| geneid | 56999 |
|---|---|
| ensemblid | ENSG00000163638.13 |
| hgncid | 13202 |
| symbol | ADAMTS9 |
| name | ADAM metallopeptidase with thrombospondin type 1 motif 9 |
| refseq_nuc | NM_182920.2 |
| refseq_prot | NP_891550.1 |
| ensembl_nuc | ENST00000498707.5 |
| ensembl_prot | ENSP00000418735.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 64515654 |
| end | 64688000 |
| strand | - |
| ver | v1.2 |
| region | chr3:64515654-64688000 |
| region5000 | chr3:64510654-64693000 |
| regionname0 | ADAMTS9_chr3_64515654_64688000 |
| regionname5000 | ADAMTS9_chr3_64510654_64693000 |
| 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 | 1935 | 166 | 52 | 24 | 70 | 6 | 12 | 48 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0002 | 0/0 | 1935 | 36 | 9 | 7 | 20 | 0 | 0 | 13 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003 | 0/0 | 1935 | 25 | 12 | 2 | 10 | 0 | 1 | 10 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0004 | 0/0 | 1935 | 8 | 3 | 4 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0005 | 0/0 | 1935 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0006 | 0/0 | 1935 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0007 | 0/0 | 1935 | 4 | 0 | 1 | 3 | 0 | 0 | 3 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0008 | 0/0 | 1935 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0009 | 0/0 | 1935 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0010 | 0/0 | 1935 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0011 | 0/0 | 1935 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0012 | 0/0 | 1935 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0013 | 0/0 | 1935 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0014 | 0/0 | 1935 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0015 | 0/0 | 1935 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0016 | 0/0 | 1935 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0017 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0018 | 0/0 | 321 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0019 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0020 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0021 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0022 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0023 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0024 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0025 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0026 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0027 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0028 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0029 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0030 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0031 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0032 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| 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 | 5808 | 126 | 23 | 19 | 67 | 5 | 10 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0002 | 0/0 | 5808 | 36 | 9 | 7 | 20 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0003 | 0/0 | 5808 | 21 | 9 | 2 | 10 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0004 | 0/0 | 5808 | 9 | 9 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0005 | 0/0 | 5808 | 7 | 2 | 4 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0006 | 0/0 | 5808 | 7 | 3 | 2 | 0 | 1 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0007 | 0/0 | 5808 | 5 | 5 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0008 | 0/0 | 5808 | 5 | 0 | 0 | 5 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0009 | 0/0 | 5808 | 5 | 4 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0010 | 0/0 | 5808 | 4 | 0 | 0 | 4 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0011 | 0/0 | 5808 | 4 | 0 | 1 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0012 | 0/0 | 5808 | 3 | 0 | 1 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0013 | 0/0 | 5808 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0014 | 0/0 | 5808 | 3 | 0 | 0 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0015 | 0/0 | 5808 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0016 | 0/0 | 5808 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0017 | 0/0 | 5808 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0018 | 0/0 | 5808 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0019 | 0/0 | 5808 | 2 | 0 | 0 | 1 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0020 | 0/0 | 5808 | 2 | 1 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0021 | 0/0 | 5808 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0022 | 0/0 | 5808 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0023 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0024 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0025 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0026 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0027 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0028 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0029 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0030 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0031 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0032 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0033 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0034 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0035 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0036 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0037 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0038 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0039 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0040 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0041 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0042 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0043 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0044 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0045 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0046 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0047 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0048 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0049 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0050 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0051 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0052 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0053 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| c0054 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| 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 | 1/1 | 1817 | 129 | 36 | 22 | 53 | 4 | 12 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0002 | 0/0 | 1817 | 75 | 23 | 5 | 43 | 1 | 3 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0003 | 0/0 | 1817 | 36 | 0 | 12 | 24 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0004 | 0/0 | 1817 | 10 | 0 | 2 | 7 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0005 | 0/0 | 1817 | 5 | 4 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0006 | 0/0 | 1817 | 4 | 4 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0007 | 0/0 | 1817 | 4 | 3 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0008 | 0/0 | 1817 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0009 | 0/0 | 1817 | 3 | 0 | 0 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0010 | 0/0 | 1817 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0011 | 0/0 | 1817 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0012 | 0/0 | 1817 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0013 | 0/0 | 1817 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0014 | 0/0 | 1817 | 2 | 1 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0015 | 0/0 | 1817 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0016 | 0/0 | 1817 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0017 | 0/0 | 1817 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0018 | 0/0 | 1817 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0019 | 0/0 | 1817 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0020 | 0/0 | 1817 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| t0021 | 0/0 | 1817 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| 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 | 5808 | 126 | 23 | 19 | 67 | 5 | 10 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0004 | 0/0 | 5808 | 9 | 9 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0006 | 0/0 | 5808 | 7 | 3 | 2 | 0 | 1 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0007 | 0/0 | 5808 | 5 | 5 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0009 | 0/0 | 5808 | 5 | 4 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0013 | 0/0 | 5808 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0014 | 0/0 | 5808 | 3 | 0 | 0 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0020 | 0/0 | 5808 | 2 | 1 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0023 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0030 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0031 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0037 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0045 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0051 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0002c0002 | 0/0 | 5808 | 36 | 9 | 7 | 20 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0003 | 0/0 | 5808 | 21 | 9 | 2 | 10 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0017 | 0/0 | 5808 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0024 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0025 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0004c0005 | 0/0 | 5808 | 7 | 2 | 4 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0004c0026 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0005c0008 | 0/0 | 5808 | 5 | 0 | 0 | 5 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0006c0010 | 0/0 | 5808 | 4 | 0 | 0 | 4 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0007c0011 | 0/0 | 5808 | 4 | 0 | 1 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0008c0021 | 0/0 | 5808 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0008c0049 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0009c0028 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0009c0029 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0009c0047 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0010c0012 | 0/0 | 5808 | 3 | 0 | 1 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0011c0022 | 0/0 | 5808 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0011c0053 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0012c0018 | 0/0 | 5808 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0013c0019 | 0/0 | 5808 | 2 | 0 | 0 | 1 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0014c0041 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0014c0054 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0015c0015 | 0/0 | 5808 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0016c0016 | 0/0 | 5808 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0017c0050 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0018c0048 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0019c0040 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0020c0034 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0021c0035 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0022c0036 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0023c0039 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0024c0038 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0025c0033 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0026c0044 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0027c0042 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0028c0043 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0029c0032 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0030c0046 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0031c0027 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0032c0052 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7624 | 72 | 7 | 16 | 37 | 3 | 7 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0002 | 0/0 | 7624 | 43 | 10 | 2 | 27 | 1 | 3 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0003 | 0/0 | 7624 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0007 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0012 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0014 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0016 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0017 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0019 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0020 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0001t0021 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0004t0001 | 0/0 | 7624 | 7 | 7 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0004t0002 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0006t0001 | 0/0 | 7624 | 4 | 0 | 2 | 0 | 1 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0006t0010 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0006t0011 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0007t0001 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0007t0002 | 0/0 | 7624 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0007t0013 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0009t0005 | 0/0 | 7624 | 5 | 4 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0013t0001 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0013t0011 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0014t0001 | 0/0 | 7624 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0014t0002 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0020t0002 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0020t0014 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0023t0001 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0030t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0031t0008 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0037t0008 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0045t0001 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0001c0051t0018 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0002c0002t0001 | 0/0 | 7624 | 9 | 7 | 1 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0002c0002t0003 | 0/0 | 7624 | 25 | 0 | 6 | 19 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0002c0002t0008 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0002c0002t0013 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0003t0001 | 0/0 | 7624 | 9 | 4 | 1 | 4 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0003t0002 | 0/0 | 7624 | 7 | 3 | 1 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0003t0007 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0003t0009 | 0/0 | 7624 | 3 | 0 | 0 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0017t0006 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0024t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0003c0025t0001 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0004c0005t0001 | 0/0 | 7624 | 3 | 2 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0004c0005t0003 | 0/0 | 7624 | 3 | 0 | 3 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0004c0005t0015 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0004c0026t0001 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0005c0008t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0005c0008t0002 | 0/0 | 7624 | 3 | 0 | 0 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0005c0008t0003 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0006c0010t0001 | 0/0 | 7624 | 3 | 0 | 0 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0006c0010t0002 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0007c0011t0004 | 0/0 | 7624 | 4 | 0 | 1 | 3 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0008c0021t0002 | 0/0 | 7624 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0008c0049t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0009c0028t0007 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0009c0029t0002 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0009c0047t0001 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0010c0012t0004 | 0/0 | 7624 | 3 | 0 | 1 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0011c0022t0001 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0011c0053t0002 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0012c0018t0006 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0013c0019t0004 | 0/0 | 7624 | 2 | 0 | 0 | 1 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0014c0041t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0014c0054t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0015c0015t0002 | 0/0 | 7624 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0016c0016t0003 | 0/0 | 7624 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0017c0050t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0018c0048t0002 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0019c0040t0002 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0020c0034t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0021c0035t0003 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0022c0036t0002 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0023c0039t0002 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0024c0038t0004 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0025c0033t0003 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0026c0044t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0027c0042t0002 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0028c0043t0003 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0029c0032t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0030c0046t0002 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0031c0027t0002 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| a0032c0052t0002 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | copy fasta | chr3 | 64510654 | 64693000 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0016g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0019g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0020g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0001t0021g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0004t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0006t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0006t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0006t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0006t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0006t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0007t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0007t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0007t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0007t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0009t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0009t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0009t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0009t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0009t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0013t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0013t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0013t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0014t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0014t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0014t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0020t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0020t0014g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0023t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0030t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0031t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0037t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0045t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0001c0051t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0002c0002t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0009g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0009g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0003t0009g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0017t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0017t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0024t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0003c0025t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0004c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0004c0005t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0004c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0004c0005t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0004c0005t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0004c0005t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0004c0005t0015g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0004c0026t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0005c0008t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0005c0008t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0005c0008t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0005c0008t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0005c0008t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0006c0010t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0006c0010t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0006c0010t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0006c0010t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0007c0011t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0007c0011t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0007c0011t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0007c0011t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0008c0021t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0008c0021t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0008c0049t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0009c0028t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0009c0029t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0009c0047t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0010c0012t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0010c0012t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0010c0012t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0011c0022t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0011c0022t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0011c0053t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0012c0018t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0012c0018t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0013c0019t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0013c0019t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0014c0041t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0014c0054t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0015c0015t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0015c0015t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0016c0016t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0016c0016t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0017c0050t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0018c0048t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0019c0040t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0020c0034t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0021c0035t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0022c0036t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0023c0039t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0024c0038t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0025c0033t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0026c0044t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0027c0042t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0028c0043t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0029c0032t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0030c0046t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0031c0027t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| a0032c0052t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00099 | hp2 | a0001 | c0006 | t0001 | g0117 | EUR | GBR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0221 | EUR | GBR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00140 | hp2 | a0001 | c0001 | t0019 | g0119 | EUR | GBR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00438 | hp1 | a0001 | c0014 | t0002 | g0126 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00609 | hp2 | a0027 | c0042 | t0002 | g0177 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00621 | hp2 | a0002 | c0002 | t0003 | g0074 | EAS | CHS | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00733 | hp1 | a0030 | c0046 | t0002 | g0252 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0059 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0031 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00738 | hp2 | a0004 | c0005 | t0001 | g0032 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00741 | hp1 | a0031 | c0027 | t0002 | g0051 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0150 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0152 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0141 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01255 | hp1 | a0021 | c0035 | t0003 | g0075 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01255 | hp2 | a0001 | c0023 | t0001 | g0020 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01257 | hp1 | a0001 | c0020 | t0014 | g0011 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01257 | hp2 | a0001 | c0006 | t0001 | g0208 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01261 | hp1 | a0001 | c0006 | t0001 | g0207 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01261 | hp2 | a0016 | c0016 | t0003 | g0048 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01496 | hp1 | a0002 | c0002 | t0003 | g0144 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01884 | hp2 | a0003 | c0003 | t0002 | g0024 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01934 | hp1 | a0001 | c0009 | t0005 | g0072 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0151 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0278 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01952 | hp2 | a0004 | c0005 | t0003 | g0040 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01978 | hp1 | a0010 | c0012 | t0004 | g0034 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02015 | hp1 | a0002 | c0002 | t0003 | g0165 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0107 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02040 | hp2 | a0024 | c0038 | t0004 | g0174 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02055 | hp1 | a0009 | c0047 | t0001 | g0274 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02071 | hp2 | a0002 | c0002 | t0003 | g0153 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02083 | hp1 | a0008 | c0021 | t0002 | g0135 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0078 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02129 | hp1 | a0008 | c0021 | t0002 | g0134 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0123 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02135 | hp1 | a0002 | c0002 | t0003 | g0154 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02135 | hp2 | a0001 | c0014 | t0001 | g0091 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0021 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02148 | hp1 | a0004 | c0005 | t0003 | g0046 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02155 | hp1 | a0019 | c0040 | t0002 | g0148 | EAS | CDX | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02257 | hp1 | a0001 | c0009 | t0005 | g0073 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02258 | hp2 | a0003 | c0003 | t0002 | g0060 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02273 | hp1 | a0002 | c0002 | t0003 | g0149 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02273 | hp2 | a0007 | c0011 | t0004 | g0179 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02280 | hp1 | a0001 | c0009 | t0005 | g0071 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02280 | hp2 | a0002 | c0002 | t0008 | g0009 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02300 | hp2 | a0004 | c0005 | t0003 | g0047 | AMR | PEL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02523 | hp1 | a0001 | c0014 | t0001 | g0115 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02572 | hp1 | a0001 | c0004 | t0002 | g0277 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02572 | hp2 | a0011 | c0022 | t0001 | g0271 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02615 | hp2 | a0001 | c0037 | t0008 | g0006 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02622 | hp1 | a0011 | c0022 | t0001 | g0270 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0242 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02698 | hp2 | a0003 | c0024 | t0001 | g0042 | SAS | PJL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0022 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02723 | hp1 | a0012 | c0018 | t0006 | g0173 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02723 | hp2 | a0001 | c0007 | t0001 | g0017 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02809 | hp2 | a0009 | c0028 | t0007 | g0275 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0063 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02886 | hp2 | a0001 | c0007 | t0013 | g0015 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02895 | hp1 | a0003 | c0003 | t0007 | g0038 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02895 | hp2 | a0004 | c0026 | t0001 | g0029 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02896 | hp1 | a0001 | c0009 | t0005 | g0069 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02897 | hp1 | a0001 | c0009 | t0005 | g0070 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02897 | hp2 | a0003 | c0003 | t0007 | g0037 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0236 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02922 | hp2 | a0001 | c0013 | t0001 | g0212 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0267 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02970 | hp2 | a0009 | c0029 | t0002 | g0237 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03098 | hp1 | a0001 | c0051 | t0018 | g0268 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03098 | hp2 | a0001 | c0007 | t0002 | g0062 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0276 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03139 | hp2 | a0001 | c0007 | t0002 | g0219 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03195 | hp1 | a0003 | c0017 | t0006 | g0028 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | ESN | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03209 | hp1 | a0022 | c0036 | t0002 | g0214 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0239 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03225 | hp2 | a0001 | c0006 | t0010 | g0003 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03453 | hp1 | a0012 | c0018 | t0006 | g0243 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03486 | hp1 | a0001 | c0031 | t0008 | g0004 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03486 | hp2 | a0011 | c0053 | t0002 | g0272 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03491 | hp1 | a0014 | c0041 | t0001 | g0280 | SAS | PJL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03540 | hp1 | a0032 | c0052 | t0002 | g0269 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | GWD | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0033 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03688 | hp2 | a0014 | c0054 | t0001 | g0283 | SAS | STU | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03927 | hp2 | a0001 | c0006 | t0001 | g0206 | SAS | BEB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | STU | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG04184 | hp1 | a0013 | c0019 | t0004 | g0200 | SAS | BEB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG04184 | hp2 | a0001 | c0030 | t0001 | g0180 | SAS | BEB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18522 | hp1 | a0004 | c0005 | t0001 | g0036 | AFR | YRI | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18522 | hp2 | a0003 | c0025 | t0001 | g0026 | AFR | YRI | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18906 | hp1 | a0001 | c0020 | t0002 | g0258 | AFR | YRI | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18906 | hp2 | a0001 | c0001 | t0017 | g0066 | AFR | YRI | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18942 | hp1 | a0003 | c0003 | t0009 | g0045 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18942 | hp2 | a0015 | c0015 | t0002 | g0055 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18946 | hp1 | a0007 | c0011 | t0004 | g0086 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18953 | hp1 | a0005 | c0008 | t0002 | g0175 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0260 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18960 | hp1 | a0002 | c0002 | t0003 | g0190 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18960 | hp2 | a0001 | c0001 | t0021 | g0284 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18961 | hp1 | a0002 | c0002 | t0003 | g0195 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18965 | hp1 | a0023 | c0039 | t0002 | g0146 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18968 | hp2 | a0018 | c0048 | t0002 | g0081 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18972 | hp2 | a0004 | c0005 | t0015 | g0010 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18974 | hp2 | a0010 | c0012 | t0004 | g0039 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18975 | hp1 | a0017 | c0050 | t0001 | g0130 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18975 | hp2 | a0003 | c0003 | t0009 | g0043 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18983 | hp1 | a0006 | c0010 | t0001 | g0245 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18984 | hp1 | a0005 | c0008 | t0002 | g0176 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18985 | hp1 | a0006 | c0010 | t0001 | g0265 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18985 | hp2 | a0005 | c0008 | t0003 | g0192 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18986 | hp1 | a0005 | c0008 | t0001 | g0094 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18988 | hp1 | a0029 | c0032 | t0001 | g0259 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18991 | hp2 | a0020 | c0034 | t0001 | g0140 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18995 | hp1 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18995 | hp2 | a0002 | c0002 | t0003 | g0196 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19001 | hp1 | a0003 | c0003 | t0001 | g0035 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19003 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0142 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19010 | hp1 | a0003 | c0003 | t0002 | g0056 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | LWK | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0238 | AFR | LWK | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0257 | AFR | LWK | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19043 | hp2 | a0002 | c0002 | t0013 | g0016 | AFR | LWK | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19056 | hp1 | a0002 | c0002 | t0003 | g0193 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19058 | hp1 | a0003 | c0003 | t0009 | g0044 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19058 | hp2 | a0007 | c0011 | t0004 | g0157 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19062 | hp1 | a0013 | c0019 | t0004 | g0161 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0160 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19065 | hp1 | a0002 | c0002 | t0003 | g0185 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19066 | hp1 | a0005 | c0008 | t0002 | g0188 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19070 | hp1 | a0028 | c0043 | t0003 | g0194 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19070 | hp2 | a0026 | c0044 | t0001 | g0098 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19077 | hp2 | a0010 | c0012 | t0004 | g0050 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19082 | hp1 | a0007 | c0011 | t0004 | g0156 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19083 | hp1 | a0006 | c0010 | t0002 | g0169 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19084 | hp1 | a0025 | c0033 | t0003 | g0261 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19085 | hp1 | a0015 | c0015 | t0002 | g0053 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19085 | hp2 | a0008 | c0049 | t0001 | g0136 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19090 | hp2 | a0003 | c0003 | t0002 | g0058 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19240 | hp1 | a0001 | c0006 | t0011 | g0008 | AFR | YRI | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA19240 | hp2 | a0004 | c0005 | t0001 | g0030 | AFR | YRI | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA20129 | hp1 | a0003 | c0017 | t0006 | g0027 | AFR | ASW | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA20129 | hp2 | a0001 | c0001 | t0020 | g0213 | AFR | ASW | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | TSI | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01123 | hp1 | a0016 | c0016 | t0003 | g0049 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02109 | hp1 | a0001 | c0007 | t0002 | g0254 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02486 | hp1 | a0001 | c0004 | t0002 | g0240 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02559 | hp1 | a0001 | c0013 | t0011 | g0005 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | ACB | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG03471 | hp2 | a0001 | c0006 | t0010 | g0007 | AFR | MSL | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG06807 | hp1 | a0003 | c0003 | t0002 | g0025 | AFR | USA | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0061 | AFR | USA | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18955 | hp1 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA18955 | hp2 | a0006 | c0010 | t0001 | g0264 | EAS | JPT | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | USA | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA20300 | hp2 | a0001 | c0045 | t0001 | g0068 | AFR | USA | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA21309 | hp1 | a0001 | c0013 | t0001 | g0145 | AFR | LWK | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0102 | REF | REF | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0249 | REF | REF | ADAMTS9_chr3_64510654_64693000 | ADAMTS9 | chr3 | 64510654 | 64693000 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:64522181
|
C | T | 4 | a0007a0010a0013others(1): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
missense_variant | MODERATE | c.5798G>A | p.Arg1933Gln | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/40 | 6141/7624 | 5798/5808 | 1933/1935 | chr3 | 64522181 | ||
| chr3:64539283
|
G | C | 1 | a0022 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.5533C>G | p.Gln1845Glu | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/40 | 5876/7624 | 5533/5808 | 1845/1935 | chr3 | 64539283 | ||
| chr3:64541139
|
C | T | 1 | a0012 | 2 | HG02723.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.5477G>A | p.Ser1826Asn | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/40 | 5820/7624 | 5477/5808 | 1826/1935 | chr3 | 64541139 | ||
| chr3:64541336
|
C | G | 1 | a0024 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.5371G>C | p.Glu1791Gln | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 35/40 | 5714/7624 | 5371/5808 | 1791/1935 | chr3 | 64541336 | ||
| chr3:64541599
|
T | C | 6 | a0007a0010a0013others(3): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
missense_variant | MODERATE | c.5219A>G | p.Lys1740Arg | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 34/40 | 5562/7624 | 5219/5808 | 1740/1935 | chr3 | 64541599 | ||
| chr3:64546800
|
G | C | 7 | a0002a0004a0005others(4): Show | 54 | HG00621.hp2 HG00738.hp2 HG01071.hp2 others(51): Show |
missense_variant | MODERATE | c.5022C>G | p.Asp1674Glu | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/40 | 5365/7624 | 5022/5808 | 1674/1935 | chr3 | 64546800 | ||
| chr3:64550972
|
C | T | 1 | a0005 | 5 | NA18953.hp1 NA18984.hp1 NA18985.hp2 others(2): Show |
missense_variant | MODERATE | c.4789G>A | p.Val1597Met | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/40 | 5132/7624 | 4789/5808 | 1597/1935 | chr3 | 64550972 | ||
| chr3:64561712
|
C | A | 1 | a0026 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.4564G>T | p.Val1522Leu | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/40 | 4907/7624 | 4564/5808 | 1522/1935 | chr3 | 64561712 | ||
| chr3:64594392
|
C | T | 7 | a0006a0007a0010others(4): Show | 17 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(14): Show |
missense_variant | MODERATE | c.4222G>A | p.Val1408Ile | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/40 | 4565/7624 | 4222/5808 | 1408/1935 | chr3 | 64594392 | ||
| chr3:64601994
|
G | A | 1 | a0019 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.3967C>T | p.Arg1323Cys | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/40 | 4310/7624 | 3967/5808 | 1323/1935 | chr3 | 64601994 | ||
| chr3:64604038
|
C | G | 1 | a0025 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.3631G>C | p.Asp1211His | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/40 | 3974/7624 | 3631/5808 | 1211/1935 | chr3 | 64604038 | ||
| chr3:64604297
|
G | A | 1 | a0014 | 2 | HG03491.hp1 HG03688.hp2 |
missense_variant | MODERATE | c.3509C>T | p.Ala1170Val | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 24/40 | 3852/7624 | 3509/5808 | 1170/1935 | chr3 | 64604297 | ||
| chr3:64615994
|
T | C | 3 | a0026a0027a0028 | 3 | HG00609.hp2 NA19070.hp1 NA19070.hp2 |
missense_variant | MODERATE | c.2990A>G | p.Asn997Ser | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 20/40 | 3333/7624 | 2990/5808 | 997/1935 | chr3 | 64615994 | ||
| chr3:64616083
|
C | G | 1 | a0029 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.2901G>C | p.Arg967Ser | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 20/40 | 3244/7624 | 2901/5808 | 967/1935 | chr3 | 64616083 | ||
| chr3:64633727
|
T | C | 1 | a0030 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.2009A>G | p.Asn670Ser | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 13/40 | 2352/7624 | 2009/5808 | 670/1935 | chr3 | 64633727 | ||
| chr3:64641870
|
T | C | 1 | a0031 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1834A>G | p.Ile612Val | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/40 | 2177/7624 | 1834/5808 | 612/1935 | chr3 | 64641870 | ||
| chr3:64641911
|
C | A | 1 | a0009 | 3 | HG02055.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1793G>T | p.Gly598Val | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/40 | 2136/7624 | 1793/5808 | 598/1935 | chr3 | 64641911 | ||
| chr3:64658506
|
G | C | 1 | a0018 | 1 | NA18968.hp2 | stop_gained | HIGH | c.965C>G | p.Ser322* | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/40 | 1308/7624 | 965/5808 | 322/1935 | chr3 | 64658506 | ||
| chr3:64681255
|
G | A | 1 | a0008 | 3 | HG02083.hp1 HG02129.hp1 NA19085.hp2 |
missense_variant | MODERATE | c.625C>T | p.Arg209Cys | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/40 | 968/7624 | 625/5808 | 209/1935 | chr3 | 64681255 | ||
| chr3:64681301
|
T | A | 1 | a0017 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.579A>T | p.Glu193Asp | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/40 | 922/7624 | 579/5808 | 193/1935 | chr3 | 64681301 | ||
| chr3:64686798
|
A | T | 6 | a0003a0004a0010others(3): Show | 41 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
missense_variant | MODERATE | c.286T>A | p.Ser96Thr | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/40 | 629/7624 | 286/5808 | 96/1935 | chr3 | 64686798 | ||
| chr3:64686825
|
C | A | 2 | a0011a0032 | 4 | HG02572.hp2 HG02622.hp1 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.259G>T | p.Ala87Ser | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/40 | 602/7624 | 259/5808 | 87/1935 | chr3 | 64686825 | ||
| chr3:64686858
|
T | C | 1 | a0011 | 3 | HG02572.hp2 HG02622.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.226A>G | p.Ile76Val | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/40 | 569/7624 | 226/5808 | 76/1935 | chr3 | 64686858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:64522219
|
T | C | 2 | a0001c0009a0001c0051 | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
synonymous_variant | LOW | c.5760A>G | p.Gly1920Gly | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/40 | 6103/7624 | 5760/5808 | 1920/1935 | chr3 | 64522219 | ||
| chr3:64541198
|
G | A | 1 | a0001c0037 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.5418C>T | p.Asn1806Asn | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/40 | 5761/7624 | 5418/5808 | 1806/1935 | chr3 | 64541198 | ||
| chr3:64546902
|
G | A | 1 | a0003c0017 | 2 | HG03195.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.4920C>T | p.Ser1640Ser | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/40 | 5263/7624 | 4920/5808 | 1640/1935 | chr3 | 64546902 | ||
| chr3:64550973
|
G | A | 1 | a0032c0052 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.4788C>T | p.Asp1596Asp | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/40 | 5131/7624 | 4788/5808 | 1596/1935 | chr3 | 64550973 | ||
| chr3:64596971
|
G | A | 1 | a0001c0014 | 3 | HG00438.hp1 HG02135.hp2 HG02523.hp1 |
synonymous_variant | LOW | c.4038C>T | p.Gly1346Gly | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/40 | 4381/7624 | 4038/5808 | 1346/1935 | chr3 | 64596971 | ||
| chr3:64602142
|
G | A | 4 | a0001c0006a0001c0007a0009c0029others(1): Show | 14 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(11): Show |
synonymous_variant | LOW | c.3819C>T | p.Ile1273Ile | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/40 | 4162/7624 | 3819/5808 | 1273/1935 | chr3 | 64602142 | ||
| chr3:64602181
|
G | A | 1 | a0001c0020 | 2 | HG01257.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.3780C>T | p.Thr1260Thr | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/40 | 4123/7624 | 3780/5808 | 1260/1935 | chr3 | 64602181 | ||
| chr3:64604284
|
C | T | 5 | a0001c0007a0001c0013a0003c0025others(2): Show | 11 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(8): Show |
synonymous_variant | LOW | c.3522G>A | p.Thr1174Thr | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 24/40 | 3865/7624 | 3522/5808 | 1174/1935 | chr3 | 64604284 | ||
| chr3:64621164
|
C | A | 1 | a0001c0020 | 2 | HG01257.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.2763G>T | p.Leu921Leu | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/40 | 3106/7624 | 2763/5808 | 921/1935 | chr3 | 64621164 | ||
| chr3:64621164
|
C | G | 1 | a0003c0024 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.2763G>C | p.Leu921Leu | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/40 | 3106/7624 | 2763/5808 | 921/1935 | chr3 | 64621164 | ||
| chr3:64622471
|
G | A | 1 | a0001c0045 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.2505C>T | p.Ala835Ala | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 17/40 | 2848/7624 | 2505/5808 | 835/1935 | chr3 | 64622471 | ||
| chr3:64622477
|
C | T | 1 | a0001c0031 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.2499G>A | p.Glu833Glu | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 17/40 | 2842/7624 | 2499/5808 | 833/1935 | chr3 | 64622477 | ||
| chr3:64622537
|
G | T | 1 | a0008c0049 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.2439C>A | p.Val813Val | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 17/40 | 2782/7624 | 2439/5808 | 813/1935 | chr3 | 64622537 | ||
| chr3:64658652
|
C | T | 1 | a0001c0030 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.819G>A | p.Thr273Thr | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/40 | 1162/7624 | 819/5808 | 273/1935 | chr3 | 64658652 | ||
| chr3:64658679
|
C | T | 4 | a0001c0004a0009c0028a0009c0029others(1): Show | 13 | HG02486.hp1 HG02572.hp1 HG02572.hp2 others(10): Show |
synonymous_variant | LOW | c.792G>A | p.Glu264Glu | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/40 | 1135/7624 | 792/5808 | 264/1935 | chr3 | 64658679 | ||
| chr3:64686610
|
G | A | 1 | a0001c0051 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.474C>T | p.Thr158Thr | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/40 | 817/7624 | 474/5808 | 158/1935 | chr3 | 64686610 | ||
| chr3:64686862
|
C | T | 1 | a0001c0023 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.222G>A | p.Arg74Arg | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/40 | 565/7624 | 222/5808 | 74/1935 | chr3 | 64686862 | ||
| chr3:64687619
|
C | A | 1 | a0014c0054 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.39G>T | p.Leu13Leu | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/40 | 382/7624 | 39/5808 | 13/1935 | chr3 | 64687619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:64515658
|
G | A | 1 | a0001c0001t0020 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1469C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 6513 | chr3 | 64515658 | |||||
| chr3:64515734
|
A | C | 1 | a0001c0009t0005 | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1393T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 6437 | chr3 | 64515734 | |||||
| chr3:64515942
|
A | G | 4 | a0001c0001t0007a0001c0006t0010a0003c0003t0007others(1): Show | 6 | HG01952.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1185T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 6229 | chr3 | 64515942 | |||||
| chr3:64515963
|
G | A | 1 | a0003c0003t0009 | 3 | NA18942.hp1 NA18975.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1164C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 6208 | chr3 | 64515963 | |||||
| chr3:64516022
|
T | C | 4 | a0007c0011t0004a0010c0012t0004a0013c0019t0004others(1): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1105A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 6149 | chr3 | 64516022 | |||||
| chr3:64516170
|
T | C | 6 | a0001c0009t0005a0001c0051t0018a0007c0011t0004others(3): Show | 16 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*957A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 6001 | chr3 | 64516170 | |||||
| chr3:64516189
|
G | T | 2 | a0003c0017t0006a0012c0018t0006 | 4 | HG02723.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*938C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 5982 | chr3 | 64516189 | |||||
| chr3:64516286
|
C | A | 1 | a0001c0001t0019 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 5885 | chr3 | 64516286 | |||||
| chr3:64516447
|
A | T | 4 | a0007c0011t0004a0010c0012t0004a0013c0019t0004others(1): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*680T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 5724 | chr3 | 64516447 | |||||
| chr3:64516512
|
C | T | 9 | a0001c0001t0003a0002c0002t0003a0004c0005t0003others(6): Show | 37 | HG00597.hp2 HG00621.hp2 HG01071.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*615G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 5659 | chr3 | 64516512 | |||||
| chr3:64516513
|
G | A | 36 | a0001c0001t0002a0001c0001t0007a0001c0001t0014others(33): Show | 105 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*614C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 5658 | chr3 | 64516513 | |||||
| chr3:64516654
|
C | G | 5 | a0001c0001t0012a0001c0001t0017a0001c0051t0018others(2): Show | 8 | HG02257.hp2 HG02723.hp1 HG03098.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*473G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 5517 | chr3 | 64516654 | |||||
| chr3:64516971
|
A | G | 1 | a0001c0001t0016 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*156T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 40/40 | 5200 | chr3 | 64516971 | |||||
| chr3:64687771
|
C | T | 5 | a0001c0001t0012a0001c0001t0014a0001c0007t0013others(2): Show | 6 | HG01257.hp1 HG02257.hp2 HG02717.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-114G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/40 | 114 | chr3 | 64687771 | |||||
| chr3:64687894
|
C | A | 1 | a0004c0005t0015 | 1 | NA18972.hp2 | 5_prime_UTR_variant | MODIFIER | c.-237G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/40 | 237 | chr3 | 64687894 | |||||
| chr3:64687895
|
A | G | 1 | a0004c0005t0015 | 1 | NA18972.hp2 | 5_prime_UTR_variant | MODIFIER | c.-238T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/40 | 238 | chr3 | 64687895 | |||||
| chr3:64687968
|
A | G | 6 | a0001c0006t0010a0001c0006t0011a0001c0013t0011others(3): Show | 7 | HG02280.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-311T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/40 | 311 | chr3 | 64687968 | |||||
| chr3:64687987
|
G | A | 1 | a0001c0001t0021 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-330C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/40 | 330 | chr3 | 64687987 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:64517209
|
A | G | 1 | a0001c0001t0003g0262 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.*6-88T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517209 | ||||||
| chr3:64517262
|
G | A | 2 | a0001c0001t0002g0253a0030c0046t0002g0252 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.*6-141C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517262 | ||||||
| chr3:64517397
|
GC | G | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-277delG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517397 | ||||||
| chr3:64517415
|
G | GTTTTT | 3 | a0001c0009t0005g0070a0001c0009t0005g0071a0001c0009t0005g0072 | 3 | HG01934.hp1 HG02280.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.*6-295_*6-294insAA others(3): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517415 | ||||||
| chr3:64517415
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.*6-295_*6-294insAA others(14): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517415 | ||||||
| chr3:64517415
|
GGTTTTTT others(3): Show |
G | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*6-304_*6-295delAA others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517415 | ||||||
| chr3:64517416
|
G | GTTTT | 6 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(3): Show | 6 | HG02040.hp2 HG02273.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-299_*6-296dupAA others(2): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTT | 27 | a0001c0001t0002g0076a0001c0001t0002g0084a0001c0001t0002g0108others(24): Show | 27 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.*6-300_*6-296dupAA others(3): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTT | 58 | a0001c0001t0001g0218a0001c0001t0002g0065a0001c0001t0002g0099others(55): Show | 58 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.*6-301_*6-296dupAA others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT | 38 | a0001c0001t0002g0083a0001c0001t0002g0088a0001c0001t0002g0089others(35): Show | 38 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.*6-302_*6-296dupAA others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(1): Show |
6 | a0001c0001t0002g0162a0001c0001t0002g0217a0001c0004t0002g0240others(3): Show | 6 | HG00735.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-303_*6-296dupAA others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.*6-296_*6-295insAA others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.*6-296_*6-295insAA others(14): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(10): Show |
1 | a0003c0003t0001g0054 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.*6-296_*6-295insAA others(15): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.*6-296_*6-295insAA others(13): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(5): Show |
4 | a0003c0017t0006g0027a0003c0017t0006g0028a0012c0018t0006g0173others(1): Show | 4 | HG02723.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*6-307_*6-296dupAA others(10): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(7): Show |
1 | a0003c0003t0001g0041 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.*6-309_*6-296dupAA others(12): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(8): Show |
10 | a0001c0001t0001g0092a0001c0001t0001g0210a0001c0001t0001g0216others(7): Show | 10 | HG00544.hp2 HG00738.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.*6-310_*6-296dupAA others(13): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(9): Show |
37 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0079others(34): Show | 38 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.*6-311_*6-296dupAA others(14): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(10): Show |
26 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0001g0102others(23): Show | 26 | HG00140.hp2 HG01123.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.*6-312_*6-296dupAA others(15): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(11): Show |
10 | a0001c0001t0001g0101a0001c0001t0001g0171a0001c0001t0001g0186others(7): Show | 10 | HG00609.hp1 HG01496.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.*6-313_*6-296dupAA others(16): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(12): Show |
4 | a0001c0001t0001g0163a0001c0001t0001g0181a0001c0031t0008g0004others(1): Show | 4 | HG00544.hp1 HG03486.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.*6-314_*6-296dupAA others(17): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(13): Show |
5 | a0001c0001t0001g0164a0001c0001t0001g0199a0001c0001t0001g0203others(2): Show | 5 | HG00558.hp1 HG00642.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.*6-315_*6-296dupAA others(18): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(14): Show |
1 | a0001c0001t0001g0096 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.*6-316_*6-296dupAA others(19): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(15): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0232 | 2 | HG01081.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.*6-317_*6-296dupAA others(20): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.*6-296_*6-295insAA others(22): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
G | T | 6 | a0001c0001t0001g0085a0001c0009t0005g0069a0001c0009t0005g0070others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-295C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517416
|
GT | G | 17 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(14): Show | 17 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.*6-296delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517416 | ||||||
| chr3:64517423
|
T | G | 1 | a0002c0002t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.*6-302A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517423 | ||||||
| chr3:64517424
|
T | G | 17 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(14): Show | 17 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.*6-303A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517424 | ||||||
| chr3:64517426
|
T | G | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*6-305A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517426 | ||||||
| chr3:64517527
|
G | A | 27 | a0001c0001t0002g0065a0001c0001t0002g0088a0001c0001t0002g0100others(24): Show | 27 | HG00438.hp1 HG00609.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.*6-406C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517527 | ||||||
| chr3:64517539
|
A | G | 4 | a0001c0004t0001g0236a0001c0004t0001g0238a0001c0004t0001g0239others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.*6-418T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517539 | ||||||
| chr3:64517550
|
C | T | 2 | a0001c0001t0001g0226a0003c0024t0001g0042 | 2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.*6-429G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517550 | ||||||
| chr3:64517655
|
C | T | 4 | a0001c0001t0002g0111a0001c0001t0002g0241a0001c0001t0002g0248others(1): Show | 4 | HG00597.hp1 NA18953.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.*6-534G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517655 | ||||||
| chr3:64517658
|
C | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-537G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517658 | ||||||
| chr3:64517667
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-546A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517667 | ||||||
| chr3:64517684
|
T | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-563A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517684 | ||||||
| chr3:64517709
|
T | C | 4 | a0003c0017t0006g0027a0003c0017t0006g0028a0012c0018t0006g0173others(1): Show | 4 | HG02723.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*6-588A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517709 | ||||||
| chr3:64517802
|
G | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.*6-681C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517802 | ||||||
| chr3:64517810
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0218 | 2 | HG00642.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.*6-689A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517810 | ||||||
| chr3:64517811
|
G | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-690C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517811 | ||||||
| chr3:64517823
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0218 | 2 | HG00642.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.*6-702A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517823 | ||||||
| chr3:64517917
|
C | A | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*6-796G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64517917 | ||||||
| chr3:64518041
|
G | T | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*6-920C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518041 | ||||||
| chr3:64518048
|
G | A | 1 | a0001c0001t0002g0184 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.*6-927C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518048 | ||||||
| chr3:64518067
|
C | T | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.*6-946G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518067 | ||||||
| chr3:64518095
|
G | C | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.*6-974C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518095 | ||||||
| chr3:64518111
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-990A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518111 | ||||||
| chr3:64518117
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.*6-996T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518117 | ||||||
| chr3:64518146
|
A | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1025T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518146 | ||||||
| chr3:64518215
|
C | T | 1 | a0028c0043t0003g0194 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.*6-1094G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518215 | ||||||
| chr3:64518254
|
T | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1133A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518254 | ||||||
| chr3:64518267
|
A | C | 1 | a0004c0026t0001g0029 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*6-1146T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518267 | ||||||
| chr3:64518282
|
C | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1161G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518282 | ||||||
| chr3:64518332
|
T | C | 1 | a0022c0036t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*6-1211A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518332 | ||||||
| chr3:64518341
|
C | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1220G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518341 | ||||||
| chr3:64518359
|
G | C | 1 | a0022c0036t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*6-1238C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518359 | ||||||
| chr3:64518395
|
T | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1274A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518395 | ||||||
| chr3:64518399
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.*6-1278A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518399 | ||||||
| chr3:64518404
|
T | C | 20 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(17): Show | 20 | HG00544.hp2 HG00609.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.*6-1283A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518404 | ||||||
| chr3:64518416
|
G | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1295C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518416 | ||||||
| chr3:64518494
|
C | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1373G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518494 | ||||||
| chr3:64518498
|
T | A | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*6-1377A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518498 | ||||||
| chr3:64518527
|
C | T | 1 | a0028c0043t0003g0194 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.*6-1406G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518527 | ||||||
| chr3:64518592
|
G | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1471C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518592 | ||||||
| chr3:64518665
|
C | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1544G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518665 | ||||||
| chr3:64518741
|
A | T | 1 | a0003c0003t0001g0041 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.*6-1620T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518741 | ||||||
| chr3:64518742
|
G | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1621C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518742 | ||||||
| chr3:64518763
|
C | CT | 28 | a0001c0001t0003g0262a0002c0002t0003g0074a0002c0002t0003g0078others(25): Show | 28 | HG00597.hp2 HG00621.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.*6-1643_*6-1642ins others(1): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518763 | ||||||
| chr3:64518763
|
C | CTT | 8 | a0001c0001t0003g0082a0002c0002t0003g0077a0002c0002t0003g0154others(5): Show | 8 | HG01952.hp2 HG02135.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.*6-1643_*6-1642ins others(2): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518763 | ||||||
| chr3:64518764
|
A | AT | 14 | a0001c0001t0001g0018a0001c0001t0001g0166a0001c0001t0001g0218others(11): Show | 14 | HG00642.hp1 HG01884.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.*6-1644dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518764 | ||||||
| chr3:64518764
|
A | ATT | 38 | a0001c0001t0001g0215a0001c0001t0002g0076a0001c0001t0002g0083others(35): Show | 38 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.*6-1645_*6-1644dup others(2): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518764 | ||||||
| chr3:64518764
|
A | ATTT | 6 | a0001c0001t0002g0089a0001c0001t0002g0184a0001c0001t0002g0202others(3): Show | 6 | HG02056.hp1 HG04184.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1646_*6-1644dup others(3): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518764 | ||||||
| chr3:64518764
|
A | T | 37 | a0001c0001t0003g0082a0001c0001t0003g0262a0002c0002t0003g0074others(34): Show | 37 | HG00597.hp2 HG00621.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.*6-1643T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518764 | ||||||
| chr3:64518764
|
AT | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.*6-1644delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518764 | ||||||
| chr3:64518764
|
ATT | A | 6 | a0001c0001t0001g0102a0001c0001t0001g0167a0001c0001t0001g0171others(3): Show | 6 | HG03130.hp2 NA18956.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1645_*6-1644del others(2): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518764 | ||||||
| chr3:64518764
|
ATTTTTTT others(5): Show |
A | 1 | a0010c0012t0004g0050 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.*6-1655_*6-1644del others(12): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518764 | ||||||
| chr3:64518765
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.*6-1644A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518765 | ||||||
| chr3:64518809
|
C | G | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1688G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518809 | ||||||
| chr3:64518888
|
C | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0279others(5): Show | 8 | HG00735.hp1 HG01884.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.*6-1767G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518888 | ||||||
| chr3:64518908
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.*6-1787C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518908 | ||||||
| chr3:64518939
|
A | G | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-1818T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518939 | ||||||
| chr3:64518962
|
G | C | 4 | a0003c0017t0006g0027a0003c0017t0006g0028a0012c0018t0006g0173others(1): Show | 4 | HG02723.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*6-1841C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64518962 | ||||||
| chr3:64519086
|
A | T | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.*6-1965T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519086 | ||||||
| chr3:64519139
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-2018A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519139 | ||||||
| chr3:64519204
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-2083A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519204 | ||||||
| chr3:64519282
|
A | G | 1 | a0001c0013t0001g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.*6-2161T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519282 | ||||||
| chr3:64519285
|
G | A | 16 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(13): Show | 16 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.*6-2164C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519285 | ||||||
| chr3:64519317
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-2196A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519317 | ||||||
| chr3:64519328
|
C | T | 1 | a0001c0013t0011g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*6-2207G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519328 | ||||||
| chr3:64519402
|
A | G | 1 | a0001c0001t0020g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*6-2281T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519402 | ||||||
| chr3:64519408
|
TC | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-2288delG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519408 | ||||||
| chr3:64519442
|
A | T | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*6-2321T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519442 | ||||||
| chr3:64519525
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6-2404A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519525 | ||||||
| chr3:64519629
|
C | T | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.*6-2508G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519629 | ||||||
| chr3:64519700
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.*5+2466A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519700 | ||||||
| chr3:64519701
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.*5+2465C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519701 | ||||||
| chr3:64519832
|
A | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.*5+2334T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519832 | ||||||
| chr3:64519862
|
C | T | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*5+2304G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519862 | ||||||
| chr3:64519866
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.*5+2300G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519866 | ||||||
| chr3:64519878
|
G | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.*5+2288C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519878 | ||||||
| chr3:64519943
|
G | A | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*5+2223C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64519943 | ||||||
| chr3:64520180
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.*5+1986G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520180 | ||||||
| chr3:64520234
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(277): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.*5+1932A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520234 | ||||||
| chr3:64520311
|
C | T | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*5+1855G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520311 | ||||||
| chr3:64520328
|
T | C | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*5+1838A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520328 | ||||||
| chr3:64520453
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+1713A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520453 | ||||||
| chr3:64520455
|
T | C | 1 | a0011c0022t0001g0270 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*5+1711A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520455 | ||||||
| chr3:64520495
|
C | A | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.*5+1671G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520495 | ||||||
| chr3:64520518
|
T | C | 5 | a0001c0001t0002g0172a0001c0001t0002g0224a0001c0001t0014g0012others(2): Show | 5 | HG00741.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.*5+1648A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520518 | ||||||
| chr3:64520548
|
A | G | 3 | a0002c0002t0003g0122a0002c0002t0003g0138a0025c0033t0003g0261 | 3 | NA18955.hp1 NA19077.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.*5+1618T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520548 | ||||||
| chr3:64520596
|
T | C | 1 | a0012c0018t0006g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*5+1570A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520596 | ||||||
| chr3:64520608
|
T | A | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*5+1558A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520608 | ||||||
| chr3:64520735
|
G | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+1431C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520735 | ||||||
| chr3:64520992
|
C | T | 3 | a0001c0001t0001g0183a0014c0041t0001g0280a0014c0054t0001g0283 | 3 | HG03491.hp1 HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.*5+1174G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64520992 | ||||||
| chr3:64521004
|
T | C | 8 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0279others(5): Show | 8 | HG00735.hp1 HG01884.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.*5+1162A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521004 | ||||||
| chr3:64521292
|
A | C | 1 | a0003c0003t0001g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.*5+874T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521292 | ||||||
| chr3:64521362
|
T | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+804A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521362 | ||||||
| chr3:64521546
|
C | T | 1 | a0002c0002t0001g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*5+620G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521546 | ||||||
| chr3:64521651
|
C | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+515G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521651 | ||||||
| chr3:64521662
|
A | C | 16 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(13): Show | 16 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.*5+504T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521662 | ||||||
| chr3:64521700
|
A | T | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*5+466T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521700 | ||||||
| chr3:64521706
|
A | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0279others(5): Show | 8 | HG00735.hp1 HG01884.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.*5+460T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521706 | ||||||
| chr3:64521761
|
C | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+405G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521761 | ||||||
| chr3:64521781
|
A | G | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+385T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521781 | ||||||
| chr3:64521818
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+348A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521818 | ||||||
| chr3:64521885
|
A | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+281T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521885 | ||||||
| chr3:64521991
|
T | C | 37 | a0001c0001t0003g0082a0001c0001t0003g0262a0002c0002t0003g0074others(34): Show | 37 | HG00597.hp2 HG00621.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.*5+175A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 39/39 | chr3 | 64521991 | ||||||
| chr3:64522290
|
C | T | 1 | a0002c0002t0003g0152 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5719-30G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522290 | ||||||
| chr3:64522345
|
A | G | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.5719-85T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522345 | ||||||
| chr3:64522346
|
C | T | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5719-86G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522346 | ||||||
| chr3:64522374
|
T | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.5719-114A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522374 | ||||||
| chr3:64522520
|
CA | C | 4 | a0001c0001t0002g0131a0001c0001t0002g0217a0001c0007t0002g0062others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.5719-261delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522520 | ||||||
| chr3:64522629
|
T | C | 7 | a0001c0001t0002g0131a0001c0001t0002g0217a0001c0006t0010g0003others(4): Show | 7 | HG00735.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5719-369A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522629 | ||||||
| chr3:64522683
|
C | T | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5719-423G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522683 | ||||||
| chr3:64522761
|
A | G | 86 | a0001c0001t0001g0215a0001c0001t0002g0065a0001c0001t0002g0076others(83): Show | 86 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.5719-501T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522761 | ||||||
| chr3:64522954
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.5719-694G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64522954 | ||||||
| chr3:64523228
|
A | T | 16 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(13): Show | 16 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.5719-968T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523228 | ||||||
| chr3:64523391
|
G | T | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.5719-1131C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523391 | ||||||
| chr3:64523461
|
A | G | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5719-1201T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523461 | ||||||
| chr3:64523516
|
C | T | 16 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(13): Show | 16 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.5719-1256G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523516 | ||||||
| chr3:64523533
|
A | G | 16 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(13): Show | 16 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.5719-1273T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523533 | ||||||
| chr3:64523569
|
C | T | 16 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(13): Show | 16 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.5719-1309G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523569 | ||||||
| chr3:64523591
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.5719-1331G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523591 | ||||||
| chr3:64523868
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5719-1608A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523868 | ||||||
| chr3:64523989
|
A | T | 3 | a0001c0001t0001g0183a0014c0041t0001g0280a0014c0054t0001g0283 | 3 | HG03491.hp1 HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.5719-1729T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523989 | ||||||
| chr3:64523992
|
G | T | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5719-1732C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64523992 | ||||||
| chr3:64524033
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.5719-1773G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64524033 | ||||||
| chr3:64524062
|
G | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.5719-1802C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64524062 | ||||||
| chr3:64524132
|
A | C | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.5719-1872T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64524132 | ||||||
| chr3:64524142
|
G | A | 2 | a0001c0001t0002g0253a0030c0046t0002g0252 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.5719-1882C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64524142 | ||||||
| chr3:64524229
|
T | A | 1 | a0002c0002t0003g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5719-1969A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64524229 | ||||||
| chr3:64524302
|
T | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.5719-2042A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64524302 | ||||||
| chr3:64524671
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.5719-2411G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64524671 | ||||||
| chr3:64524805
|
A | C | 4 | a0001c0001t0003g0262a0002c0002t0003g0190a0002c0002t0003g0196others(1): Show | 4 | HG00597.hp2 NA18960.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.5719-2545T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64524805 | ||||||
| chr3:64525013
|
C | A | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5719-2753G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525013 | ||||||
| chr3:64525036
|
G | A | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.5719-2776C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525036 | ||||||
| chr3:64525138
|
G | A | 4 | a0001c0001t0001g0233a0001c0007t0013g0015a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5719-2878C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525138 | ||||||
| chr3:64525278
|
T | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.5719-3018A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525278 | ||||||
| chr3:64525341
|
A | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.5719-3081T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525341 | ||||||
| chr3:64525421
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(102): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.5719-3161A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525421 | ||||||
| chr3:64525607
|
T | G | 6 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.5719-3347A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525607 | ||||||
| chr3:64525659
|
G | A | 1 | a0005c0008t0002g0176 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5719-3399C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525659 | ||||||
| chr3:64525676
|
T | A | 1 | a0002c0002t0003g0155 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.5719-3416A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525676 | ||||||
| chr3:64525704
|
G | T | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.5719-3444C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525704 | ||||||
| chr3:64525786
|
T | G | 35 | a0002c0002t0003g0074a0002c0002t0003g0077a0002c0002t0003g0078others(32): Show | 35 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.5719-3526A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525786 | ||||||
| chr3:64525797
|
G | C | 1 | a0001c0001t0001g0159 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.5719-3537C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525797 | ||||||
| chr3:64525846
|
A | G | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5719-3586T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525846 | ||||||
| chr3:64525868
|
C | T | 1 | a0003c0003t0002g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5719-3608G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525868 | ||||||
| chr3:64525878
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5719-3618G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525878 | ||||||
| chr3:64525929
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.5719-3669T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525929 | ||||||
| chr3:64525931
|
CAATAT | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(163): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.5719-3676_5719-367 others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525931 | ||||||
| chr3:64525954
|
A | G | 8 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(5): Show | 8 | HG01952.hp1 HG02258.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.5719-3694T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64525954 | ||||||
| chr3:64526044
|
ATCT | A | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.5719-3787_5719-378 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526044 | ||||||
| chr3:64526049
|
A | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(147): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.5719-3789T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526049 | ||||||
| chr3:64526070
|
A | G | 4 | a0003c0003t0002g0058a0003c0003t0009g0043a0003c0003t0009g0044others(1): Show | 4 | NA18942.hp1 NA18975.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.5719-3810T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526070 | ||||||
| chr3:64526081
|
AAAT | A | 63 | a0001c0001t0002g0065a0001c0001t0002g0076a0001c0001t0002g0083others(60): Show | 63 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.5719-3824_5719-382 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526081 | ||||||
| chr3:64526167
|
GAGA | G | 41 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0093others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.5719-3910_5719-390 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526167 | ||||||
| chr3:64526236
|
G | A | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5719-3976C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526236 | ||||||
| chr3:64526254
|
A | C | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5719-3994T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526254 | ||||||
| chr3:64526256
|
T | C | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5719-3996A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526256 | ||||||
| chr3:64526264
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.5719-4004G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526264 | ||||||
| chr3:64526265
|
G | A | 18 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(15): Show | 18 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.5719-4005C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526265 | ||||||
| chr3:64526299
|
C | T | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5719-4039G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526299 | ||||||
| chr3:64526405
|
G | A | 1 | a0012c0018t0006g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5719-4145C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526405 | ||||||
| chr3:64526406
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(112): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.5719-4146A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526406 | ||||||
| chr3:64526412
|
T | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0279others(7): Show | 10 | HG00735.hp1 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.5719-4152A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526412 | ||||||
| chr3:64526429
|
C | A | 1 | a0003c0003t0002g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5719-4169G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526429 | ||||||
| chr3:64526553
|
A | G | 51 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(48): Show | 51 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.5719-4293T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526553 | ||||||
| chr3:64526555
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5719-4295T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526555 | ||||||
| chr3:64526781
|
C | A | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5719-4521G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526781 | ||||||
| chr3:64526782
|
G | A | 1 | a0003c0003t0002g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5719-4522C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526782 | ||||||
| chr3:64526820
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5719-4560T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526820 | ||||||
| chr3:64526887
|
A | T | 15 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(12): Show | 15 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.5719-4627T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64526887 | ||||||
| chr3:64527012
|
G | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(163): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.5719-4752C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527012 | ||||||
| chr3:64527196
|
C | A | 1 | a0001c0001t0001g0181 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5719-4936G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527196 | ||||||
| chr3:64527316
|
A | G | 7 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(4): Show | 7 | HG01952.hp1 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5719-5056T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527316 | ||||||
| chr3:64527319
|
C | G | 8 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(5): Show | 8 | HG01952.hp1 HG02258.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.5719-5059G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527319 | ||||||
| chr3:64527338
|
T | C | 2 | a0007c0011t0004g0086a0010c0012t0004g0050 | 2 | NA18946.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.5719-5078A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527338 | ||||||
| chr3:64527500
|
A | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(102): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.5719-5240T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527500 | ||||||
| chr3:64527551
|
A | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(102): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.5719-5291T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527551 | ||||||
| chr3:64527567
|
T | TA | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.5719-5308_5719-530 others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527567 | ||||||
| chr3:64527585
|
G | C | 4 | a0001c0001t0001g0233a0001c0007t0013g0015a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5719-5325C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527585 | ||||||
| chr3:64527646
|
C | T | 2 | a0001c0001t0002g0083a0001c0001t0002g0282 | 2 | NA18940.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.5719-5386G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527646 | ||||||
| chr3:64527690
|
T | C | 11 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(8): Show | 11 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.5719-5430A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527690 | ||||||
| chr3:64527704
|
T | C | 1 | a0001c0013t0001g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5719-5444A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527704 | ||||||
| chr3:64527848
|
A | C | 35 | a0002c0002t0003g0074a0002c0002t0003g0077a0002c0002t0003g0078others(32): Show | 35 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.5718+5318T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527848 | ||||||
| chr3:64527978
|
C | G | 1 | a0011c0022t0001g0270 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5718+5188G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527978 | ||||||
| chr3:64527996
|
C | T | 50 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(47): Show | 50 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.5718+5170G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64527996 | ||||||
| chr3:64528028
|
A | G | 58 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(55): Show | 58 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.5718+5138T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528028 | ||||||
| chr3:64528155
|
G | A | 136 | a0001c0001t0002g0065a0001c0001t0002g0076a0001c0001t0002g0083others(133): Show | 136 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.5718+5011C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528155 | ||||||
| chr3:64528191
|
C | A | 2 | a0016c0016t0003g0048a0016c0016t0003g0049 | 2 | HG01123.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.5718+4975G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528191 | ||||||
| chr3:64528328
|
A | G | 58 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(55): Show | 58 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.5718+4838T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528328 | ||||||
| chr3:64528332
|
G | A | 58 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(55): Show | 58 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.5718+4834C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528332 | ||||||
| chr3:64528475
|
T | G | 1 | a0001c0001t0001g0181 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5718+4691A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528475 | ||||||
| chr3:64528550
|
C | T | 3 | a0001c0001t0002g0111a0001c0001t0002g0241a0001c0001t0002g0248 | 3 | HG00597.hp1 NA18953.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.5718+4616G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528550 | ||||||
| chr3:64528662
|
A | C | 35 | a0002c0002t0003g0074a0002c0002t0003g0077a0002c0002t0003g0078others(32): Show | 35 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.5718+4504T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528662 | ||||||
| chr3:64528712
|
G | A | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5718+4454C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528712 | ||||||
| chr3:64528717
|
A | G | 58 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(55): Show | 58 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.5718+4449T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528717 | ||||||
| chr3:64528801
|
C | T | 9 | a0001c0001t0002g0172a0001c0001t0002g0224a0001c0001t0014g0012others(6): Show | 9 | HG00741.hp1 HG01257.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.5718+4365G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528801 | ||||||
| chr3:64528811
|
A | G | 4 | a0001c0001t0001g0233a0001c0007t0013g0015a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5718+4355T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528811 | ||||||
| chr3:64528813
|
G | A | 1 | a0003c0003t0002g0031 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5718+4353C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528813 | ||||||
| chr3:64528834
|
C | T | 1 | a0022c0036t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5718+4332G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528834 | ||||||
| chr3:64528953
|
G | C | 3 | a0001c0009t0005g0071a0001c0009t0005g0072a0001c0009t0005g0073 | 3 | HG01934.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5718+4213C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528953 | ||||||
| chr3:64528961
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5718+4205C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64528961 | ||||||
| chr3:64529006
|
G | A | 1 | a0022c0036t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5718+4160C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529006 | ||||||
| chr3:64529031
|
T | C | 15 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(12): Show | 15 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5718+4135A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529031 | ||||||
| chr3:64529032
|
T | G | 35 | a0002c0002t0003g0074a0002c0002t0003g0077a0002c0002t0003g0078others(32): Show | 35 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.5718+4134A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529032 | ||||||
| chr3:64529142
|
G | C | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5718+4024C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529142 | ||||||
| chr3:64529147
|
AATGT | A | 10 | a0001c0001t0002g0116a0001c0001t0002g0247a0003c0003t0002g0058others(7): Show | 10 | HG00438.hp2 HG00558.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.5718+4015_5718+401 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529147 | ||||||
| chr3:64529330
|
C | G | 11 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(8): Show | 11 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.5718+3836G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529330 | ||||||
| chr3:64529351
|
C | T | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5718+3815G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529351 | ||||||
| chr3:64529420
|
A | AT | 9 | a0001c0001t0016g0063a0007c0011t0004g0156a0007c0011t0004g0157others(6): Show | 9 | HG01978.hp1 HG02273.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.5718+3745dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529420 | ||||||
| chr3:64529435
|
T | C | 59 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(56): Show | 59 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.5718+3731A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529435 | ||||||
| chr3:64529467
|
G | A | 1 | a0019c0040t0002g0148 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.5718+3699C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529467 | ||||||
| chr3:64529534
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5718+3632C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529534 | ||||||
| chr3:64529575
|
G | C | 1 | a0002c0002t0008g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5718+3591C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529575 | ||||||
| chr3:64529670
|
C | G | 1 | a0002c0002t0003g0165 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5718+3496G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529670 | ||||||
| chr3:64529687
|
A | C | 1 | a0001c0001t0003g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.5718+3479T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529687 | ||||||
| chr3:64529817
|
G | GGTTTT | 3 | a0001c0001t0002g0178a0002c0002t0001g0227a0002c0002t0001g0229 | 3 | HG01243.hp2 HG03453.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.5718+3344_5718+334 others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529817 | ||||||
| chr3:64529920
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.5718+3246G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529920 | ||||||
| chr3:64529982
|
A | AT | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0067others(85): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.5718+3183dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529982 | ||||||
| chr3:64529982
|
A | ATT | 80 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0168others(77): Show | 80 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.5718+3182_5718+318 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529982 | ||||||
| chr3:64529982
|
A | ATTT | 8 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0137others(5): Show | 8 | HG02257.hp1 HG03098.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.5718+3181_5718+318 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529982 | ||||||
| chr3:64529982
|
AT | A | 43 | a0001c0001t0012g0014a0001c0001t0017g0066a0001c0051t0018g0268others(40): Show | 43 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.5718+3183delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529982 | ||||||
| chr3:64529982
|
ATTTTT | A | 10 | a0001c0001t0002g0065a0001c0001t0002g0118a0001c0001t0002g0253others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.5718+3179_5718+318 others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529982 | ||||||
| chr3:64529982
|
ATTTTTT | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0087a0001c0001t0001g0128others(9): Show | 12 | HG00735.hp1 HG01884.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.5718+3178_5718+318 others(10): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529982 | ||||||
| chr3:64529982
|
ATTTTTTT others(1): Show |
A | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5718+3176_5718+318 others(12): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64529982 | ||||||
| chr3:64530018
|
C | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0279others(7): Show | 10 | HG00735.hp1 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.5718+3148G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530018 | ||||||
| chr3:64530041
|
C | G | 39 | a0002c0002t0003g0074a0002c0002t0003g0077a0002c0002t0003g0078others(36): Show | 39 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.5718+3125G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530041 | ||||||
| chr3:64530042
|
T | C | 3 | a0002c0002t0003g0141a0002c0002t0003g0150a0002c0002t0003g0151 | 3 | HG01071.hp2 HG01099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.5718+3124A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530042 | ||||||
| chr3:64530059
|
A | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0221 | 2 | HG00140.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.5718+3107T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530059 | ||||||
| chr3:64530164
|
G | A | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5718+3002C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530164 | ||||||
| chr3:64530292
|
AT | A | 54 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0087others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.5718+2873delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530292 | ||||||
| chr3:64530368
|
C | G | 15 | a0001c0051t0018g0268a0002c0002t0001g0064a0002c0002t0001g0220others(12): Show | 15 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.5718+2798G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530368 | ||||||
| chr3:64530416
|
G | T | 4 | a0002c0002t0003g0141a0002c0002t0003g0150a0002c0002t0003g0151others(1): Show | 4 | HG01071.hp2 HG01099.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.5718+2750C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530416 | ||||||
| chr3:64530453
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.5718+2713C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530453 | ||||||
| chr3:64530494
|
C | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.5718+2672G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530494 | ||||||
| chr3:64530504
|
A | G | 24 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(21): Show | 24 | HG00738.hp2 HG01243.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.5718+2662T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530504 | ||||||
| chr3:64530526
|
T | TA | 26 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0183others(23): Show | 26 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.5718+2639dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530526 | ||||||
| chr3:64530526
|
TA | T | 59 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0222others(56): Show | 59 | HG00099.hp1 HG00621.hp2 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.5718+2639delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530526 | ||||||
| chr3:64530526
|
TAAA | T | 15 | a0002c0002t0001g0225a0002c0002t0001g0227a0002c0002t0001g0229others(12): Show | 15 | HG00738.hp2 HG01243.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.5718+2637_5718+263 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530526 | ||||||
| chr3:64530526
|
TAAAA | T | 10 | a0001c0051t0018g0268a0002c0002t0001g0064a0002c0002t0001g0220others(7): Show | 10 | HG02486.hp2 HG02559.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.5718+2636_5718+263 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530526 | ||||||
| chr3:64530554
|
G | A | 2 | a0003c0017t0006g0027a0003c0017t0006g0028 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5718+2612C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530554 | ||||||
| chr3:64530755
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5718+2411T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530755 | ||||||
| chr3:64530873
|
C | G | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5718+2293G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530873 | ||||||
| chr3:64530950
|
T | C | 1 | a0001c0001t0002g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.5718+2216A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64530950 | ||||||
| chr3:64531018
|
ACT | A | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5718+2146_5718+214 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531018 | ||||||
| chr3:64531108
|
C | T | 2 | a0001c0006t0010g0003a0001c0006t0010g0007 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5718+2058G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531108 | ||||||
| chr3:64531147
|
G | T | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5718+2019C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531147 | ||||||
| chr3:64531160
|
C | CT | 39 | a0002c0002t0003g0074a0002c0002t0003g0077a0002c0002t0003g0078others(36): Show | 39 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.5718+2005dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531160 | ||||||
| chr3:64531160
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.5718+2006G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531160 | ||||||
| chr3:64531174
|
C | G | 1 | a0011c0022t0001g0270 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5718+1992G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531174 | ||||||
| chr3:64531244
|
G | A | 1 | a0001c0014t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5718+1922C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531244 | ||||||
| chr3:64531320
|
T | C | 1 | a0011c0053t0002g0272 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5718+1846A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531320 | ||||||
| chr3:64531416
|
T | C | 1 | a0011c0053t0002g0272 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5718+1750A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531416 | ||||||
| chr3:64531470
|
T | TA | 23 | a0001c0001t0002g0187a0001c0001t0007g0278a0001c0006t0010g0003others(20): Show | 23 | HG00738.hp2 HG01243.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.5718+1695dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531470 | ||||||
| chr3:64531470
|
T | TAA | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5718+1694_5718+169 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531470 | ||||||
| chr3:64531470
|
TA | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0201others(3): Show | 6 | HG00544.hp2 HG02523.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.5718+1695delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531470 | ||||||
| chr3:64531487
|
A | T | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5718+1679T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531487 | ||||||
| chr3:64531527
|
G | A | 3 | a0001c0001t0002g0111a0001c0001t0002g0241a0001c0001t0002g0248 | 3 | HG00597.hp1 NA18953.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.5718+1639C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531527 | ||||||
| chr3:64531580
|
A | G | 22 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(19): Show | 22 | HG00738.hp2 HG01243.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.5718+1586T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531580 | ||||||
| chr3:64531723
|
G | C | 4 | a0001c0001t0001g0233a0001c0007t0013g0015a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5718+1443C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531723 | ||||||
| chr3:64531763
|
C | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(146): Show | 151 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.5718+1403G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531763 | ||||||
| chr3:64531850
|
C | T | 8 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(5): Show | 8 | HG01952.hp1 HG02258.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.5718+1316G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531850 | ||||||
| chr3:64531862
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5718+1304C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531862 | ||||||
| chr3:64531920
|
C | T | 3 | a0003c0003t0001g0059a0012c0018t0006g0173a0012c0018t0006g0243 | 3 | HG00735.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5718+1246G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64531920 | ||||||
| chr3:64532038
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(275): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.5718+1128A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532038 | ||||||
| chr3:64532124
|
C | T | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0104others(7): Show | 10 | HG02523.hp2 NA18955.hp2 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.5718+1042G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532124 | ||||||
| chr3:64532265
|
A | G | 15 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0279others(12): Show | 15 | HG00735.hp1 HG01884.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.5718+901T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532265 | ||||||
| chr3:64532402
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5718+764G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532402 | ||||||
| chr3:64532445
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(177): Show | 182 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.5718+721G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532445 | ||||||
| chr3:64532607
|
G | A | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5718+559C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532607 | ||||||
| chr3:64532617
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.5718+549G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532617 | ||||||
| chr3:64532634
|
C | A | 1 | a0001c0001t0007g0278 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5718+532G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532634 | ||||||
| chr3:64532718
|
T | G | 10 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.5718+448A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532718 | ||||||
| chr3:64532946
|
G | A | 2 | a0003c0017t0006g0027a0003c0017t0006g0028 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5718+220C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532946 | ||||||
| chr3:64532984
|
T | G | 4 | a0001c0001t0001g0233a0001c0007t0013g0015a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5718+182A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 38/39 | chr3 | 64532984 | ||||||
| chr3:64533318
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(275): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.5614-48A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64533318 | ||||||
| chr3:64533358
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5614-88A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64533358 | ||||||
| chr3:64533480
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.5614-210G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64533480 | ||||||
| chr3:64533854
|
A | G | 3 | a0001c0001t0001g0233a0003c0003t0001g0022a0003c0003t0001g0033 | 3 | HG01070.hp1 HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5614-584T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64533854 | ||||||
| chr3:64533858
|
T | C | 14 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.5614-588A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64533858 | ||||||
| chr3:64534004
|
T | G | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5614-734A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534004 | ||||||
| chr3:64534238
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(178): Show | 183 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.5614-968C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534238 | ||||||
| chr3:64534247
|
C | A | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5614-977G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534247 | ||||||
| chr3:64534268
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.5614-998C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534268 | ||||||
| chr3:64534364
|
C | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5614-1094G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534364 | ||||||
| chr3:64534421
|
A | G | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.5614-1151T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534421 | ||||||
| chr3:64534444
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(178): Show | 183 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.5614-1174C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534444 | ||||||
| chr3:64534776
|
TG | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.5614-1507delC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534776 | ||||||
| chr3:64534813
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.5614-1543G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534813 | ||||||
| chr3:64534813
|
C | T | 54 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(51): Show | 54 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.5614-1543G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534813 | ||||||
| chr3:64534908
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5614-1638A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534908 | ||||||
| chr3:64534915
|
G | T | 14 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.5614-1645C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64534915 | ||||||
| chr3:64535161
|
T | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0279others(7): Show | 10 | HG00735.hp1 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.5614-1891A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535161 | ||||||
| chr3:64535195
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.5614-1925C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535195 | ||||||
| chr3:64535240
|
A | C | 11 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(8): Show | 11 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.5614-1970T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535240 | ||||||
| chr3:64535414
|
G | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0201others(3): Show | 6 | HG00544.hp2 HG02523.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.5614-2144C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535414 | ||||||
| chr3:64535429
|
G | T | 39 | a0002c0002t0003g0074a0002c0002t0003g0077a0002c0002t0003g0078others(36): Show | 39 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.5614-2159C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535429 | ||||||
| chr3:64535483
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5614-2213C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535483 | ||||||
| chr3:64535552
|
CT | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.5614-2283delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535552 | ||||||
| chr3:64535552
|
CTT | C | 17 | a0001c0001t0001g0201a0001c0001t0001g0222a0002c0002t0001g0064others(14): Show | 17 | HG00099.hp1 HG00738.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.5614-2284_5614-228 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535552 | ||||||
| chr3:64535552
|
CTTTTTT | C | 38 | a0002c0002t0003g0077a0002c0002t0003g0078a0002c0002t0003g0107others(35): Show | 38 | HG01071.hp2 HG01099.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.5614-2288_5614-228 others(10): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535552 | ||||||
| chr3:64535553
|
T | TTTTC | 9 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0279others(6): Show | 9 | HG01884.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.5614-2284_5614-228 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535553 | ||||||
| chr3:64535554
|
T | TTTCTTTT others(6): Show |
1 | a0003c0003t0001g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5614-2285_5614-228 others(17): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535554 | ||||||
| chr3:64535558
|
T | C | 12 | a0001c0013t0001g0212a0007c0011t0004g0086a0007c0011t0004g0156others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5614-2288A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535558 | ||||||
| chr3:64535640
|
G | C | 16 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(13): Show | 16 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.5614-2370C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535640 | ||||||
| chr3:64535711
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5614-2441C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535711 | ||||||
| chr3:64535732
|
G | A | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5614-2462C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535732 | ||||||
| chr3:64535829
|
C | T | 39 | a0002c0002t0003g0074a0002c0002t0003g0077a0002c0002t0003g0078others(36): Show | 39 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.5614-2559G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535829 | ||||||
| chr3:64535995
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.5614-2725G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64535995 | ||||||
| chr3:64536045
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(116): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.5614-2775T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64536045 | ||||||
| chr3:64536397
|
G | C | 55 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(52): Show | 55 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.5613+2806C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64536397 | ||||||
| chr3:64536694
|
G | C | 42 | a0001c0001t0001g0233a0002c0002t0003g0074a0002c0002t0003g0077others(39): Show | 42 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.5613+2509C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64536694 | ||||||
| chr3:64536699
|
C | A | 1 | a0019c0040t0002g0148 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.5613+2504G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64536699 | ||||||
| chr3:64536725
|
G | A | 3 | a0003c0003t0009g0043a0003c0003t0009g0044a0003c0003t0009g0045 | 3 | NA18942.hp1 NA18975.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.5613+2478C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64536725 | ||||||
| chr3:64536760
|
C | T | 4 | a0001c0004t0001g0276a0001c0045t0001g0068a0011c0022t0001g0270others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5613+2443G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64536760 | ||||||
| chr3:64536832
|
T | C | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.5613+2371A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64536832 | ||||||
| chr3:64537022
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.5613+2181G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537022 | ||||||
| chr3:64537181
|
G | C | 3 | a0003c0003t0009g0043a0003c0003t0009g0044a0003c0003t0009g0045 | 3 | NA18942.hp1 NA18975.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.5613+2022C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537181 | ||||||
| chr3:64537377
|
A | T | 1 | a0022c0036t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5613+1826T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537377 | ||||||
| chr3:64537499
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5613+1704A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537499 | ||||||
| chr3:64537573
|
TG | T | 14 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.5613+1629delC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537573 | ||||||
| chr3:64537579
|
C | T | 2 | a0001c0006t0010g0003a0001c0006t0010g0007 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5613+1624G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537579 | ||||||
| chr3:64537584
|
A | C | 3 | a0001c0001t0002g0118a0001c0001t0002g0253a0030c0046t0002g0252 | 3 | HG00733.hp1 HG01106.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.5613+1619T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537584 | ||||||
| chr3:64537612
|
G | C | 3 | a0001c0001t0002g0118a0001c0001t0002g0253a0030c0046t0002g0252 | 3 | HG00733.hp1 HG01106.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.5613+1591C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537612 | ||||||
| chr3:64537627
|
C | G | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5613+1576G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537627 | ||||||
| chr3:64537648
|
A | AAC | 3 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG03139.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5613+1554_5613+155 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537648 | ||||||
| chr3:64537665
|
CAG | C | 5 | a0001c0001t0002g0172a0001c0001t0002g0224a0001c0001t0014g0012others(2): Show | 5 | HG00741.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.5613+1536_5613+153 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537665 | ||||||
| chr3:64537667
|
G | C | 43 | a0001c0001t0001g0233a0002c0002t0001g0121a0002c0002t0003g0074others(40): Show | 43 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.5613+1536C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537667 | ||||||
| chr3:64537675
|
G | A | 1 | a0002c0002t0003g0196 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5613+1528C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537675 | ||||||
| chr3:64537707
|
A | C | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5613+1496T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537707 | ||||||
| chr3:64537733
|
T | C | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5613+1470A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537733 | ||||||
| chr3:64537832
|
A | G | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5613+1371T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537832 | ||||||
| chr3:64537923
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0263 | 2 | NA18982.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.5613+1280C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64537923 | ||||||
| chr3:64538064
|
G | A | 8 | a0001c0001t0001g0183a0001c0001t0016g0063a0001c0037t0008g0006others(5): Show | 8 | HG00735.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.5613+1139C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538064 | ||||||
| chr3:64538183
|
C | T | 1 | a0001c0013t0001g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5613+1020G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538183 | ||||||
| chr3:64538190
|
C | T | 2 | a0003c0017t0006g0027a0003c0017t0006g0028 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5613+1013G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538190 | ||||||
| chr3:64538254
|
A | G | 1 | a0004c0005t0003g0040 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5613+949T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538254 | ||||||
| chr3:64538478
|
TA | T | 12 | a0001c0001t0001g0191a0001c0014t0001g0115a0007c0011t0004g0086others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5613+724delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538478 | ||||||
| chr3:64538507
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0210 | 2 | NA18747.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.5613+696G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538507 | ||||||
| chr3:64538543
|
C | G | 27 | a0001c0001t0002g0065a0001c0001t0002g0100a0001c0001t0002g0118others(24): Show | 27 | HG00438.hp1 HG00609.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.5613+660G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538543 | ||||||
| chr3:64538725
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.5613+478A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538725 | ||||||
| chr3:64538777
|
A | T | 11 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(8): Show | 11 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.5613+426T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538777 | ||||||
| chr3:64538884
|
C | T | 40 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(37): Show | 40 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.5613+319G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64538884 | ||||||
| chr3:64539038
|
C | T | 1 | a0001c0014t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5613+165G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 37/39 | chr3 | 64539038 | ||||||
| chr3:64539299
|
G | A | 1 | a0002c0002t0003g0149 | 1 | HG02273.hp1 | splice_region_variant&intron_variant | LOW | c.5522-5C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539299 | ||||||
| chr3:64539495
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(167): Show | 172 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.5522-201C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539495 | ||||||
| chr3:64539501
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(114): Show | 119 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.5522-207G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539501 | ||||||
| chr3:64539508
|
C | T | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5522-214G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539508 | ||||||
| chr3:64539744
|
C | T | 54 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(51): Show | 54 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.5522-450G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539744 | ||||||
| chr3:64539750
|
T | C | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5522-456A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539750 | ||||||
| chr3:64539789
|
C | T | 1 | a0001c0014t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5522-495G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539789 | ||||||
| chr3:64539790
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0246 | 2 | NA18999.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.5522-496C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539790 | ||||||
| chr3:64539875
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.5522-581T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539875 | ||||||
| chr3:64539954
|
G | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0256a0001c0051t0018g0268 | 3 | HG03098.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5522-660C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64539954 | ||||||
| chr3:64540000
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5522-706A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540000 | ||||||
| chr3:64540016
|
G | A | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5522-722C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540016 | ||||||
| chr3:64540037
|
T | A | 57 | a0001c0001t0001g0233a0002c0002t0001g0121a0002c0002t0003g0074others(54): Show | 57 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.5522-743A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540037 | ||||||
| chr3:64540063
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5522-769G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540063 | ||||||
| chr3:64540363
|
T | C | 5 | a0001c0001t0002g0065a0001c0004t0002g0277a0001c0006t0011g0008others(2): Show | 5 | HG02109.hp1 HG02572.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.5521+732A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540363 | ||||||
| chr3:64540483
|
T | C | 8 | a0007c0011t0004g0156a0007c0011t0004g0157a0007c0011t0004g0179others(5): Show | 8 | HG01978.hp1 HG02273.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.5521+612A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540483 | ||||||
| chr3:64540539
|
T | C | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5521+556A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540539 | ||||||
| chr3:64540671
|
C | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0201others(3): Show | 6 | HG00544.hp2 HG02523.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.5521+424G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540671 | ||||||
| chr3:64540722
|
T | C | 1 | a0028c0043t0003g0194 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5521+373A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540722 | ||||||
| chr3:64540798
|
C | CTTCA | 5 | a0001c0001t0002g0065a0001c0004t0001g0236a0001c0004t0001g0238others(2): Show | 5 | HG02622.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.5521+293_5521+296d others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540798 | ||||||
| chr3:64540798
|
C | CTTCATTC others(1): Show |
21 | a0001c0001t0001g0018a0001c0001t0001g0085a0001c0001t0001g0092others(18): Show | 21 | HG00544.hp2 HG01884.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.5521+289_5521+296d others(10): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540798 | ||||||
| chr3:64540798
|
C | CTTCATTC others(5): Show |
1 | a0003c0003t0001g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5521+285_5521+296d others(14): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540798 | ||||||
| chr3:64540840
|
C | T | 1 | a0001c0007t0002g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5521+255G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540840 | ||||||
| chr3:64540862
|
C | T | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5521+233G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540862 | ||||||
| chr3:64540891
|
A | G | 149 | a0001c0001t0001g0233a0001c0001t0002g0065a0001c0001t0002g0076others(146): Show | 149 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.5521+204T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540891 | ||||||
| chr3:64540934
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.5521+161C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540934 | ||||||
| chr3:64540936
|
T | C | 45 | a0001c0001t0001g0233a0002c0002t0001g0121a0002c0002t0003g0074others(42): Show | 45 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.5521+159A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540936 | ||||||
| chr3:64540975
|
CCAATGTG | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.5521+113_5521+119d others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540975 | ||||||
| chr3:64540993
|
T | C | 1 | a0010c0012t0004g0050 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.5521+102A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64540993 | ||||||
| chr3:64541041
|
G | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.5521+54C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64541041 | ||||||
| chr3:64541060
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0002g0281a0017c0050t0001g0130 | 3 | HG00544.hp1 HG03942.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.5521+35G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 36/39 | chr3 | 64541060 | ||||||
| chr3:64541266
|
A | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.5388-38T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 35/39 | chr3 | 64541266 | ||||||
| chr3:64541267
|
G | A | 48 | a0001c0001t0001g0233a0001c0001t0002g0228a0001c0001t0002g0255others(45): Show | 48 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.5388-39C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 35/39 | chr3 | 64541267 | ||||||
| chr3:64541425
|
A | G | 1 | a0001c0001t0002g0100 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.5293-11T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 34/39 | chr3 | 64541425 | ||||||
| chr3:64541452
|
A | C | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5293-38T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 34/39 | chr3 | 64541452 | ||||||
| chr3:64541511
|
G | A | 1 | a0002c0002t0003g0195 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5292+15C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 34/39 | chr3 | 64541511 | ||||||
| chr3:64541645
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.5198-25A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 33/39 | chr3 | 64541645 | ||||||
| chr3:64541660
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.5198-40G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 33/39 | chr3 | 64541660 | ||||||
| chr3:64541702
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.5198-82C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 33/39 | chr3 | 64541702 | ||||||
| chr3:64541748
|
T | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0217a0001c0007t0002g0062others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.5197+90A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 33/39 | chr3 | 64541748 | ||||||
| chr3:64541789
|
C | A | 87 | a0001c0001t0002g0065a0001c0001t0002g0076a0001c0001t0002g0083others(84): Show | 87 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.5197+49G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 33/39 | chr3 | 64541789 | ||||||
| chr3:64541789
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.5197+49G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 33/39 | chr3 | 64541789 | ||||||
| chr3:64541825
|
T | C | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5197+13A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 33/39 | chr3 | 64541825 | ||||||
| chr3:64542128
|
C | T | 6 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066others(3): Show | 6 | HG02257.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.5065-158G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542128 | ||||||
| chr3:64542159
|
G | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(114): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.5065-189C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542159 | ||||||
| chr3:64542220
|
T | TAC | 53 | a0001c0001t0001g0067a0001c0001t0001g0233a0002c0002t0001g0064others(50): Show | 53 | HG00621.hp2 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.5065-252_5065-251d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542220 | ||||||
| chr3:64542220
|
T | TACAC | 5 | a0002c0002t0001g0227a0002c0002t0001g0229a0002c0002t0001g0266others(2): Show | 5 | HG01243.hp2 HG02559.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5065-254_5065-251d others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542220 | ||||||
| chr3:64542231
|
A | T | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5065-261T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542231 | ||||||
| chr3:64542241
|
A | ACACG | 6 | a0001c0001t0001g0113a0001c0009t0005g0069a0001c0009t0005g0070others(3): Show | 6 | HG01934.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5065-272_5065-271i others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542241 | ||||||
| chr3:64542241
|
A | ACG | 62 | a0001c0001t0001g0019a0001c0001t0001g0079a0001c0001t0001g0080others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.5065-272_5065-271i others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542241 | ||||||
| chr3:64542241
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(46): Show | 51 | HG00099.hp2 HG00544.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.5065-271T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542241 | ||||||
| chr3:64542269
|
C | T | 44 | a0001c0001t0001g0067a0001c0001t0001g0233a0002c0002t0001g0121others(41): Show | 44 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.5065-299G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542269 | ||||||
| chr3:64542363
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5065-393C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542363 | ||||||
| chr3:64542387
|
G | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.5065-417C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542387 | ||||||
| chr3:64542407
|
G | A | 9 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(6): Show | 9 | HG02257.hp2 HG03098.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.5065-437C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542407 | ||||||
| chr3:64542430
|
C | CTTTCTT | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.5065-461_5065-460i others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542430 | ||||||
| chr3:64542430
|
C | CTTTTT | 100 | a0001c0001t0002g0065a0001c0001t0002g0076a0001c0001t0002g0083others(97): Show | 100 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.5065-465_5065-461d others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542430 | ||||||
| chr3:64542430
|
C | CTTTTTTT others(1): Show |
38 | a0001c0001t0001g0067a0002c0002t0001g0121a0002c0002t0003g0074others(35): Show | 38 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.5065-468_5065-461d others(10): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542430 | ||||||
| chr3:64542476
|
G | A | 2 | a0005c0008t0002g0188a0010c0012t0004g0039 | 2 | NA18974.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.5065-506C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542476 | ||||||
| chr3:64542490
|
C | A | 1 | a0001c0001t0019g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5065-520G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542490 | ||||||
| chr3:64542495
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(116): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.5065-525T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542495 | ||||||
| chr3:64542521
|
A | G | 10 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(7): Show | 10 | HG02257.hp2 HG02258.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.5065-551T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542521 | ||||||
| chr3:64542558
|
T | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5065-588A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542558 | ||||||
| chr3:64542594
|
A | T | 40 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(37): Show | 40 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.5065-624T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542594 | ||||||
| chr3:64542706
|
C | A | 108 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0065others(105): Show | 108 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.5065-736G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542706 | ||||||
| chr3:64542742
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5065-772T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542742 | ||||||
| chr3:64542836
|
T | C | 82 | a0001c0001t0002g0065a0001c0001t0002g0076a0001c0001t0002g0083others(79): Show | 82 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.5065-866A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542836 | ||||||
| chr3:64542864
|
A | C | 1 | a0001c0013t0001g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5065-894T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542864 | ||||||
| chr3:64542890
|
G | C | 2 | a0001c0001t0002g0241a0001c0001t0002g0248 | 2 | NA18953.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.5065-920C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542890 | ||||||
| chr3:64542904
|
A | G | 1 | a0014c0041t0001g0280 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5065-934T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542904 | ||||||
| chr3:64542914
|
T | TA | 96 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0065others(93): Show | 96 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.5065-945dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542914 | ||||||
| chr3:64542929
|
G | A | 1 | a0030c0046t0002g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.5065-959C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542929 | ||||||
| chr3:64542943
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5065-973T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64542943 | ||||||
| chr3:64543207
|
TA | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.5065-1238delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543207 | ||||||
| chr3:64543220
|
C | G | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5065-1250G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543220 | ||||||
| chr3:64543233
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.5065-1263A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543233 | ||||||
| chr3:64543306
|
C | T | 2 | a0001c0001t0002g0241a0001c0001t0002g0248 | 2 | NA18953.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.5065-1336G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543306 | ||||||
| chr3:64543351
|
C | T | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.5065-1381G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543351 | ||||||
| chr3:64543465
|
A | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.5065-1495T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543465 | ||||||
| chr3:64543494
|
C | T | 1 | a0001c0009t0005g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5065-1524G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543494 | ||||||
| chr3:64543596
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5065-1626A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543596 | ||||||
| chr3:64543723
|
C | T | 1 | a0003c0003t0001g0041 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.5065-1753G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543723 | ||||||
| chr3:64543725
|
T | C | 3 | a0001c0009t0005g0071a0001c0009t0005g0072a0001c0009t0005g0073 | 3 | HG01934.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5065-1755A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543725 | ||||||
| chr3:64543906
|
C | G | 3 | a0002c0002t0003g0190a0002c0002t0003g0196a0004c0005t0015g0010 | 3 | NA18960.hp1 NA18972.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.5065-1936G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543906 | ||||||
| chr3:64543925
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(98): Show | 103 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.5065-1955C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543925 | ||||||
| chr3:64543968
|
C | T | 9 | a0002c0002t0003g0123a0002c0002t0003g0144a0002c0002t0003g0149others(6): Show | 9 | HG01099.hp1 HG01123.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.5065-1998G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64543968 | ||||||
| chr3:64544115
|
G | C | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5065-2145C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544115 | ||||||
| chr3:64544164
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.5065-2194T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544164 | ||||||
| chr3:64544165
|
A | G | 4 | a0001c0001t0001g0067a0001c0001t0001g0233a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5065-2195T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544165 | ||||||
| chr3:64544170
|
A | G | 4 | a0001c0001t0001g0067a0001c0001t0001g0233a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5065-2200T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544170 | ||||||
| chr3:64544171
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.5065-2201A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544171 | ||||||
| chr3:64544175
|
C | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0233a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5065-2205G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544175 | ||||||
| chr3:64544202
|
A | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.5065-2232T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544202 | ||||||
| chr3:64544321
|
G | A | 3 | a0001c0051t0018g0268a0003c0017t0006g0027a0003c0017t0006g0028 | 3 | HG03098.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5065-2351C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544321 | ||||||
| chr3:64544396
|
C | G | 3 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG03139.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5064+2362G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544396 | ||||||
| chr3:64544443
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.5064+2315A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544443 | ||||||
| chr3:64544637
|
G | A | 85 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0065others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.5064+2121C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544637 | ||||||
| chr3:64544686
|
T | C | 87 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0065others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.5064+2072A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544686 | ||||||
| chr3:64544785
|
G | A | 1 | a0001c0007t0002g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5064+1973C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544785 | ||||||
| chr3:64544949
|
T | C | 3 | a0001c0001t0002g0108a0001c0001t0002g0221a0001c0006t0001g0117 | 3 | HG00099.hp2 HG00140.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.5064+1809A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544949 | ||||||
| chr3:64544955
|
T | C | 4 | a0001c0001t0001g0067a0001c0001t0001g0233a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5064+1803A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64544955 | ||||||
| chr3:64545010
|
A | AATGC | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5064+1747_5064+174 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545010 | ||||||
| chr3:64545012
|
G | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5064+1746C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545012 | ||||||
| chr3:64545012
|
G | GCTC | 40 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(37): Show | 40 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.5064+1743_5064+174 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545012 | ||||||
| chr3:64545058
|
A | T | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.5064+1700T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545058 | ||||||
| chr3:64545078
|
G | C | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5064+1680C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545078 | ||||||
| chr3:64545138
|
G | C | 40 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(37): Show | 40 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.5064+1620C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545138 | ||||||
| chr3:64545141
|
C | T | 1 | a0002c0002t0003g0122 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.5064+1617G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545141 | ||||||
| chr3:64545143
|
C | G | 40 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(37): Show | 40 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.5064+1615G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545143 | ||||||
| chr3:64545201
|
T | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5064+1557A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545201 | ||||||
| chr3:64545215
|
CT | C | 4 | a0003c0003t0001g0035a0006c0010t0001g0245a0006c0010t0001g0264others(1): Show | 4 | NA18955.hp2 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.5064+1542delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545215 | ||||||
| chr3:64545221
|
C | T | 1 | a0001c0001t0019g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5064+1537G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545221 | ||||||
| chr3:64545367
|
A | G | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5064+1391T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545367 | ||||||
| chr3:64545454
|
T | C | 1 | a0001c0007t0002g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5064+1304A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545454 | ||||||
| chr3:64545491
|
A | T | 1 | a0008c0049t0001g0136 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.5064+1267T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545491 | ||||||
| chr3:64545577
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5064+1181C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545577 | ||||||
| chr3:64545894
|
C | T | 6 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(3): Show | 6 | HG01952.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.5064+864G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545894 | ||||||
| chr3:64545902
|
C | A | 40 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(37): Show | 40 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.5064+856G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64545902 | ||||||
| chr3:64546152
|
A | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(116): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.5064+606T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546152 | ||||||
| chr3:64546188
|
G | C | 1 | a0001c0001t0002g0244 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.5064+570C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546188 | ||||||
| chr3:64546352
|
C | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5064+406G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546352 | ||||||
| chr3:64546352
|
C | T | 69 | a0001c0001t0002g0065a0001c0001t0002g0076a0001c0001t0002g0083others(66): Show | 69 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.5064+406G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546352 | ||||||
| chr3:64546411
|
A | C | 1 | a0001c0001t0001g0002 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.5064+347T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546411 | ||||||
| chr3:64546453
|
G | C | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.5064+305C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546453 | ||||||
| chr3:64546490
|
C | T | 40 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(37): Show | 40 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.5064+268G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546490 | ||||||
| chr3:64546578
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5064+180T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546578 | ||||||
| chr3:64546598
|
A | G | 40 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(37): Show | 40 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.5064+160T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546598 | ||||||
| chr3:64546646
|
A | G | 4 | a0001c0001t0001g0067a0001c0001t0001g0233a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5064+112T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 32/39 | chr3 | 64546646 | ||||||
| chr3:64547030
|
C | G | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4870-78G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547030 | ||||||
| chr3:64547044
|
G | T | 1 | a0005c0008t0002g0175 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4870-92C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547044 | ||||||
| chr3:64547097
|
T | G | 20 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0095others(17): Show | 20 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.4870-145A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547097 | ||||||
| chr3:64547226
|
G | A | 10 | a0001c0001t0002g0172a0001c0001t0002g0211a0001c0001t0002g0224others(7): Show | 10 | HG00741.hp1 HG01257.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4870-274C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547226 | ||||||
| chr3:64547353
|
ACAG | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.4870-404_4870-402d others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547353 | ||||||
| chr3:64547377
|
G | A | 3 | a0001c0001t0001g0233a0003c0003t0001g0022a0003c0003t0001g0033 | 3 | HG01070.hp1 HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4870-425C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547377 | ||||||
| chr3:64547509
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4870-557A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547509 | ||||||
| chr3:64547512
|
A | ATT | 54 | a0001c0001t0001g0067a0001c0001t0001g0090a0001c0001t0001g0114others(51): Show | 54 | HG00140.hp2 HG00609.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.4870-562_4870-561d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547512 | ||||||
| chr3:64547512
|
A | ATTT | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.4870-563_4870-561d others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547512 | ||||||
| chr3:64547512
|
A | ATTTT | 12 | a0001c0001t0001g0101a0001c0001t0001g0209a0001c0001t0001g0222others(9): Show | 12 | HG00099.hp1 HG00733.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.4870-564_4870-561d others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547512 | ||||||
| chr3:64547512
|
A | ATTTTTTT others(2449): Show |
1 | a0001c0001t0002g0147 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4870-561_4870-560i others(2458): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547512 | ||||||
| chr3:64547512
|
A | ATTTTTTT others(2450): Show |
10 | a0001c0001t0002g0100a0001c0001t0002g0162a0001c0001t0002g0170others(7): Show | 10 | HG00438.hp1 HG02071.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.4870-561_4870-560i others(2459): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547512 | ||||||
| chr3:64547512
|
A | ATTTTTTT others(2451): Show |
4 | a0001c0004t0002g0277a0001c0006t0011g0008a0001c0007t0002g0219others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4870-561_4870-560i others(2460): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547512 | ||||||
| chr3:64547512
|
AT | A | 65 | a0002c0002t0001g0064a0002c0002t0001g0121a0002c0002t0001g0220others(62): Show | 65 | HG00621.hp2 HG00738.hp2 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.4870-561delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547512 | ||||||
| chr3:64547538
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.4870-586A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547538 | ||||||
| chr3:64547669
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(111): Show | 116 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.4870-717G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547669 | ||||||
| chr3:64547814
|
T | G | 1 | a0001c0001t0002g0099 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4870-862A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547814 | ||||||
| chr3:64547820
|
T | C | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.4870-868A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547820 | ||||||
| chr3:64547857
|
G | GT | 26 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(23): Show | 26 | HG00738.hp2 HG01243.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.4870-906dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547857 | ||||||
| chr3:64547857
|
GT | G | 9 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066others(6): Show | 9 | HG01934.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4870-906delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547857 | ||||||
| chr3:64547882
|
T | C | 10 | a0001c0001t0002g0172a0001c0001t0002g0211a0001c0001t0002g0224others(7): Show | 10 | HG00741.hp1 HG01257.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4870-930A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547882 | ||||||
| chr3:64547895
|
A | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4870-943T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64547895 | ||||||
| chr3:64548014
|
G | A | 1 | a0003c0003t0002g0057 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4870-1062C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548014 | ||||||
| chr3:64548184
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4870-1232G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548184 | ||||||
| chr3:64548263
|
C | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4870-1311G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548263 | ||||||
| chr3:64548308
|
T | C | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4870-1356A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548308 | ||||||
| chr3:64548418
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4870-1466A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548418 | ||||||
| chr3:64548491
|
A | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(186): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.4870-1539T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548491 | ||||||
| chr3:64548578
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4870-1626C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548578 | ||||||
| chr3:64548596
|
T | TG | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.4870-1645dupC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548596 | ||||||
| chr3:64548603
|
GA | G | 17 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(14): Show | 17 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.4870-1652delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548603 | ||||||
| chr3:64548604
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.4870-1652T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548604 | ||||||
| chr3:64548710
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.4870-1758G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548710 | ||||||
| chr3:64548742
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.4870-1790A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548742 | ||||||
| chr3:64548742
|
T | TGTTGACT others(2449): Show |
1 | a0001c0004t0002g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4870-1791_4870-179 others(2460): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548742 | ||||||
| chr3:64548838
|
C | T | 17 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(14): Show | 17 | HG01934.hp1 HG01978.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.4870-1886G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548838 | ||||||
| chr3:64548872
|
G | A | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4870-1920C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64548872 | ||||||
| chr3:64549108
|
C | T | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.4869+1784G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64549108 | ||||||
| chr3:64549652
|
A | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0233a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4869+1240T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64549652 | ||||||
| chr3:64549674
|
T | C | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4869+1218A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64549674 | ||||||
| chr3:64549692
|
G | A | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4869+1200C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64549692 | ||||||
| chr3:64549808
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0139 | 2 | NA18972.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.4869+1084G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64549808 | ||||||
| chr3:64549839
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0189a0001c0001t0001g0191others(1): Show | 4 | HG02056.hp2 NA18950.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.4869+1053C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64549839 | ||||||
| chr3:64549930
|
A | G | 1 | a0011c0022t0001g0270 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4869+962T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64549930 | ||||||
| chr3:64550011
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.4869+881T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550011 | ||||||
| chr3:64550121
|
C | T | 61 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0228others(58): Show | 61 | HG00621.hp2 HG00738.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.4869+771G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550121 | ||||||
| chr3:64550127
|
T | G | 14 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4869+765A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550127 | ||||||
| chr3:64550195
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.4869+697G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550195 | ||||||
| chr3:64550292
|
C | G | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4869+600G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550292 | ||||||
| chr3:64550434
|
G | A | 10 | a0007c0011t0004g0156a0007c0011t0004g0157a0007c0011t0004g0179others(7): Show | 10 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.4869+458C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550434 | ||||||
| chr3:64550551
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.4869+341C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550551 | ||||||
| chr3:64550661
|
A | T | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.4869+231T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550661 | ||||||
| chr3:64550785
|
G | A | 2 | a0002c0002t0003g0077a0002c0002t0003g0078 | 2 | HG02083.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.4869+107C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550785 | ||||||
| chr3:64550810
|
C | T | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4869+82G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 31/39 | chr3 | 64550810 | ||||||
| chr3:64551066
|
T | A | 1 | a0001c0001t0002g0131 | 1 | HG03041.hp2 | splice_region_variant&intron_variant | LOW | c.4699-4A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551066 | ||||||
| chr3:64551096
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4699-34C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551096 | ||||||
| chr3:64551142
|
C | T | 5 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(2): Show | 5 | HG03139.hp1 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.4699-80G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551142 | ||||||
| chr3:64551251
|
C | T | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4699-189G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551251 | ||||||
| chr3:64551426
|
A | G | 1 | a0002c0002t0003g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4699-364T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551426 | ||||||
| chr3:64551489
|
G | A | 14 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4699-427C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551489 | ||||||
| chr3:64551669
|
A | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4699-607T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551669 | ||||||
| chr3:64551680
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4699-618A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551680 | ||||||
| chr3:64551725
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4699-663C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551725 | ||||||
| chr3:64551746
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(187): Show | 192 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.4699-684T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551746 | ||||||
| chr3:64551788
|
T | C | 3 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG03139.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4699-726A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551788 | ||||||
| chr3:64551804
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(187): Show | 192 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.4699-742G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551804 | ||||||
| chr3:64551824
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.4699-762T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551824 | ||||||
| chr3:64551933
|
C | T | 1 | a0010c0012t0004g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4699-871G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64551933 | ||||||
| chr3:64552249
|
A | C | 1 | a0001c0001t0014g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4699-1187T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552249 | ||||||
| chr3:64552326
|
A | G | 1 | a0002c0002t0003g0150 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4699-1264T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552326 | ||||||
| chr3:64552340
|
T | C | 3 | a0007c0011t0004g0156a0007c0011t0004g0157a0013c0019t0004g0161 | 3 | NA19058.hp2 NA19062.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.4699-1278A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552340 | ||||||
| chr3:64552380
|
T | C | 16 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0106others(13): Show | 16 | HG00597.hp2 HG02015.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.4699-1318A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552380 | ||||||
| chr3:64552473
|
T | C | 3 | a0002c0002t0003g0077a0002c0002t0003g0078a0002c0002t0003g0142 | 3 | HG02083.hp2 NA19004.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.4699-1411A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552473 | ||||||
| chr3:64552484
|
G | C | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4699-1422C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552484 | ||||||
| chr3:64552512
|
C | T | 14 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4699-1450G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552512 | ||||||
| chr3:64552559
|
T | C | 14 | a0002c0002t0001g0064a0002c0002t0001g0220a0002c0002t0001g0225others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4699-1497A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552559 | ||||||
| chr3:64552575
|
C | CT | 6 | a0001c0001t0001g0080a0001c0001t0001g0233a0002c0002t0003g0196others(3): Show | 6 | HG01070.hp1 HG02717.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.4699-1514dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552575 | ||||||
| chr3:64552575
|
C | CTT | 49 | a0002c0002t0001g0121a0002c0002t0003g0074a0002c0002t0003g0077others(46): Show | 49 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.4699-1515_4699-151 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552575 | ||||||
| chr3:64552585
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4699-1523A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552585 | ||||||
| chr3:64552714
|
C | T | 58 | a0001c0001t0001g0233a0002c0002t0001g0064a0002c0002t0001g0121others(55): Show | 58 | HG00621.hp2 HG00738.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.4699-1652G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552714 | ||||||
| chr3:64552780
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4699-1718G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64552780 | ||||||
| chr3:64553007
|
G | A | 2 | a0001c0001t0001g0112a0003c0003t0001g0054 | 2 | NA18956.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4699-1945C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553007 | ||||||
| chr3:64553022
|
C | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.4699-1960G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553022 | ||||||
| chr3:64553095
|
G | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.4699-2033C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553095 | ||||||
| chr3:64553113
|
G | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.4699-2051C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553113 | ||||||
| chr3:64553190
|
C | T | 2 | a0012c0018t0006g0173a0012c0018t0006g0243 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4699-2128G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553190 | ||||||
| chr3:64553196
|
C | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(127): Show | 132 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.4699-2134G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553196 | ||||||
| chr3:64553418
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(185): Show | 190 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.4699-2356G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553418 | ||||||
| chr3:64553729
|
T | C | 13 | a0001c0001t0002g0100a0001c0001t0002g0137a0001c0001t0002g0147others(10): Show | 13 | HG00438.hp1 HG02027.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.4699-2667A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553729 | ||||||
| chr3:64553812
|
A | G | 4 | a0001c0001t0001g0183a0001c0001t0016g0063a0014c0041t0001g0280others(1): Show | 4 | HG02886.hp1 HG03491.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.4699-2750T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553812 | ||||||
| chr3:64553889
|
A | G | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.4699-2827T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553889 | ||||||
| chr3:64553913
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0263 | 2 | NA18982.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.4699-2851A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553913 | ||||||
| chr3:64553938
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(186): Show | 191 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.4699-2876G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553938 | ||||||
| chr3:64553987
|
A | G | 5 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(2): Show | 5 | HG03139.hp1 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.4699-2925T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64553987 | ||||||
| chr3:64554043
|
T | C | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4699-2981A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554043 | ||||||
| chr3:64554059
|
A | G | 5 | a0005c0008t0001g0094a0005c0008t0002g0175a0005c0008t0002g0176others(2): Show | 5 | NA18953.hp1 NA18984.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.4699-2997T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554059 | ||||||
| chr3:64554099
|
C | T | 79 | a0001c0001t0002g0065a0001c0001t0002g0076a0001c0001t0002g0083others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.4699-3037G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554099 | ||||||
| chr3:64554196
|
T | C | 12 | a0007c0011t0004g0086a0007c0011t0004g0156a0007c0011t0004g0157others(9): Show | 12 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.4699-3134A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554196 | ||||||
| chr3:64554208
|
G | A | 1 | a0006c0010t0002g0169 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4699-3146C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554208 | ||||||
| chr3:64554216
|
C | G | 24 | a0001c0001t0002g0065a0001c0001t0002g0100a0001c0001t0002g0118others(21): Show | 24 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.4699-3154G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554216 | ||||||
| chr3:64554371
|
G | A | 1 | a0002c0002t0003g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4699-3309C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554371 | ||||||
| chr3:64554460
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(186): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.4699-3398C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554460 | ||||||
| chr3:64554695
|
A | G | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4699-3633T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554695 | ||||||
| chr3:64554746
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4699-3684G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554746 | ||||||
| chr3:64554747
|
G | A | 1 | a0003c0025t0001g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4699-3685C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554747 | ||||||
| chr3:64554777
|
T | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.4699-3715A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554777 | ||||||
| chr3:64554839
|
A | G | 3 | a0001c0001t0001g0233a0003c0003t0001g0022a0003c0003t0001g0033 | 3 | HG01070.hp1 HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4699-3777T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554839 | ||||||
| chr3:64554839
|
AAAGTAAA others(5): Show |
A | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01978.hp1 HG02040.hp2 HG02273.hp2 others(11): Show |
intron_variant | MODIFIER | c.4699-3789_4699-377 others(16): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554839 | ||||||
| chr3:64554876
|
T | G | 10 | a0001c0001t0002g0172a0001c0001t0002g0211a0001c0001t0002g0224others(7): Show | 10 | HG00741.hp1 HG01257.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4699-3814A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554876 | ||||||
| chr3:64554891
|
G | A | 2 | a0001c0001t0002g0217a0003c0003t0002g0031 | 2 | HG00735.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.4699-3829C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554891 | ||||||
| chr3:64554976
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(127): Show | 132 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.4699-3914T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64554976 | ||||||
| chr3:64555012
|
G | A | 1 | a0001c0004t0001g0276 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4699-3950C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555012 | ||||||
| chr3:64555021
|
C | T | 65 | a0001c0001t0002g0076a0001c0001t0002g0083a0001c0001t0002g0084others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.4699-3959G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555021 | ||||||
| chr3:64555022
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(188): Show | 193 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.4699-3960C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555022 | ||||||
| chr3:64555281
|
C | G | 1 | a0003c0025t0001g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4699-4219G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555281 | ||||||
| chr3:64555374
|
GTCAT | G | 10 | a0001c0001t0002g0065a0001c0004t0002g0277a0001c0006t0011g0008others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.4699-4316_4699-431 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555374 | ||||||
| chr3:64555386
|
TTCAA | T | 46 | a0001c0001t0001g0189a0001c0001t0002g0111a0001c0009t0005g0071others(43): Show | 46 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.4699-4328_4699-432 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555386 | ||||||
| chr3:64555390
|
A | T | 2 | a0002c0002t0003g0107a0002c0002t0003g0155 | 2 | HG02040.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.4699-4328T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555390 | ||||||
| chr3:64555408
|
A | G | 1 | a0001c0013t0011g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4699-4346T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555408 | ||||||
| chr3:64555446
|
T | C | 48 | a0001c0001t0001g0189a0001c0001t0002g0111a0001c0009t0005g0071others(45): Show | 48 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.4699-4384A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555446 | ||||||
| chr3:64555456
|
C | T | 49 | a0001c0001t0001g0189a0001c0001t0002g0111a0001c0009t0005g0071others(46): Show | 49 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.4699-4394G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555456 | ||||||
| chr3:64555465
|
T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.4699-4403A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555465 | ||||||
| chr3:64555577
|
GTGCAGTT others(5): Show |
G | 55 | a0001c0001t0001g0189a0001c0001t0001g0233a0001c0001t0002g0088others(52): Show | 55 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.4699-4527_4699-451 others(16): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555577 | ||||||
| chr3:64555578
|
T | G | 132 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.4699-4516A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555578 | ||||||
| chr3:64555590
|
A | G | 55 | a0001c0001t0001g0189a0001c0001t0001g0233a0001c0001t0002g0088others(52): Show | 55 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.4699-4528T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555590 | ||||||
| chr3:64555613
|
A | G | 55 | a0001c0001t0001g0189a0001c0001t0001g0233a0001c0001t0002g0088others(52): Show | 55 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.4699-4551T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555613 | ||||||
| chr3:64555686
|
T | C | 172 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(169): Show | 172 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.4699-4624A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555686 | ||||||
| chr3:64555697
|
A | G | 15 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(12): Show | 15 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.4699-4635T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555697 | ||||||
| chr3:64555806
|
T | C | 2 | a0001c0001t0002g0083a0001c0001t0002g0282 | 2 | NA18940.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.4699-4744A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555806 | ||||||
| chr3:64555824
|
G | C | 163 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.4699-4762C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555824 | ||||||
| chr3:64555853
|
G | A | 9 | a0001c0001t0002g0065a0001c0004t0002g0277a0001c0006t0011g0008others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.4699-4791C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555853 | ||||||
| chr3:64555909
|
A | C | 1 | a0002c0002t0003g0142 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4699-4847T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555909 | ||||||
| chr3:64555963
|
T | C | 4 | a0001c0001t0001g0067a0001c0001t0001g0233a0003c0003t0001g0022others(1): Show | 4 | HG01070.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4699-4901A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555963 | ||||||
| chr3:64555979
|
C | T | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4699-4917G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555979 | ||||||
| chr3:64555993
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(82): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.4699-4931A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64555993 | ||||||
| chr3:64556101
|
T | G | 1 | a0001c0001t0001g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4699-5039A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556101 | ||||||
| chr3:64556135
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4699-5073T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556135 | ||||||
| chr3:64556216
|
G | C | 1 | a0002c0002t0003g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4699-5154C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556216 | ||||||
| chr3:64556439
|
G | C | 2 | a0001c0001t0001g0223a0031c0027t0002g0051 | 2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4698+5139C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556439 | ||||||
| chr3:64556707
|
A | G | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0045t0001g0068others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4698+4871T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556707 | ||||||
| chr3:64556709
|
G | T | 5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0045t0001g0068others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4698+4869C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556709 | ||||||
| chr3:64556714
|
T | TCCTTCCT others(11): Show |
2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4698+4863_4698+486 others(22): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556714 | ||||||
| chr3:64556714
|
T | TTTCC | 114 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(111): Show | 114 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.4698+4860_4698+486 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556714 | ||||||
| chr3:64556714
|
T | TTTCCTTC others(1): Show |
55 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0101others(52): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.4698+4856_4698+486 others(12): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556714 | ||||||
| chr3:64556714
|
T | TTTCCTTC others(5): Show |
26 | a0001c0001t0001g0001a0001c0001t0001g0096a0001c0001t0001g0102others(23): Show | 27 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.4698+4852_4698+486 others(16): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556714 | ||||||
| chr3:64556714
|
T | TTTCCTTC others(9): Show |
6 | a0001c0001t0001g0019a0001c0001t0001g0166a0001c0001t0001g0168others(3): Show | 6 | HG01081.hp2 HG02148.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.4698+4848_4698+486 others(20): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556714 | ||||||
| chr3:64556714
|
TTTCC | T | 3 | a0001c0001t0002g0184a0001c0014t0001g0091a0002c0002t0003g0074 | 3 | HG00621.hp2 HG02135.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.4698+4860_4698+486 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556714 | ||||||
| chr3:64556714
|
TTTCCTTC others(1): Show |
T | 30 | a0001c0001t0001g0067a0001c0001t0001g0189a0001c0001t0001g0201others(27): Show | 30 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.4698+4856_4698+486 others(12): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556714 | ||||||
| chr3:64556714
|
TTTCCTTC others(5): Show |
T | 4 | a0005c0008t0001g0094a0005c0008t0002g0175a0005c0008t0002g0176others(1): Show | 4 | NA18953.hp1 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.4698+4852_4698+486 others(16): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64556714 | ||||||
| chr3:64557094
|
G | A | 1 | a0001c0001t0007g0278 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4698+4484C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557094 | ||||||
| chr3:64557142
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18971.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.4698+4436C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557142 | ||||||
| chr3:64557306
|
C | A | 4 | a0001c0001t0016g0063a0001c0004t0001g0061a0001c0013t0011g0005others(1): Show | 4 | HG02559.hp1 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.4698+4272G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557306 | ||||||
| chr3:64557529
|
G | A | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4698+4049C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557529 | ||||||
| chr3:64557575
|
T | C | 8 | a0001c0001t0002g0211a0001c0004t0001g0257a0001c0004t0001g0276others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.4698+4003A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557575 | ||||||
| chr3:64557582
|
A | G | 103 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.4698+3996T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557582 | ||||||
| chr3:64557655
|
G | A | 1 | a0002c0002t0003g0077 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4698+3923C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557655 | ||||||
| chr3:64557808
|
C | A | 1 | a0001c0001t0001g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4698+3770G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557808 | ||||||
| chr3:64557847
|
G | A | 32 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0002g0111others(29): Show | 32 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.4698+3731C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557847 | ||||||
| chr3:64557887
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(218): Show | 222 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.4698+3691T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557887 | ||||||
| chr3:64557939
|
T | C | 113 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.4698+3639A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64557939 | ||||||
| chr3:64558054
|
A | T | 10 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(7): Show | 10 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4698+3524T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558054 | ||||||
| chr3:64558173
|
G | A | 2 | a0001c0001t0001g0103a0003c0003t0002g0057 | 2 | NA18946.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.4698+3405C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558173 | ||||||
| chr3:64558218
|
G | A | 8 | a0001c0001t0001g0133a0002c0002t0001g0064a0002c0002t0001g0220others(5): Show | 8 | HG00738.hp2 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.4698+3360C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558218 | ||||||
| chr3:64558228
|
G | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(254): Show | 258 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.4698+3350C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558228 | ||||||
| chr3:64558238
|
G | A | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4698+3340C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558238 | ||||||
| chr3:64558304
|
C | T | 1 | a0002c0002t0003g0165 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4698+3274G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558304 | ||||||
| chr3:64558322
|
A | T | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4698+3256T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558322 | ||||||
| chr3:64558681
|
A | T | 14 | a0001c0001t0001g0085a0006c0010t0002g0169a0007c0011t0004g0086others(11): Show | 14 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4698+2897T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558681 | ||||||
| chr3:64558813
|
G | A | 13 | a0001c0001t0001g0279a0001c0001t0002g0131a0001c0001t0002g0217others(10): Show | 13 | HG01257.hp1 HG01884.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.4698+2765C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558813 | ||||||
| chr3:64558822
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(197): Show | 201 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.4698+2756T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558822 | ||||||
| chr3:64558970
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4698+2608C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64558970 | ||||||
| chr3:64559130
|
A | G | 4 | a0005c0008t0001g0094a0005c0008t0002g0175a0005c0008t0002g0176others(1): Show | 4 | NA18953.hp1 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.4698+2448T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559130 | ||||||
| chr3:64559153
|
G | A | 4 | a0003c0003t0007g0037a0003c0003t0007g0038a0003c0017t0006g0027others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4698+2425C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559153 | ||||||
| chr3:64559194
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4698+2384G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559194 | ||||||
| chr3:64559205
|
C | T | 5 | a0001c0013t0001g0145a0003c0003t0001g0021a0003c0025t0001g0026others(2): Show | 5 | HG02145.hp2 HG02895.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.4698+2373G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559205 | ||||||
| chr3:64559304
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4698+2274A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559304 | ||||||
| chr3:64559365
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.4698+2213A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559365 | ||||||
| chr3:64559378
|
G | A | 6 | a0001c0001t0002g0065a0001c0004t0002g0277a0001c0006t0011g0008others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4698+2200C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559378 | ||||||
| chr3:64559393
|
A | T | 15 | a0001c0001t0001g0085a0001c0001t0001g0171a0006c0010t0002g0169others(12): Show | 15 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.4698+2185T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559393 | ||||||
| chr3:64559413
|
A | G | 1 | a0009c0047t0001g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4698+2165T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559413 | ||||||
| chr3:64559467
|
C | T | 1 | a0002c0002t0003g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4698+2111G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559467 | ||||||
| chr3:64559495
|
T | G | 1 | a0001c0013t0011g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4698+2083A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559495 | ||||||
| chr3:64559702
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4698+1876T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559702 | ||||||
| chr3:64559805
|
T | C | 4 | a0001c0006t0001g0117a0001c0006t0001g0206a0001c0006t0001g0207others(1): Show | 4 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.4698+1773A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559805 | ||||||
| chr3:64559887
|
G | A | 1 | a0009c0047t0001g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4698+1691C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559887 | ||||||
| chr3:64559987
|
C | T | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4698+1591G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559987 | ||||||
| chr3:64559988
|
G | A | 7 | a0001c0001t0001g0018a0001c0006t0001g0117a0001c0006t0001g0206others(4): Show | 7 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.4698+1590C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64559988 | ||||||
| chr3:64560287
|
A | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4698+1291T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64560287 | ||||||
| chr3:64560407
|
A | C | 15 | a0001c0001t0001g0085a0001c0001t0001g0171a0006c0010t0002g0169others(12): Show | 15 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.4698+1171T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64560407 | ||||||
| chr3:64560545
|
G | A | 2 | a0001c0006t0001g0117a0001c0006t0001g0206 | 2 | HG00099.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4698+1033C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64560545 | ||||||
| chr3:64560726
|
C | A | 7 | a0001c0001t0002g0131a0001c0001t0002g0217a0001c0001t0020g0213others(4): Show | 7 | HG00735.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4698+852G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64560726 | ||||||
| chr3:64560783
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(87): Show | 91 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.4698+795G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64560783 | ||||||
| chr3:64560840
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4698+738G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64560840 | ||||||
| chr3:64560869
|
T | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0092others(43): Show | 47 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.4698+709A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64560869 | ||||||
| chr3:64560879
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4698+699G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64560879 | ||||||
| chr3:64561064
|
C | CCTT | 69 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(66): Show | 70 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.4698+511_4698+513d others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561064 | ||||||
| chr3:64561065
|
C | CTT | 13 | a0001c0001t0001g0132a0001c0001t0001g0183a0001c0001t0002g0084others(10): Show | 13 | HG00438.hp1 HG01257.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.4698+511_4698+512d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561065 | ||||||
| chr3:64561065
|
C | CTTCT | 14 | a0001c0001t0001g0085a0001c0001t0001g0171a0006c0010t0002g0169others(11): Show | 14 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4698+512_4698+513i others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561065 | ||||||
| chr3:64561065
|
C | CTTT | 106 | a0001c0001t0001g0018a0001c0001t0001g0090a0001c0001t0001g0093others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.4698+510_4698+512d others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561065 | ||||||
| chr3:64561065
|
C | CTTTT | 15 | a0001c0001t0001g0279a0001c0001t0002g0065a0001c0001t0002g0131others(12): Show | 15 | HG00735.hp2 HG01884.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.4698+509_4698+512d others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561065 | ||||||
| chr3:64561081
|
A | T | 12 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0009t0005g0071others(9): Show | 12 | HG01070.hp1 HG01243.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.4698+497T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561081 | ||||||
| chr3:64561220
|
C | G | 43 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0002g0111others(40): Show | 43 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.4698+358G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561220 | ||||||
| chr3:64561239
|
G | C | 10 | a0001c0001t0001g0279a0001c0001t0002g0131a0001c0001t0002g0217others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.4698+339C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561239 | ||||||
| chr3:64561321
|
G | GT | 110 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0085others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.4698+256dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561321 | ||||||
| chr3:64561321
|
G | GTT | 50 | a0001c0001t0001g0183a0001c0001t0001g0189a0001c0001t0001g0198others(47): Show | 50 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.4698+255_4698+256d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561321 | ||||||
| chr3:64561321
|
G | GTTT | 7 | a0001c0014t0001g0091a0001c0014t0001g0115a0001c0014t0002g0126others(4): Show | 7 | HG00438.hp1 HG02135.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.4698+254_4698+256d others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561321 | ||||||
| chr3:64561400
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4698+178C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561400 | ||||||
| chr3:64561502
|
T | C | 43 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0002g0111others(40): Show | 43 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.4698+76A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561502 | ||||||
| chr3:64561511
|
G | GA | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4698+66dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561511 | ||||||
| chr3:64561515
|
T | A | 1 | a0001c0001t0002g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4698+63A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 30/39 | chr3 | 64561515 | ||||||
| chr3:64561801
|
G | C | 7 | a0001c0001t0001g0199a0001c0001t0001g0216a0001c0001t0001g0218others(4): Show | 7 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.4525-50C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64561801 | ||||||
| chr3:64561826
|
C | T | 4 | a0001c0013t0001g0145a0003c0003t0001g0021a0003c0025t0001g0026others(1): Show | 4 | HG02145.hp2 HG02895.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.4525-75G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64561826 | ||||||
| chr3:64561904
|
C | A | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4525-153G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64561904 | ||||||
| chr3:64561962
|
G | A | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4525-211C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64561962 | ||||||
| chr3:64561996
|
T | A | 4 | a0001c0014t0001g0091a0001c0014t0001g0115a0001c0014t0002g0126others(1): Show | 4 | HG00438.hp1 HG02135.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.4525-245A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64561996 | ||||||
| chr3:64562383
|
C | T | 1 | a0003c0003t0002g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4525-632G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64562383 | ||||||
| chr3:64562488
|
A | G | 30 | a0001c0001t0001g0067a0001c0001t0001g0133a0001c0001t0001g0233others(27): Show | 30 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.4525-737T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64562488 | ||||||
| chr3:64562556
|
A | C | 15 | a0001c0001t0001g0085a0001c0001t0001g0171a0006c0010t0002g0169others(12): Show | 15 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.4525-805T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64562556 | ||||||
| chr3:64562595
|
C | T | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4525-844G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64562595 | ||||||
| chr3:64562883
|
A | C | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4525-1132T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64562883 | ||||||
| chr3:64562908
|
G | C | 10 | a0001c0001t0001g0279a0001c0001t0002g0131a0001c0001t0002g0217others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.4525-1157C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64562908 | ||||||
| chr3:64562919
|
A | G | 2 | a0001c0001t0001g0223a0031c0027t0002g0051 | 2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4525-1168T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64562919 | ||||||
| chr3:64563055
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(98): Show | 102 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.4525-1304G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563055 | ||||||
| chr3:64563128
|
G | C | 3 | a0001c0009t0005g0071a0001c0009t0005g0072a0001c0009t0005g0073 | 3 | HG01934.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.4525-1377C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563128 | ||||||
| chr3:64563164
|
C | T | 1 | a0003c0003t0001g0041 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4525-1413G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563164 | ||||||
| chr3:64563228
|
T | C | 10 | a0001c0001t0001g0279a0001c0001t0002g0131a0001c0001t0002g0217others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.4525-1477A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563228 | ||||||
| chr3:64563292
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(171): Show | 175 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.4525-1541A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563292 | ||||||
| chr3:64563494
|
CAT | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0092others(44): Show | 48 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.4525-1745_4525-174 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563494 | ||||||
| chr3:64563562
|
G | A | 11 | a0001c0001t0001g0171a0006c0010t0002g0169a0007c0011t0004g0156others(8): Show | 11 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.4525-1811C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563562 | ||||||
| chr3:64563604
|
C | A | 4 | a0001c0014t0001g0091a0001c0014t0001g0115a0001c0014t0002g0126others(1): Show | 4 | HG00438.hp1 HG02135.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.4525-1853G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563604 | ||||||
| chr3:64563778
|
C | T | 1 | a0002c0002t0003g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4525-2027G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563778 | ||||||
| chr3:64563809
|
C | T | 1 | a0001c0014t0001g0091 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4525-2058G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563809 | ||||||
| chr3:64563869
|
G | A | 8 | a0001c0001t0001g0133a0002c0002t0001g0064a0002c0002t0001g0220others(5): Show | 8 | HG00738.hp2 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.4525-2118C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64563869 | ||||||
| chr3:64564037
|
G | A | 29 | a0001c0001t0001g0067a0001c0001t0001g0133a0001c0001t0001g0233others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.4525-2286C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564037 | ||||||
| chr3:64564202
|
G | A | 2 | a0001c0013t0011g0005a0003c0003t0002g0060 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.4525-2451C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564202 | ||||||
| chr3:64564210
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(96): Show | 100 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.4525-2459G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564210 | ||||||
| chr3:64564352
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0092others(43): Show | 47 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.4525-2601C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564352 | ||||||
| chr3:64564477
|
A | G | 9 | a0001c0001t0016g0063a0001c0004t0001g0061a0001c0009t0005g0069others(6): Show | 9 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.4525-2726T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564477 | ||||||
| chr3:64564517
|
A | G | 1 | a0001c0001t0002g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4525-2766T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564517 | ||||||
| chr3:64564517
|
A | T | 1 | a0004c0005t0001g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4525-2766T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564517 | ||||||
| chr3:64564618
|
T | TG | 26 | a0001c0001t0001g0067a0001c0001t0001g0133a0001c0001t0001g0233others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.4525-2868dupC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564618 | ||||||
| chr3:64564619
|
G | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(92): Show | 97 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.4525-2868C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564619 | ||||||
| chr3:64564634
|
G | A | 1 | a0009c0047t0001g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4525-2883C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564634 | ||||||
| chr3:64564641
|
T | C | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4525-2890A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564641 | ||||||
| chr3:64564674
|
A | C | 29 | a0001c0001t0001g0067a0001c0001t0001g0133a0001c0001t0001g0233others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.4525-2923T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564674 | ||||||
| chr3:64564702
|
C | G | 10 | a0001c0001t0001g0133a0002c0002t0001g0064a0002c0002t0001g0220others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4525-2951G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564702 | ||||||
| chr3:64564776
|
A | G | 29 | a0001c0001t0001g0067a0001c0001t0001g0133a0001c0001t0001g0233others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.4525-3025T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564776 | ||||||
| chr3:64564889
|
G | A | 1 | a0028c0043t0003g0194 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4525-3138C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564889 | ||||||
| chr3:64564973
|
G | A | 1 | a0027c0042t0002g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4525-3222C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64564973 | ||||||
| chr3:64565135
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4524+3233G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565135 | ||||||
| chr3:64565190
|
C | A | 1 | a0002c0002t0003g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4524+3178G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565190 | ||||||
| chr3:64565282
|
T | C | 67 | a0001c0001t0001g0018a0001c0001t0001g0085a0001c0001t0001g0090others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.4524+3086A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565282 | ||||||
| chr3:64565287
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4524+3081G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565287 | ||||||
| chr3:64565472
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4524+2896T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565472 | ||||||
| chr3:64565600
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4524+2768A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565600 | ||||||
| chr3:64565633
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4524+2735G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565633 | ||||||
| chr3:64565951
|
G | A | 1 | a0001c0001t0001g0102 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4524+2417C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565951 | ||||||
| chr3:64565952
|
C | A | 1 | a0001c0001t0001g0102 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4524+2416G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64565952 | ||||||
| chr3:64566015
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4524+2353A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566015 | ||||||
| chr3:64566031
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4524+2337G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566031 | ||||||
| chr3:64566165
|
C | G | 1 | a0003c0025t0001g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4524+2203G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566165 | ||||||
| chr3:64566214
|
T | A | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4524+2154A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566214 | ||||||
| chr3:64566405
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.4524+1963A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566405 | ||||||
| chr3:64566789
|
C | T | 55 | a0001c0001t0001g0018a0001c0001t0001g0085a0001c0001t0001g0090others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.4524+1579G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566789 | ||||||
| chr3:64566809
|
G | A | 1 | a0001c0030t0001g0180 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4524+1559C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566809 | ||||||
| chr3:64566809
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4524+1559C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566809 | ||||||
| chr3:64566810
|
T | A | 39 | a0001c0001t0001g0133a0001c0001t0001g0279a0001c0001t0002g0131others(36): Show | 39 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.4524+1558A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566810 | ||||||
| chr3:64566861
|
C | CA | 56 | a0001c0001t0001g0018a0001c0001t0001g0085a0001c0001t0001g0090others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.4524+1506dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566861 | ||||||
| chr3:64566863
|
A | G | 3 | a0001c0001t0001g0279a0001c0001t0007g0278a0002c0002t0008g0009 | 3 | HG01884.hp1 HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.4524+1505T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566863 | ||||||
| chr3:64566873
|
G | A | 1 | a0005c0008t0002g0175 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4524+1495C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566873 | ||||||
| chr3:64566953
|
T | C | 3 | a0001c0001t0001g0279a0001c0001t0007g0278a0002c0002t0008g0009 | 3 | HG01884.hp1 HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.4524+1415A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566953 | ||||||
| chr3:64566964
|
G | A | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4524+1404C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64566964 | ||||||
| chr3:64567074
|
G | A | 34 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0002g0111others(31): Show | 34 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.4524+1294C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567074 | ||||||
| chr3:64567080
|
A | C | 10 | a0001c0001t0001g0133a0002c0002t0001g0064a0002c0002t0001g0220others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4524+1288T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567080 | ||||||
| chr3:64567142
|
A | G | 1 | a0028c0043t0003g0194 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4524+1226T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567142 | ||||||
| chr3:64567296
|
G | A | 5 | a0001c0001t0002g0211a0001c0004t0001g0257a0001c0004t0001g0276others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4524+1072C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567296 | ||||||
| chr3:64567347
|
T | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0279a0001c0001t0007g0278others(1): Show | 4 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.4524+1021A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567347 | ||||||
| chr3:64567368
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4524+1000C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567368 | ||||||
| chr3:64567541
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0085others(84): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.4524+827G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567541 | ||||||
| chr3:64567676
|
T | TAATCAGT others(30): Show |
1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4524+655_4524+691d others(39): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567676 | ||||||
| chr3:64567713
|
C | T | 3 | a0001c0001t0001g0279a0001c0001t0007g0278a0002c0002t0008g0009 | 3 | HG01884.hp1 HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.4524+655G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567713 | ||||||
| chr3:64567767
|
T | C | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4524+601A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567767 | ||||||
| chr3:64567776
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(10): Show | 14 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.4524+592G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567776 | ||||||
| chr3:64567951
|
T | C | 37 | a0001c0001t0001g0133a0001c0001t0002g0131a0001c0001t0002g0217others(34): Show | 37 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.4524+417A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64567951 | ||||||
| chr3:64568045
|
T | C | 34 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0002g0111others(31): Show | 34 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.4524+323A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64568045 | ||||||
| chr3:64568269
|
T | C | 2 | a0026c0044t0001g0098a0027c0042t0002g0177 | 2 | HG00609.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.4524+99A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64568269 | ||||||
| chr3:64568287
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(10): Show | 14 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.4524+81A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64568287 | ||||||
| chr3:64568330
|
CG | C | 4 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(1): Show | 4 | HG02970.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4524+37delC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 29/39 | chr3 | 64568330 | ||||||
| chr3:64568578
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4357-43A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64568578 | ||||||
| chr3:64568583
|
G | A | 41 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0002g0111others(38): Show | 41 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.4357-48C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64568583 | ||||||
| chr3:64568981
|
G | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0079others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.4357-446C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64568981 | ||||||
| chr3:64569008
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4357-473C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569008 | ||||||
| chr3:64569201
|
T | C | 3 | a0001c0001t0001g0279a0001c0001t0007g0278a0002c0002t0008g0009 | 3 | HG01884.hp1 HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.4357-666A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569201 | ||||||
| chr3:64569456
|
A | T | 74 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(71): Show | 74 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.4357-921T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569456 | ||||||
| chr3:64569635
|
G | GTT | 3 | a0001c0009t0005g0071a0001c0009t0005g0072a0001c0009t0005g0073 | 3 | HG01934.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.4357-1101_4357-110 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569635 | ||||||
| chr3:64569637
|
T | A | 3 | a0001c0009t0005g0071a0001c0009t0005g0072a0001c0009t0005g0073 | 3 | HG01934.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.4357-1102A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569637 | ||||||
| chr3:64569637
|
T | TCA | 131 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(128): Show | 131 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.4357-1104_4357-110 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569637 | ||||||
| chr3:64569734
|
G | A | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4357-1199C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569734 | ||||||
| chr3:64569761
|
T | G | 1 | a0001c0001t0002g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4357-1226A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569761 | ||||||
| chr3:64569826
|
T | G | 3 | a0007c0011t0004g0156a0007c0011t0004g0157a0020c0034t0001g0140 | 3 | NA18991.hp2 NA19058.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.4357-1291A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569826 | ||||||
| chr3:64569830
|
G | C | 1 | a0001c0001t0002g0129 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4357-1295C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569830 | ||||||
| chr3:64569970
|
A | G | 6 | a0001c0001t0001g0067a0001c0013t0001g0145a0003c0003t0001g0021others(3): Show | 6 | HG02145.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.4357-1435T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64569970 | ||||||
| chr3:64570023
|
A | G | 94 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(91): Show | 94 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.4357-1488T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570023 | ||||||
| chr3:64570128
|
G | A | 10 | a0001c0001t0001g0133a0002c0002t0001g0064a0002c0002t0001g0220others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4357-1593C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570128 | ||||||
| chr3:64570145
|
T | TATAA | 10 | a0001c0001t0001g0133a0002c0002t0001g0064a0002c0002t0001g0220others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4357-1611_4357-161 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570145 | ||||||
| chr3:64570150
|
G | A | 45 | a0001c0001t0001g0133a0001c0001t0001g0233a0001c0001t0002g0131others(42): Show | 45 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.4357-1615C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570150 | ||||||
| chr3:64570162
|
T | C | 94 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(91): Show | 94 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.4357-1627A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570162 | ||||||
| chr3:64570364
|
C | T | 10 | a0001c0001t0001g0133a0002c0002t0001g0064a0002c0002t0001g0220others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4357-1829G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570364 | ||||||
| chr3:64570474
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4357-1939C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570474 | ||||||
| chr3:64570658
|
T | C | 10 | a0001c0001t0001g0133a0002c0002t0001g0064a0002c0002t0001g0220others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4357-2123A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570658 | ||||||
| chr3:64570690
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4357-2155G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570690 | ||||||
| chr3:64570691
|
GTC | G | 36 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0087others(33): Show | 36 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.4357-2158_4357-215 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570691 | ||||||
| chr3:64570693
|
CTCA | C | 13 | a0001c0001t0002g0224a0001c0001t0002g0273a0001c0004t0002g0277others(10): Show | 13 | HG02109.hp1 HG02129.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.4357-2161_4357-215 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570693 | ||||||
| chr3:64570694
|
T | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0104a0001c0001t0001g0124others(8): Show | 11 | HG02145.hp2 HG02148.hp1 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.4357-2159A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570694 | ||||||
| chr3:64570695
|
C | CA | 38 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0189others(35): Show | 38 | HG00438.hp1 HG01071.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4357-2161dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570695 | ||||||
| chr3:64570695
|
CA | C | 24 | a0001c0001t0001g0080a0001c0001t0001g0104a0001c0001t0001g0124others(21): Show | 24 | HG00438.hp2 HG00558.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.4357-2161delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570695 | ||||||
| chr3:64570695
|
CAA | C | 31 | a0001c0001t0001g0133a0001c0001t0002g0099a0001c0001t0002g0217others(28): Show | 31 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.4357-2162_4357-216 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570695 | ||||||
| chr3:64570695
|
CAAA | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(23): Show | 27 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.4357-2163_4357-216 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570695 | ||||||
| chr3:64570695
|
CAAAA | C | 17 | a0001c0001t0001g0085a0001c0001t0001g0171a0001c0001t0001g0183others(14): Show | 17 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.4357-2164_4357-216 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570695 | ||||||
| chr3:64570697
|
A | C | 36 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0087others(33): Show | 36 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.4357-2162T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570697 | ||||||
| chr3:64570698
|
A | C | 13 | a0001c0001t0002g0224a0001c0001t0002g0273a0001c0004t0002g0277others(10): Show | 13 | HG02109.hp1 HG02129.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.4357-2163T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570698 | ||||||
| chr3:64570849
|
G | A | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4357-2314C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64570849 | ||||||
| chr3:64571021
|
T | C | 4 | a0001c0014t0001g0091a0001c0014t0001g0115a0001c0014t0002g0126others(1): Show | 4 | HG00438.hp1 HG02135.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.4357-2486A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571021 | ||||||
| chr3:64571022
|
A | C | 98 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(95): Show | 98 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.4357-2487T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571022 | ||||||
| chr3:64571161
|
A | C | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4357-2626T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571161 | ||||||
| chr3:64571305
|
G | A | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4357-2770C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571305 | ||||||
| chr3:64571310
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4357-2775A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571310 | ||||||
| chr3:64571336
|
C | T | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4357-2801G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571336 | ||||||
| chr3:64571348
|
T | C | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4357-2813A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571348 | ||||||
| chr3:64571363
|
G | T | 4 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(1): Show | 4 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.4357-2828C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571363 | ||||||
| chr3:64571474
|
T | C | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4357-2939A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571474 | ||||||
| chr3:64571627
|
T | C | 97 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(94): Show | 97 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.4357-3092A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571627 | ||||||
| chr3:64571710
|
T | C | 1 | a0001c0001t0014g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4357-3175A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571710 | ||||||
| chr3:64571800
|
T | C | 97 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(94): Show | 97 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.4357-3265A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571800 | ||||||
| chr3:64571958
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.4357-3423G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64571958 | ||||||
| chr3:64572040
|
A | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0093others(79): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.4357-3505T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572040 | ||||||
| chr3:64572043
|
T | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(16): Show | 20 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.4357-3508A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572043 | ||||||
| chr3:64572059
|
C | CA | 96 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(93): Show | 96 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.4357-3525_4357-352 others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572059 | ||||||
| chr3:64572060
|
T | A | 96 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(93): Show | 96 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.4357-3525A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572060 | ||||||
| chr3:64572061
|
C | A | 96 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(93): Show | 96 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.4357-3526G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572061 | ||||||
| chr3:64572062
|
C | G | 96 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(93): Show | 96 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.4357-3527G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572062 | ||||||
| chr3:64572064
|
A | AGG | 96 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(93): Show | 96 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.4357-3530_4357-352 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572064 | ||||||
| chr3:64572077
|
G | A | 1 | a0002c0002t0003g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4357-3542C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572077 | ||||||
| chr3:64572117
|
G | A | 53 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0103others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.4357-3582C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572117 | ||||||
| chr3:64572286
|
T | C | 144 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(141): Show | 144 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.4357-3751A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572286 | ||||||
| chr3:64572444
|
A | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4357-3909T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572444 | ||||||
| chr3:64572479
|
C | T | 37 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0002g0111others(34): Show | 37 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.4357-3944G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572479 | ||||||
| chr3:64572486
|
T | C | 7 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066others(4): Show | 7 | HG00438.hp1 HG02135.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4357-3951A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572486 | ||||||
| chr3:64572596
|
G | T | 1 | a0001c0001t0002g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4357-4061C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572596 | ||||||
| chr3:64572802
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0002g0108a0001c0001t0002g0221others(1): Show | 4 | HG00140.hp1 HG01123.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.4357-4267C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572802 | ||||||
| chr3:64572832
|
G | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.4357-4297C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572832 | ||||||
| chr3:64572885
|
C | T | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4357-4350G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572885 | ||||||
| chr3:64572905
|
C | T | 42 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0103others(39): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.4357-4370G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572905 | ||||||
| chr3:64572912
|
T | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(113): Show | 117 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.4357-4377A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572912 | ||||||
| chr3:64572993
|
G | A | 4 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(1): Show | 4 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.4357-4458C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64572993 | ||||||
| chr3:64573062
|
T | C | 1 | a0001c0013t0011g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4357-4527A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573062 | ||||||
| chr3:64573079
|
T | TA | 7 | a0001c0001t0001g0018a0001c0001t0002g0187a0001c0001t0002g0224others(4): Show | 7 | HG02647.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4357-4545dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573079 | ||||||
| chr3:64573079
|
T | TAA | 44 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0201others(41): Show | 44 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.4357-4546_4357-454 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573079 | ||||||
| chr3:64573079
|
T | TAAA | 46 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(43): Show | 46 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.4357-4547_4357-454 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573079 | ||||||
| chr3:64573079
|
TA | T | 21 | a0001c0001t0001g0183a0001c0001t0001g0279a0001c0001t0007g0278others(18): Show | 21 | HG00099.hp2 HG00438.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.4357-4545delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573079 | ||||||
| chr3:64573079
|
TAA | T | 84 | a0001c0001t0001g0067a0001c0001t0001g0090a0001c0001t0001g0093others(81): Show | 84 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.4357-4546_4357-454 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573079 | ||||||
| chr3:64573079
|
TAAAAA | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(18): Show | 22 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.4357-4549_4357-454 others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573079 | ||||||
| chr3:64573108
|
G | GA | 101 | a0001c0001t0001g0067a0001c0001t0001g0090a0001c0001t0001g0093others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.4357-4574dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573108 | ||||||
| chr3:64573126
|
G | A | 3 | a0003c0003t0002g0060a0003c0017t0006g0027a0003c0017t0006g0028 | 3 | HG02258.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4357-4591C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573126 | ||||||
| chr3:64573138
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4357-4603T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573138 | ||||||
| chr3:64573279
|
T | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.4357-4744A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573279 | ||||||
| chr3:64573332
|
G | T | 14 | a0001c0001t0001g0171a0006c0010t0002g0169a0007c0011t0004g0086others(11): Show | 14 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4357-4797C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573332 | ||||||
| chr3:64573436
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4357-4901A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573436 | ||||||
| chr3:64573662
|
T | G | 1 | a0005c0008t0001g0094 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4357-5127A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573662 | ||||||
| chr3:64573714
|
A | C | 34 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0002g0111others(31): Show | 34 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.4357-5179T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573714 | ||||||
| chr3:64573793
|
G | A | 15 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0211others(12): Show | 15 | HG01070.hp1 HG02258.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.4357-5258C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573793 | ||||||
| chr3:64573971
|
A | T | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4357-5436T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573971 | ||||||
| chr3:64573983
|
G | T | 8 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0104others(5): Show | 8 | NA18955.hp1 NA18974.hp1 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.4357-5448C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64573983 | ||||||
| chr3:64574022
|
G | A | 14 | a0001c0001t0001g0171a0006c0010t0002g0169a0007c0011t0004g0086others(11): Show | 14 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4357-5487C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574022 | ||||||
| chr3:64574047
|
T | C | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4357-5512A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574047 | ||||||
| chr3:64574091
|
A | G | 3 | a0003c0003t0002g0060a0003c0017t0006g0027a0003c0017t0006g0028 | 3 | HG02258.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4357-5556T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574091 | ||||||
| chr3:64574092
|
A | G | 3 | a0003c0003t0002g0060a0003c0017t0006g0027a0003c0017t0006g0028 | 3 | HG02258.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4357-5557T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574092 | ||||||
| chr3:64574123
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4357-5588C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574123 | ||||||
| chr3:64574134
|
C | T | 1 | a0001c0007t0013g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4357-5599G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574134 | ||||||
| chr3:64574337
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(63): Show | 67 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.4357-5802C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574337 | ||||||
| chr3:64574381
|
C | T | 13 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0211others(10): Show | 13 | HG01070.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.4357-5846G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574381 | ||||||
| chr3:64574441
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4357-5906C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574441 | ||||||
| chr3:64574511
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(19): Show | 23 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4357-5976G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574511 | ||||||
| chr3:64574529
|
C | T | 1 | a0002c0002t0003g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4357-5994G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574529 | ||||||
| chr3:64574559
|
C | CA | 16 | a0001c0001t0001g0171a0003c0003t0002g0060a0003c0017t0006g0027others(13): Show | 16 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.4357-6025dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574559 | ||||||
| chr3:64574559
|
C | CAA | 139 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.4357-6026_4357-602 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574559 | ||||||
| chr3:64574559
|
C | CAAA | 39 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0133others(36): Show | 39 | HG00438.hp1 HG00544.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.4357-6027_4357-602 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574559 | ||||||
| chr3:64574559
|
C | CAAAA | 8 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0007g0278others(5): Show | 8 | HG01952.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4357-6028_4357-602 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574559 | ||||||
| chr3:64574559
|
C | CAAAAA | 11 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0211others(8): Show | 11 | HG01070.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4357-6029_4357-602 others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574559 | ||||||
| chr3:64574669
|
G | T | 49 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(46): Show | 49 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.4357-6134C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574669 | ||||||
| chr3:64574706
|
G | T | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4357-6171C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574706 | ||||||
| chr3:64574720
|
G | GAC | 239 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4357-6187_4357-618 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574720 | ||||||
| chr3:64574853
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4357-6318C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64574853 | ||||||
| chr3:64575152
|
C | G | 1 | a0013c0019t0004g0200 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4357-6617G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575152 | ||||||
| chr3:64575177
|
G | T | 1 | a0005c0008t0001g0094 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4357-6642C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575177 | ||||||
| chr3:64575369
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.4357-6834A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575369 | ||||||
| chr3:64575399
|
C | T | 1 | a0008c0049t0001g0136 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.4357-6864G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575399 | ||||||
| chr3:64575538
|
G | A | 1 | a0001c0001t0014g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4357-7003C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575538 | ||||||
| chr3:64575539
|
G | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4357-7004C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575539 | ||||||
| chr3:64575574
|
T | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0104others(5): Show | 8 | NA18955.hp1 NA18974.hp1 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.4357-7039A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575574 | ||||||
| chr3:64575728
|
C | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG03139.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4357-7193G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575728 | ||||||
| chr3:64575743
|
G | A | 1 | a0026c0044t0001g0098 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4357-7208C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575743 | ||||||
| chr3:64575750
|
A | G | 14 | a0001c0001t0001g0171a0006c0010t0002g0169a0007c0011t0004g0086others(11): Show | 14 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4357-7215T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575750 | ||||||
| chr3:64575771
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0251 | 2 | HG01978.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.4357-7236A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575771 | ||||||
| chr3:64575842
|
AT | A | 7 | a0001c0001t0001g0233a0001c0004t0001g0257a0002c0002t0001g0266others(4): Show | 7 | HG01070.hp1 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4357-7308delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575842 | ||||||
| chr3:64575908
|
G | A | 1 | a0010c0012t0004g0039 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4357-7373C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575908 | ||||||
| chr3:64575943
|
A | G | 5 | a0001c0001t0002g0088a0003c0003t0001g0035a0006c0010t0001g0245others(2): Show | 5 | NA18955.hp2 NA18983.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.4357-7408T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575943 | ||||||
| chr3:64575961
|
T | C | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4357-7426A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64575961 | ||||||
| chr3:64576014
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4357-7479C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576014 | ||||||
| chr3:64576080
|
C | T | 8 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0104others(5): Show | 8 | NA18955.hp1 NA18974.hp1 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.4357-7545G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576080 | ||||||
| chr3:64576178
|
A | G | 7 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066others(4): Show | 7 | HG00438.hp1 HG02135.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4357-7643T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576178 | ||||||
| chr3:64576393
|
C | G | 1 | a0001c0001t0002g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4357-7858G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576393 | ||||||
| chr3:64576429
|
C | T | 77 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(74): Show | 77 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.4357-7894G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576429 | ||||||
| chr3:64576520
|
C | A | 14 | a0001c0001t0001g0171a0006c0010t0002g0169a0007c0011t0004g0086others(11): Show | 14 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4357-7985G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576520 | ||||||
| chr3:64576651
|
T | C | 1 | a0002c0002t0001g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4357-8116A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576651 | ||||||
| chr3:64576699
|
C | G | 61 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(58): Show | 61 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.4357-8164G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576699 | ||||||
| chr3:64576710
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4357-8175C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576710 | ||||||
| chr3:64576749
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4357-8214T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576749 | ||||||
| chr3:64576949
|
C | T | 9 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066others(6): Show | 9 | HG00438.hp1 HG02135.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4357-8414G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576949 | ||||||
| chr3:64576965
|
G | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0090others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.4357-8430C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64576965 | ||||||
| chr3:64577077
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0166 | 2 | HG03490.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.4357-8542C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577077 | ||||||
| chr3:64577111
|
C | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4357-8576G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577111 | ||||||
| chr3:64577204
|
G | A | 1 | a0002c0002t0003g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4357-8669C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577204 | ||||||
| chr3:64577269
|
T | C | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4357-8734A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577269 | ||||||
| chr3:64577324
|
T | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4357-8789A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577324 | ||||||
| chr3:64577362
|
G | T | 16 | a0001c0001t0001g0171a0003c0017t0006g0027a0003c0017t0006g0028others(13): Show | 16 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.4357-8827C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577362 | ||||||
| chr3:64577391
|
G | C | 9 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4357-8856C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577391 | ||||||
| chr3:64577498
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.4357-8963G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577498 | ||||||
| chr3:64577499
|
G | C | 9 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256others(6): Show | 9 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.4357-8964C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577499 | ||||||
| chr3:64577701
|
TTGACA | T | 16 | a0001c0001t0001g0171a0003c0017t0006g0027a0003c0017t0006g0028others(13): Show | 16 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.4357-9171_4357-916 others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577701 | ||||||
| chr3:64577892
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4357-9357A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577892 | ||||||
| chr3:64577976
|
C | G | 1 | a0002c0002t0003g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4357-9441G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64577976 | ||||||
| chr3:64578020
|
G | A | 1 | a0009c0047t0001g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4357-9485C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578020 | ||||||
| chr3:64578022
|
G | T | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4357-9487C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578022 | ||||||
| chr3:64578092
|
C | T | 43 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0103others(40): Show | 43 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.4357-9557G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578092 | ||||||
| chr3:64578170
|
C | T | 3 | a0001c0009t0005g0071a0001c0009t0005g0072a0001c0009t0005g0073 | 3 | HG01934.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.4357-9635G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578170 | ||||||
| chr3:64578289
|
TA | T | 52 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0103others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.4357-9755delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578289 | ||||||
| chr3:64578329
|
C | T | 6 | a0001c0001t0001g0183a0001c0001t0020g0213a0001c0037t0008g0006others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.4357-9794G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578329 | ||||||
| chr3:64578481
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4357-9946A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578481 | ||||||
| chr3:64578512
|
C | T | 2 | a0001c0001t0001g0183a0001c0037t0008g0006 | 2 | HG02615.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.4357-9977G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578512 | ||||||
| chr3:64578549
|
ATCTT | A | 14 | a0001c0001t0001g0171a0006c0010t0002g0169a0007c0011t0004g0086others(11): Show | 14 | HG01255.hp1 HG01978.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4357-10018_4357-10 others(10): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578549 | ||||||
| chr3:64578620
|
A | G | 1 | a0001c0001t0014g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4357-10085T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578620 | ||||||
| chr3:64578657
|
A | G | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4357-10122T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578657 | ||||||
| chr3:64578738
|
A | G | 7 | a0001c0001t0002g0065a0001c0006t0010g0003a0001c0006t0010g0007others(4): Show | 7 | HG02109.hp1 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.4357-10203T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578738 | ||||||
| chr3:64578803
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4357-10268T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64578803 | ||||||
| chr3:64579196
|
G | A | 1 | a0001c0007t0013g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4357-10661C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579196 | ||||||
| chr3:64579202
|
T | G | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4357-10667A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579202 | ||||||
| chr3:64579303
|
A | G | 2 | a0003c0017t0006g0027a0003c0017t0006g0028 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4357-10768T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579303 | ||||||
| chr3:64579326
|
T | C | 13 | a0001c0001t0001g0171a0006c0010t0002g0169a0007c0011t0004g0086others(10): Show | 13 | HG01255.hp1 HG01978.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.4357-10791A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579326 | ||||||
| chr3:64579351
|
C | T | 4 | a0001c0001t0001g0183a0001c0001t0020g0213a0001c0037t0008g0006others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.4357-10816G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579351 | ||||||
| chr3:64579673
|
A | G | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4357-11138T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579673 | ||||||
| chr3:64579825
|
A | C | 57 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0080others(54): Show | 57 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.4357-11290T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579825 | ||||||
| chr3:64579840
|
T | C | 81 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(78): Show | 81 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.4357-11305A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579840 | ||||||
| chr3:64579842
|
G | A | 9 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4357-11307C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64579842 | ||||||
| chr3:64580034
|
C | T | 1 | a0003c0003t0001g0041 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4357-11499G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580034 | ||||||
| chr3:64580112
|
A | ATG | 6 | a0001c0001t0001g0067a0001c0013t0001g0145a0003c0003t0001g0021others(3): Show | 6 | HG02145.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.4357-11579_4357-11 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580112 | ||||||
| chr3:64580132
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4357-11597C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580132 | ||||||
| chr3:64580213
|
A | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(15): Show | 19 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.4357-11678T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580213 | ||||||
| chr3:64580290
|
A | T | 8 | a0001c0001t0001g0183a0001c0001t0020g0213a0001c0014t0001g0091others(5): Show | 8 | HG00438.hp1 HG02135.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4357-11755T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580290 | ||||||
| chr3:64580369
|
A | G | 1 | a0005c0008t0002g0188 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4357-11834T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580369 | ||||||
| chr3:64580379
|
A | C | 139 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.4357-11844T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580379 | ||||||
| chr3:64580385
|
A | G | 129 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.4357-11850T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580385 | ||||||
| chr3:64580578
|
A | G | 1 | a0001c0006t0001g0207 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4357-12043T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580578 | ||||||
| chr3:64580611
|
T | C | 9 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4357-12076A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580611 | ||||||
| chr3:64580727
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4357-12192G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64580727 | ||||||
| chr3:64581042
|
C | T | 13 | a0001c0001t0001g0171a0006c0010t0002g0169a0007c0011t0004g0086others(10): Show | 13 | HG01255.hp1 HG01978.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.4357-12507G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581042 | ||||||
| chr3:64581132
|
C | T | 9 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4357-12597G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581132 | ||||||
| chr3:64581173
|
T | A | 1 | a0003c0003t0001g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4357-12638A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581173 | ||||||
| chr3:64581338
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4357-12803C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581338 | ||||||
| chr3:64581372
|
T | C | 56 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(53): Show | 56 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.4357-12837A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581372 | ||||||
| chr3:64581386
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4357-12851G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581386 | ||||||
| chr3:64581452
|
G | A | 43 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(40): Show | 43 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.4356+12806C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581452 | ||||||
| chr3:64581906
|
C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0090others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.4356+12352G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581906 | ||||||
| chr3:64581952
|
C | A | 70 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0103others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.4356+12306G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581952 | ||||||
| chr3:64581961
|
C | G | 4 | a0003c0003t0001g0023a0003c0003t0002g0060a0003c0017t0006g0027others(1): Show | 4 | HG02258.hp2 HG03195.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.4356+12297G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64581961 | ||||||
| chr3:64582106
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0093others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.4356+12152C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582106 | ||||||
| chr3:64582401
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0095others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.4356+11857G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582401 | ||||||
| chr3:64582430
|
A | T | 3 | a0001c0001t0002g0065a0001c0009t0005g0069a0001c0009t0005g0070 | 3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4356+11828T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582430 | ||||||
| chr3:64582515
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4356+11743A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582515 | ||||||
| chr3:64582523
|
T | C | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+11735A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582523 | ||||||
| chr3:64582567
|
C | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4356+11691G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582567 | ||||||
| chr3:64582580
|
G | C | 3 | a0001c0001t0001g0189a0002c0002t0003g0077a0002c0002t0003g0078 | 3 | HG02083.hp2 NA19011.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.4356+11678C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582580 | ||||||
| chr3:64582611
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(10): Show | 14 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+11647G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582611 | ||||||
| chr3:64582818
|
G | A | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4356+11440C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582818 | ||||||
| chr3:64582839
|
T | C | 40 | a0001c0001t0001g0167a0001c0001t0001g0189a0001c0001t0001g0201others(37): Show | 40 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.4356+11419A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582839 | ||||||
| chr3:64582861
|
G | C | 1 | a0001c0001t0002g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4356+11397C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582861 | ||||||
| chr3:64582912
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4356+11346T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582912 | ||||||
| chr3:64582937
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.4356+11321G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582937 | ||||||
| chr3:64582983
|
T | C | 5 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.4356+11275A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64582983 | ||||||
| chr3:64583017
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4356+11241T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583017 | ||||||
| chr3:64583054
|
A | G | 1 | a0001c0001t0019g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4356+11204T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583054 | ||||||
| chr3:64583098
|
T | C | 82 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0103others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.4356+11160A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583098 | ||||||
| chr3:64583207
|
T | G | 9 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066others(6): Show | 9 | HG00438.hp1 HG02135.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4356+11051A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583207 | ||||||
| chr3:64583234
|
C | T | 10 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(7): Show | 10 | HG02109.hp1 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4356+11024G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583234 | ||||||
| chr3:64583260
|
T | C | 1 | a0012c0018t0006g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4356+10998A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583260 | ||||||
| chr3:64583339
|
G | A | 6 | a0001c0001t0001g0233a0002c0002t0001g0266a0002c0002t0001g0267others(3): Show | 6 | HG01070.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4356+10919C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583339 | ||||||
| chr3:64583350
|
C | T | 1 | a0001c0001t0014g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4356+10908G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583350 | ||||||
| chr3:64583407
|
A | C | 55 | a0001c0001t0001g0019a0001c0001t0001g0092a0001c0001t0001g0113others(52): Show | 55 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.4356+10851T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583407 | ||||||
| chr3:64583426
|
T | C | 1 | a0028c0043t0003g0194 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4356+10832A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583426 | ||||||
| chr3:64583442
|
G | A | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+10816C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583442 | ||||||
| chr3:64583520
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0002g0184 | 2 | NA18968.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.4356+10738T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583520 | ||||||
| chr3:64583526
|
T | C | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4356+10732A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583526 | ||||||
| chr3:64583679
|
A | G | 4 | a0001c0001t0002g0211a0001c0004t0001g0276a0001c0004t0002g0277others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.4356+10579T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583679 | ||||||
| chr3:64583811
|
C | A | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4356+10447G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583811 | ||||||
| chr3:64583869
|
C | T | 2 | a0001c0001t0002g0246a0025c0033t0003g0261 | 2 | NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.4356+10389G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64583869 | ||||||
| chr3:64584006
|
CG | C | 38 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0103others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.4356+10251delC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584006 | ||||||
| chr3:64584026
|
C | T | 63 | a0001c0001t0001g0019a0001c0001t0001g0092a0001c0001t0001g0113others(60): Show | 63 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.4356+10232G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584026 | ||||||
| chr3:64584123
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0002g0137 | 2 | HG02015.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.4356+10135A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584123 | ||||||
| chr3:64584170
|
C | T | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+10088G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584170 | ||||||
| chr3:64584224
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4356+10034C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584224 | ||||||
| chr3:64584390
|
C | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4356+9868G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584390 | ||||||
| chr3:64584405
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4356+9853T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584405 | ||||||
| chr3:64584677
|
A | T | 3 | a0003c0003t0001g0023a0003c0017t0006g0027a0003c0017t0006g0028 | 3 | HG03195.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4356+9581T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584677 | ||||||
| chr3:64584723
|
A | G | 3 | a0002c0002t0001g0266a0002c0002t0001g0267a0002c0002t0013g0016 | 3 | HG02559.hp2 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4356+9535T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584723 | ||||||
| chr3:64584752
|
C | T | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+9506G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584752 | ||||||
| chr3:64584772
|
CTAT | C | 3 | a0001c0001t0002g0065a0001c0009t0005g0069a0001c0009t0005g0070 | 3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4356+9483_4356+948 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584772 | ||||||
| chr3:64584850
|
T | G | 1 | a0001c0037t0008g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4356+9408A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584850 | ||||||
| chr3:64584973
|
A | C | 9 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4356+9285T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64584973 | ||||||
| chr3:64585012
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.4356+9246T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64585012 | ||||||
| chr3:64585300
|
C | T | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+8958G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64585300 | ||||||
| chr3:64585343
|
C | A | 1 | a0001c0013t0001g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4356+8915G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64585343 | ||||||
| chr3:64585623
|
C | T | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+8635G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64585623 | ||||||
| chr3:64585688
|
C | A | 1 | a0002c0002t0003g0078 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4356+8570G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64585688 | ||||||
| chr3:64585774
|
T | G | 7 | a0001c0001t0001g0067a0001c0013t0001g0145a0001c0013t0001g0212others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4356+8484A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64585774 | ||||||
| chr3:64585804
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4356+8454A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64585804 | ||||||
| chr3:64585814
|
A | C | 2 | a0001c0007t0002g0254a0011c0053t0002g0272 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4356+8444T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64585814 | ||||||
| chr3:64586086
|
T | G | 2 | a0011c0022t0001g0270a0011c0022t0001g0271 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.4356+8172A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586086 | ||||||
| chr3:64586089
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.4356+8169T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586089 | ||||||
| chr3:64586125
|
A | G | 45 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(42): Show | 45 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.4356+8133T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586125 | ||||||
| chr3:64586147
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(11): Show | 15 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.4356+8111C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586147 | ||||||
| chr3:64586150
|
A | G | 22 | a0001c0001t0001g0233a0001c0001t0002g0131a0001c0001t0002g0211others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.4356+8108T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586150 | ||||||
| chr3:64586282
|
T | C | 1 | a0003c0017t0006g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4356+7976A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586282 | ||||||
| chr3:64586339
|
C | A | 135 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0090others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.4356+7919G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586339 | ||||||
| chr3:64586515
|
A | C | 1 | a0009c0028t0007g0275 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4356+7743T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586515 | ||||||
| chr3:64586646
|
G | A | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+7612C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586646 | ||||||
| chr3:64586751
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0209 | 3 | HG01070.hp2 HG01071.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.4356+7507T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586751 | ||||||
| chr3:64586861
|
A | G | 1 | a0001c0013t0011g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4356+7397T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586861 | ||||||
| chr3:64586966
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4356+7292G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586966 | ||||||
| chr3:64586985
|
T | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.4356+7273A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64586985 | ||||||
| chr3:64587038
|
C | G | 10 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(7): Show | 10 | HG02109.hp1 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4356+7220G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587038 | ||||||
| chr3:64587041
|
A | C | 10 | a0001c0001t0001g0133a0001c0001t0020g0213a0002c0002t0001g0220others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4356+7217T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587041 | ||||||
| chr3:64587083
|
G | C | 9 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4356+7175C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587083 | ||||||
| chr3:64587237
|
C | T | 2 | a0001c0001t0001g0103a0003c0003t0002g0057 | 2 | NA18946.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.4356+7021G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587237 | ||||||
| chr3:64587263
|
C | T | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+6995G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587263 | ||||||
| chr3:64587278
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4356+6980T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587278 | ||||||
| chr3:64587351
|
T | G | 1 | a0008c0021t0002g0135 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4356+6907A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587351 | ||||||
| chr3:64587525
|
A | G | 2 | a0001c0007t0002g0254a0011c0053t0002g0272 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4356+6733T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587525 | ||||||
| chr3:64587600
|
T | C | 64 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(61): Show | 64 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.4356+6658A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587600 | ||||||
| chr3:64587650
|
T | C | 3 | a0001c0001t0002g0065a0001c0009t0005g0069a0001c0009t0005g0070 | 3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4356+6608A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587650 | ||||||
| chr3:64587704
|
C | A | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4356+6554G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587704 | ||||||
| chr3:64587809
|
A | G | 23 | a0001c0001t0002g0065a0001c0001t0012g0013a0001c0001t0012g0014others(20): Show | 23 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.4356+6449T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587809 | ||||||
| chr3:64587843
|
A | T | 2 | a0001c0001t0001g0109a0001c0001t0002g0221 | 2 | HG00140.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.4356+6415T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64587843 | ||||||
| chr3:64588075
|
G | A | 6 | a0001c0013t0001g0145a0001c0013t0001g0212a0001c0013t0011g0005others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.4356+6183C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588075 | ||||||
| chr3:64588185
|
T | C | 16 | a0001c0001t0002g0202a0003c0003t0002g0056a0006c0010t0002g0169others(13): Show | 16 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.4356+6073A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588185 | ||||||
| chr3:64588210
|
T | C | 1 | a0001c0001t0002g0129 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4356+6048A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588210 | ||||||
| chr3:64588419
|
A | AT | 15 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.4356+5838dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588419 | ||||||
| chr3:64588419
|
AT | A | 26 | a0001c0001t0001g0092a0001c0001t0002g0065a0001c0001t0002g0100others(23): Show | 26 | HG00544.hp2 HG01123.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.4356+5838delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588419 | ||||||
| chr3:64588466
|
A | G | 10 | a0001c0001t0002g0088a0001c0001t0002g0116a0003c0003t0001g0035others(7): Show | 10 | HG00438.hp2 NA18942.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.4356+5792T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588466 | ||||||
| chr3:64588501
|
C | T | 2 | a0001c0001t0002g0083a0001c0001t0002g0282 | 2 | NA18940.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.4356+5757G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588501 | ||||||
| chr3:64588518
|
C | T | 8 | a0001c0001t0002g0211a0001c0001t0014g0012a0001c0004t0001g0257others(5): Show | 8 | HG02258.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.4356+5740G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588518 | ||||||
| chr3:64588520
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4356+5738G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588520 | ||||||
| chr3:64588625
|
G | T | 6 | a0001c0013t0001g0145a0001c0013t0001g0212a0001c0013t0011g0005others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.4356+5633C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588625 | ||||||
| chr3:64588684
|
C | T | 10 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(7): Show | 10 | HG02109.hp1 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4356+5574G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588684 | ||||||
| chr3:64588846
|
T | G | 16 | a0001c0001t0002g0202a0003c0003t0002g0056a0006c0010t0002g0169others(13): Show | 16 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.4356+5412A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588846 | ||||||
| chr3:64588955
|
A | G | 6 | a0001c0001t0002g0131a0001c0001t0002g0217a0003c0003t0002g0031others(3): Show | 6 | HG00735.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.4356+5303T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588955 | ||||||
| chr3:64588970
|
C | T | 2 | a0002c0002t0003g0107a0003c0003t0001g0041 | 2 | HG02040.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.4356+5288G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588970 | ||||||
| chr3:64588990
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(21): Show | 25 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.4356+5268T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64588990 | ||||||
| chr3:64589166
|
A | T | 4 | a0001c0001t0001g0080a0006c0010t0001g0245a0006c0010t0001g0264others(1): Show | 4 | NA18955.hp2 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.4356+5092T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589166 | ||||||
| chr3:64589248
|
T | G | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4356+5010A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589248 | ||||||
| chr3:64589302
|
A | G | 44 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(41): Show | 44 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.4356+4956T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589302 | ||||||
| chr3:64589433
|
C | T | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4356+4825G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589433 | ||||||
| chr3:64589463
|
C | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4356+4795G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589463 | ||||||
| chr3:64589478
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4356+4780C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589478 | ||||||
| chr3:64589690
|
T | C | 16 | a0001c0001t0002g0202a0003c0003t0002g0056a0006c0010t0002g0169others(13): Show | 16 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.4356+4568A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589690 | ||||||
| chr3:64589774
|
G | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG03139.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4356+4484C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589774 | ||||||
| chr3:64589793
|
G | A | 2 | a0001c0001t0001g0279a0001c0001t0007g0278 | 2 | HG01884.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.4356+4465C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589793 | ||||||
| chr3:64589879
|
A | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0205a0017c0050t0001g0130 | 3 | HG00609.hp1 NA18975.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.4356+4379T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589879 | ||||||
| chr3:64589953
|
G | A | 107 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0090others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.4356+4305C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64589953 | ||||||
| chr3:64590070
|
T | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4356+4188A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590070 | ||||||
| chr3:64590124
|
C | T | 107 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0090others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.4356+4134G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590124 | ||||||
| chr3:64590170
|
T | C | 1 | a0003c0003t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4356+4088A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590170 | ||||||
| chr3:64590409
|
A | T | 2 | a0001c0001t0002g0089a0001c0001t0002g0204 | 2 | HG02056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.4356+3849T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590409 | ||||||
| chr3:64590434
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4356+3824A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590434 | ||||||
| chr3:64590474
|
T | C | 1 | a0012c0018t0006g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4356+3784A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590474 | ||||||
| chr3:64590571
|
A | G | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4356+3687T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590571 | ||||||
| chr3:64590638
|
T | C | 1 | a0001c0009t0005g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4356+3620A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590638 | ||||||
| chr3:64590715
|
A | G | 1 | a0002c0002t0003g0141 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4356+3543T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590715 | ||||||
| chr3:64590837
|
C | T | 4 | a0001c0014t0001g0091a0001c0014t0001g0115a0001c0014t0002g0126others(1): Show | 4 | HG00438.hp1 HG02135.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.4356+3421G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64590837 | ||||||
| chr3:64591091
|
T | C | 16 | a0001c0001t0002g0202a0003c0003t0002g0056a0006c0010t0002g0169others(13): Show | 16 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.4356+3167A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591091 | ||||||
| chr3:64591214
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4356+3044G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591214 | ||||||
| chr3:64591265
|
C | A | 1 | a0002c0002t0003g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4356+2993G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591265 | ||||||
| chr3:64591269
|
G | A | 1 | a0001c0001t0002g0137 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4356+2989C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591269 | ||||||
| chr3:64591311
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4356+2947C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591311 | ||||||
| chr3:64591439
|
C | CA | 7 | a0001c0001t0001g0067a0001c0001t0001g0106a0001c0013t0001g0145others(4): Show | 7 | HG02145.hp2 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4356+2818dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591439 | ||||||
| chr3:64591553
|
A | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4356+2705T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591553 | ||||||
| chr3:64591684
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(10): Show | 14 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+2574A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591684 | ||||||
| chr3:64591790
|
A | G | 16 | a0001c0001t0002g0202a0003c0003t0002g0056a0006c0010t0002g0169others(13): Show | 16 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.4356+2468T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591790 | ||||||
| chr3:64591918
|
G | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(10): Show | 14 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+2340C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64591918 | ||||||
| chr3:64592203
|
C | T | 10 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(7): Show | 10 | HG02109.hp1 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4356+2055G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592203 | ||||||
| chr3:64592229
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0002g0065a0002c0002t0003g0077others(1): Show | 4 | HG02083.hp2 HG03579.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.4356+2029C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592229 | ||||||
| chr3:64592241
|
A | C | 1 | a0001c0001t0003g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4356+2017T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592241 | ||||||
| chr3:64592426
|
T | G | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4356+1832A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592426 | ||||||
| chr3:64592529
|
G | A | 6 | a0001c0001t0001g0233a0002c0002t0001g0266a0002c0002t0001g0267others(3): Show | 6 | HG01070.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4356+1729C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592529 | ||||||
| chr3:64592537
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0007g0278 | 2 | HG01884.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.4356+1721T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592537 | ||||||
| chr3:64592557
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4356+1701A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592557 | ||||||
| chr3:64592640
|
A | G | 1 | a0001c0014t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4356+1618T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592640 | ||||||
| chr3:64592731
|
G | A | 14 | a0006c0010t0002g0169a0007c0011t0004g0086a0007c0011t0004g0156others(11): Show | 14 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356+1527C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592731 | ||||||
| chr3:64592772
|
A | AT | 9 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0233others(6): Show | 9 | HG01070.hp1 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.4356+1485dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592772 | ||||||
| chr3:64592772
|
AT | A | 7 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(4): Show | 7 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.4356+1485delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592772 | ||||||
| chr3:64592785
|
T | G | 1 | a0022c0036t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4356+1473A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592785 | ||||||
| chr3:64592806
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4356+1452G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64592806 | ||||||
| chr3:64593316
|
G | A | 10 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(7): Show | 10 | HG02109.hp1 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4356+942C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593316 | ||||||
| chr3:64593318
|
T | C | 10 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(7): Show | 10 | HG02109.hp1 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4356+940A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593318 | ||||||
| chr3:64593504
|
T | C | 2 | a0001c0001t0020g0213a0003c0003t0002g0060 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4356+754A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593504 | ||||||
| chr3:64593515
|
G | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0226 | 2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4356+743C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593515 | ||||||
| chr3:64593622
|
A | G | 2 | a0001c0007t0002g0254a0011c0053t0002g0272 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4356+636T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593622 | ||||||
| chr3:64593673
|
G | A | 2 | a0014c0041t0001g0280a0014c0054t0001g0283 | 2 | HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.4356+585C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593673 | ||||||
| chr3:64593950
|
GTGTGTGT others(4): Show |
G | 1 | a0001c0001t0003g0262 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4356+297_4356+307d others(13): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593950 | ||||||
| chr3:64593957
|
TATG | T | 3 | a0001c0001t0014g0012a0001c0037t0008g0006a0022c0036t0002g0214 | 3 | HG02615.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4356+298_4356+300d others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593957 | ||||||
| chr3:64593958
|
ATGATG | A | 13 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0004t0001g0061others(10): Show | 13 | HG01070.hp1 HG01255.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.4356+295_4356+299d others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593958 | ||||||
| chr3:64593958
|
ATGATGTG | A | 17 | a0001c0001t0001g0018a0001c0001t0002g0089a0001c0001t0002g0204others(14): Show | 17 | HG00099.hp2 HG00735.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4356+293_4356+299d others(9): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593958 | ||||||
| chr3:64593958
|
ATGATGTG others(2): Show |
A | 51 | a0001c0001t0001g0093a0001c0001t0001g0106a0001c0001t0001g0109others(48): Show | 51 | HG00140.hp1 HG00438.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.4356+291_4356+299d others(11): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593958 | ||||||
| chr3:64593958
|
ATGATGTG others(4): Show |
A | 13 | a0001c0001t0001g0090a0001c0001t0001g0114a0001c0001t0001g0139others(10): Show | 13 | HG00558.hp2 HG02559.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.4356+289_4356+299d others(13): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593958 | ||||||
| chr3:64593958
|
ATGATGTG others(6): Show |
A | 5 | a0001c0001t0002g0137a0001c0020t0002g0258a0001c0020t0014g0011others(2): Show | 5 | HG01257.hp1 NA18906.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.4356+287_4356+299d others(15): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593958 | ||||||
| chr3:64593960
|
GA | G | 5 | a0001c0001t0002g0211a0001c0004t0002g0277a0001c0014t0001g0115others(2): Show | 5 | HG02258.hp1 HG02523.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.4356+297delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593960 | ||||||
| chr3:64593960
|
GATGTGT | G | 8 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(5): Show | 8 | HG02109.hp1 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.4356+292_4356+297d others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593960 | ||||||
| chr3:64593961
|
A | ATG | 53 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0095others(50): Show | 54 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.4356+295_4356+296d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593961 | ||||||
| chr3:64593961
|
A | ATGTG | 22 | a0001c0001t0001g0019a0001c0001t0001g0133a0001c0001t0001g0166others(19): Show | 22 | HG00140.hp2 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.4356+293_4356+296d others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593961 | ||||||
| chr3:64593961
|
A | ATGTGTG | 3 | a0001c0001t0001g0105a0001c0001t0001g0125a0001c0001t0001g0163 | 3 | HG00544.hp1 HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.4356+291_4356+296d others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593961 | ||||||
| chr3:64593961
|
A | G | 2 | a0001c0004t0001g0276a0009c0028t0007g0275 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4356+297T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593961 | ||||||
| chr3:64593961
|
ATG | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0102a0001c0001t0016g0063others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.4356+295_4356+296d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593961 | ||||||
| chr3:64593961
|
ATGTG | A | 9 | a0001c0001t0001g0080a0001c0001t0001g0235a0001c0001t0002g0065others(6): Show | 9 | HG03579.hp2 HG03688.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.4356+293_4356+296d others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64593961 | ||||||
| chr3:64594003
|
A | G | 20 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0211others(17): Show | 20 | HG01070.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.4356+255T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64594003 | ||||||
| chr3:64594105
|
T | C | 3 | a0003c0003t0001g0023a0003c0017t0006g0027a0003c0017t0006g0028 | 3 | HG03195.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4356+153A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64594105 | ||||||
| chr3:64594158
|
T | C | 3 | a0001c0001t0001g0120a0002c0002t0003g0107a0003c0003t0001g0041 | 3 | HG02040.hp1 HG02155.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.4356+100A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 28/39 | chr3 | 64594158 | ||||||
| chr3:64594451
|
GA | G | 17 | a0006c0010t0001g0245a0006c0010t0001g0264a0006c0010t0001g0265others(14): Show | 17 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.4180-18delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594451 | ||||||
| chr3:64594459
|
C | A | 6 | a0002c0002t0003g0141a0002c0002t0003g0144a0002c0002t0003g0149others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.4180-25G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594459 | ||||||
| chr3:64594493
|
C | T | 193 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0080others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.4180-59G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594493 | ||||||
| chr3:64594494
|
C | G | 2 | a0026c0044t0001g0098a0027c0042t0002g0177 | 2 | HG00609.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.4180-60G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594494 | ||||||
| chr3:64594532
|
T | C | 9 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4180-98A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594532 | ||||||
| chr3:64594532
|
T | G | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4180-98A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594532 | ||||||
| chr3:64594545
|
G | A | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4180-111C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594545 | ||||||
| chr3:64594675
|
T | C | 3 | a0001c0014t0001g0091a0001c0014t0001g0115a0001c0014t0002g0126 | 3 | HG00438.hp1 HG02135.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.4180-241A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594675 | ||||||
| chr3:64594739
|
G | A | 3 | a0003c0003t0001g0023a0003c0017t0006g0027a0003c0017t0006g0028 | 3 | HG03195.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4180-305C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594739 | ||||||
| chr3:64594761
|
A | T | 17 | a0006c0010t0001g0245a0006c0010t0001g0264a0006c0010t0001g0265others(14): Show | 17 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.4180-327T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594761 | ||||||
| chr3:64594870
|
T | A | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4180-436A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594870 | ||||||
| chr3:64594873
|
G | A | 3 | a0001c0009t0005g0069a0001c0009t0005g0070a0003c0003t0001g0021 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4180-439C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594873 | ||||||
| chr3:64594953
|
AT | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.4180-520delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594953 | ||||||
| chr3:64594977
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.4180-543A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594977 | ||||||
| chr3:64594978
|
G | A | 1 | a0001c0030t0001g0180 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4180-544C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64594978 | ||||||
| chr3:64595025
|
G | A | 38 | a0001c0001t0001g0103a0001c0001t0001g0167a0001c0001t0001g0189others(35): Show | 38 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.4180-591C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64595025 | ||||||
| chr3:64595079
|
C | CCAAAA | 207 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.4180-650_4180-646d others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64595079 | ||||||
| chr3:64595208
|
G | A | 9 | a0001c0001t0002g0131a0001c0001t0002g0217a0001c0009t0005g0069others(6): Show | 9 | HG00735.hp2 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4180-774C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64595208 | ||||||
| chr3:64595209
|
T | C | 32 | a0001c0001t0001g0067a0001c0001t0001g0133a0001c0001t0001g0233others(29): Show | 32 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.4180-775A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64595209 | ||||||
| chr3:64595515
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0002g0253a0030c0046t0002g0252others(1): Show | 4 | HG00733.hp1 HG00741.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.4180-1081G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64595515 | ||||||
| chr3:64595684
|
G | A | 44 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0102others(41): Show | 44 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.4179+1146C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64595684 | ||||||
| chr3:64595759
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4179+1071C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64595759 | ||||||
| chr3:64595798
|
TC | T | 134 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.4179+1031delG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64595798 | ||||||
| chr3:64596039
|
T | C | 4 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4179+791A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64596039 | ||||||
| chr3:64596057
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(20): Show | 24 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.4179+773C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64596057 | ||||||
| chr3:64596082
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4179+748A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64596082 | ||||||
| chr3:64596227
|
C | A | 2 | a0003c0003t0007g0037a0003c0003t0007g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4179+603G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64596227 | ||||||
| chr3:64596405
|
C | T | 174 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0080others(171): Show | 174 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.4179+425G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64596405 | ||||||
| chr3:64596489
|
TGAA | T | 6 | a0001c0001t0001g0067a0001c0013t0001g0145a0001c0013t0001g0212others(3): Show | 6 | HG02559.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.4179+338_4179+340d others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64596489 | ||||||
| chr3:64596510
|
C | T | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4179+320G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64596510 | ||||||
| chr3:64596812
|
C | G | 6 | a0001c0001t0001g0067a0001c0013t0001g0145a0001c0013t0001g0212others(3): Show | 6 | HG02559.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.4179+18G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 27/39 | chr3 | 64596812 | ||||||
| chr3:64597075
|
A | G | 4 | a0001c0006t0001g0117a0001c0006t0001g0206a0001c0006t0001g0207others(1): Show | 4 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.4018-84T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597075 | ||||||
| chr3:64597176
|
A | G | 6 | a0001c0001t0001g0067a0001c0013t0001g0145a0001c0013t0001g0212others(3): Show | 6 | HG02559.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.4018-185T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597176 | ||||||
| chr3:64597201
|
G | T | 2 | a0003c0003t0007g0037a0003c0003t0007g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4018-210C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597201 | ||||||
| chr3:64597292
|
C | A | 1 | a0001c0001t0001g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4018-301G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597292 | ||||||
| chr3:64597294
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0002g0224others(10): Show | 13 | HG02257.hp2 HG02559.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.4018-303G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597294 | ||||||
| chr3:64597524
|
G | A | 6 | a0001c0001t0001g0128a0001c0001t0001g0171a0002c0002t0003g0123others(3): Show | 6 | HG01099.hp1 HG02056.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.4018-533C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597524 | ||||||
| chr3:64597590
|
C | G | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4018-599G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597590 | ||||||
| chr3:64597656
|
C | T | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4018-665G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597656 | ||||||
| chr3:64597837
|
G | T | 3 | a0001c0014t0001g0091a0001c0014t0001g0115a0001c0014t0002g0126 | 3 | HG00438.hp1 HG02135.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.4018-846C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597837 | ||||||
| chr3:64597880
|
C | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG00544.hp1 HG00558.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.4018-889G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64597880 | ||||||
| chr3:64598020
|
T | C | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4018-1029A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598020 | ||||||
| chr3:64598030
|
C | T | 56 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0106others(53): Show | 56 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4018-1039G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598030 | ||||||
| chr3:64598075
|
T | C | 2 | a0001c0031t0008g0004a0009c0047t0001g0274 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4018-1084A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598075 | ||||||
| chr3:64598082
|
A | T | 14 | a0001c0006t0001g0117a0001c0006t0001g0206a0001c0006t0001g0207others(11): Show | 14 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.4018-1091T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598082 | ||||||
| chr3:64598272
|
T | C | 7 | a0001c0001t0002g0217a0001c0001t0020g0213a0001c0004t0001g0257others(4): Show | 7 | HG00735.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4018-1281A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598272 | ||||||
| chr3:64598274
|
A | T | 11 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(8): Show | 11 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.4018-1283T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598274 | ||||||
| chr3:64598293
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4018-1302A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598293 | ||||||
| chr3:64598319
|
A | AT | 18 | a0001c0001t0001g0133a0001c0001t0002g0065a0001c0001t0002g0184others(15): Show | 18 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.4018-1329dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598319 | ||||||
| chr3:64598319
|
AT | A | 61 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0106others(58): Show | 61 | HG00558.hp2 HG00597.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.4018-1329delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598319 | ||||||
| chr3:64598319
|
ATTTT | A | 10 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(7): Show | 10 | HG02109.hp1 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4018-1332_4018-132 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598319 | ||||||
| chr3:64598345
|
T | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0085others(68): Show | 72 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.4018-1354A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598345 | ||||||
| chr3:64598406
|
C | G | 14 | a0001c0006t0001g0117a0001c0006t0001g0206a0001c0006t0001g0207others(11): Show | 14 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.4018-1415G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598406 | ||||||
| chr3:64598456
|
C | T | 5 | a0001c0001t0001g0079a0002c0002t0001g0121a0002c0002t0003g0122others(2): Show | 5 | NA18955.hp1 NA18974.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.4018-1465G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598456 | ||||||
| chr3:64598494
|
AT | A | 4 | a0001c0001t0001g0092a0001c0001t0002g0147a0008c0021t0002g0134others(1): Show | 4 | HG00544.hp2 HG02027.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.4018-1504delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598494 | ||||||
| chr3:64598501
|
G | C | 4 | a0001c0001t0001g0092a0001c0001t0002g0147a0008c0021t0002g0134others(1): Show | 4 | HG00544.hp2 HG02027.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.4018-1510C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598501 | ||||||
| chr3:64598576
|
T | G | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.4018-1585A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598576 | ||||||
| chr3:64598720
|
T | C | 1 | a0001c0013t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4018-1729A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598720 | ||||||
| chr3:64598780
|
C | T | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.4018-1789G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598780 | ||||||
| chr3:64598971
|
CT | C | 8 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(5): Show | 8 | HG02257.hp2 HG02647.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.4018-1981delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64598971 | ||||||
| chr3:64599104
|
T | C | 50 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0106others(47): Show | 50 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.4018-2113A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599104 | ||||||
| chr3:64599186
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(14): Show | 18 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(15): Show |
intron_variant | MODIFIER | c.4018-2195G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599186 | ||||||
| chr3:64599301
|
T | C | 1 | a0001c0004t0002g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4018-2310A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599301 | ||||||
| chr3:64599302
|
T | C | 1 | a0002c0002t0001g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4018-2311A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599302 | ||||||
| chr3:64599362
|
A | G | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.4018-2371T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599362 | ||||||
| chr3:64599611
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(24): Show | 28 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.4017+2333G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599611 | ||||||
| chr3:64599652
|
A | G | 9 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4017+2292T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599652 | ||||||
| chr3:64599841
|
T | C | 3 | a0001c0009t0005g0069a0001c0009t0005g0070a0003c0003t0001g0021 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4017+2103A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599841 | ||||||
| chr3:64599998
|
C | T | 5 | a0001c0001t0002g0211a0001c0004t0001g0276a0001c0004t0002g0277others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4017+1946G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64599998 | ||||||
| chr3:64600051
|
C | CT | 27 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0109others(24): Show | 27 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.4017+1892dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600051 | ||||||
| chr3:64600051
|
C | CTT | 75 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0085others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.4017+1891_4017+189 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600051 | ||||||
| chr3:64600051
|
C | CTTT | 6 | a0001c0001t0001g0120a0001c0001t0001g0199a0001c0001t0002g0065others(3): Show | 6 | HG02155.hp2 HG02257.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.4017+1890_4017+189 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600051 | ||||||
| chr3:64600051
|
CT | C | 67 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0114others(64): Show | 67 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.4017+1892delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600051 | ||||||
| chr3:64600051
|
CTT | C | 9 | a0001c0001t0002g0202a0003c0003t0001g0023a0003c0003t0002g0056others(6): Show | 9 | HG02258.hp2 HG03195.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.4017+1891_4017+189 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600051 | ||||||
| chr3:64600051
|
CTTT | C | 14 | a0001c0006t0001g0117a0001c0006t0001g0206a0001c0006t0001g0207others(11): Show | 14 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.4017+1890_4017+189 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600051 | ||||||
| chr3:64600115
|
G | T | 8 | a0001c0001t0001g0133a0002c0002t0001g0220a0002c0002t0001g0225others(5): Show | 8 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.4017+1829C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600115 | ||||||
| chr3:64600355
|
G | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.4017+1589C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600355 | ||||||
| chr3:64600654
|
C | T | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.4017+1290G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600654 | ||||||
| chr3:64600775
|
G | C | 5 | a0005c0008t0001g0094a0005c0008t0002g0175a0005c0008t0002g0176others(2): Show | 5 | NA18953.hp1 NA18984.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.4017+1169C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600775 | ||||||
| chr3:64600984
|
G | T | 6 | a0001c0001t0001g0067a0001c0013t0001g0145a0001c0013t0001g0212others(3): Show | 6 | HG02559.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.4017+960C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64600984 | ||||||
| chr3:64601045
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0085others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.4017+899T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64601045 | ||||||
| chr3:64601059
|
T | A | 2 | a0001c0013t0001g0145a0001c0013t0001g0212 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4017+885A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64601059 | ||||||
| chr3:64601136
|
C | T | 1 | a0001c0001t0014g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4017+808G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64601136 | ||||||
| chr3:64601167
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4017+777T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64601167 | ||||||
| chr3:64601431
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4017+513T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64601431 | ||||||
| chr3:64601512
|
C | G | 1 | a0001c0001t0001g0231 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4017+432G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64601512 | ||||||
| chr3:64601870
|
G | T | 1 | a0022c0036t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4017+74C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64601870 | ||||||
| chr3:64601886
|
T | G | 17 | a0001c0001t0001g0067a0001c0001t0001g0133a0001c0001t0020g0213others(14): Show | 17 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.4017+58A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 26/39 | chr3 | 64601886 | ||||||
| chr3:64602498
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.3748-285G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602498 | ||||||
| chr3:64602529
|
T | A | 1 | a0001c0001t0014g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3748-316A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602529 | ||||||
| chr3:64602564
|
C | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3748-351G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602564 | ||||||
| chr3:64602632
|
T | A | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3748-419A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602632 | ||||||
| chr3:64602679
|
T | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(25): Show | 29 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.3748-466A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602679 | ||||||
| chr3:64602825
|
T | C | 1 | a0002c0002t0003g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3748-612A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602825 | ||||||
| chr3:64602849
|
A | G | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3748-636T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602849 | ||||||
| chr3:64602890
|
G | A | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3748-677C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602890 | ||||||
| chr3:64602915
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3748-702G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602915 | ||||||
| chr3:64602937
|
C | G | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3748-724G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64602937 | ||||||
| chr3:64603085
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3747+837C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64603085 | ||||||
| chr3:64603244
|
G | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.3747+678C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64603244 | ||||||
| chr3:64603286
|
T | A | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3747+636A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64603286 | ||||||
| chr3:64603331
|
T | A | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.3747+591A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64603331 | ||||||
| chr3:64603419
|
T | TA | 122 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.3747+502dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64603419 | ||||||
| chr3:64603419
|
T | TAA | 15 | a0001c0001t0001g0133a0001c0001t0020g0213a0001c0013t0001g0145others(12): Show | 15 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.3747+501_3747+502d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64603419 | ||||||
| chr3:64603472
|
G | A | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3747+450C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 25/39 | chr3 | 64603472 | ||||||
| chr3:64604131
|
T | C | 8 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(5): Show | 8 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3580-42A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 24/39 | chr3 | 64604131 | ||||||
| chr3:64604175
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.3579+52T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 24/39 | chr3 | 64604175 | ||||||
| chr3:64604596
|
T | A | 2 | a0014c0041t0001g0280a0014c0054t0001g0283 | 2 | HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.3475-265A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64604596 | ||||||
| chr3:64604687
|
C | T | 26 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(23): Show | 26 | HG01257.hp1 HG01884.hp1 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.3475-356G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64604687 | ||||||
| chr3:64604690
|
T | C | 10 | a0001c0001t0001g0133a0001c0001t0020g0213a0002c0002t0001g0220others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.3475-359A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64604690 | ||||||
| chr3:64604732
|
TC | T | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.3475-402delG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64604732 | ||||||
| chr3:64604904
|
C | T | 26 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(23): Show | 26 | HG01257.hp1 HG01884.hp1 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.3475-573G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64604904 | ||||||
| chr3:64605024
|
G | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.3475-693C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605024 | ||||||
| chr3:64605067
|
C | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.3475-736G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605067 | ||||||
| chr3:64605121
|
T | C | 1 | a0001c0007t0002g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3475-790A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605121 | ||||||
| chr3:64605292
|
G | A | 8 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(5): Show | 8 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3475-961C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605292 | ||||||
| chr3:64605401
|
G | A | 2 | a0001c0037t0008g0006a0002c0002t0001g0220 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.3475-1070C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605401 | ||||||
| chr3:64605405
|
CAT | C | 40 | a0001c0001t0001g0103a0001c0001t0001g0168a0001c0001t0001g0189others(37): Show | 40 | HG00597.hp1 HG00621.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.3475-1076_3475-107 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605405 | ||||||
| chr3:64605437
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3475-1106T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605437 | ||||||
| chr3:64605505
|
G | A | 11 | a0001c0007t0001g0017a0001c0007t0002g0062a0001c0007t0002g0219others(8): Show | 11 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.3475-1174C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605505 | ||||||
| chr3:64605637
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(7): Show | 11 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.3475-1306C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64605637 | ||||||
| chr3:64606135
|
T | A | 3 | a0001c0009t0005g0071a0001c0009t0005g0072a0001c0009t0005g0073 | 3 | HG01934.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3474+825A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64606135 | ||||||
| chr3:64606152
|
A | G | 6 | a0001c0001t0002g0211a0001c0004t0001g0276a0001c0004t0002g0277others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3474+808T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64606152 | ||||||
| chr3:64606237
|
A | T | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3474+723T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64606237 | ||||||
| chr3:64606322
|
C | T | 43 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(40): Show | 43 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.3474+638G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64606322 | ||||||
| chr3:64606376
|
A | G | 2 | a0001c0037t0008g0006a0002c0002t0001g0220 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.3474+584T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64606376 | ||||||
| chr3:64606757
|
C | T | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3474+203G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64606757 | ||||||
| chr3:64606902
|
G | A | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3474+58C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 23/39 | chr3 | 64606902 | ||||||
| chr3:64607208
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3355-129G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607208 | ||||||
| chr3:64607251
|
T | A | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3355-172A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607251 | ||||||
| chr3:64607318
|
C | T | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3355-239G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607318 | ||||||
| chr3:64607342
|
G | T | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3355-263C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607342 | ||||||
| chr3:64607393
|
G | A | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3355-314C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607393 | ||||||
| chr3:64607451
|
A | G | 2 | a0001c0001t0001g0201a0002c0002t0003g0165 | 2 | HG02015.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.3355-372T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607451 | ||||||
| chr3:64607641
|
A | C | 1 | a0001c0001t0001g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3355-562T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607641 | ||||||
| chr3:64607808
|
T | C | 1 | a0001c0001t0002g0244 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3355-729A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607808 | ||||||
| chr3:64607855
|
C | T | 6 | a0001c0001t0001g0128a0001c0001t0001g0171a0002c0002t0003g0123others(3): Show | 6 | HG01099.hp1 HG02056.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.3355-776G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607855 | ||||||
| chr3:64607856
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3355-777C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607856 | ||||||
| chr3:64607964
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3355-885G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607964 | ||||||
| chr3:64607972
|
G | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.3355-893C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64607972 | ||||||
| chr3:64608173
|
GA | G | 129 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(126): Show | 129 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.3355-1095delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608173 | ||||||
| chr3:64608173
|
GAA | G | 9 | a0001c0001t0001g0133a0001c0006t0010g0007a0002c0002t0001g0225others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.3355-1096_3355-109 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608173 | ||||||
| chr3:64608258
|
C | CA | 68 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(65): Show | 68 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.3355-1180dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608258 | ||||||
| chr3:64608258
|
C | CAA | 13 | a0001c0001t0001g0120a0001c0001t0001g0167a0001c0001t0001g0168others(10): Show | 13 | HG02109.hp1 HG02148.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.3355-1181_3355-118 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608258 | ||||||
| chr3:64608258
|
CA | C | 30 | a0001c0001t0001g0018a0001c0001t0001g0096a0001c0001t0001g0279others(27): Show | 30 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.3355-1180delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608258 | ||||||
| chr3:64608258
|
CAA | C | 8 | a0001c0001t0002g0202a0001c0004t0001g0257a0001c0009t0005g0069others(5): Show | 8 | HG02135.hp2 HG02896.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.3355-1181_3355-118 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608258 | ||||||
| chr3:64608415
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3355-1336G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608415 | ||||||
| chr3:64608450
|
G | A | 138 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(135): Show | 138 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.3355-1371C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608450 | ||||||
| chr3:64608455
|
T | A | 1 | a0018c0048t0002g0081 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3355-1376A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608455 | ||||||
| chr3:64608616
|
T | C | 2 | a0001c0001t0002g0246a0025c0033t0003g0261 | 2 | NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3355-1537A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608616 | ||||||
| chr3:64608686
|
A | G | 55 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(52): Show | 55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.3355-1607T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608686 | ||||||
| chr3:64608740
|
G | GA | 18 | a0001c0001t0001g0209a0001c0001t0002g0065a0001c0001t0002g0217others(15): Show | 18 | HG00438.hp1 HG00735.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.3355-1662dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608740 | ||||||
| chr3:64608740
|
GA | G | 8 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG00558.hp1 HG02027.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3355-1662delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608740 | ||||||
| chr3:64608784
|
C | G | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3355-1705G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608784 | ||||||
| chr3:64608798
|
T | C | 144 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(141): Show | 144 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3355-1719A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608798 | ||||||
| chr3:64608807
|
C | A | 143 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(140): Show | 143 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.3355-1728G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608807 | ||||||
| chr3:64608853
|
T | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.3355-1774A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608853 | ||||||
| chr3:64608927
|
T | C | 144 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(141): Show | 144 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3355-1848A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608927 | ||||||
| chr3:64608994
|
C | T | 2 | a0001c0007t0001g0017a0001c0007t0002g0062 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3355-1915G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64608994 | ||||||
| chr3:64609024
|
AC | A | 42 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0106others(39): Show | 42 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.3355-1946delG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609024 | ||||||
| chr3:64609025
|
C | A | 48 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(45): Show | 48 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.3355-1946G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609025 | ||||||
| chr3:64609077
|
T | C | 2 | a0001c0001t0002g0172a0012c0018t0006g0173 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3355-1998A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609077 | ||||||
| chr3:64609090
|
C | T | 2 | a0001c0037t0008g0006a0002c0002t0001g0220 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.3355-2011G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609090 | ||||||
| chr3:64609161
|
C | T | 1 | a0025c0033t0003g0261 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3355-2082G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609161 | ||||||
| chr3:64609173
|
T | C | 2 | a0003c0025t0001g0026a0004c0026t0001g0029 | 2 | HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3355-2094A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609173 | ||||||
| chr3:64609286
|
G | C | 1 | a0009c0029t0002g0237 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3355-2207C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609286 | ||||||
| chr3:64609510
|
A | T | 136 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0080others(133): Show | 136 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.3355-2431T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609510 | ||||||
| chr3:64609703
|
G | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.3355-2624C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609703 | ||||||
| chr3:64609776
|
C | T | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3355-2697G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609776 | ||||||
| chr3:64609830
|
T | C | 49 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(46): Show | 49 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.3355-2751A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609830 | ||||||
| chr3:64609895
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0095others(21): Show | 25 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(22): Show |
intron_variant | MODIFIER | c.3355-2816G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609895 | ||||||
| chr3:64609914
|
T | C | 111 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(108): Show | 111 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.3355-2835A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64609914 | ||||||
| chr3:64610080
|
T | G | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3355-3001A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610080 | ||||||
| chr3:64610140
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.3355-3061T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610140 | ||||||
| chr3:64610153
|
C | G | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3355-3074G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610153 | ||||||
| chr3:64610202
|
C | T | 2 | a0001c0031t0008g0004a0009c0047t0001g0274 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3355-3123G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610202 | ||||||
| chr3:64610207
|
A | ATGACTTC others(19): Show |
1 | a0001c0001t0001g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3354+3112_3355-312 others(30): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610207 | ||||||
| chr3:64610207
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3355-3128T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610207 | ||||||
| chr3:64610211
|
C | T | 1 | a0002c0002t0003g0150 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3355-3132G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610211 | ||||||
| chr3:64610223
|
C | T | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3354+3122G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610223 | ||||||
| chr3:64610229
|
C | A | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3354+3116G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610229 | ||||||
| chr3:64610251
|
A | T | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3354+3094T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610251 | ||||||
| chr3:64610396
|
C | T | 15 | a0001c0001t0002g0065a0001c0001t0002g0217a0001c0001t0020g0213others(12): Show | 15 | HG00438.hp1 HG00735.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.3354+2949G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610396 | ||||||
| chr3:64610505
|
AT | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.3354+2839delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610505 | ||||||
| chr3:64610514
|
T | A | 3 | a0001c0014t0001g0115a0002c0002t0003g0160a0013c0019t0004g0161 | 3 | HG02523.hp1 NA19062.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.3354+2831A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610514 | ||||||
| chr3:64610544
|
C | G | 101 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(98): Show | 101 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.3354+2801G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610544 | ||||||
| chr3:64610602
|
C | A | 4 | a0001c0006t0001g0117a0001c0006t0001g0206a0001c0006t0001g0207others(1): Show | 4 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.3354+2743G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610602 | ||||||
| chr3:64610667
|
A | T | 13 | a0001c0001t0002g0241a0001c0001t0002g0248a0006c0010t0001g0245others(10): Show | 13 | HG01123.hp1 HG01255.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.3354+2678T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610667 | ||||||
| chr3:64610858
|
C | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3354+2487G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610858 | ||||||
| chr3:64610934
|
G | A | 4 | a0001c0006t0001g0117a0001c0006t0001g0206a0001c0006t0001g0207others(1): Show | 4 | HG00099.hp2 HG01257.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.3354+2411C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610934 | ||||||
| chr3:64610995
|
G | C | 3 | a0001c0001t0001g0120a0002c0002t0003g0107a0003c0003t0001g0041 | 3 | HG02040.hp1 HG02155.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.3354+2350C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64610995 | ||||||
| chr3:64611075
|
C | CA | 11 | a0001c0001t0001g0096a0001c0001t0001g0113a0001c0001t0001g0159others(8): Show | 11 | HG00741.hp2 HG02145.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.3354+2269dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611075 | ||||||
| chr3:64611075
|
CAA | C | 21 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0002g0131others(18): Show | 21 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.3354+2268_3354+226 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611075 | ||||||
| chr3:64611075
|
CAAA | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0080others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.3354+2267_3354+226 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611075 | ||||||
| chr3:64611075
|
CAAAA | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0090a0001c0001t0001g0105others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.3354+2266_3354+226 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611075 | ||||||
| chr3:64611135
|
C | T | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3354+2210G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611135 | ||||||
| chr3:64611282
|
G | T | 8 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0131others(5): Show | 8 | HG01070.hp1 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.3354+2063C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611282 | ||||||
| chr3:64611355
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.3354+1990G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611355 | ||||||
| chr3:64611430
|
C | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.3354+1915G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611430 | ||||||
| chr3:64611671
|
T | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.3354+1674A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611671 | ||||||
| chr3:64611750
|
A | C | 4 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3354+1595T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611750 | ||||||
| chr3:64611929
|
T | C | 14 | a0001c0001t0002g0217a0001c0001t0020g0213a0001c0009t0005g0069others(11): Show | 14 | HG00438.hp1 HG00735.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.3354+1416A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611929 | ||||||
| chr3:64611932
|
G | A | 18 | a0001c0001t0001g0279a0001c0001t0002g0202a0001c0001t0007g0278others(15): Show | 18 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3354+1413C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611932 | ||||||
| chr3:64611974
|
A | G | 18 | a0001c0001t0001g0279a0001c0001t0002g0202a0001c0001t0007g0278others(15): Show | 18 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3354+1371T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64611974 | ||||||
| chr3:64612098
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3354+1247A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612098 | ||||||
| chr3:64612146
|
C | T | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3354+1199G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612146 | ||||||
| chr3:64612204
|
GA | G | 14 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(11): Show | 14 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3354+1140delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612204 | ||||||
| chr3:64612287
|
C | T | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3354+1058G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612287 | ||||||
| chr3:64612424
|
A | T | 3 | a0001c0001t0002g0211a0001c0004t0001g0276a0001c0004t0002g0277 | 3 | HG02258.hp1 HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3354+921T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612424 | ||||||
| chr3:64612433
|
A | T | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3354+912T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612433 | ||||||
| chr3:64612444
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3354+901A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612444 | ||||||
| chr3:64612571
|
A | T | 1 | a0001c0001t0001g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3354+774T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612571 | ||||||
| chr3:64612627
|
C | T | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3354+718G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612627 | ||||||
| chr3:64612643
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3354+702C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612643 | ||||||
| chr3:64612644
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3354+701G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612644 | ||||||
| chr3:64612646
|
G | A | 1 | a0001c0001t0020g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3354+699C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612646 | ||||||
| chr3:64612851
|
A | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3354+494T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612851 | ||||||
| chr3:64612978
|
C | A | 3 | a0001c0001t0001g0233a0003c0003t0001g0022a0003c0003t0001g0033 | 3 | HG01070.hp1 HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3354+367G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612978 | ||||||
| chr3:64612996
|
G | A | 1 | a0003c0003t0002g0057 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3354+349C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612996 | ||||||
| chr3:64612999
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3354+346C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64612999 | ||||||
| chr3:64613001
|
A | G | 1 | a0027c0042t0002g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3354+344T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613001 | ||||||
| chr3:64613083
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3354+262G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613083 | ||||||
| chr3:64613084
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3354+261T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613084 | ||||||
| chr3:64613084
|
A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.3354+261T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613084 | ||||||
| chr3:64613085
|
C | G | 4 | a0001c0001t0001g0090a0001c0009t0005g0071a0001c0009t0005g0072others(1): Show | 4 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3354+260G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613085 | ||||||
| chr3:64613178
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3354+167C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613178 | ||||||
| chr3:64613180
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3354+165G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613180 | ||||||
| chr3:64613188
|
T | C | 131 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(128): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.3354+157A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613188 | ||||||
| chr3:64613235
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3354+110A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613235 | ||||||
| chr3:64613333
|
C | T | 2 | a0001c0037t0008g0006a0002c0002t0001g0220 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.3354+12G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613333 | ||||||
| chr3:64613337
|
C | A | 5 | a0001c0004t0001g0236a0001c0004t0001g0238a0001c0004t0001g0239others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02922.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.3354+8G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 22/39 | chr3 | 64613337 | ||||||
| chr3:64613542
|
T | G | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3190-33A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64613542 | ||||||
| chr3:64613603
|
T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0095others(34): Show | 38 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.3190-94A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64613603 | ||||||
| chr3:64613673
|
G | A | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3190-164C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64613673 | ||||||
| chr3:64613710
|
G | A | 2 | a0001c0037t0008g0006a0002c0002t0001g0220 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.3190-201C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64613710 | ||||||
| chr3:64613753
|
A | C | 18 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0131others(15): Show | 18 | HG01070.hp1 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.3190-244T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64613753 | ||||||
| chr3:64613859
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(14): Show | 18 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(15): Show |
intron_variant | MODIFIER | c.3190-350C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64613859 | ||||||
| chr3:64613878
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3190-369A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64613878 | ||||||
| chr3:64613944
|
A | G | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3190-435T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64613944 | ||||||
| chr3:64614077
|
G | A | 8 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(5): Show | 8 | HG00438.hp1 HG01934.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.3190-568C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614077 | ||||||
| chr3:64614123
|
G | A | 12 | a0001c0001t0001g0067a0001c0007t0001g0017a0001c0007t0002g0062others(9): Show | 12 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.3190-614C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614123 | ||||||
| chr3:64614310
|
C | A | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3190-801G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614310 | ||||||
| chr3:64614484
|
G | C | 3 | a0001c0001t0001g0120a0002c0002t0003g0107a0003c0003t0001g0041 | 3 | HG02040.hp1 HG02155.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.3189+837C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614484 | ||||||
| chr3:64614508
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3189+813C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614508 | ||||||
| chr3:64614616
|
G | A | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3189+705C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614616 | ||||||
| chr3:64614674
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3189+647A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614674 | ||||||
| chr3:64614726
|
CTT | C | 10 | a0001c0001t0001g0233a0001c0001t0002g0131a0001c0001t0012g0013others(7): Show | 10 | HG01070.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3189+593_3189+594d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614726 | ||||||
| chr3:64614829
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3189+492G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614829 | ||||||
| chr3:64614839
|
CT | C | 134 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(131): Show | 134 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.3189+481delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614839 | ||||||
| chr3:64614854
|
C | T | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.3189+467G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64614854 | ||||||
| chr3:64615144
|
C | T | 1 | a0002c0002t0003g0150 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3189+177G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64615144 | ||||||
| chr3:64615153
|
C | T | 98 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3189+168G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64615153 | ||||||
| chr3:64615182
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3189+139T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64615182 | ||||||
| chr3:64615291
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0003g0262 | 2 | HG00597.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.3189+30G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 21/39 | chr3 | 64615291 | ||||||
| chr3:64615564
|
C | G | 1 | a0001c0001t0001g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3025-79G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 20/39 | chr3 | 64615564 | ||||||
| chr3:64615645
|
T | A | 5 | a0001c0004t0001g0236a0001c0004t0001g0238a0001c0004t0001g0239others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3025-160A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 20/39 | chr3 | 64615645 | ||||||
| chr3:64615699
|
C | T | 115 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(112): Show | 115 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.3025-214G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 20/39 | chr3 | 64615699 | ||||||
| chr3:64615748
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3024+212A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 20/39 | chr3 | 64615748 | ||||||
| chr3:64615866
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3024+94C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 20/39 | chr3 | 64615866 | ||||||
| chr3:64615874
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.3024+86A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 20/39 | chr3 | 64615874 | ||||||
| chr3:64616186
|
G | A | 1 | a0018c0048t0002g0081 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2814-16C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616186 | ||||||
| chr3:64616227
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2814-57A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616227 | ||||||
| chr3:64616330
|
A | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0095others(31): Show | 35 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.2814-160T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616330 | ||||||
| chr3:64616370
|
T | C | 8 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(5): Show | 8 | HG00438.hp1 HG01934.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2814-200A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616370 | ||||||
| chr3:64616402
|
C | T | 1 | a0002c0002t0003g0149 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2814-232G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616402 | ||||||
| chr3:64616460
|
C | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2814-290G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616460 | ||||||
| chr3:64616462
|
T | A | 13 | a0001c0001t0001g0183a0001c0001t0001g0279a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2814-292A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616462 | ||||||
| chr3:64616527
|
GAAGACAT others(3): Show |
G | 29 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(26): Show | 30 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.2814-367_2814-358d others(12): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616527 | ||||||
| chr3:64616549
|
A | G | 2 | a0001c0004t0001g0061a0002c0002t0008g0009 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2814-379T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616549 | ||||||
| chr3:64616634
|
G | T | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2814-464C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616634 | ||||||
| chr3:64616691
|
C | A | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2814-521G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616691 | ||||||
| chr3:64616725
|
A | G | 2 | a0003c0003t0002g0031a0004c0005t0001g0030 | 2 | HG00735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2814-555T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616725 | ||||||
| chr3:64616926
|
T | C | 8 | a0001c0001t0002g0211a0001c0001t0014g0012a0001c0004t0001g0276others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2814-756A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64616926 | ||||||
| chr3:64617210
|
T | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.2814-1040A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64617210 | ||||||
| chr3:64617239
|
C | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2814-1069G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64617239 | ||||||
| chr3:64617297
|
A | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2814-1127T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64617297 | ||||||
| chr3:64617338
|
C | T | 1 | a0017c0050t0001g0130 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2814-1168G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64617338 | ||||||
| chr3:64617555
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2814-1385A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64617555 | ||||||
| chr3:64617629
|
G | GA | 6 | a0001c0001t0002g0202a0003c0003t0002g0056a0003c0003t0002g0058others(3): Show | 6 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.2814-1460dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64617629 | ||||||
| chr3:64617905
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(180): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2814-1735A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64617905 | ||||||
| chr3:64617978
|
C | T | 43 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0087others(40): Show | 43 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2814-1808G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64617978 | ||||||
| chr3:64618182
|
T | C | 1 | a0015c0015t0002g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2814-2012A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64618182 | ||||||
| chr3:64618312
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2814-2142C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64618312 | ||||||
| chr3:64618357
|
T | C | 1 | a0004c0005t0001g0032 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2814-2187A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64618357 | ||||||
| chr3:64618503
|
G | A | 4 | a0001c0001t0002g0129a0002c0002t0003g0142a0005c0008t0003g0192others(1): Show | 4 | NA18968.hp2 NA18985.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814-2333C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64618503 | ||||||
| chr3:64618853
|
G | A | 1 | a0003c0003t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2813+2261C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64618853 | ||||||
| chr3:64618931
|
T | C | 2 | a0003c0025t0001g0026a0004c0026t0001g0029 | 2 | HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2813+2183A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64618931 | ||||||
| chr3:64618983
|
T | G | 4 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2813+2131A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64618983 | ||||||
| chr3:64619125
|
C | T | 2 | a0001c0001t0001g0234a0001c0023t0001g0020 | 2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2813+1989G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619125 | ||||||
| chr3:64619228
|
C | G | 4 | a0001c0001t0002g0129a0002c0002t0003g0142a0005c0008t0003g0192others(1): Show | 4 | NA18968.hp2 NA18985.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2813+1886G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619228 | ||||||
| chr3:64619233
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2813+1881A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619233 | ||||||
| chr3:64619256
|
A | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0187 | 2 | NA19003.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2813+1858T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619256 | ||||||
| chr3:64619312
|
T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(17): Show | 21 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(18): Show |
intron_variant | MODIFIER | c.2813+1802A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619312 | ||||||
| chr3:64619443
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(28): Show | 32 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.2813+1671T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619443 | ||||||
| chr3:64619497
|
G | A | 6 | a0001c0001t0002g0076a0001c0001t0002g0083a0001c0001t0002g0084others(3): Show | 6 | NA18940.hp1 NA18960.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.2813+1617C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619497 | ||||||
| chr3:64619503
|
C | T | 1 | a0017c0050t0001g0130 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2813+1611G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619503 | ||||||
| chr3:64619570
|
G | T | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2813+1544C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619570 | ||||||
| chr3:64619652
|
G | T | 5 | a0005c0008t0001g0094a0005c0008t0002g0175a0005c0008t0002g0176others(2): Show | 5 | NA18953.hp1 NA18984.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813+1462C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619652 | ||||||
| chr3:64619682
|
G | A | 92 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(89): Show | 92 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.2813+1432C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619682 | ||||||
| chr3:64619705
|
G | T | 1 | a0002c0002t0003g0149 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2813+1409C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619705 | ||||||
| chr3:64619721
|
T | C | 1 | a0002c0002t0003g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2813+1393A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619721 | ||||||
| chr3:64619721
|
T | G | 8 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0002g0131others(5): Show | 8 | HG01070.hp1 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2813+1393A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619721 | ||||||
| chr3:64619724
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2813+1390G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619724 | ||||||
| chr3:64619845
|
C | A | 24 | a0001c0001t0001g0067a0001c0001t0001g0233a0001c0001t0001g0279others(21): Show | 24 | HG01070.hp1 HG01884.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.2813+1269G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64619845 | ||||||
| chr3:64620010
|
CT | C | 3 | a0001c0007t0001g0017a0001c0007t0002g0062a0001c0007t0013g0015 | 3 | HG02723.hp2 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2813+1103delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620010 | ||||||
| chr3:64620016
|
G | GT | 8 | a0001c0001t0001g0183a0001c0001t0002g0202a0001c0045t0001g0068others(5): Show | 8 | HG02040.hp1 HG03927.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.2813+1097dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620016 | ||||||
| chr3:64620157
|
G | A | 7 | a0001c0001t0002g0217a0001c0001t0020g0213a0001c0004t0001g0257others(4): Show | 7 | HG00735.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2813+957C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620157 | ||||||
| chr3:64620179
|
A | G | 123 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0080others(120): Show | 123 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.2813+935T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620179 | ||||||
| chr3:64620236
|
A | G | 2 | a0001c0037t0008g0006a0002c0002t0001g0220 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2813+878T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620236 | ||||||
| chr3:64620272
|
C | A | 181 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(178): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2813+842G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620272 | ||||||
| chr3:64620387
|
T | C | 1 | a0001c0007t0001g0017 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2813+727A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620387 | ||||||
| chr3:64620420
|
T | TAAAAGGA others(330): Show |
1 | a0003c0003t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2813+693_2813+694i others(339): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620420 | ||||||
| chr3:64620420
|
T | TAAAAGGA others(328): Show |
5 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813+693_2813+694i others(337): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620420 | ||||||
| chr3:64620420
|
T | TAAAAGGA others(330): Show |
2 | a0001c0014t0001g0091a0001c0014t0002g0126 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2813+693_2813+694i others(339): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620420 | ||||||
| chr3:64620491
|
C | T | 112 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0080others(109): Show | 112 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2813+623G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620491 | ||||||
| chr3:64620555
|
C | T | 4 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0282others(1): Show | 4 | NA18940.hp1 NA18960.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.2813+559G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620555 | ||||||
| chr3:64620665
|
C | T | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2813+449G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620665 | ||||||
| chr3:64620666
|
G | A | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2813+448C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620666 | ||||||
| chr3:64620715
|
G | C | 12 | a0001c0001t0001g0109a0001c0001t0002g0211a0001c0001t0002g0221others(9): Show | 12 | HG00140.hp1 HG01123.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2813+399C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620715 | ||||||
| chr3:64620772
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2813+342G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620772 | ||||||
| chr3:64620806
|
T | C | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2813+308A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620806 | ||||||
| chr3:64620821
|
C | T | 1 | a0023c0039t0002g0146 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2813+293G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620821 | ||||||
| chr3:64620991
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2813+123A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 19/39 | chr3 | 64620991 | ||||||
| chr3:64621254
|
GA | G | 9 | a0001c0007t0001g0017a0001c0007t0002g0062a0001c0007t0002g0219others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2687-15delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621254 | ||||||
| chr3:64621636
|
C | A | 6 | a0001c0001t0002g0217a0001c0004t0001g0257a0003c0003t0002g0031others(3): Show | 6 | HG00735.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2687-396G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621636 | ||||||
| chr3:64621637
|
C | G | 6 | a0001c0001t0002g0217a0001c0004t0001g0257a0003c0003t0002g0031others(3): Show | 6 | HG00735.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2687-397G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621637 | ||||||
| chr3:64621761
|
CAAAAAAA others(1): Show |
C | 9 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0009t0005g0071others(6): Show | 9 | HG00438.hp1 HG01934.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.2686+429_2686+436d others(10): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621761 | ||||||
| chr3:64621777
|
T | G | 6 | a0001c0001t0002g0217a0001c0004t0001g0257a0003c0003t0002g0031others(3): Show | 6 | HG00735.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2686+421A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621777 | ||||||
| chr3:64621785
|
T | G | 14 | a0001c0001t0002g0202a0001c0001t0002g0217a0001c0004t0001g0257others(11): Show | 14 | HG00735.hp2 HG01257.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2686+413A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621785 | ||||||
| chr3:64621785
|
T | TA | 17 | a0001c0001t0001g0133a0001c0001t0002g0065a0001c0001t0020g0213others(14): Show | 17 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2686+412dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621785 | ||||||
| chr3:64621787
|
AAAAAAT | A | 29 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0106others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.2686+405_2686+410d others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621787 | ||||||
| chr3:64621792
|
AT | A | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2686+405delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621792 | ||||||
| chr3:64621793
|
T | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0095others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.2686+405A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621793 | ||||||
| chr3:64621793
|
T | TA | 70 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0085others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.2686+404dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621793 | ||||||
| chr3:64621798
|
A | AG | 4 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2686+399dupC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621798 | ||||||
| chr3:64621811
|
A | C | 1 | a0001c0001t0002g0108 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2686+387T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621811 | ||||||
| chr3:64621940
|
A | G | 13 | a0001c0001t0002g0217a0001c0009t0005g0069a0001c0009t0005g0070others(10): Show | 13 | HG00438.hp1 HG00735.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2686+258T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64621940 | ||||||
| chr3:64622011
|
T | A | 12 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0061others(9): Show | 12 | HG01884.hp1 HG01952.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2686+187A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 18/39 | chr3 | 64622011 | ||||||
| chr3:64622879
|
T | A | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2390-293A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64622879 | ||||||
| chr3:64622909
|
A | G | 11 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0236others(8): Show | 11 | HG01884.hp1 HG01952.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2390-323T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64622909 | ||||||
| chr3:64622990
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(28): Show | 32 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.2390-404T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64622990 | ||||||
| chr3:64623006
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2390-420T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64623006 | ||||||
| chr3:64623050
|
C | G | 2 | a0001c0014t0001g0091a0001c0014t0002g0126 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2390-464G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64623050 | ||||||
| chr3:64623276
|
G | A | 4 | a0001c0004t0001g0061a0003c0003t0001g0023a0003c0017t0006g0027others(1): Show | 4 | HG03195.hp1 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2390-690C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64623276 | ||||||
| chr3:64623523
|
G | A | 138 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(135): Show | 138 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.2390-937C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64623523 | ||||||
| chr3:64623558
|
T | C | 139 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(136): Show | 139 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.2390-972A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64623558 | ||||||
| chr3:64623634
|
C | T | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2390-1048G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64623634 | ||||||
| chr3:64623635
|
C | A | 134 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(131): Show | 134 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.2390-1049G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64623635 | ||||||
| chr3:64623697
|
C | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2390-1111G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64623697 | ||||||
| chr3:64624264
|
A | C | 9 | a0001c0001t0001g0132a0001c0001t0001g0163a0001c0001t0002g0089others(6): Show | 9 | HG00544.hp1 HG02015.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2390-1678T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624264 | ||||||
| chr3:64624278
|
G | A | 3 | a0001c0001t0001g0189a0002c0002t0003g0077a0002c0002t0003g0078 | 3 | HG02083.hp2 NA19011.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2390-1692C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624278 | ||||||
| chr3:64624345
|
A | C | 1 | a0001c0001t0002g0110 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2390-1759T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624345 | ||||||
| chr3:64624437
|
T | C | 1 | a0003c0003t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2390-1851A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624437 | ||||||
| chr3:64624440
|
G | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(15): Show | 19 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(16): Show |
intron_variant | MODIFIER | c.2390-1854C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624440 | ||||||
| chr3:64624498
|
A | G | 3 | a0001c0001t0002g0228a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG03139.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2390-1912T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624498 | ||||||
| chr3:64624609
|
T | C | 14 | a0001c0001t0001g0133a0001c0001t0002g0065a0001c0001t0012g0013others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2390-2023A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624609 | ||||||
| chr3:64624636
|
A | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2390-2050T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624636 | ||||||
| chr3:64624789
|
AAATT | A | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2390-2207_2390-220 others(8): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624789 | ||||||
| chr3:64624805
|
T | G | 2 | a0001c0001t0002g0172a0012c0018t0006g0173 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2390-2219A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624805 | ||||||
| chr3:64624850
|
T | A | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2390-2264A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624850 | ||||||
| chr3:64624854
|
A | G | 8 | a0001c0007t0002g0062a0001c0007t0002g0219a0001c0007t0002g0254others(5): Show | 8 | HG02109.hp1 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2390-2268T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624854 | ||||||
| chr3:64624878
|
G | A | 17 | a0001c0001t0002g0217a0001c0009t0005g0069a0001c0009t0005g0070others(14): Show | 17 | HG00438.hp1 HG00735.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.2390-2292C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624878 | ||||||
| chr3:64624905
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2390-2319G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624905 | ||||||
| chr3:64624908
|
C | A | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2390-2322G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624908 | ||||||
| chr3:64624909
|
T | G | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2390-2323A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624909 | ||||||
| chr3:64624910
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2390-2324G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624910 | ||||||
| chr3:64624911
|
C | G | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2390-2325G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64624911 | ||||||
| chr3:64625012
|
C | T | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2390-2426G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625012 | ||||||
| chr3:64625086
|
A | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2390-2500T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625086 | ||||||
| chr3:64625088
|
A | G | 1 | a0002c0002t0001g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2390-2502T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625088 | ||||||
| chr3:64625148
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0002g0099 | 2 | HG01243.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2390-2562G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625148 | ||||||
| chr3:64625181
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2390-2595G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625181 | ||||||
| chr3:64625288
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2390-2702C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625288 | ||||||
| chr3:64625318
|
T | C | 2 | a0003c0003t0002g0057a0008c0049t0001g0136 | 2 | NA18995.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2390-2732A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625318 | ||||||
| chr3:64625382
|
T | C | 2 | a0001c0014t0001g0091a0001c0014t0002g0126 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2390-2796A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625382 | ||||||
| chr3:64625558
|
G | A | 8 | a0001c0001t0001g0233a0001c0001t0002g0131a0001c0009t0005g0069others(5): Show | 8 | HG01070.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2390-2972C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625558 | ||||||
| chr3:64625570
|
A | G | 140 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(137): Show | 140 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.2390-2984T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625570 | ||||||
| chr3:64625656
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2390-3070G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625656 | ||||||
| chr3:64625802
|
AC | A | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2390-3217delG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625802 | ||||||
| chr3:64625881
|
C | A | 2 | a0001c0001t0001g0095a0001c0001t0002g0099 | 2 | HG01243.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2390-3295G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625881 | ||||||
| chr3:64625938
|
T | G | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2390-3352A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625938 | ||||||
| chr3:64625987
|
G | A | 8 | a0001c0001t0001g0233a0001c0001t0002g0131a0001c0009t0005g0069others(5): Show | 8 | HG01070.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2390-3401C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64625987 | ||||||
| chr3:64626002
|
C | T | 3 | a0001c0009t0005g0069a0001c0009t0005g0070a0003c0003t0001g0021 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2390-3416G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626002 | ||||||
| chr3:64626096
|
G | C | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2390-3510C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626096 | ||||||
| chr3:64626179
|
C | A | 116 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(113): Show | 116 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.2390-3593G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626179 | ||||||
| chr3:64626387
|
G | A | 1 | a0002c0002t0003g0138 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2390-3801C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626387 | ||||||
| chr3:64626474
|
G | A | 1 | a0001c0001t0020g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2390-3888C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626474 | ||||||
| chr3:64626503
|
C | T | 2 | a0003c0025t0001g0026a0004c0026t0001g0029 | 2 | HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2390-3917G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626503 | ||||||
| chr3:64626575
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(24): Show | 28 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.2390-3989G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626575 | ||||||
| chr3:64626613
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2390-4027C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626613 | ||||||
| chr3:64626689
|
T | C | 17 | a0001c0001t0001g0133a0001c0001t0012g0013a0001c0001t0012g0014others(14): Show | 17 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2390-4103A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626689 | ||||||
| chr3:64626726
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(25): Show | 29 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.2390-4140T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626726 | ||||||
| chr3:64626849
|
A | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(11): Show | 15 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.2390-4263T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626849 | ||||||
| chr3:64626893
|
C | G | 14 | a0001c0001t0001g0133a0001c0001t0012g0013a0001c0001t0012g0014others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2390-4307G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626893 | ||||||
| chr3:64626996
|
G | A | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2390-4410C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64626996 | ||||||
| chr3:64627320
|
C | T | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2389+4135G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627320 | ||||||
| chr3:64627333
|
C | G | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2389+4122G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627333 | ||||||
| chr3:64627385
|
G | GA | 13 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0236others(10): Show | 13 | HG01884.hp1 HG01952.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2389+4069dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627385 | ||||||
| chr3:64627385
|
GA | G | 127 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(124): Show | 127 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.2389+4069delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627385 | ||||||
| chr3:64627470
|
A | G | 1 | a0002c0002t0003g0193 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2389+3985T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627470 | ||||||
| chr3:64627480
|
G | A | 1 | a0002c0002t0008g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2389+3975C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627480 | ||||||
| chr3:64627602
|
G | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0085others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.2389+3853C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627602 | ||||||
| chr3:64627602
|
G | T | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2389+3853C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627602 | ||||||
| chr3:64627686
|
G | A | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2389+3769C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627686 | ||||||
| chr3:64627715
|
C | T | 2 | a0001c0037t0008g0006a0002c0002t0001g0220 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2389+3740G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627715 | ||||||
| chr3:64627768
|
C | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2389+3687G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627768 | ||||||
| chr3:64627888
|
G | C | 95 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(92): Show | 95 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.2389+3567C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627888 | ||||||
| chr3:64627906
|
T | C | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2389+3549A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627906 | ||||||
| chr3:64627955
|
A | C | 7 | a0001c0001t0002g0211a0001c0004t0001g0276a0001c0004t0002g0277others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2389+3500T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627955 | ||||||
| chr3:64627966
|
T | C | 1 | a0001c0023t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2389+3489A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64627966 | ||||||
| chr3:64628154
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2389+3301T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628154 | ||||||
| chr3:64628173
|
T | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(40): Show | 44 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.2389+3282A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628173 | ||||||
| chr3:64628281
|
G | A | 1 | a0004c0026t0001g0029 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2389+3174C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628281 | ||||||
| chr3:64628386
|
G | C | 1 | a0002c0002t0003g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2389+3069C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628386 | ||||||
| chr3:64628524
|
G | A | 24 | a0001c0001t0002g0217a0001c0004t0001g0061a0001c0004t0001g0257others(21): Show | 24 | HG00438.hp1 HG00735.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.2389+2931C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628524 | ||||||
| chr3:64628538
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127 | 3 | NA18963.hp2 NA18971.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2389+2917T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628538 | ||||||
| chr3:64628578
|
T | TC | 14 | a0001c0001t0001g0133a0001c0001t0012g0013a0001c0001t0012g0014others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2389+2876dupG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628578 | ||||||
| chr3:64628637
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(16): Show | 20 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(17): Show |
intron_variant | MODIFIER | c.2389+2818C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628637 | ||||||
| chr3:64628751
|
C | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2389+2704G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628751 | ||||||
| chr3:64628808
|
C | T | 3 | a0001c0001t0001g0067a0003c0003t0001g0022a0012c0018t0006g0243 | 3 | HG02717.hp1 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2389+2647G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628808 | ||||||
| chr3:64628893
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2389+2562G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64628893 | ||||||
| chr3:64629083
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.2389+2372T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629083 | ||||||
| chr3:64629106
|
C | T | 4 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008others(1): Show | 4 | HG02970.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2389+2349G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629106 | ||||||
| chr3:64629147
|
T | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.2389+2308A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629147 | ||||||
| chr3:64629193
|
G | A | 1 | a0015c0015t0002g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2389+2262C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629193 | ||||||
| chr3:64629207
|
A | T | 1 | a0015c0015t0002g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2389+2248T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629207 | ||||||
| chr3:64629444
|
C | T | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2389+2011G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629444 | ||||||
| chr3:64629570
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2389+1885G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629570 | ||||||
| chr3:64629630
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2389+1825T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629630 | ||||||
| chr3:64629631
|
T | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2389+1824A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629631 | ||||||
| chr3:64629652
|
T | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2389+1803A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629652 | ||||||
| chr3:64629676
|
A | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2389+1779T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629676 | ||||||
| chr3:64629883
|
G | A | 126 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(123): Show | 126 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.2389+1572C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629883 | ||||||
| chr3:64629904
|
T | C | 3 | a0001c0013t0001g0145a0001c0013t0001g0212a0032c0052t0002g0269 | 3 | HG02922.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2389+1551A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64629904 | ||||||
| chr3:64630064
|
T | TC | 188 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2389+1390_2389+139 others(5): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630064 | ||||||
| chr3:64630132
|
G | GTTGCTCT others(3): Show |
177 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2389+1322_2389+132 others(14): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630132 | ||||||
| chr3:64630133
|
C | T | 1 | a0001c0007t0002g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2389+1322G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630133 | ||||||
| chr3:64630197
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.2389+1258T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630197 | ||||||
| chr3:64630494
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2389+961A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630494 | ||||||
| chr3:64630757
|
A | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2389+698T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630757 | ||||||
| chr3:64630792
|
A | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2389+663T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630792 | ||||||
| chr3:64630803
|
A | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(19): Show | 23 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(20): Show |
intron_variant | MODIFIER | c.2389+652T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630803 | ||||||
| chr3:64630809
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2389+646A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630809 | ||||||
| chr3:64630906
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.2389+549T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630906 | ||||||
| chr3:64630988
|
A | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(31): Show | 35 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.2389+467T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64630988 | ||||||
| chr3:64631016
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(4): Show | 7 | HG02647.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2389+439A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64631016 | ||||||
| chr3:64631094
|
A | C | 1 | a0003c0003t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2389+361T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64631094 | ||||||
| chr3:64631100
|
T | C | 3 | a0001c0001t0002g0129a0002c0002t0003g0142a0005c0008t0003g0192 | 3 | NA18985.hp2 NA19001.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2389+355A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64631100 | ||||||
| chr3:64631361
|
G | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0164a0001c0001t0001g0235others(1): Show | 4 | HG00642.hp2 HG01081.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2389+94C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64631361 | ||||||
| chr3:64631366
|
G | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2389+89C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64631366 | ||||||
| chr3:64631394
|
C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2389+61G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 16/39 | chr3 | 64631394 | ||||||
| chr3:64631624
|
A | T | 9 | a0001c0001t0002g0202a0001c0020t0002g0258a0001c0020t0014g0011others(6): Show | 9 | HG01257.hp1 HG03491.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.2294-74T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 15/39 | chr3 | 64631624 | ||||||
| chr3:64631695
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(20): Show | 24 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(21): Show |
intron_variant | MODIFIER | c.2293+113A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 15/39 | chr3 | 64631695 | ||||||
| chr3:64631699
|
G | A | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2293+109C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 15/39 | chr3 | 64631699 | ||||||
| chr3:64631747
|
G | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0095others(34): Show | 38 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.2293+61C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 15/39 | chr3 | 64631747 | ||||||
| chr3:64631973
|
A | G | 1 | a0001c0014t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2176-48T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64631973 | ||||||
| chr3:64631993
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0004c0005t0015g0010 | 3 | NA18946.hp2 NA18972.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2176-68A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64631993 | ||||||
| chr3:64632014
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(16): Show | 20 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(17): Show |
intron_variant | MODIFIER | c.2176-89T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632014 | ||||||
| chr3:64632023
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2176-98T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632023 | ||||||
| chr3:64632517
|
A | T | 1 | a0001c0014t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2176-592T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632517 | ||||||
| chr3:64632736
|
G | A | 1 | a0003c0017t0006g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2175+736C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632736 | ||||||
| chr3:64632749
|
G | A | 1 | a0012c0018t0006g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2175+723C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632749 | ||||||
| chr3:64632828
|
C | CA | 14 | a0001c0001t0001g0216a0001c0001t0001g0233a0001c0001t0002g0116others(11): Show | 14 | HG00438.hp2 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.2175+643dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632828 | ||||||
| chr3:64632828
|
C | CAA | 24 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(21): Show | 25 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(22): Show |
intron_variant | MODIFIER | c.2175+642_2175+643d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632828 | ||||||
| chr3:64632828
|
CA | C | 12 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0004t0001g0236others(9): Show | 12 | HG01884.hp1 HG01952.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2175+643delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632828 | ||||||
| chr3:64632836
|
A | T | 7 | a0001c0001t0002g0211a0001c0004t0001g0276a0001c0004t0002g0277others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2175+636T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632836 | ||||||
| chr3:64632838
|
A | C | 7 | a0001c0009t0005g0069a0001c0009t0005g0070a0001c0014t0001g0091others(4): Show | 7 | HG00438.hp1 HG02135.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2175+634T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632838 | ||||||
| chr3:64632854
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2175+618T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632854 | ||||||
| chr3:64632884
|
C | A | 1 | a0002c0002t0003g0196 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2175+588G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64632884 | ||||||
| chr3:64633163
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2175+309G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64633163 | ||||||
| chr3:64633299
|
C | G | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2175+173G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64633299 | ||||||
| chr3:64633372
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2175+100G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 14/39 | chr3 | 64633372 | ||||||
| chr3:64633669
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2038+29G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 13/39 | chr3 | 64633669 | ||||||
| chr3:64633682
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2038+16G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 13/39 | chr3 | 64633682 | ||||||
| chr3:64634041
|
C | A | 4 | a0001c0001t0016g0063a0003c0003t0002g0025a0003c0003t0007g0037others(1): Show | 4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857-162G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634041 | ||||||
| chr3:64634088
|
C | T | 1 | a0030c0046t0002g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1857-209G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634088 | ||||||
| chr3:64634153
|
G | A | 1 | a0001c0013t0011g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1857-274C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634153 | ||||||
| chr3:64634197
|
G | C | 144 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(141): Show | 144 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1857-318C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634197 | ||||||
| chr3:64634252
|
T | C | 1 | a0004c0005t0001g0032 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1857-373A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634252 | ||||||
| chr3:64634346
|
T | A | 3 | a0001c0001t0001g0067a0003c0003t0001g0022a0012c0018t0006g0243 | 3 | HG02717.hp1 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1857-467A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634346 | ||||||
| chr3:64634371
|
T | C | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1857-492A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634371 | ||||||
| chr3:64634399
|
A | G | 1 | a0001c0013t0011g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1857-520T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634399 | ||||||
| chr3:64634422
|
T | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857-543A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634422 | ||||||
| chr3:64634432
|
A | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(17): Show | 21 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(18): Show |
intron_variant | MODIFIER | c.1857-553T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634432 | ||||||
| chr3:64634443
|
A | G | 1 | a0002c0002t0008g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1857-564T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634443 | ||||||
| chr3:64634662
|
A | T | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1857-783T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634662 | ||||||
| chr3:64634695
|
T | C | 144 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(141): Show | 144 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1857-816A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634695 | ||||||
| chr3:64634702
|
T | A | 4 | a0001c0001t0001g0113a0001c0001t0002g0172a0003c0024t0001g0042others(1): Show | 4 | HG02145.hp1 HG02698.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857-823A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634702 | ||||||
| chr3:64634702
|
T | C | 1 | a0001c0020t0014g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1857-823A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64634702 | ||||||
| chr3:64635125
|
G | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(15): Show | 19 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(16): Show |
intron_variant | MODIFIER | c.1857-1246C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635125 | ||||||
| chr3:64635161
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1857-1282G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635161 | ||||||
| chr3:64635207
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(25): Show | 29 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.1857-1328A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635207 | ||||||
| chr3:64635253
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(24): Show | 28 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.1857-1374T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635253 | ||||||
| chr3:64635257
|
G | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1857-1378C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635257 | ||||||
| chr3:64635320
|
C | T | 3 | a0001c0001t0002g0065a0001c0001t0020g0213a0003c0003t0002g0060 | 3 | HG02258.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1857-1441G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635320 | ||||||
| chr3:64635436
|
A | G | 1 | a0009c0047t0001g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1857-1557T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635436 | ||||||
| chr3:64635461
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1857-1582A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635461 | ||||||
| chr3:64635533
|
G | A | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1857-1654C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635533 | ||||||
| chr3:64635573
|
A | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1857-1694T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635573 | ||||||
| chr3:64635752
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0164 | 2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1857-1873T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635752 | ||||||
| chr3:64635760
|
T | C | 1 | a0003c0024t0001g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1857-1881A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635760 | ||||||
| chr3:64635797
|
A | G | 144 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(141): Show | 144 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1857-1918T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635797 | ||||||
| chr3:64635883
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(25): Show | 29 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.1857-2004A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64635883 | ||||||
| chr3:64636086
|
A | AT | 175 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1857-2208dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636086 | ||||||
| chr3:64636103
|
A | G | 144 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0085others(141): Show | 144 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1857-2224T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636103 | ||||||
| chr3:64636155
|
G | C | 2 | a0001c0013t0001g0145a0001c0013t0001g0212 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1857-2276C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636155 | ||||||
| chr3:64636212
|
C | G | 1 | a0001c0001t0001g0139 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1857-2333G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636212 | ||||||
| chr3:64636375
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1857-2496A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636375 | ||||||
| chr3:64636507
|
A | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857-2628T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636507 | ||||||
| chr3:64636554
|
A | C | 6 | a0001c0001t0001g0233a0001c0001t0002g0131a0002c0002t0001g0266others(3): Show | 6 | HG01070.hp1 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1857-2675T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636554 | ||||||
| chr3:64636643
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0002g0273others(3): Show | 6 | HG02647.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1857-2764T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636643 | ||||||
| chr3:64636653
|
A | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1857-2774T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636653 | ||||||
| chr3:64636872
|
T | C | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1857-2993A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636872 | ||||||
| chr3:64636913
|
G | A | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857-3034C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64636913 | ||||||
| chr3:64637040
|
T | C | 1 | a0001c0006t0001g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1857-3161A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637040 | ||||||
| chr3:64637112
|
T | A | 1 | a0029c0032t0001g0259 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1857-3233A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637112 | ||||||
| chr3:64637157
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0002g0246a0025c0033t0003g0261 | 3 | NA18983.hp2 NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1857-3278G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637157 | ||||||
| chr3:64637165
|
C | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1857-3286G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637165 | ||||||
| chr3:64637220
|
A | G | 14 | a0001c0001t0001g0133a0001c0001t0012g0013a0001c0001t0012g0014others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857-3341T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637220 | ||||||
| chr3:64637251
|
T | A | 2 | a0001c0001t0001g0234a0001c0023t0001g0020 | 2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1857-3372A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637251 | ||||||
| chr3:64637303
|
T | C | 1 | a0001c0001t0002g0187 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1857-3424A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637303 | ||||||
| chr3:64637431
|
T | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0282 | 3 | NA18940.hp1 NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1857-3552A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637431 | ||||||
| chr3:64637537
|
A | G | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857-3658T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637537 | ||||||
| chr3:64637680
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1857-3801A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637680 | ||||||
| chr3:64637703
|
C | T | 7 | a0001c0007t0002g0062a0001c0007t0002g0219a0001c0007t0002g0254others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1857-3824G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637703 | ||||||
| chr3:64637926
|
C | T | 1 | a0001c0001t0002g0187 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1856+3922G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637926 | ||||||
| chr3:64637957
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1856+3891C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64637957 | ||||||
| chr3:64638025
|
G | A | 1 | a0002c0002t0008g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1856+3823C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638025 | ||||||
| chr3:64638030
|
A | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1856+3818T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638030 | ||||||
| chr3:64638075
|
G | A | 6 | a0001c0001t0002g0202a0002c0002t0003g0153a0003c0003t0002g0056others(3): Show | 6 | HG02071.hp2 NA18939.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.1856+3773C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638075 | ||||||
| chr3:64638113
|
A | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1856+3735T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638113 | ||||||
| chr3:64638130
|
T | A | 1 | a0002c0002t0003g0195 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1856+3718A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638130 | ||||||
| chr3:64638259
|
C | T | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1856+3589G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638259 | ||||||
| chr3:64638291
|
T | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1856+3557A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638291 | ||||||
| chr3:64638350
|
T | C | 1 | a0002c0002t0008g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1856+3498A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638350 | ||||||
| chr3:64638452
|
G | A | 31 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0093others(28): Show | 31 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1856+3396C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638452 | ||||||
| chr3:64638530
|
G | C | 7 | a0001c0001t0001g0018a0001c0001t0002g0065a0001c0001t0002g0224others(4): Show | 7 | HG02647.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1856+3318C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638530 | ||||||
| chr3:64638533
|
C | A | 1 | a0001c0007t0002g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1856+3315G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638533 | ||||||
| chr3:64638534
|
A | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1856+3314T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638534 | ||||||
| chr3:64638540
|
C | A | 1 | a0001c0007t0002g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1856+3308G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638540 | ||||||
| chr3:64638576
|
G | T | 6 | a0001c0001t0001g0279a0001c0001t0007g0278a0001c0006t0010g0003others(3): Show | 6 | HG01884.hp1 HG01952.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1856+3272C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638576 | ||||||
| chr3:64638602
|
A | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0087others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1856+3246T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638602 | ||||||
| chr3:64638701
|
G | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1856+3147C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638701 | ||||||
| chr3:64638750
|
C | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1856+3098G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638750 | ||||||
| chr3:64638876
|
G | GA | 6 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(3): Show | 6 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1856+2971dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64638876 | ||||||
| chr3:64639293
|
G | GT | 39 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0109others(36): Show | 39 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1856+2554dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639293 | ||||||
| chr3:64639293
|
G | GTT | 47 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0097others(44): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.1856+2553_1856+255 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639293 | ||||||
| chr3:64639293
|
G | GTTT | 67 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0087others(64): Show | 67 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1856+2552_1856+255 others(7): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639293 | ||||||
| chr3:64639293
|
GT | G | 13 | a0001c0001t0001g0166a0001c0001t0002g0162a0001c0001t0002g0217others(10): Show | 13 | HG00735.hp2 HG01099.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1856+2554delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639293 | ||||||
| chr3:64639312
|
TA | T | 7 | a0001c0001t0002g0108a0001c0001t0002g0170a0001c0001t0002g0202others(4): Show | 7 | HG02071.hp1 HG02273.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.1856+2535delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639312 | ||||||
| chr3:64639313
|
A | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1856+2535T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639313 | ||||||
| chr3:64639314
|
A | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0087others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.1856+2534T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639314 | ||||||
| chr3:64639315
|
A | T | 15 | a0001c0001t0001g0124a0001c0001t0014g0012a0001c0001t0020g0213others(12): Show | 15 | HG01934.hp1 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1856+2533T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639315 | ||||||
| chr3:64639316
|
A | T | 1 | a0001c0001t0001g0124 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1856+2532T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639316 | ||||||
| chr3:64639567
|
T | TA | 165 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0080others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1856+2280dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639567 | ||||||
| chr3:64639601
|
T | C | 1 | a0006c0010t0002g0169 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1856+2247A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639601 | ||||||
| chr3:64639660
|
C | T | 7 | a0001c0001t0002g0202a0001c0020t0002g0258a0001c0020t0014g0011others(4): Show | 7 | HG01257.hp1 NA18906.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1856+2188G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639660 | ||||||
| chr3:64639715
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1856+2133A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639715 | ||||||
| chr3:64639815
|
T | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1856+2033A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639815 | ||||||
| chr3:64639969
|
T | C | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1856+1879A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639969 | ||||||
| chr3:64639984
|
A | G | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1856+1864T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64639984 | ||||||
| chr3:64640091
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0002g0065a0001c0001t0002g0224others(4): Show | 7 | HG02647.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1856+1757A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64640091 | ||||||
| chr3:64640238
|
C | G | 122 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0087others(119): Show | 122 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1856+1610G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64640238 | ||||||
| chr3:64640447
|
A | G | 1 | a0002c0002t0003g0190 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1856+1401T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64640447 | ||||||
| chr3:64640522
|
C | T | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1856+1326G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64640522 | ||||||
| chr3:64640691
|
G | T | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1856+1157C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64640691 | ||||||
| chr3:64640799
|
T | C | 2 | a0001c0014t0001g0091a0001c0014t0002g0126 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1856+1049A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64640799 | ||||||
| chr3:64640921
|
G | A | 25 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0106others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.1856+927C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64640921 | ||||||
| chr3:64641123
|
T | G | 6 | a0001c0001t0002g0217a0001c0001t0020g0213a0003c0003t0002g0031others(3): Show | 6 | HG00735.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1856+725A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641123 | ||||||
| chr3:64641126
|
G | T | 2 | a0001c0001t0001g0201a0002c0002t0003g0165 | 2 | HG02015.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1856+722C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641126 | ||||||
| chr3:64641179
|
G | A | 1 | a0001c0001t0002g0137 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1856+669C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641179 | ||||||
| chr3:64641246
|
C | CT | 13 | a0001c0001t0001g0133a0001c0001t0012g0013a0001c0001t0012g0014others(10): Show | 13 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1856+601dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641246 | ||||||
| chr3:64641246
|
CTT | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0087others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1856+600_1856+601d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641246 | ||||||
| chr3:64641470
|
C | T | 2 | a0002c0002t0003g0144a0004c0005t0003g0040 | 2 | HG01496.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1856+378G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641470 | ||||||
| chr3:64641471
|
G | T | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1856+377C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641471 | ||||||
| chr3:64641522
|
C | T | 14 | a0001c0001t0001g0133a0001c0001t0012g0013a0001c0001t0012g0014others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1856+326G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641522 | ||||||
| chr3:64641523
|
G | A | 142 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0087others(139): Show | 142 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.1856+325C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641523 | ||||||
| chr3:64641598
|
C | T | 126 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0087others(123): Show | 126 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1856+250G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641598 | ||||||
| chr3:64641629
|
T | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG00558.hp1 HG02027.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1856+219A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641629 | ||||||
| chr3:64641641
|
T | A | 131 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0087others(128): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.1856+207A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641641 | ||||||
| chr3:64641711
|
G | C | 2 | a0001c0020t0002g0258a0001c0020t0014g0011 | 2 | HG01257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1856+137C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641711 | ||||||
| chr3:64641767
|
C | T | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1856+81G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641767 | ||||||
| chr3:64641772
|
C | T | 102 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0102others(99): Show | 102 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1856+76G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641772 | ||||||
| chr3:64641788
|
C | A | 1 | a0001c0007t0002g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1856+60G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641788 | ||||||
| chr3:64641828
|
T | C | 1 | a0003c0003t0002g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1856+20A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 12/39 | chr3 | 64641828 | ||||||
| chr3:64642076
|
C | T | 101 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0102others(98): Show | 101 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.1711-83G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642076 | ||||||
| chr3:64642141
|
G | A | 100 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0102others(97): Show | 100 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.1711-148C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642141 | ||||||
| chr3:64642196
|
G | C | 29 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0106others(26): Show | 29 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1711-203C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642196 | ||||||
| chr3:64642242
|
G | C | 5 | a0001c0001t0002g0202a0003c0003t0002g0056a0007c0011t0004g0086others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1711-249C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642242 | ||||||
| chr3:64642346
|
A | T | 1 | a0001c0001t0002g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1711-353T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642346 | ||||||
| chr3:64642441
|
AG | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1711-449delC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642441 | ||||||
| chr3:64642446
|
GGA | G | 16 | a0001c0001t0001g0279a0001c0001t0002g0217a0001c0001t0007g0278others(13): Show | 16 | HG00735.hp2 HG01884.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1711-455_1711-454d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642446 | ||||||
| chr3:64642447
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1711-454C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642447 | ||||||
| chr3:64642494
|
G | GC | 204 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(201): Show | 204 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.1711-502dupG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642494 | ||||||
| chr3:64642534
|
G | A | 3 | a0001c0001t0002g0202a0001c0004t0001g0257a0003c0003t0002g0056 | 3 | NA18939.hp1 NA19010.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1711-541C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642534 | ||||||
| chr3:64642601
|
G | C | 3 | a0001c0020t0002g0258a0001c0020t0014g0011a0003c0003t0002g0060 | 3 | HG01257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1711-608C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642601 | ||||||
| chr3:64642760
|
G | A | 1 | a0001c0001t0017g0066 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1711-767C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642760 | ||||||
| chr3:64642776
|
C | T | 2 | a0001c0001t0002g0253a0030c0046t0002g0252 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1711-783G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642776 | ||||||
| chr3:64642777
|
G | A | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1711-784C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642777 | ||||||
| chr3:64642878
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1711-885G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64642878 | ||||||
| chr3:64643086
|
C | T | 6 | a0001c0004t0001g0061a0001c0007t0002g0062a0001c0007t0002g0254others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1711-1093G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643086 | ||||||
| chr3:64643150
|
C | T | 9 | a0001c0001t0002g0202a0001c0004t0001g0257a0002c0002t0003g0185others(6): Show | 9 | HG02040.hp2 NA18939.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.1711-1157G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643150 | ||||||
| chr3:64643164
|
G | C | 1 | a0013c0019t0004g0200 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1711-1171C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643164 | ||||||
| chr3:64643261
|
T | C | 8 | a0001c0001t0002g0202a0002c0002t0003g0185a0003c0003t0001g0054others(5): Show | 8 | NA18939.hp1 NA18946.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.1711-1268A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643261 | ||||||
| chr3:64643391
|
A | G | 2 | a0001c0013t0001g0145a0001c0013t0001g0212 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1711-1398T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643391 | ||||||
| chr3:64643430
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1711-1437A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643430 | ||||||
| chr3:64643445
|
A | AT | 9 | a0001c0001t0002g0273a0001c0001t0016g0063a0001c0004t0002g0277others(6): Show | 9 | HG02040.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1711-1453dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643445
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0020g0213a0032c0052t0002g0269 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1711-1462_1711-145 others(14): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643445
|
A | ATTTTTTT others(4): Show |
1 | a0002c0002t0008g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1711-1463_1711-145 others(15): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643445
|
A | ATTTTTTT others(5): Show |
16 | a0001c0001t0001g0101a0001c0001t0001g0164a0001c0001t0001g0222others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.1711-1464_1711-145 others(16): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643445
|
A | ATTTTTTT others(6): Show |
12 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0218others(9): Show | 13 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1711-1465_1711-145 others(17): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643445
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0095a0001c0001t0012g0013a0003c0003t0001g0059 | 3 | HG00735.hp1 HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1711-1466_1711-145 others(18): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643445
|
A | ATTTTTTT others(8): Show |
1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1711-1467_1711-145 others(19): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643445
|
AT | A | 182 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(179): Show | 182 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.1711-1453delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643445
|
ATT | A | 10 | a0001c0001t0014g0012a0001c0031t0008g0004a0003c0003t0001g0033others(7): Show | 10 | HG02273.hp2 HG02300.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1711-1454_1711-145 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643445 | ||||||
| chr3:64643529
|
T | G | 5 | a0001c0001t0016g0063a0001c0007t0002g0219a0003c0003t0002g0025others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1711-1536A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643529 | ||||||
| chr3:64643554
|
C | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1711-1561G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643554 | ||||||
| chr3:64643728
|
C | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1711-1735G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643728 | ||||||
| chr3:64643753
|
A | C | 236 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1711-1760T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643753 | ||||||
| chr3:64643909
|
A | T | 2 | a0003c0025t0001g0026a0004c0026t0001g0029 | 2 | HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1711-1916T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64643909 | ||||||
| chr3:64644010
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0210 | 2 | NA18747.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1711-2017A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644010 | ||||||
| chr3:64644022
|
C | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1711-2029G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644022 | ||||||
| chr3:64644115
|
C | A | 1 | a0001c0001t0002g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1711-2122G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644115 | ||||||
| chr3:64644164
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1711-2171G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644164 | ||||||
| chr3:64644228
|
C | T | 106 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1711-2235G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644228 | ||||||
| chr3:64644323
|
T | C | 6 | a0001c0001t0002g0211a0001c0009t0005g0071a0001c0009t0005g0072others(3): Show | 6 | HG01934.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1711-2330A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644323 | ||||||
| chr3:64644406
|
C | T | 8 | a0001c0001t0002g0099a0001c0001t0002g0202a0003c0003t0001g0054others(5): Show | 8 | HG02300.hp1 NA18939.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1711-2413G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644406 | ||||||
| chr3:64644551
|
G | A | 8 | a0001c0001t0002g0099a0001c0001t0002g0202a0003c0003t0001g0054others(5): Show | 8 | HG02300.hp1 NA18939.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1711-2558C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644551 | ||||||
| chr3:64644678
|
T | C | 3 | a0001c0001t0016g0063a0001c0007t0002g0219a0003c0003t0002g0025 | 3 | HG02886.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1711-2685A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644678 | ||||||
| chr3:64644695
|
A | G | 3 | a0001c0001t0016g0063a0001c0007t0002g0219a0003c0003t0002g0025 | 3 | HG02886.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1711-2702T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644695 | ||||||
| chr3:64644929
|
C | A | 1 | a0003c0003t0002g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1711-2936G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644929 | ||||||
| chr3:64644935
|
C | T | 2 | a0003c0025t0001g0026a0004c0026t0001g0029 | 2 | HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1711-2942G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64644935 | ||||||
| chr3:64645051
|
G | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(184): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1710+2889C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645051 | ||||||
| chr3:64645203
|
A | G | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1710+2737T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645203 | ||||||
| chr3:64645464
|
G | A | 2 | a0001c0001t0002g0211a0001c0013t0001g0212 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1710+2476C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645464 | ||||||
| chr3:64645521
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1710+2419G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645521 | ||||||
| chr3:64645530
|
A | G | 2 | a0003c0025t0001g0026a0004c0026t0001g0029 | 2 | HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1710+2410T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645530 | ||||||
| chr3:64645542
|
C | T | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1710+2398G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645542 | ||||||
| chr3:64645564
|
A | G | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1710+2376T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645564 | ||||||
| chr3:64645570
|
C | G | 17 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0012g0013others(14): Show | 17 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1710+2370G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645570 | ||||||
| chr3:64645598
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0090others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1710+2342A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645598 | ||||||
| chr3:64645603
|
T | A | 1 | a0023c0039t0002g0146 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1710+2337A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645603 | ||||||
| chr3:64645759
|
T | C | 3 | a0001c0001t0016g0063a0001c0007t0002g0219a0003c0003t0002g0025 | 3 | HG02886.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1710+2181A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645759 | ||||||
| chr3:64645763
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0002g0247 | 2 | HG00558.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1710+2177G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645763 | ||||||
| chr3:64645778
|
C | T | 3 | a0001c0001t0016g0063a0001c0007t0002g0219a0003c0003t0002g0025 | 3 | HG02886.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1710+2162G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645778 | ||||||
| chr3:64645797
|
T | C | 3 | a0001c0001t0016g0063a0001c0007t0002g0219a0003c0003t0002g0025 | 3 | HG02886.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1710+2143A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645797 | ||||||
| chr3:64645978
|
G | A | 1 | a0002c0002t0003g0195 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1710+1962C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64645978 | ||||||
| chr3:64646025
|
A | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(201): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1710+1915T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64646025 | ||||||
| chr3:64646054
|
CAT | C | 8 | a0001c0001t0002g0099a0001c0001t0002g0202a0003c0003t0001g0054others(5): Show | 8 | HG02300.hp1 NA18939.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1710+1884_1710+188 others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64646054 | ||||||
| chr3:64646580
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(194): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1710+1360C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64646580 | ||||||
| chr3:64646631
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0233a0003c0003t0001g0022others(2): Show | 5 | HG01070.hp1 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1710+1309G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64646631 | ||||||
| chr3:64646738
|
A | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(176): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1710+1202T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64646738 | ||||||
| chr3:64646772
|
T | C | 2 | a0001c0001t0020g0213a0032c0052t0002g0269 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1710+1168A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64646772 | ||||||
| chr3:64646783
|
T | A | 1 | a0001c0001t0001g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1710+1157A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64646783 | ||||||
| chr3:64647017
|
A | G | 9 | a0001c0001t0007g0278a0001c0004t0001g0236a0001c0004t0001g0238others(6): Show | 9 | HG01952.hp1 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1710+923T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647017 | ||||||
| chr3:64647114
|
T | C | 1 | a0001c0023t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1710+826A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647114 | ||||||
| chr3:64647210
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1710+730A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647210 | ||||||
| chr3:64647241
|
T | G | 1 | a0001c0001t0002g0129 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1710+699A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647241 | ||||||
| chr3:64647271
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1710+669G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647271 | ||||||
| chr3:64647463
|
A | T | 4 | a0005c0008t0002g0175a0005c0008t0002g0176a0008c0049t0001g0136others(1): Show | 4 | HG00609.hp2 NA18953.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1710+477T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647463 | ||||||
| chr3:64647762
|
A | C | 1 | a0003c0003t0002g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1710+178T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647762 | ||||||
| chr3:64647771
|
T | A | 1 | a0018c0048t0002g0081 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1710+169A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647771 | ||||||
| chr3:64647777
|
A | G | 15 | a0001c0001t0001g0090a0001c0001t0001g0183a0001c0001t0002g0089others(12): Show | 15 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1710+163T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647777 | ||||||
| chr3:64647828
|
A | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(197): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1710+112T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647828 | ||||||
| chr3:64647860
|
A | G | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1710+80T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 11/39 | chr3 | 64647860 | ||||||
| chr3:64648127
|
A | T | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1606-83T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648127 | ||||||
| chr3:64648186
|
T | C | 1 | a0001c0001t0003g0262 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1606-142A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648186 | ||||||
| chr3:64648195
|
A | G | 8 | a0001c0001t0002g0099a0001c0001t0002g0202a0003c0003t0001g0054others(5): Show | 8 | HG02300.hp1 NA18939.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1606-151T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648195 | ||||||
| chr3:64648523
|
C | T | 1 | a0012c0018t0006g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1606-479G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648523 | ||||||
| chr3:64648664
|
C | A | 39 | a0001c0001t0001g0019a0001c0001t0001g0097a0001c0001t0001g0133others(36): Show | 39 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1606-620G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648664 | ||||||
| chr3:64648735
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1606-691A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648735 | ||||||
| chr3:64648821
|
A | G | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1606-777T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648821 | ||||||
| chr3:64648901
|
A | G | 1 | a0001c0001t0019g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1605+736T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648901 | ||||||
| chr3:64648902
|
A | G | 105 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(102): Show | 105 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1605+735T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64648902 | ||||||
| chr3:64649000
|
A | G | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1605+637T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649000 | ||||||
| chr3:64649004
|
G | A | 27 | a0001c0001t0001g0019a0001c0001t0001g0097a0001c0001t0001g0133others(24): Show | 27 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1605+633C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649004 | ||||||
| chr3:64649060
|
T | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1605+577A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649060 | ||||||
| chr3:64649065
|
G | A | 5 | a0001c0001t0002g0131a0001c0001t0002g0228a0001c0001t0002g0255others(2): Show | 5 | HG03041.hp2 HG03139.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1605+572C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649065 | ||||||
| chr3:64649242
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1605+395A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649242 | ||||||
| chr3:64649261
|
A | G | 4 | a0001c0001t0007g0278a0001c0006t0010g0003a0001c0006t0010g0007others(1): Show | 4 | HG01952.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1605+376T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649261 | ||||||
| chr3:64649325
|
C | T | 104 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(101): Show | 104 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1605+312G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649325 | ||||||
| chr3:64649440
|
G | A | 2 | a0001c0001t0020g0213a0032c0052t0002g0269 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1605+197C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649440 | ||||||
| chr3:64649463
|
T | C | 2 | a0001c0001t0016g0063a0003c0003t0002g0025 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1605+174A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649463 | ||||||
| chr3:64649576
|
T | A | 14 | a0001c0001t0002g0211a0001c0001t0020g0213a0001c0007t0002g0062others(11): Show | 14 | HG01934.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1605+61A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649576 | ||||||
| chr3:64649612
|
G | A | 1 | a0002c0002t0003g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1605+25C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 10/39 | chr3 | 64649612 | ||||||
| chr3:64649783
|
G | A | 1 | a0002c0002t0003g0153 | 1 | HG02071.hp2 | splice_region_variant&intron_variant | LOW | c.1464-5C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64649783 | ||||||
| chr3:64650065
|
C | G | 2 | a0006c0010t0002g0169a0015c0015t0002g0055 | 2 | NA18942.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1464-287G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650065 | ||||||
| chr3:64650182
|
C | A | 99 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(96): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1464-404G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650182 | ||||||
| chr3:64650338
|
C | G | 2 | a0001c0009t0005g0069a0001c0009t0005g0070 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1464-560G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650338 | ||||||
| chr3:64650452
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0090others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1463+565C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650452 | ||||||
| chr3:64650540
|
A | C | 1 | a0001c0001t0002g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1463+477T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650540 | ||||||
| chr3:64650590
|
G | A | 3 | a0001c0006t0010g0003a0001c0006t0010g0007a0001c0006t0011g0008 | 3 | HG03225.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1463+427C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650590 | ||||||
| chr3:64650621
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1463+396C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650621 | ||||||
| chr3:64650799
|
T | C | 15 | a0001c0001t0001g0090a0001c0001t0001g0183a0001c0001t0002g0089others(12): Show | 15 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1463+218A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650799 | ||||||
| chr3:64650867
|
C | CT | 36 | a0001c0001t0001g0019a0001c0001t0001g0092a0001c0001t0001g0097others(33): Show | 36 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1463+149dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650867 | ||||||
| chr3:64650867
|
CT | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0090others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1463+149delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 9/39 | chr3 | 64650867 | ||||||
| chr3:64651238
|
G | C | 1 | a0001c0001t0002g0244 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1317-75C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64651238 | ||||||
| chr3:64651366
|
C | T | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066 | 3 | HG02257.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1317-203G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64651366 | ||||||
| chr3:64651699
|
G | T | 1 | a0002c0002t0001g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1317-536C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64651699 | ||||||
| chr3:64651914
|
C | A | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1317-751G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64651914 | ||||||
| chr3:64651940
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1317-777G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64651940 | ||||||
| chr3:64652090
|
A | G | 105 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(102): Show | 105 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1317-927T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652090 | ||||||
| chr3:64652127
|
T | C | 12 | a0001c0001t0002g0211a0001c0007t0002g0062a0001c0007t0002g0254others(9): Show | 12 | HG01934.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1317-964A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652127 | ||||||
| chr3:64652147
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1317-984A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652147 | ||||||
| chr3:64652172
|
T | C | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1317-1009A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652172 | ||||||
| chr3:64652211
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1317-1048T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652211 | ||||||
| chr3:64652254
|
A | T | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1317-1091T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652254 | ||||||
| chr3:64652492
|
C | G | 14 | a0001c0001t0001g0018a0001c0001t0002g0224a0001c0001t0012g0013others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1317-1329G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652492 | ||||||
| chr3:64652591
|
C | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0090others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1317-1428G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652591 | ||||||
| chr3:64652688
|
C | T | 7 | a0001c0001t0002g0131a0001c0001t0002g0228a0001c0001t0002g0255others(4): Show | 7 | HG02486.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317-1525G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652688 | ||||||
| chr3:64652757
|
C | T | 15 | a0001c0001t0001g0090a0001c0001t0001g0183a0001c0001t0002g0089others(12): Show | 15 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1317-1594G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652757 | ||||||
| chr3:64652793
|
A | T | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1316+1560T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652793 | ||||||
| chr3:64652964
|
G | A | 1 | a0001c0013t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1316+1389C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64652964 | ||||||
| chr3:64653083
|
A | G | 3 | a0001c0004t0001g0061a0001c0004t0001g0257a0001c0013t0001g0145 | 3 | HG06807.hp2 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1316+1270T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653083 | ||||||
| chr3:64653204
|
G | C | 15 | a0001c0001t0001g0090a0001c0001t0001g0183a0001c0001t0002g0089others(12): Show | 15 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1316+1149C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653204 | ||||||
| chr3:64653274
|
G | C | 7 | a0001c0001t0002g0099a0001c0001t0002g0202a0003c0003t0001g0054others(4): Show | 7 | HG02300.hp1 NA18939.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+1079C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653274 | ||||||
| chr3:64653473
|
T | C | 6 | a0001c0007t0002g0062a0001c0007t0002g0254a0001c0007t0013g0015others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316+880A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653473 | ||||||
| chr3:64653595
|
C | T | 98 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(95): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1316+758G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653595 | ||||||
| chr3:64653645
|
G | A | 111 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(108): Show | 111 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1316+708C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653645 | ||||||
| chr3:64653760
|
T | G | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1316+593A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653760 | ||||||
| chr3:64653783
|
G | C | 2 | a0001c0001t0001g0218a0001c0006t0001g0206 | 2 | HG00642.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1316+570C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653783 | ||||||
| chr3:64653899
|
A | G | 96 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(93): Show | 96 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1316+454T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653899 | ||||||
| chr3:64653908
|
A | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1316+445T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653908 | ||||||
| chr3:64653925
|
G | A | 97 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(94): Show | 97 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1316+428C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653925 | ||||||
| chr3:64653979
|
CT | C | 96 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(93): Show | 96 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1316+373delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64653979 | ||||||
| chr3:64654227
|
C | A | 15 | a0001c0001t0001g0090a0001c0001t0001g0183a0001c0001t0002g0089others(12): Show | 15 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1316+126G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 8/39 | chr3 | 64654227 | ||||||
| chr3:64654505
|
T | C | 1 | a0003c0003t0002g0056 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1211-47A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 7/39 | chr3 | 64654505 | ||||||
| chr3:64654525
|
T | C | 15 | a0001c0001t0002g0217a0001c0001t0016g0063a0001c0013t0001g0145others(12): Show | 15 | HG00735.hp2 HG01884.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1210+47A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 7/39 | chr3 | 64654525 | ||||||
| chr3:64654530
|
TA | T | 280 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1210+41delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 7/39 | chr3 | 64654530 | ||||||
| chr3:64654536
|
G | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1210+36C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 7/39 | chr3 | 64654536 | ||||||
| chr3:64654556
|
C | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0002g0224others(8): Show | 11 | HG00738.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1210+16G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 7/39 | chr3 | 64654556 | ||||||
| chr3:64654752
|
A | G | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1170-140T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64654752 | ||||||
| chr3:64654859
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1170-247G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64654859 | ||||||
| chr3:64655022
|
T | A | 14 | a0001c0001t0002g0217a0001c0001t0002g0273a0001c0001t0020g0213others(11): Show | 14 | HG00735.hp2 HG01884.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1170-410A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64655022 | ||||||
| chr3:64655116
|
T | C | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1169+460A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64655116 | ||||||
| chr3:64655183
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1169+393C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64655183 | ||||||
| chr3:64655407
|
G | A | 1 | a0001c0001t0021g0284 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1169+169C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64655407 | ||||||
| chr3:64655474
|
C | G | 42 | a0001c0001t0001g0112a0001c0001t0001g0139a0001c0001t0001g0164others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1169+102G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64655474 | ||||||
| chr3:64655550
|
A | G | 2 | a0001c0001t0001g0168a0002c0002t0003g0152 | 2 | HG01099.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1169+26T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64655550 | ||||||
| chr3:64655555
|
A | T | 1 | a0003c0003t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1169+21T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 6/39 | chr3 | 64655555 | ||||||
| chr3:64655700
|
A | G | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1054-9T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 5/39 | chr3 | 64655700 | ||||||
| chr3:64655702
|
A | G | 7 | a0001c0001t0002g0224a0001c0006t0010g0003a0001c0006t0010g0007others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054-11T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 5/39 | chr3 | 64655702 | ||||||
| chr3:64655952
|
C | T | 1 | a0005c0008t0002g0175 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.970-77G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64655952 | ||||||
| chr3:64655985
|
G | C | 1 | a0001c0004t0001g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.970-110C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64655985 | ||||||
| chr3:64656022
|
C | T | 55 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0112others(52): Show | 55 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.970-147G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656022 | ||||||
| chr3:64656129
|
A | G | 5 | a0001c0001t0001g0279a0001c0009t0005g0069a0001c0009t0005g0070others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.970-254T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656129 | ||||||
| chr3:64656230
|
C | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0067others(253): Show | 257 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.970-355G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656230 | ||||||
| chr3:64656294
|
C | A | 1 | a0001c0001t0019g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.970-419G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656294 | ||||||
| chr3:64656380
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(186): Show | 190 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.970-505C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656380 | ||||||
| chr3:64656410
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.970-535C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656410 | ||||||
| chr3:64656418
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.970-543G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656418 | ||||||
| chr3:64656427
|
A | C | 1 | a0001c0007t0002g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.970-552T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656427 | ||||||
| chr3:64656637
|
G | A | 37 | a0001c0001t0001g0112a0001c0001t0001g0164a0001c0001t0001g0166others(34): Show | 37 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.970-762C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656637 | ||||||
| chr3:64656641
|
A | T | 11 | a0001c0001t0001g0158a0001c0001t0001g0263a0002c0002t0003g0153others(8): Show | 11 | HG02071.hp2 HG02135.hp1 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.970-766T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656641 | ||||||
| chr3:64656666
|
G | A | 37 | a0001c0001t0001g0112a0001c0001t0001g0164a0001c0001t0001g0166others(34): Show | 37 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.970-791C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656666 | ||||||
| chr3:64656678
|
C | T | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.970-803G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656678 | ||||||
| chr3:64656704
|
C | A | 1 | a0001c0004t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.970-829G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656704 | ||||||
| chr3:64656847
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.970-972T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656847 | ||||||
| chr3:64656851
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.970-976C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656851 | ||||||
| chr3:64656918
|
A | G | 1 | a0001c0001t0002g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.970-1043T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656918 | ||||||
| chr3:64656925
|
A | G | 10 | a0001c0001t0001g0158a0001c0001t0001g0263a0002c0002t0003g0153others(7): Show | 10 | HG02071.hp2 HG02135.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.970-1050T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656925 | ||||||
| chr3:64656947
|
C | T | 16 | a0001c0001t0001g0158a0001c0001t0001g0263a0001c0001t0020g0213others(13): Show | 16 | HG02071.hp2 HG02109.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.970-1072G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656947 | ||||||
| chr3:64656956
|
T | TC | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(224): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.970-1082dupG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64656956 | ||||||
| chr3:64657024
|
C | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0096others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.970-1149G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657024 | ||||||
| chr3:64657491
|
A | G | 10 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0250others(7): Show | 10 | HG02071.hp2 HG02135.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+1011T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657491 | ||||||
| chr3:64657509
|
G | GT | 96 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0114others(93): Show | 96 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.969+992dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657509 | ||||||
| chr3:64657509
|
G | GTT | 12 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0263others(9): Show | 12 | HG00597.hp2 HG00735.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.969+991_969+992dup others(2): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657509 | ||||||
| chr3:64657549
|
C | T | 1 | a0019c0040t0002g0148 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.969+953G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657549 | ||||||
| chr3:64657591
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.969+911C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657591 | ||||||
| chr3:64657611
|
T | G | 3 | a0001c0007t0002g0062a0001c0007t0002g0254a0001c0007t0013g0015 | 3 | HG02109.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.969+891A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657611 | ||||||
| chr3:64657618
|
A | G | 36 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0067others(33): Show | 36 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.969+884T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657618 | ||||||
| chr3:64657693
|
A | AT | 107 | a0001c0001t0001g0114a0001c0001t0001g0132a0001c0001t0001g0158others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.969+808dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657693 | ||||||
| chr3:64657816
|
G | A | 1 | a0012c0018t0006g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.969+686C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657816 | ||||||
| chr3:64657857
|
A | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.969+645T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657857 | ||||||
| chr3:64657974
|
A | G | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0020g0213others(1): Show | 4 | HG03540.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.969+528T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657974 | ||||||
| chr3:64657992
|
T | G | 28 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0279others(25): Show | 28 | HG00735.hp2 HG00738.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.969+510A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64657992 | ||||||
| chr3:64658103
|
C | T | 1 | a0001c0004t0001g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.969+399G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64658103 | ||||||
| chr3:64658105
|
G | C | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0020g0213others(1): Show | 4 | HG03540.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.969+397C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64658105 | ||||||
| chr3:64658247
|
G | A | 35 | a0001c0001t0001g0114a0001c0001t0001g0167a0001c0001t0001g0181others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.969+255C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64658247 | ||||||
| chr3:64658270
|
T | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0143a0001c0001t0002g0110others(1): Show | 4 | HG00597.hp1 HG00621.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.969+232A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64658270 | ||||||
| chr3:64658470
|
C | T | 2 | a0002c0002t0013g0016a0022c0036t0002g0214 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.969+32G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 4/39 | chr3 | 64658470 | ||||||
| chr3:64658873
|
T | C | 13 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0250others(10): Show | 13 | HG00609.hp2 HG02071.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.680-82A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64658873 | ||||||
| chr3:64658877
|
C | T | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.680-86G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64658877 | ||||||
| chr3:64658942
|
G | A | 3 | a0001c0007t0002g0062a0001c0007t0002g0254a0001c0007t0013g0015 | 3 | HG02109.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.680-151C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64658942 | ||||||
| chr3:64659032
|
G | A | 2 | a0002c0002t0013g0016a0022c0036t0002g0214 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680-241C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659032 | ||||||
| chr3:64659046
|
C | A | 1 | a0002c0002t0013g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.680-255G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659046 | ||||||
| chr3:64659055
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.680-264C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659055 | ||||||
| chr3:64659101
|
A | G | 2 | a0001c0001t0001g0218a0001c0006t0001g0206 | 2 | HG00642.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.680-310T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659101 | ||||||
| chr3:64659153
|
C | T | 1 | a0007c0011t0004g0179 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.680-362G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659153 | ||||||
| chr3:64659225
|
T | C | 7 | a0001c0004t0001g0236a0001c0004t0001g0238a0001c0004t0001g0239others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-434A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659225 | ||||||
| chr3:64659289
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0095others(14): Show | 18 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.680-498C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659289 | ||||||
| chr3:64659371
|
C | T | 2 | a0001c0051t0018g0268a0003c0003t0001g0059 | 2 | HG00735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.680-580G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659371 | ||||||
| chr3:64659473
|
C | CA | 7 | a0001c0001t0001g0113a0001c0001t0001g0199a0001c0001t0002g0088others(4): Show | 7 | HG02145.hp1 HG03195.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.680-683dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659473 | ||||||
| chr3:64659473
|
CA | C | 52 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0166others(49): Show | 52 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.680-683delT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659473 | ||||||
| chr3:64659499
|
G | A | 24 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0279others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.680-708C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659499 | ||||||
| chr3:64659701
|
C | A | 13 | a0001c0004t0001g0061a0001c0004t0001g0236a0001c0004t0001g0238others(10): Show | 13 | HG02486.hp1 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.680-910G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659701 | ||||||
| chr3:64659815
|
G | A | 7 | a0003c0003t0001g0023a0003c0003t0002g0024a0003c0003t0002g0025others(4): Show | 7 | HG01884.hp2 HG02895.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-1024C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659815 | ||||||
| chr3:64659823
|
C | T | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.680-1032G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659823 | ||||||
| chr3:64659870
|
T | A | 3 | a0001c0007t0002g0062a0001c0007t0002g0254a0001c0007t0013g0015 | 3 | HG02109.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.680-1079A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659870 | ||||||
| chr3:64659938
|
C | T | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0020g0213others(1): Show | 4 | HG03540.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-1147G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64659938 | ||||||
| chr3:64660004
|
A | G | 10 | a0001c0004t0001g0061a0001c0004t0001g0236a0001c0004t0001g0238others(7): Show | 10 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-1213T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660004 | ||||||
| chr3:64660012
|
T | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0095others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.680-1221A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660012 | ||||||
| chr3:64660042
|
A | G | 1 | a0001c0001t0002g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.680-1251T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660042 | ||||||
| chr3:64660197
|
T | C | 26 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0250others(23): Show | 26 | HG00609.hp2 HG02071.hp2 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.680-1406A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660197 | ||||||
| chr3:64660409
|
C | T | 3 | a0001c0004t0001g0276a0001c0004t0002g0277a0009c0028t0007g0275 | 3 | HG02572.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.680-1618G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660409 | ||||||
| chr3:64660454
|
A | C | 1 | a0001c0013t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.680-1663T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660454 | ||||||
| chr3:64660549
|
C | G | 7 | a0001c0001t0001g0279a0001c0001t0012g0013a0001c0001t0012g0014others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-1758G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660549 | ||||||
| chr3:64660812
|
A | G | 1 | a0002c0002t0001g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.680-2021T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660812 | ||||||
| chr3:64660891
|
A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0095others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.680-2100T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660891 | ||||||
| chr3:64660949
|
G | A | 11 | a0001c0004t0001g0061a0001c0004t0001g0236a0001c0004t0001g0238others(8): Show | 11 | HG02258.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.680-2158C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64660949 | ||||||
| chr3:64661005
|
A | G | 1 | a0002c0002t0003g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.680-2214T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661005 | ||||||
| chr3:64661095
|
A | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0090others(112): Show | 116 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.680-2304T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661095 | ||||||
| chr3:64661121
|
G | A | 13 | a0001c0001t0001g0067a0003c0003t0001g0022a0003c0003t0001g0023others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.680-2330C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661121 | ||||||
| chr3:64661159
|
T | G | 28 | a0001c0001t0001g0114a0001c0001t0001g0163a0001c0001t0001g0168others(25): Show | 28 | HG00544.hp1 HG00621.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.680-2368A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661159 | ||||||
| chr3:64661259
|
C | T | 32 | a0001c0001t0001g0018a0001c0001t0001g0143a0001c0001t0001g0197others(29): Show | 32 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-2468G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661259 | ||||||
| chr3:64661303
|
A | ACCAGTTG others(17): Show |
58 | a0001c0001t0001g0114a0001c0001t0001g0163a0001c0001t0001g0167others(55): Show | 58 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.680-2513_680-2512i others(26): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661303 | ||||||
| chr3:64661313
|
G | A | 137 | a0001c0001t0001g0090a0001c0001t0001g0114a0001c0001t0001g0120others(134): Show | 137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.680-2522C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661313 | ||||||
| chr3:64661395
|
T | C | 3 | a0001c0001t0002g0224a0001c0001t0007g0278a0002c0002t0001g0225 | 3 | HG01952.hp1 HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.680-2604A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661395 | ||||||
| chr3:64661477
|
C | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.680-2686G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661477 | ||||||
| chr3:64661480
|
G | A | 21 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0209others(18): Show | 21 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.680-2689C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661480 | ||||||
| chr3:64661709
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(103): Show | 107 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.680-2918T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661709 | ||||||
| chr3:64661854
|
T | G | 2 | a0001c0001t0002g0211a0001c0013t0001g0212 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.680-3063A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661854 | ||||||
| chr3:64661935
|
A | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.680-3144T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64661935 | ||||||
| chr3:64662155
|
C | G | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-3364G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64662155 | ||||||
| chr3:64662221
|
T | C | 1 | a0002c0002t0001g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.680-3430A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64662221 | ||||||
| chr3:64662391
|
G | A | 1 | a0001c0004t0001g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.680-3600C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64662391 | ||||||
| chr3:64662424
|
T | C | 34 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(31): Show | 34 | HG00099.hp2 HG01070.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.680-3633A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64662424 | ||||||
| chr3:64662480
|
A | G | 6 | a0001c0001t0002g0065a0001c0009t0005g0071a0001c0009t0005g0072others(3): Show | 6 | HG01934.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.680-3689T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64662480 | ||||||
| chr3:64662862
|
C | T | 1 | a0002c0002t0003g0196 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.680-4071G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64662862 | ||||||
| chr3:64662932
|
G | C | 4 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0006t0001g0207others(1): Show | 4 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-4141C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64662932 | ||||||
| chr3:64662932
|
G | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.680-4141C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64662932 | ||||||
| chr3:64663044
|
C | T | 4 | a0001c0004t0001g0276a0001c0004t0002g0277a0001c0013t0011g0005others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-4253G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663044 | ||||||
| chr3:64663102
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.680-4311C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663102 | ||||||
| chr3:64663208
|
T | C | 4 | a0001c0004t0001g0276a0001c0004t0002g0277a0001c0013t0011g0005others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-4417A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663208 | ||||||
| chr3:64663239
|
A | G | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-4448T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663239 | ||||||
| chr3:64663428
|
C | CT | 34 | a0001c0001t0001g0067a0001c0001t0001g0226a0001c0001t0002g0131others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.680-4638dupA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663428 | ||||||
| chr3:64663428
|
CT | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.680-4638delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663428 | ||||||
| chr3:64663453
|
A | AAGGGGAA others(27): Show |
1 | a0007c0011t0004g0086 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.680-4696_680-4663d others(36): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663453 | ||||||
| chr3:64663512
|
G | A | 2 | a0011c0022t0001g0270a0011c0022t0001g0271 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.680-4721C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663512 | ||||||
| chr3:64663518
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.680-4727A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663518 | ||||||
| chr3:64663642
|
C | A | 1 | a0001c0001t0001g0002 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.680-4851G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663642 | ||||||
| chr3:64663707
|
C | T | 12 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0250others(9): Show | 12 | HG00609.hp2 HG02071.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.680-4916G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663707 | ||||||
| chr3:64663752
|
C | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(104): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.680-4961G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663752 | ||||||
| chr3:64663794
|
C | T | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-5003G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663794 | ||||||
| chr3:64663836
|
T | C | 1 | a0003c0003t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.680-5045A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663836 | ||||||
| chr3:64663843
|
T | A | 2 | a0001c0007t0002g0062a0001c0007t0002g0254 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.680-5052A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663843 | ||||||
| chr3:64663906
|
A | G | 3 | a0001c0045t0001g0068a0002c0002t0013g0016a0022c0036t0002g0214 | 3 | HG03209.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.680-5115T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663906 | ||||||
| chr3:64663908
|
C | G | 28 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0120others(25): Show | 28 | HG00438.hp1 HG00544.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.680-5117G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64663908 | ||||||
| chr3:64664145
|
A | G | 1 | a0001c0001t0002g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.680-5354T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664145 | ||||||
| chr3:64664273
|
T | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.680-5482A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664273 | ||||||
| chr3:64664614
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0133others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.680-5823G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664614 | ||||||
| chr3:64664650
|
C | T | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-5859G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664650 | ||||||
| chr3:64664783
|
T | C | 23 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(20): Show | 23 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.680-5992A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664783 | ||||||
| chr3:64664791
|
C | T | 6 | a0001c0001t0002g0065a0001c0009t0005g0071a0001c0009t0005g0072others(3): Show | 6 | HG01934.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.680-6000G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664791 | ||||||
| chr3:64664866
|
T | C | 23 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(20): Show | 23 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.680-6075A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664866 | ||||||
| chr3:64664911
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0133others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.680-6120C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664911 | ||||||
| chr3:64664987
|
T | C | 8 | a0001c0001t0001g0158a0001c0001t0001g0159a0002c0002t0003g0153others(5): Show | 8 | HG02071.hp2 HG02135.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-6196A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64664987 | ||||||
| chr3:64665148
|
C | A | 1 | a0002c0002t0001g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.680-6357G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665148 | ||||||
| chr3:64665183
|
G | A | 3 | a0001c0001t0001g0263a0006c0010t0001g0264a0006c0010t0001g0265 | 3 | NA18955.hp2 NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.680-6392C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665183 | ||||||
| chr3:64665196
|
C | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.680-6405G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665196 | ||||||
| chr3:64665204
|
A | G | 30 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0120others(27): Show | 30 | HG00438.hp1 HG00544.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.680-6413T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665204 | ||||||
| chr3:64665251
|
C | T | 27 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0124others(24): Show | 27 | HG00438.hp1 HG01255.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.680-6460G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665251 | ||||||
| chr3:64665320
|
A | G | 53 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0079others(50): Show | 53 | HG00099.hp2 HG01070.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.680-6529T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665320 | ||||||
| chr3:64665334
|
G | A | 5 | a0001c0001t0002g0065a0001c0009t0005g0071a0001c0009t0005g0072others(2): Show | 5 | HG01934.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-6543C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665334 | ||||||
| chr3:64665377
|
C | T | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-6586G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665377 | ||||||
| chr3:64665426
|
C | T | 27 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0124others(24): Show | 27 | HG00438.hp1 HG01255.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.680-6635G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665426 | ||||||
| chr3:64665713
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.680-6922G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665713 | ||||||
| chr3:64665733
|
T | C | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.680-6942A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665733 | ||||||
| chr3:64665786
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.680-6995T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665786 | ||||||
| chr3:64665960
|
G | A | 6 | a0001c0001t0002g0065a0001c0009t0005g0071a0001c0009t0005g0072others(3): Show | 6 | HG01934.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.680-7169C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64665960 | ||||||
| chr3:64666005
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.680-7214T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666005 | ||||||
| chr3:64666006
|
T | G | 1 | a0001c0001t0002g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.680-7215A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666006 | ||||||
| chr3:64666038
|
C | T | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-7247G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666038 | ||||||
| chr3:64666080
|
A | T | 20 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(17): Show | 20 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.680-7289T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666080 | ||||||
| chr3:64666197
|
T | C | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-7406A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666197 | ||||||
| chr3:64666214
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.680-7423T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666214 | ||||||
| chr3:64666244
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0133others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.680-7453C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666244 | ||||||
| chr3:64666248
|
T | A | 2 | a0001c0001t0001g0133a0031c0027t0002g0051 | 2 | HG00741.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.680-7457A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666248 | ||||||
| chr3:64666432
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0014g0012 | 2 | HG02717.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.680-7641T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666432 | ||||||
| chr3:64666628
|
T | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0079others(47): Show | 50 | HG00099.hp2 HG01070.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.680-7837A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666628 | ||||||
| chr3:64666646
|
T | A | 1 | a0001c0001t0003g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.680-7855A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666646 | ||||||
| chr3:64666653
|
AT | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0133others(96): Show | 100 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.680-7863delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666653 | ||||||
| chr3:64666726
|
A | G | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-7935T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666726 | ||||||
| chr3:64666803
|
A | T | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.680-8012T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666803 | ||||||
| chr3:64666929
|
C | T | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-8138G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64666929 | ||||||
| chr3:64667416
|
C | G | 2 | a0002c0002t0013g0016a0022c0036t0002g0214 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680-8625G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64667416 | ||||||
| chr3:64667436
|
G | A | 1 | a0001c0004t0001g0276 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.680-8645C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64667436 | ||||||
| chr3:64667522
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.680-8731A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64667522 | ||||||
| chr3:64667641
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.680-8850C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64667641 | ||||||
| chr3:64667772
|
T | C | 23 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(20): Show | 23 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.680-8981A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64667772 | ||||||
| chr3:64667836
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.680-9045A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64667836 | ||||||
| chr3:64667979
|
G | C | 31 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(28): Show | 31 | HG00735.hp2 HG00738.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.680-9188C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64667979 | ||||||
| chr3:64668070
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.680-9279G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668070 | ||||||
| chr3:64668220
|
T | A | 44 | a0001c0001t0001g0019a0001c0001t0001g0197a0001c0001t0001g0198others(41): Show | 44 | HG00099.hp2 HG01070.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.680-9429A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668220 | ||||||
| chr3:64668292
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0133others(63): Show | 67 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.680-9501A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668292 | ||||||
| chr3:64668381
|
T | C | 1 | a0001c0007t0013g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.680-9590A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668381 | ||||||
| chr3:64668427
|
A | G | 202 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.680-9636T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668427 | ||||||
| chr3:64668450
|
G | A | 20 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(17): Show | 20 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.680-9659C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668450 | ||||||
| chr3:64668592
|
T | C | 1 | a0001c0006t0001g0206 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.680-9801A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668592 | ||||||
| chr3:64668628
|
C | T | 26 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(23): Show | 26 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.680-9837G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668628 | ||||||
| chr3:64668640
|
T | C | 2 | a0002c0002t0003g0077a0002c0002t0003g0078 | 2 | HG02083.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.680-9849A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668640 | ||||||
| chr3:64668699
|
G | A | 1 | a0001c0001t0020g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.680-9908C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668699 | ||||||
| chr3:64668743
|
C | G | 18 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(15): Show | 18 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.680-9952G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668743 | ||||||
| chr3:64668747
|
G | T | 1 | a0001c0006t0001g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.680-9956C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668747 | ||||||
| chr3:64668852
|
A | G | 1 | a0002c0002t0001g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.680-10061T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668852 | ||||||
| chr3:64668953
|
C | T | 23 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(20): Show | 23 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.680-10162G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668953 | ||||||
| chr3:64668967
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.680-10176T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64668967 | ||||||
| chr3:64669003
|
G | A | 28 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0124others(25): Show | 28 | HG00438.hp1 HG01255.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.680-10212C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64669003 | ||||||
| chr3:64669134
|
G | C | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.680-10343C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64669134 | ||||||
| chr3:64669188
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.680-10397A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64669188 | ||||||
| chr3:64669421
|
A | G | 2 | a0001c0004t0001g0276a0001c0004t0002g0277 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.680-10630T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64669421 | ||||||
| chr3:64669640
|
C | T | 4 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0017g0066others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-10849G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64669640 | ||||||
| chr3:64669654
|
C | T | 3 | a0001c0001t0002g0244a0001c0001t0002g0246a0006c0010t0001g0245 | 3 | NA18982.hp2 NA18983.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.680-10863G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64669654 | ||||||
| chr3:64669681
|
T | G | 99 | a0001c0001t0001g0067a0001c0001t0001g0090a0001c0001t0001g0120others(96): Show | 99 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.680-10890A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64669681 | ||||||
| chr3:64670004
|
C | A | 4 | a0001c0004t0001g0276a0001c0004t0002g0277a0001c0013t0011g0005others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+11197G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670004 | ||||||
| chr3:64670011
|
C | T | 28 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0124others(25): Show | 28 | HG00438.hp1 HG00738.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.679+11190G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670011 | ||||||
| chr3:64670048
|
A | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.679+11153T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670048 | ||||||
| chr3:64670083
|
T | C | 23 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(20): Show | 23 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.679+11118A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670083 | ||||||
| chr3:64670118
|
T | C | 2 | a0003c0003t0002g0031a0004c0005t0001g0030 | 2 | HG00735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.679+11083A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670118 | ||||||
| chr3:64670133
|
TGTCTCA | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.679+11062_679+1106 others(10): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670133 | ||||||
| chr3:64670243
|
G | A | 9 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0250others(6): Show | 9 | HG02071.hp2 HG02135.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+10958C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670243 | ||||||
| chr3:64670421
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.679+10780T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670421 | ||||||
| chr3:64670447
|
C | T | 4 | a0001c0004t0001g0276a0001c0004t0002g0277a0001c0013t0011g0005others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+10754G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670447 | ||||||
| chr3:64670534
|
A | G | 30 | a0001c0001t0001g0067a0001c0001t0002g0217a0001c0001t0002g0228others(27): Show | 30 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.679+10667T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670534 | ||||||
| chr3:64670543
|
T | A | 5 | a0001c0001t0001g0186a0001c0001t0002g0187a0002c0002t0003g0185others(2): Show | 5 | HG02040.hp2 NA19004.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+10658A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670543 | ||||||
| chr3:64670610
|
A | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.679+10591T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64670610 | ||||||
| chr3:64671001
|
C | T | 18 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(15): Show | 18 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.679+10200G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64671001 | ||||||
| chr3:64671103
|
G | A | 2 | a0001c0004t0001g0276a0001c0004t0002g0277 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.679+10098C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64671103 | ||||||
| chr3:64671619
|
G | A | 2 | a0001c0007t0002g0062a0001c0007t0002g0254 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.679+9582C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64671619 | ||||||
| chr3:64671963
|
C | T | 2 | a0001c0001t0002g0172a0012c0018t0006g0173 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.679+9238G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64671963 | ||||||
| chr3:64672129
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.679+9072A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64672129 | ||||||
| chr3:64672340
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.679+8861C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64672340 | ||||||
| chr3:64672415
|
G | A | 2 | a0001c0001t0001g0127a0001c0014t0002g0126 | 2 | HG00438.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.679+8786C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64672415 | ||||||
| chr3:64672640
|
G | A | 40 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0197others(37): Show | 40 | HG00099.hp2 HG01934.hp1 HG01978.hp2 others(37): Show |
intron_variant | MODIFIER | c.679+8561C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64672640 | ||||||
| chr3:64672673
|
ACT | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0133others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.679+8526_679+8527d others(4): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64672673 | ||||||
| chr3:64672676
|
C | T | 1 | a0001c0014t0001g0091 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.679+8525G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64672676 | ||||||
| chr3:64672737
|
T | C | 95 | a0001c0001t0001g0067a0001c0001t0001g0158a0001c0001t0001g0159others(92): Show | 95 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.679+8464A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64672737 | ||||||
| chr3:64672764
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.679+8437G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64672764 | ||||||
| chr3:64673010
|
T | TGTAGCCT others(23): Show |
23 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(20): Show | 23 | HG00099.hp2 HG01978.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.679+8161_679+8190d others(32): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673010 | ||||||
| chr3:64673070
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.679+8131G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673070 | ||||||
| chr3:64673167
|
A | T | 2 | a0001c0001t0002g0217a0001c0001t0002g0273 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.679+8034T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673167 | ||||||
| chr3:64673182
|
C | T | 1 | a0004c0005t0015g0010 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.679+8019G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673182 | ||||||
| chr3:64673208
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.679+7993T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673208 | ||||||
| chr3:64673431
|
G | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.679+7770C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673431 | ||||||
| chr3:64673436
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(102): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.679+7765C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673436 | ||||||
| chr3:64673454
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.679+7747C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673454 | ||||||
| chr3:64673598
|
T | C | 27 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0124others(24): Show | 27 | HG00438.hp1 HG01255.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.679+7603A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673598 | ||||||
| chr3:64673650
|
G | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0006t0001g0207others(1): Show | 4 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+7551C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673650 | ||||||
| chr3:64673716
|
A | G | 1 | a0001c0007t0002g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.679+7485T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673716 | ||||||
| chr3:64673816
|
A | T | 1 | a0003c0003t0001g0035 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.679+7385T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673816 | ||||||
| chr3:64673996
|
G | A | 1 | a0001c0051t0018g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.679+7205C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673996 | ||||||
| chr3:64673996
|
G | T | 1 | a0003c0003t0001g0035 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.679+7205C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64673996 | ||||||
| chr3:64674026
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.679+7175A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674026 | ||||||
| chr3:64674065
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.679+7136A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674065 | ||||||
| chr3:64674082
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0222others(10): Show | 14 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.679+7119A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674082 | ||||||
| chr3:64674091
|
AG | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.679+7109delC | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674091 | ||||||
| chr3:64674093
|
T | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0114others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.679+7108A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674093 | ||||||
| chr3:64674094
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.679+7107A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674094 | ||||||
| chr3:64674276
|
G | GA | 24 | a0001c0001t0001g0143a0001c0001t0001g0167a0001c0001t0001g0191others(21): Show | 24 | HG00597.hp2 HG00621.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.679+6924dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674276 | ||||||
| chr3:64674662
|
A | G | 4 | a0001c0001t0001g0085a0001c0001t0002g0083a0001c0001t0002g0084others(1): Show | 4 | NA18960.hp2 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+6539T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674662 | ||||||
| chr3:64674697
|
T | C | 6 | a0001c0001t0002g0065a0001c0009t0005g0071a0001c0009t0005g0072others(3): Show | 6 | HG01934.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+6504A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64674697 | ||||||
| chr3:64675085
|
A | G | 30 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0124others(27): Show | 30 | HG00438.hp1 HG01255.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.679+6116T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64675085 | ||||||
| chr3:64675124
|
C | T | 2 | a0001c0001t0001g0171a0029c0032t0001g0259 | 2 | NA18988.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.679+6077G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64675124 | ||||||
| chr3:64675232
|
G | A | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.679+5969C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64675232 | ||||||
| chr3:64675438
|
G | T | 2 | a0002c0002t0003g0160a0013c0019t0004g0161 | 2 | NA19062.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.679+5763C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64675438 | ||||||
| chr3:64675560
|
A | G | 22 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(19): Show | 22 | HG00642.hp2 HG01257.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.679+5641T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64675560 | ||||||
| chr3:64675772
|
C | G | 13 | a0001c0001t0001g0067a0003c0003t0001g0022a0003c0003t0001g0023others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.679+5429G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64675772 | ||||||
| chr3:64675899
|
A | G | 1 | a0014c0041t0001g0280 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.679+5302T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64675899 | ||||||
| chr3:64675929
|
A | G | 15 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0139others(12): Show | 15 | HG00558.hp2 HG02027.hp2 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.679+5272T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64675929 | ||||||
| chr3:64676023
|
C | T | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.679+5178G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676023 | ||||||
| chr3:64676377
|
G | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0133others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.679+4824C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676377 | ||||||
| chr3:64676492
|
C | T | 6 | a0001c0004t0001g0276a0001c0004t0002g0277a0001c0007t0002g0062others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+4709G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676492 | ||||||
| chr3:64676521
|
T | TA | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.679+4679dupT | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676521 | ||||||
| chr3:64676621
|
T | C | 2 | a0001c0001t0002g0253a0030c0046t0002g0252 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.679+4580A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676621 | ||||||
| chr3:64676652
|
GC | G | 14 | a0001c0001t0002g0228a0001c0001t0012g0013a0001c0001t0012g0014others(11): Show | 14 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.679+4548delG | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676652 | ||||||
| chr3:64676688
|
G | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0079others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.679+4513C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676688 | ||||||
| chr3:64676707
|
G | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0080others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.679+4494C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676707 | ||||||
| chr3:64676851
|
C | G | 3 | a0001c0045t0001g0068a0002c0002t0013g0016a0022c0036t0002g0214 | 3 | HG03209.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.679+4350G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676851 | ||||||
| chr3:64676939
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.679+4262G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676939 | ||||||
| chr3:64676953
|
C | G | 80 | a0001c0001t0001g0067a0001c0001t0001g0120a0001c0001t0001g0124others(77): Show | 80 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.679+4248G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64676953 | ||||||
| chr3:64677047
|
C | T | 8 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0250others(5): Show | 8 | HG02071.hp2 HG02135.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.679+4154G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64677047 | ||||||
| chr3:64677164
|
G | T | 8 | a0001c0001t0001g0139a0001c0001t0002g0244a0001c0001t0002g0246others(5): Show | 8 | HG00558.hp2 NA18953.hp2 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.679+4037C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64677164 | ||||||
| chr3:64677232
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.679+3969T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64677232 | ||||||
| chr3:64677375
|
C | T | 6 | a0001c0004t0001g0276a0001c0004t0002g0277a0001c0007t0002g0062others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+3826G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64677375 | ||||||
| chr3:64677780
|
A | G | 14 | a0001c0001t0002g0228a0001c0001t0012g0013a0001c0001t0012g0014others(11): Show | 14 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.679+3421T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64677780 | ||||||
| chr3:64677888
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.679+3313C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64677888 | ||||||
| chr3:64678039
|
G | A | 1 | a0003c0003t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.679+3162C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678039 | ||||||
| chr3:64678056
|
T | A | 2 | a0001c0007t0002g0219a0002c0002t0001g0220 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.679+3145A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678056 | ||||||
| chr3:64678093
|
G | C | 1 | a0012c0018t0006g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.679+3108C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678093 | ||||||
| chr3:64678187
|
T | C | 1 | a0001c0004t0002g0277 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.679+3014A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678187 | ||||||
| chr3:64678212
|
C | T | 47 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0125others(44): Show | 47 | HG00438.hp1 HG00642.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.679+2989G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678212 | ||||||
| chr3:64678427
|
C | A | 1 | a0004c0005t0015g0010 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.679+2774G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678427 | ||||||
| chr3:64678638
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0167others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.679+2563C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678638 | ||||||
| chr3:64678772
|
C | T | 5 | a0001c0001t0002g0065a0001c0009t0005g0071a0001c0009t0005g0072others(2): Show | 5 | HG01934.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+2429G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678772 | ||||||
| chr3:64678780
|
G | A | 37 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(34): Show | 37 | HG00099.hp2 HG01070.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.679+2421C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678780 | ||||||
| chr3:64678862
|
C | A | 1 | a0001c0001t0019g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.679+2339G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64678862 | ||||||
| chr3:64679049
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.679+2152G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64679049 | ||||||
| chr3:64679093
|
C | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0067others(210): Show | 214 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.679+2108G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64679093 | ||||||
| chr3:64679201
|
T | C | 2 | a0001c0001t0002g0250a0014c0054t0001g0283 | 2 | HG03688.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.679+2000A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64679201 | ||||||
| chr3:64679340
|
C | T | 1 | a0003c0003t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.679+1861G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64679340 | ||||||
| chr3:64679430
|
T | C | 4 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0007t0013g0015others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+1771A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64679430 | ||||||
| chr3:64679625
|
A | C | 3 | a0003c0003t0007g0037a0003c0003t0007g0038a0004c0005t0001g0036 | 3 | HG02895.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.679+1576T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64679625 | ||||||
| chr3:64679678
|
G | A | 13 | a0001c0001t0001g0067a0003c0003t0001g0022a0003c0003t0001g0023others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.679+1523C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64679678 | ||||||
| chr3:64679992
|
G | A | 40 | a0001c0001t0002g0282a0003c0003t0001g0021a0003c0003t0001g0022others(37): Show | 40 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.679+1209C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64679992 | ||||||
| chr3:64680055
|
T | C | 1 | a0003c0003t0001g0035 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.679+1146A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680055 | ||||||
| chr3:64680057
|
A | T | 1 | a0003c0003t0001g0035 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.679+1144T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680057 | ||||||
| chr3:64680263
|
T | C | 4 | a0001c0001t0002g0131a0011c0022t0001g0270a0011c0022t0001g0271others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+938A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680263 | ||||||
| chr3:64680374
|
G | A | 4 | a0001c0001t0002g0131a0011c0022t0001g0270a0011c0022t0001g0271others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+827C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680374 | ||||||
| chr3:64680398
|
G | A | 2 | a0003c0003t0002g0057a0003c0003t0002g0058 | 2 | NA18995.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.679+803C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680398 | ||||||
| chr3:64680489
|
A | G | 1 | a0001c0045t0001g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.679+712T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680489 | ||||||
| chr3:64680505
|
C | A | 10 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0125others(7): Show | 10 | HG00438.hp1 HG02056.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.679+696G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680505 | ||||||
| chr3:64680545
|
C | A | 2 | a0001c0001t0001g0251a0001c0023t0001g0020 | 2 | HG01255.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.679+656G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680545 | ||||||
| chr3:64680545
|
C | G | 82 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0143others(79): Show | 82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.679+656G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680545 | ||||||
| chr3:64680552
|
A | G | 45 | a0001c0001t0001g0067a0001c0001t0002g0131a0001c0001t0002g0282others(42): Show | 45 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.679+649T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680552 | ||||||
| chr3:64680559
|
A | C | 2 | a0001c0001t0001g0018a0001c0007t0001g0017 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.679+642T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680559 | ||||||
| chr3:64680570
|
G | A | 28 | a0001c0001t0002g0282a0003c0003t0001g0021a0003c0003t0001g0035others(25): Show | 28 | HG00741.hp1 HG01123.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.679+631C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680570 | ||||||
| chr3:64680593
|
A | T | 41 | a0001c0001t0001g0067a0001c0001t0002g0282a0003c0003t0001g0021others(38): Show | 41 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.679+608T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680593 | ||||||
| chr3:64680739
|
A | G | 2 | a0001c0001t0001g0018a0001c0007t0001g0017 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.679+462T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680739 | ||||||
| chr3:64680750
|
C | T | 1 | a0010c0012t0004g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.679+451G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680750 | ||||||
| chr3:64680772
|
T | A | 2 | a0001c0001t0002g0253a0030c0046t0002g0252 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.679+429A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64680772 | ||||||
| chr3:64681048
|
A | C | 1 | a0014c0054t0001g0283 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.679+153T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64681048 | ||||||
| chr3:64681127
|
A | G | 4 | a0001c0001t0002g0131a0011c0022t0001g0270a0011c0022t0001g0271others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+74T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 3/39 | chr3 | 64681127 | ||||||
| chr3:64681383
|
G | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(64): Show | 68 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.517-20C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64681383 | ||||||
| chr3:64681431
|
G | T | 1 | a0002c0002t0003g0165 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.517-68C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64681431 | ||||||
| chr3:64681455
|
T | C | 1 | a0003c0003t0001g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.517-92A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64681455 | ||||||
| chr3:64681495
|
T | G | 1 | a0014c0054t0001g0283 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.517-132A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64681495 | ||||||
| chr3:64681697
|
T | C | 3 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0007t0002g0254 | 3 | HG02109.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.517-334A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64681697 | ||||||
| chr3:64681716
|
T | C | 3 | a0001c0001t0001g0018a0001c0007t0001g0017a0014c0054t0001g0283 | 3 | HG02723.hp2 HG03471.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.517-353A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64681716 | ||||||
| chr3:64681912
|
T | C | 1 | a0001c0004t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517-549A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64681912 | ||||||
| chr3:64681968
|
A | AAGCTGGC others(6): Show |
2 | a0001c0001t0001g0143a0002c0002t0003g0142 | 2 | NA19004.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.517-618_517-606dup others(13): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64681968 | ||||||
| chr3:64682184
|
G | A | 41 | a0001c0001t0002g0282a0003c0003t0001g0021a0003c0003t0001g0022others(38): Show | 41 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.517-821C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682184 | ||||||
| chr3:64682260
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.517-897G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682260 | ||||||
| chr3:64682272
|
G | T | 11 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0163others(8): Show | 11 | HG00544.hp1 HG02071.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-909C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682272 | ||||||
| chr3:64682387
|
C | T | 1 | a0002c0002t0003g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.517-1024G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682387 | ||||||
| chr3:64682473
|
C | G | 13 | a0001c0001t0001g0067a0003c0003t0001g0022a0003c0003t0001g0023others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.517-1110G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682473 | ||||||
| chr3:64682583
|
G | A | 1 | a0001c0001t0002g0137 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.517-1220C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682583 | ||||||
| chr3:64682771
|
C | T | 2 | a0001c0001t0002g0065a0001c0001t0017g0066 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.517-1408G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682771 | ||||||
| chr3:64682850
|
G | T | 1 | a0003c0003t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.517-1487C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682850 | ||||||
| chr3:64682935
|
C | A | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.517-1572G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64682935 | ||||||
| chr3:64683043
|
G | T | 19 | a0001c0001t0001g0143a0001c0001t0001g0263a0001c0001t0002g0147others(16): Show | 19 | HG00597.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.517-1680C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683043 | ||||||
| chr3:64683187
|
G | C | 49 | a0001c0001t0002g0282a0001c0001t0012g0013a0001c0001t0012g0014others(46): Show | 49 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.517-1824C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683187 | ||||||
| chr3:64683302
|
C | G | 1 | a0002c0002t0003g0141 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.517-1939G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683302 | ||||||
| chr3:64683448
|
G | A | 1 | a0003c0003t0001g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.517-2085C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683448 | ||||||
| chr3:64683631
|
A | G | 1 | a0014c0054t0001g0283 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.517-2268T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683631 | ||||||
| chr3:64683640
|
AT | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0279a0001c0001t0007g0278others(6): Show | 9 | HG01884.hp1 HG01952.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-2278delA | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683640 | ||||||
| chr3:64683656
|
T | G | 50 | a0001c0001t0001g0067a0001c0001t0002g0282a0001c0001t0012g0013others(47): Show | 50 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.517-2293A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683656 | ||||||
| chr3:64683664
|
A | C | 3 | a0001c0001t0001g0139a0002c0002t0003g0138a0020c0034t0001g0140 | 3 | NA18983.hp2 NA18991.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.517-2301T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683664 | ||||||
| chr3:64683939
|
G | A | 49 | a0001c0001t0002g0282a0001c0001t0012g0013a0001c0001t0012g0014others(46): Show | 49 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.517-2576C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64683939 | ||||||
| chr3:64684015
|
T | C | 7 | a0001c0001t0001g0263a0001c0001t0003g0262a0002c0002t0003g0260others(4): Show | 7 | HG00597.hp2 NA18955.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+2553A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684015 | ||||||
| chr3:64684235
|
G | A | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.516+2333C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684235 | ||||||
| chr3:64684335
|
G | A | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.516+2233C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684335 | ||||||
| chr3:64684337
|
C | T | 4 | a0011c0022t0001g0270a0011c0022t0001g0271a0011c0053t0002g0272others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+2231G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684337 | ||||||
| chr3:64684338
|
G | GA | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2229_516+2230i others(3): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684338 | ||||||
| chr3:64684339
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2229C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684339 | ||||||
| chr3:64684341
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2227G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684341 | ||||||
| chr3:64684342
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2226C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684342 | ||||||
| chr3:64684344
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2224G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684344 | ||||||
| chr3:64684345
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2223G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684345 | ||||||
| chr3:64684346
|
C | CAGAA | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2221_516+2222i others(6): Show |
ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684346 | ||||||
| chr3:64684348
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2220A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684348 | ||||||
| chr3:64684349
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.516+2219G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684349 | ||||||
| chr3:64684363
|
A | C | 3 | a0001c0009t0005g0071a0001c0009t0005g0072a0001c0009t0005g0073 | 3 | HG01934.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.516+2205T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684363 | ||||||
| chr3:64684729
|
A | C | 44 | a0001c0001t0001g0067a0001c0009t0005g0069a0001c0009t0005g0070others(41): Show | 44 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.516+1839T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64684729 | ||||||
| chr3:64685205
|
C | T | 1 | a0014c0054t0001g0283 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.516+1363G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685205 | ||||||
| chr3:64685206
|
C | T | 2 | a0001c0001t0002g0065a0001c0001t0017g0066 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.516+1362G>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685206 | ||||||
| chr3:64685208
|
C | G | 1 | a0002c0002t0001g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.516+1360G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685208 | ||||||
| chr3:64685240
|
C | A | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.516+1328G>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685240 | ||||||
| chr3:64685347
|
C | G | 1 | a0032c0052t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.516+1221G>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685347 | ||||||
| chr3:64685482
|
T | G | 2 | a0002c0002t0001g0266a0002c0002t0001g0267 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.516+1086A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685482 | ||||||
| chr3:64685687
|
G | A | 4 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0007t0013g0015others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+881C>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685687 | ||||||
| chr3:64685691
|
G | T | 2 | a0001c0001t0001g0018a0001c0007t0001g0017 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.516+877C>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685691 | ||||||
| chr3:64685799
|
A | C | 1 | a0001c0001t0016g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.516+769T>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685799 | ||||||
| chr3:64685893
|
T | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0012g0013others(6): Show | 9 | HG01257.hp1 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.516+675A>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685893 | ||||||
| chr3:64685994
|
A | G | 1 | a0001c0006t0010g0003 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.516+574T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64685994 | ||||||
| chr3:64686061
|
A | T | 2 | a0001c0004t0001g0061a0001c0007t0002g0062 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.516+507T>A | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 2/39 | chr3 | 64686061 | ||||||
| chr3:64687048
|
G | C | 7 | a0001c0001t0001g0279a0001c0001t0002g0273a0001c0001t0007g0278others(4): Show | 7 | HG01884.hp1 HG01952.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.116-80C>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/39 | chr3 | 64687048 | ||||||
| chr3:64687099
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0012g0013others(7): Show | 10 | HG01257.hp1 HG02257.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-131T>C | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/39 | chr3 | 64687099 | ||||||
| chr3:64687219
|
T | C | 2 | a0001c0001t0002g0281a0014c0041t0001g0280 | 2 | HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.116-251A>G | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/39 | chr3 | 64687219 | ||||||
| chr3:64687318
|
T | A | 1 | a0001c0001t0002g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.115+225A>T | ADAMTS9 | ENSG00000163638.13 | transcript | ENST00000498707.5 | protein_coding | 1/39 | chr3 | 64687318 |