001g0196a0001c0001t0002g0050a0001c0001t0002g0052others(269): Show | 272 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.2905-44C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 30/41 | chr9 | 99052344 | ||||||
| chr9:99052448
|
CT | C | 24 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0019t0003g0054others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.2950+17delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr9 | 99052448 | |||||
| chr9:99052511
|
G | T | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2950+78G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052511 | ||||||
| chr9:99052562
|
A | G | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2950+129A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052562 | ||||||
| chr9:99052570
|
T | C | 58 | a0001c0001t0002g0191a0001c0013t0001g0015a0001c0013t0001g0046others(55): Show | 58 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.2950+137T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052570 | ||||||
| chr9:99052570
|
T | G | 3 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0007g0003 | 3 | HG02572.hp1 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2950+137T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052570 | ||||||
| chr9:99052774
|
G | A | 24 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0019t0003g0054others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.2950+341G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052774 | ||||||
| chr9:99052780
|
C | A | 1 | a0002c0010t0009g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2950+347C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052780 | ||||||
| chr9:99052896
|
G | A | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2950+463G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052896 | ||||||
| chr9:99052926
|
G | T | 3 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0007g0003 | 3 | HG02572.hp1 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2950+493G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052926 | ||||||
| chr9:99052985
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2950+552C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99052985 | ||||||
| chr9:99053057
|
G | T | 166 | a0001c0001t0002g0192a0001c0013t0001g0015a0001c0013t0001g0046others(163): Show | 166 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.2950+624G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053057 | ||||||
| chr9:99053164
|
C | A | 1 | a0001c0013t0001g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2950+731C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053164 | ||||||
| chr9:99053188
|
C | T | 24 | a0002c0003t0003g0147a0003c0004t0003g0263a0005c0019t0003g0054others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.2950+755C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053188 | ||||||
| chr9:99053189
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2950+756G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053189 | ||||||
| chr9:99053224
|
C | G | 1 | a0057c0080t0002g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2950+791C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053224 | ||||||
| chr9:99053253
|
T | C | 1 | a0002c0067t0002g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2950+820T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053253 | ||||||
| chr9:99053460
|
C | T | 1 | a0005c0015t0001g0163 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2950+1027C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053460 | ||||||
| chr9:99053494
|
C | G | 1 | a0002c0010t0001g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2950+1061C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053494 | ||||||
| chr9:99053564
|
C | T | 3 | a0002c0077t0002g0174a0010c0012t0002g0220a0010c0012t0002g0221 | 3 | HG02970.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2951-1012C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053564 | ||||||
| chr9:99053596
|
T | G | 1 | a0036c0045t0003g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2951-980T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053596 | ||||||
| chr9:99053634
|
G | A | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2951-942G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053634 | ||||||
| chr9:99053647
|
C | A | 1 | a0008c0009t0002g0001 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2951-929C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053647 | ||||||
| chr9:99053718
|
G | A | 2 | a0002c0067t0002g0206a0036c0045t0003g0212 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2951-858G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053718 | ||||||
| chr9:99053778
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2951-798C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053778 | ||||||
| chr9:99053796
|
C | G | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2951-780C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053796 | ||||||
| chr9:99053821
|
C | A | 2 | a0010c0012t0002g0220a0010c0012t0002g0221 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2951-755C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053821 | ||||||
| chr9:99053877
|
G | A | 2 | a0020c0029t0004g0156a0020c0046t0007g0004 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2951-699G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053877 | ||||||
| chr9:99053981
|
C | G | 3 | a0002c0067t0002g0206a0036c0045t0003g0212a0037c0044t0003g0138 | 3 | HG02258.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2951-595C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99053981 | ||||||
| chr9:99054086
|
A | C | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2951-490A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054086 | ||||||
| chr9:99054117
|
C | T | 53 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(50): Show | 53 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2951-459C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054117 | ||||||
| chr9:99054119
|
C | A | 1 | a0002c0002t0001g0076 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2951-457C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054119 | ||||||
| chr9:99054178
|
T | C | 167 | a0001c0001t0002g0192a0001c0013t0001g0015a0001c0013t0001g0046others(164): Show | 167 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.2951-398T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054178 | ||||||
| chr9:99054199
|
A | C | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2951-377A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054199 | ||||||
| chr9:99054259
|
C | A | 1 | a0024c0028t0002g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2951-317C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054259 | ||||||
| chr9:99054270
|
C | T | 72 | a0001c0001t0002g0192a0001c0031t0001g0205a0002c0010t0001g0008others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2951-306C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054270 | ||||||
| chr9:99054271
|
G | A | 2 | a0003c0004t0002g0299a0010c0012t0002g0277 | 2 | HG01358.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2951-305G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054271 | ||||||
| chr9:99054290
|
C | T | 3 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0007g0003 | 3 | HG02572.hp1 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2951-286C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054290 | ||||||
| chr9:99054316
|
A | G | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2951-260A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054316 | ||||||
| chr9:99054323
|
A | C | 23 | a0001c0001t0002g0050a0001c0001t0002g0089a0001c0001t0002g0123others(20): Show | 23 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.2951-253A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054323 | ||||||
| chr9:99054562
|
G | A | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2951-14G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 31/41 | chr9 | 99054562 | ||||||
| chr9:99054715
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3031+59G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 32/41 | chr9 | 99054715 | ||||||
| chr9:99054803
|
A | G | 9 | a0002c0003t0003g0100a0002c0010t0009g0204a0002c0067t0002g0206others(6): Show | 9 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3031+147A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 32/41 | chr9 | 99054803 | ||||||
| chr9:99054817
|
T | A | 9 | a0002c0003t0003g0100a0002c0010t0009g0204a0002c0067t0002g0206others(6): Show | 9 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3031+161T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 32/41 | chr9 | 99054817 | ||||||
| chr9:99054931
|
T | G | 1 | a0016c0064t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3032-171T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 32/41 | chr9 | 99054931 | ||||||
| chr9:99055072
|
C | T | 1 | a0003c0004t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3032-30C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 32/41 | chr9 | 99055072 | ||||||
| chr9:99055423
|
C | T | 3 | a0002c0003t0002g0179a0002c0003t0002g0184a0020c0029t0002g0049 | 3 | HG01081.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3192+51C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/41 | chr9 | 99055423 | ||||||
| chr9:99055485
|
G | A | 1 | a0004c0005t0001g0006 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3192+113G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/41 | chr9 | 99055485 | ||||||
| chr9:99055737
|
T | C | 1 | a0002c0003t0002g0193 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3192+365T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/41 | chr9 | 99055737 | ||||||
| chr9:99055767
|
G | T | 4 | a0001c0001t0002g0089a0001c0001t0002g0123a0001c0001t0002g0219others(1): Show | 4 | HG02622.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+395G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/41 | chr9 | 99055767 | ||||||
| chr9:99055789
|
G | A | 1 | a0010c0012t0002g0087 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3192+417G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/41 | chr9 | 99055789 | ||||||
| chr9:99055971
|
C | G | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3193-289C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/41 | chr9 | 99055971 | ||||||
| chr9:99056211
|
G | T | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3193-49G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 34/41 | chr9 | 99056211 | ||||||
| chr9:99056434
|
T | C | 170 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0013t0001g0015others(167): Show | 170 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.3337+30T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99056434 | ||||||
| chr9:99056514
|
G | A | 72 | a0001c0001t0002g0192a0001c0031t0001g0205a0002c0010t0001g0008others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.3337+110G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99056514 | ||||||
| chr9:99056543
|
T | G | 2 | a0001c0001t0002g0253a0001c0001t0002g0254 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3337+139T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99056543 | ||||||
| chr9:99056631
|
T | C | 3 | a0002c0077t0002g0174a0010c0012t0002g0220a0010c0012t0002g0221 | 3 | HG02970.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3337+227T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99056631 | ||||||
| chr9:99056648
|
T | G | 56 | a0001c0001t0002g0191a0001c0013t0001g0015a0001c0013t0001g0046others(53): Show | 56 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.3337+244T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99056648 | ||||||
| chr9:99057044
|
G | A | 7 | a0002c0077t0002g0174a0010c0012t0002g0220a0010c0012t0002g0221others(4): Show | 7 | HG02723.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.3337+640G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057044 | ||||||
| chr9:99057107
|
T | C | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3337+703T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057107 | ||||||
| chr9:99057138
|
G | C | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3337+734G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057138 | ||||||
| chr9:99057250
|
G | T | 65 | a0001c0001t0002g0191a0001c0013t0001g0015a0001c0013t0001g0046others(62): Show | 65 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.3337+846G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057250 | ||||||
| chr9:99057368
|
C | T | 1 | a0009c0011t0002g0159 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3337+964C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057368 | ||||||
| chr9:99057543
|
A | G | 5 | a0004c0005t0001g0042a0004c0005t0001g0045a0004c0005t0001g0094others(2): Show | 5 | HG01261.hp1 HG01928.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.3337+1139A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057543 | ||||||
| chr9:99057557
|
A | G | 1 | a0003c0006t0001g0097 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3337+1153A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057557 | ||||||
| chr9:99057558
|
C | T | 1 | a0022c0026t0004g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3337+1154C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057558 | ||||||
| chr9:99057562
|
A | G | 170 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0013t0001g0015others(167): Show | 170 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.3337+1158A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057562 | ||||||
| chr9:99057752
|
T | A | 1 | a0002c0010t0001g0021 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3337+1348T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99057752 | ||||||
| chr9:99058263
|
G | A | 55 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.3338-1626G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058263 | ||||||
| chr9:99058410
|
C | T | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3338-1479C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058410 | ||||||
| chr9:99058420
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3338-1469A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058420 | ||||||
| chr9:99058436
|
T | G | 141 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0013t0001g0015others(138): Show | 141 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.3338-1453T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058436 | ||||||
| chr9:99058528
|
A | T | 63 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3338-1361A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058528 | ||||||
| chr9:99058637
|
T | C | 1 | a0020c0029t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3338-1252T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058637 | ||||||
| chr9:99058735
|
C | A | 6 | a0002c0003t0003g0100a0002c0010t0009g0204a0024c0028t0002g0088others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3338-1154C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058735 | ||||||
| chr9:99058834
|
C | T | 1 | a0002c0003t0003g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3338-1055C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058834 | ||||||
| chr9:99058839
|
G | A | 63 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3338-1050G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058839 | ||||||
| chr9:99058887
|
C | T | 63 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3338-1002C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058887 | ||||||
| chr9:99058897
|
G | A | 63 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3338-992G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058897 | ||||||
| chr9:99058977
|
G | A | 1 | a0012c0014t0002g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3338-912G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99058977 | ||||||
| chr9:99059094
|
A | C | 63 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3338-795A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059094 | ||||||
| chr9:99059194
|
G | C | 1 | a0007c0008t0002g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3338-695G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059194 | ||||||
| chr9:99059279
|
G | T | 1 | a0010c0012t0002g0277 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3338-610G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059279 | ||||||
| chr9:99059282
|
C | T | 1 | a0002c0010t0001g0161 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3338-607C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059282 | ||||||
| chr9:99059287
|
C | T | 1 | a0036c0045t0003g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3338-602C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059287 | ||||||
| chr9:99059392
|
CT | C | 63 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3338-495delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr9 | 99059392 | |||||
| chr9:99059449
|
A | C | 8 | a0002c0003t0003g0100a0002c0010t0009g0204a0002c0067t0002g0206others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3338-440A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059449 | ||||||
| chr9:99059484
|
T | C | 1 | a0054c0063t0001g0023 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3338-405T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059484 | ||||||
| chr9:99059514
|
G | A | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3338-375G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059514 | ||||||
| chr9:99059601
|
G | A | 59 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(56): Show | 59 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.3338-288G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059601 | ||||||
| chr9:99059823
|
G | T | 2 | a0001c0001t0002g0119a0001c0001t0002g0198 | 2 | HG01109.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3338-66G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 35/41 | chr9 | 99059823 | ||||||
| chr9:99060020
|
C | T | 143 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(140): Show | 143 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.3402+67C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060020 | ||||||
| chr9:99060118
|
A | G | 148 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(145): Show | 148 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.3402+165A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060118 | ||||||
| chr9:99060140
|
G | A | 148 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(145): Show | 148 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.3402+187G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060140 | ||||||
| chr9:99060142
|
GA | G | 155 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(152): Show | 155 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.3402+195delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | INFO_REALIGN_3_PRIME | chr9 | 99060142 | |||||
| chr9:99060180
|
G | A | 147 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(144): Show | 147 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.3402+227G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060180 | ||||||
| chr9:99060226
|
A | C | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3402+273A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060226 | ||||||
| chr9:99060232
|
TTTTATA | T | 88 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(85): Show | 88 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.3402+281_3402+286d others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | INFO_REALIGN_3_PRIME | chr9 | 99060232 | |||||
| chr9:99060233
|
TTTA | T | 3 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088 | 3 | HG02809.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3402+282_3402+284d others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | INFO_REALIGN_3_PRIME | chr9 | 99060233 | |||||
| chr9:99060234
|
T | A | 61 | a0001c0031t0001g0157a0001c0031t0001g0205a0002c0002t0001g0235others(58): Show | 61 | HG00621.hp2 HG01074.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.3402+281T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060234 | ||||||
| chr9:99060238
|
A | T | 1 | a0002c0077t0002g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3402+285A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060238 | ||||||
| chr9:99060241
|
TATATA | T | 5 | a0004c0005t0001g0017a0004c0005t0001g0101a0004c0005t0001g0121others(2): Show | 5 | HG01261.hp1 HG03704.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.3402+289_3402+293d others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060241 | ||||||
| chr9:99060241
|
TATATATA | T | 24 | a0001c0031t0001g0205a0002c0010t0001g0170a0003c0006t0001g0072others(21): Show | 24 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.3402+289_3402+295d others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060241 | ||||||
| chr9:99060245
|
TATATATA | T | 8 | a0006c0007t0001g0216a0006c0078t0001g0231a0011c0016t0001g0086others(5): Show | 8 | HG01243.hp1 HG02451.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3402+293_3402+299d others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060245 | ||||||
| chr9:99060247
|
TATATA | T | 16 | a0001c0031t0001g0157a0002c0002t0001g0302a0002c0010t0001g0161others(13): Show | 16 | HG00621.hp2 HG01074.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.3402+295_3402+299d others(7): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060247 | ||||||
| chr9:99060248
|
A | T | 47 | a0002c0010t0001g0008a0002c0010t0001g0021a0002c0010t0001g0107others(44): Show | 47 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.3402+295A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060248 | ||||||
| chr9:99060250
|
A | T | 73 | a0001c0031t0001g0205a0002c0010t0001g0008a0002c0010t0001g0021others(70): Show | 73 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.3402+297A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060250 | ||||||
| chr9:99060252
|
A | T | 112 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(109): Show | 112 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.3402+299A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060252 | ||||||
| chr9:99060253
|
TATA | T | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3402+301_3402+303d others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060253 | ||||||
| chr9:99060254
|
A | T | 145 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(142): Show | 145 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.3402+301A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060254 | ||||||
| chr9:99060256
|
A | ATTT | 14 | a0002c0003t0003g0100a0002c0003t0003g0147a0003c0004t0003g0263others(11): Show | 14 | HG00558.hp2 HG02027.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.3402+311_3402+313d others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | INFO_REALIGN_3_PRIME | chr9 | 99060256 | |||||
| chr9:99060256
|
A | T | 179 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0057others(176): Show | 179 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.3402+303A>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060256 | ||||||
| chr9:99060257
|
T | TATA | 3 | a0010c0012t0005g0304a0030c0030t0005g0127a0030c0030t0005g0128 | 3 | HG01081.hp1 HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.3402+304_3402+305i others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060257 | ||||||
| chr9:99060258
|
T | A | 9 | a0002c0010t0009g0204a0003c0004t0002g0132a0003c0004t0002g0142others(6): Show | 9 | HG00408.hp2 HG01109.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3402+305T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060258 | ||||||
| chr9:99060288
|
G | A | 1 | a0036c0045t0003g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3402+335G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060288 | ||||||
| chr9:99060429
|
AT | A | 28 | a0001c0001t0002g0061a0001c0001t0003g0234a0002c0002t0001g0176others(25): Show | 28 | HG00558.hp2 HG01081.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.3402+495delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | INFO_REALIGN_3_PRIME | chr9 | 99060429 | |||||
| chr9:99060429
|
ATT | A | 6 | a0001c0001t0002g0172a0002c0002t0001g0178a0003c0004t0002g0189others(3): Show | 6 | HG01516.hp1 HG01516.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.3402+494_3402+495d others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | INFO_REALIGN_3_PRIME | chr9 | 99060429 | |||||
| chr9:99060429
|
ATTT | A | 143 | a0001c0013t0001g0015a0001c0013t0001g0046a0001c0013t0001g0064others(140): Show | 143 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.3402+493_3402+495d others(5): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | INFO_REALIGN_3_PRIME | chr9 | 99060429 | |||||
| chr9:99060500
|
C | T | 1 | a0001c0013t0001g0015 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3402+547C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060500 | ||||||
| chr9:99060613
|
C | T | 1 | a0010c0012t0002g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3402+660C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060613 | ||||||
| chr9:99060829
|
A | C | 3 | a0015c0018t0001g0033a0015c0018t0001g0035a0035c0043t0001g0063 | 3 | NA18964.hp1 NA18968.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3402+876A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060829 | ||||||
| chr9:99060878
|
T | G | 1 | a0019c0024t0006g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3402+925T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99060878 | ||||||
| chr9:99061045
|
G | A | 62 | a0001c0001t0002g0191a0001c0013t0001g0015a0001c0013t0001g0046others(59): Show | 62 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.3403-926G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061045 | ||||||
| chr9:99061091
|
A | G | 155 | a0001c0001t0002g0191a0001c0013t0001g0015a0001c0013t0001g0046others(152): Show | 155 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.3403-880A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061091 | ||||||
| chr9:99061127
|
T | C | 1 | a0048c0068t0002g0079 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3403-844T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061127 | ||||||
| chr9:99061208
|
C | G | 62 | a0001c0001t0002g0191a0001c0013t0001g0015a0001c0013t0001g0046others(59): Show | 62 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.3403-763C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061208 | ||||||
| chr9:99061323
|
T | A | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3403-648T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061323 | ||||||
| chr9:99061374
|
G | A | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3403-597G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061374 | ||||||
| chr9:99061491
|
T | C | 3 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088 | 3 | HG02809.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3403-480T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061491 | ||||||
| chr9:99061492
|
T | A | 2 | a0002c0010t0009g0204a0055c0082t0009g0005 | 2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3403-479T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061492 | ||||||
| chr9:99061528
|
T | G | 2 | a0022c0026t0004g0139a0022c0026t0004g0201 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3403-443T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061528 | ||||||
| chr9:99061651
|
G | T | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3403-320G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061651 | ||||||
| chr9:99061713
|
C | T | 2 | a0020c0029t0004g0156a0020c0046t0007g0004 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3403-258C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061713 | ||||||
| chr9:99061776
|
C | T | 3 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088 | 3 | HG02809.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3403-195C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061776 | ||||||
| chr9:99061856
|
C | T | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3403-115C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 36/41 | chr9 | 99061856 | ||||||
| chr9:99062113
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3531+14T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 37/41 | chr9 | 99062113 | ||||||
| chr9:99062224
|
A | G | 3 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088 | 3 | HG02809.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3532-21A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 37/41 | chr9 | 99062224 | ||||||
| chr9:99062380
|
C | G | 10 | a0004c0005t0001g0307a0006c0007t0001g0216a0006c0007t0001g0217others(7): Show | 10 | HG01243.hp1 HG02451.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3591+76C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 38/41 | chr9 | 99062380 | ||||||
| chr9:99062647
|
C | G | 6 | a0002c0010t0009g0204a0024c0028t0004g0165a0036c0045t0003g0212others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3591+343C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 38/41 | chr9 | 99062647 | ||||||
| chr9:99062830
|
C | G | 17 | a0001c0001t0003g0234a0002c0003t0003g0100a0002c0003t0003g0147others(14): Show | 17 | HG00558.hp2 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.3592-220C>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 38/41 | chr9 | 99062830 | ||||||
| chr9:99062862
|
T | C | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3592-188T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 38/41 | chr9 | 99062862 | ||||||
| chr9:99063126
|
C | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0308 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3651+17C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99063126 | ||||||
| chr9:99063267
|
G | T | 2 | a0002c0010t0009g0204a0055c0082t0009g0005 | 2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3651+158G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99063267 | ||||||
| chr9:99063307
|
A | G | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3651+198A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99063307 | ||||||
| chr9:99063329
|
G | A | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3651+220G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99063329 | ||||||
| chr9:99063473
|
A | G | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3651+364A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99063473 | ||||||
| chr9:99063852
|
G | T | 1 | a0010c0075t0007g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3651+743G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99063852 | ||||||
| chr9:99063929
|
G | A | 1 | a0005c0015t0001g0163 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3651+820G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99063929 | ||||||
| chr9:99063976
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3651+867G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99063976 | ||||||
| chr9:99064111
|
AC | A | 3 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0007g0003 | 3 | HG02572.hp1 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3651+1006delC | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99064111 | |||||
| chr9:99064157
|
G | T | 2 | a0001c0001t0002g0119a0001c0001t0002g0198 | 2 | HG01109.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3651+1048G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99064157 | ||||||
| chr9:99064735
|
T | C | 1 | a0006c0007t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3651+1626T>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99064735 | ||||||
| chr9:99064912
|
C | T | 1 | a0002c0002t0001g0043 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3651+1803C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99064912 | ||||||
| chr9:99065220
|
G | A | 2 | a0007c0008t0002g0268a0010c0012t0002g0277 | 2 | HG01169.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.3652-1662G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065220 | ||||||
| chr9:99065297
|
C | T | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-1585C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065297 | ||||||
| chr9:99065309
|
G | A | 2 | a0001c0001t0002g0119a0001c0001t0002g0198 | 2 | HG01109.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3652-1573G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065309 | ||||||
| chr9:99065504
|
G | A | 17 | a0001c0001t0003g0234a0002c0003t0003g0147a0003c0004t0003g0263others(14): Show | 17 | HG00558.hp2 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.3652-1378G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065504 | ||||||
| chr9:99065546
|
T | G | 4 | a0001c0001t0002g0191a0010c0012t0002g0087a0016c0022t0002g0226others(1): Show | 4 | HG00280.hp2 HG00733.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-1336T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065546 | ||||||
| chr9:99065590
|
C | T | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-1292C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065590 | ||||||
| chr9:99065797
|
T | A | 5 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088others(2): Show | 5 | HG02717.hp1 HG02809.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3652-1085T>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065797 | ||||||
| chr9:99065859
|
T | G | 2 | a0036c0045t0003g0212a0037c0044t0003g0138 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3652-1023T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065859 | ||||||
| chr9:99065883
|
G | A | 3 | a0017c0021t0001g0099a0017c0021t0001g0213a0017c0021t0001g0230 | 3 | HG02109.hp1 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3652-999G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065883 | ||||||
| chr9:99065942
|
C | T | 1 | a0020c0029t0002g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3652-940C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065942 | ||||||
| chr9:99065973
|
G | A | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-909G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99065973 | ||||||
| chr9:99066189
|
T | TGA | 190 | a0001c0001t0001g0196a0001c0001t0002g0191a0001c0001t0003g0234others(187): Show | 190 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3652-687_3652-686d others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066189 | |||||
| chr9:99066346
|
G | T | 13 | a0001c0001t0003g0234a0002c0003t0003g0147a0003c0004t0003g0263others(10): Show | 13 | HG00558.hp2 HG02027.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.3652-536G>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066346 | ||||||
| chr9:99066490
|
G | A | 150 | a0001c0001t0001g0196a0001c0013t0001g0015a0001c0013t0001g0046others(147): Show | 150 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.3652-392G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066490 | ||||||
| chr9:99066536
|
C | A | 2 | a0033c0038t0001g0028a0049c0071t0001g0278 | 2 | HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3652-346C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066536 | ||||||
| chr9:99066541
|
G | A | 1 | a0002c0002t0001g0043 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3652-341G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066541 | ||||||
| chr9:99066569
|
C | A | 4 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3652-313C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066569 | ||||||
| chr9:99066599
|
G | GGTTTTTT others(15): Show |
3 | a0002c0002t0001g0007a0002c0002t0001g0176a0002c0002t0001g0235 | 3 | NA18991.hp2 NA19076.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.3652-283_3652-282i others(24): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066599 | ||||||
| chr9:99066599
|
G | GT | 37 | a0001c0001t0001g0196a0001c0001t0002g0061a0001c0001t0002g0067others(34): Show | 37 | HG00642.hp1 HG00642.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.3652-258dupT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTT | 8 | a0001c0001t0002g0168a0001c0001t0002g0177a0001c0001t0003g0234others(5): Show | 8 | HG02055.hp1 HG02602.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3652-259_3652-258d others(4): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTT | 19 | a0002c0010t0001g0170a0003c0006t0001g0072a0003c0006t0001g0080others(16): Show | 19 | HG02129.hp2 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.3652-263_3652-258d others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT | 11 | a0001c0031t0001g0205a0003c0006t0001g0081a0003c0006t0001g0085others(8): Show | 11 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3652-264_3652-258d others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(13): Show |
2 | a0005c0015t0001g0040a0005c0015t0001g0163 | 2 | HG01993.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.3652-272_3652-271i others(22): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(14): Show |
3 | a0005c0015t0001g0029a0005c0015t0001g0154a0005c0015t0001g0273 | 3 | HG01928.hp1 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3652-272_3652-271i others(23): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(15): Show |
1 | a0005c0061t0001g0041 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3652-272_3652-271i others(24): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(5): Show |
2 | a0010c0012t0005g0304a0030c0030t0005g0127 | 2 | HG01081.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3652-269_3652-258d others(14): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(6): Show |
1 | a0030c0030t0005g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3652-270_3652-258d others(15): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(8): Show |
1 | a0010c0012t0005g0215 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3652-272_3652-258d others(17): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(12): Show |
2 | a0001c0013t0001g0015a0005c0059t0001g0112 | 2 | HG04228.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3652-276_3652-258d others(21): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(13): Show |
7 | a0001c0013t0001g0064a0001c0013t0001g0242a0002c0002t0001g0043others(4): Show | 7 | HG03239.hp2 HG03710.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.3652-277_3652-258d others(22): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(14): Show |
21 | a0001c0013t0001g0068a0001c0013t0001g0257a0001c0031t0001g0157others(18): Show | 21 | HG00280.hp1 HG00558.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.3652-278_3652-258d others(23): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(15): Show |
5 | a0002c0002t0001g0111a0003c0006t0001g0146a0003c0036t0001g0274others(2): Show | 5 | HG00408.hp1 NA18992.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.3652-279_3652-258d others(24): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(16): Show |
5 | a0002c0002t0001g0310a0003c0004t0001g0030a0008c0009t0001g0208others(2): Show | 5 | HG02071.hp1 HG02129.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.3652-280_3652-258d others(25): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(17): Show |
1 | a0002c0002t0001g0018 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3652-281_3652-258d others(26): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(18): Show |
1 | a0008c0033t0001g0134 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3652-282_3652-258d others(27): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(19): Show |
1 | a0049c0071t0001g0278 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3652-258_3652-257i others(28): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(20): Show |
1 | a0002c0002t0001g0053 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3652-258_3652-257i others(29): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(21): Show |
1 | a0014c0020t0001g0131 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3652-258_3652-257i others(30): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
G | GTTTTTTT others(22): Show |
1 | a0002c0002t0001g0195 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3652-258_3652-257i others(31): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
GT | G | 11 | a0001c0001t0002g0186a0001c0001t0002g0198a0002c0002t0001g0150others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.3652-258delT | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
GTTTTTTT | G | 42 | a0002c0010t0001g0008a0002c0010t0001g0107a0002c0010t0001g0125others(39): Show | 42 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.3652-264_3652-258d others(9): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066599
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0013t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3652-267_3652-258d others(12): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066599 | |||||
| chr9:99066607
|
T | TTGTTTGT others(11): Show |
4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-274_3652-273i others(20): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr9 | 99066607 | |||||
| chr9:99066608
|
T | TGTTTGTT others(6): Show |
4 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3652-274_3652-273i others(15): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066608 | ||||||
| chr9:99066611
|
T | G | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-271T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066611 | ||||||
| chr9:99066612
|
T | G | 4 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3652-270T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066612 | ||||||
| chr9:99066615
|
T | G | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-267T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066615 | ||||||
| chr9:99066616
|
T | G | 4 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3652-266T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066616 | ||||||
| chr9:99066619
|
T | G | 4 | a0019c0024t0006g0122a0019c0024t0006g0124a0019c0024t0006g0166others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-263T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066619 | ||||||
| chr9:99066620
|
T | G | 4 | a0010c0012t0002g0220a0010c0012t0002g0221a0024c0028t0002g0088others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3652-262T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066620 | ||||||
| chr9:99066633
|
G | A | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3652-249G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 39/41 | chr9 | 99066633 | ||||||
| chr9:99067260
|
G | A | 150 | a0001c0001t0001g0196a0001c0013t0001g0015a0001c0013t0001g0046others(147): Show | 150 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.3837+193G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | chr9 | 99067260 | ||||||
| chr9:99067275
|
G | C | 1 | a0036c0045t0003g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3837+208G>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | chr9 | 99067275 | ||||||
| chr9:99067917
|
G | A | 144 | a0001c0001t0001g0196a0001c0013t0001g0015a0001c0013t0001g0046others(141): Show | 144 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.3838-638G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | chr9 | 99067917 | ||||||
| chr9:99067942
|
C | A | 6 | a0001c0001t0002g0171a0001c0001t0002g0186a0001c0001t0002g0190others(3): Show | 6 | HG00741.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.3838-613C>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | chr9 | 99067942 | ||||||
| chr9:99068152
|
G | A | 1 | a0007c0008t0002g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3838-403G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | chr9 | 99068152 | ||||||
| chr9:99068181
|
A | G | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3838-374A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | chr9 | 99068181 | ||||||
| chr9:99068322
|
G | A | 1 | a0003c0006t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3838-233G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | chr9 | 99068322 | ||||||
| chr9:99068467
|
C | CA | 14 | a0001c0001t0002g0113a0002c0003t0002g0223a0002c0003t0002g0224others(11): Show | 14 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3838-69dupA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr9 | 99068467 | |||||
| chr9:99068467
|
C | CAA | 147 | a0001c0001t0001g0196a0001c0013t0001g0015a0001c0013t0001g0046others(144): Show | 147 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.3838-70_3838-69dup others(2): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr9 | 99068467 | |||||
| chr9:99068467
|
CA | C | 17 | a0001c0001t0003g0234a0002c0003t0002g0118a0002c0003t0003g0100others(14): Show | 17 | HG00558.hp2 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.3838-69delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr9 | 99068467 | |||||
| chr9:99068831
|
G | A | 144 | a0001c0001t0001g0196a0001c0013t0001g0015a0001c0013t0001g0046others(141): Show | 144 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.3953+161G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99068831 | ||||||
| chr9:99068984
|
C | T | 1 | a0001c0013t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3953+314C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99068984 | ||||||
| chr9:99068987
|
A | G | 156 | a0001c0001t0001g0196a0001c0013t0001g0015a0001c0013t0001g0046others(153): Show | 156 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.3953+317A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99068987 | ||||||
| chr9:99069244
|
A | G | 1 | a0047c0070t0011g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3954-429A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99069244 | ||||||
| chr9:99069248
|
TATTGTA | T | 148 | a0001c0001t0001g0196a0001c0013t0001g0015a0001c0013t0001g0046others(145): Show | 148 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.3954-417_3954-412d others(8): Show |
COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr9 | 99069248 | |||||
| chr9:99069266
|
A | G | 2 | a0002c0010t0009g0204a0055c0082t0009g0005 | 2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3954-407A>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99069266 | ||||||
| chr9:99069312
|
TA | T | 9 | a0001c0001t0002g0171a0001c0001t0002g0186a0001c0001t0002g0190others(6): Show | 9 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3954-360delA | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99069312 | ||||||
| chr9:99069314
|
C | T | 9 | a0001c0001t0002g0171a0001c0001t0002g0186a0001c0001t0002g0190others(6): Show | 9 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3954-359C>T | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99069314 | ||||||
| chr9:99069480
|
A | C | 4 | a0010c0012t0005g0215a0010c0012t0005g0304a0030c0030t0005g0127others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3954-193A>C | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99069480 | ||||||
| chr9:99069497
|
G | A | 164 | a0001c0001t0001g0196a0001c0013t0001g0015a0001c0013t0001g0046others(161): Show | 164 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.3954-176G>A | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99069497 | ||||||
| chr9:99069610
|
T | G | 2 | a0036c0045t0003g0212a0037c0044t0003g0138 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3954-63T>G | COL15A1 | ENSG00000204291.12 | transcript | ENST00000375001.8 | protein_coding | 41/41 | chr9 | 99069610 |