Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8754 |
|---|---|
| ensemblid | ENSG00000168615.13 |
| hgncid | 216 |
| symbol | ADAM9 |
| name | ADAM metallopeptidase domain 9 |
| refseq_nuc | NM_003816.3 |
| refseq_prot | NP_003807.1 |
| ensembl_nuc | ENST00000487273.7 |
| ensembl_prot | ENSP00000419446.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 38996973 |
| end | 39105261 |
| strand | + |
| ver | v1.2 |
| region | chr8:38996973-39105261 |
| region5000 | chr8:38991973-39110261 |
| regionname0 | ADAM9_chr8_38996973_39105261 |
| regionname5000 | ADAM9_chr8_38991973_39110261 |
| 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 | 819 | 313 | 71 | 59 | 129 | 10 | 42 | 101 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0002 | 0/0 | 819 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0003 | 0/0 | 819 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0004 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0005 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0006 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| 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 | 2460 | 304 | 70 | 54 | 127 | 9 | 42 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0002 | 0/0 | 2460 | 13 | 13 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0003 | 0/0 | 2460 | 7 | 1 | 5 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0004 | 0/0 | 2460 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0005 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0006 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0007 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0008 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0009 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| c0010 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1653 | 315 | 70 | 60 | 132 | 10 | 42 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| t0002 | 1/0 | 1653 | 15 | 14 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| t0003 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| t0004 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| 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 | 2460 | 304 | 70 | 54 | 127 | 9 | 42 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0003 | 0/0 | 2460 | 7 | 1 | 5 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0006 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0007 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0002c0002 | 0/0 | 2460 | 13 | 13 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0002c0010 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0003c0004 | 0/0 | 2460 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0004c0008 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0005c0009 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0006c0005 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4112 | 301 | 68 | 54 | 127 | 9 | 42 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0001t0002 | 1/0 | 4112 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0001t0003 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0001t0004 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0003t0001 | 0/0 | 4112 | 7 | 1 | 5 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0006t0001 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0001c0007t0001 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0002c0002t0002 | 0/0 | 4112 | 13 | 13 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0002c0010t0002 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0003c0004t0001 | 0/0 | 4112 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0004c0008t0001 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0005c0009t0001 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| a0006c0005t0001 | 0/0 | 4112 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | copy fasta | chr8 | 38991973 | 39110261 |
| 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 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0002g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0007t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0010t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0003c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0003c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0004c0008t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0005c0009t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0006c0005t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | GBR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0294 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0290 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0206 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0258 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0245 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02165 | hp1 | a0001 | c0007 | t0001 | g0267 | EAS | CDX | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0187 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0188 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0197 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0332 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02717 | hp2 | a0004 | c0008 | t0001 | g0120 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0194 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0193 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0189 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0130 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18945 | hp1 | a0001 | c0006 | t0001 | g0256 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18963 | hp2 | a0003 | c0004 | t0001 | g0302 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19064 | hp1 | a0003 | c0004 | t0001 | g0301 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19066 | hp1 | a0005 | c0009 | t0001 | g0163 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20129 | hp1 | a0002 | c0010 | t0002 | g0198 | AFR | ASW | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ASW | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0295 | EUR | TSI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01123 | hp2 | a0006 | c0005 | t0001 | g0292 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0293 | AFR | USA | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0190 | AFR | USA | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | USA | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0110 | REF | REF | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0168 | REF | REF | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38997149
|
C | T | 1 | a0006 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.86C>T | p.Ala29Val | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/22 | 177/4112 | 86/2460 | 29/819 | chr8 | 38997149 | ||
| chr8:39021671
|
C | T | 1 | a0002 | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
missense_variant | MODERATE | c.701C>T | p.Ala234Val | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/22 | 792/4112 | 701/2460 | 234/819 | chr8 | 39021671 | ||
| chr8:39026784
|
G | T | 1 | a0005 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.1104G>T | p.Lys368Asn | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/22 | 1195/4112 | 1104/2460 | 368/819 | chr8 | 39026784 | ||
| chr8:39054572
|
G | A | 1 | a0003 | 2 | NA18963.hp2 NA19064.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1394G>A | p.Arg465Gln | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/22 | 1485/4112 | 1394/2460 | 465/819 | chr8 | 39054572 | ||
| chr8:39090082
|
T | G | 1 | a0004 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2104T>G | p.Phe702Val | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/22 | 2195/4112 | 2104/2460 | 702/819 | chr8 | 39090082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38997141
|
C | A | 2 | a0001c0003a0006c0005 | 8 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(5): Show |
synonymous_variant | LOW | c.78C>A | p.Val26Val | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/22 | 169/4112 | 78/2460 | 26/819 | chr8 | 38997141 | ||
| chr8:39042033
|
A | G | 1 | a0002c0002 | 13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.1218A>G | p.Pro406Pro | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/22 | 1309/4112 | 1218/2460 | 406/819 | chr8 | 39042033 | ||
| chr8:39042051
|
T | C | 1 | a0001c0006 | 1 | NA18945.hp1 | synonymous_variant | LOW | c.1236T>C | p.Tyr412Tyr | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/22 | 1327/4112 | 1236/2460 | 412/819 | chr8 | 39042051 | ||
| chr8:39077258
|
G | A | 1 | a0001c0007 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.1728G>A | p.Glu576Glu | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/22 | 1819/4112 | 1728/2460 | 576/819 | chr8 | 39077258 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38997060
|
C | T | 1 | a0001c0001t0004 | 1 | HG02647.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-4C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/22 | chr8 | 38997060 | ||||||
| chr8:39104031
|
G | T | 10 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 22/22 | 331 | chr8 | 39104031 | |||||
| chr8:39104186
|
A | G | 1 | a0001c0001t0003 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 22/22 | 486 | chr8 | 39104186 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38997399
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+239C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997399 | ||||||
| chr8:38997440
|
C | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+280C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997440 | ||||||
| chr8:38997450
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.97+290C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997450 | ||||||
| chr8:38997543
|
G | T | 127 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.97+383G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997543 | ||||||
| chr8:38997651
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.97+491T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997651 | ||||||
| chr8:38997857
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.97+697C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997857 | ||||||
| chr8:38998026
|
T | C | 1 | a0001c0003t0001g0206 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.97+866T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998026 | ||||||
| chr8:38998181
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.97+1021A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998181 | ||||||
| chr8:38998192
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.97+1032G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998192 | ||||||
| chr8:38998228
|
G | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(1): Show | 4 | HG01346.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1068G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998228 | ||||||
| chr8:38998246
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.97+1086G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998246 | ||||||
| chr8:38998263
|
G | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+1103G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998263 | ||||||
| chr8:38998328
|
T | C | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.97+1168T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998328 | ||||||
| chr8:38998340
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.97+1180A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998340 | ||||||
| chr8:38998396
|
AT | A | 106 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(103): Show | 106 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.97+1245delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 38998396 | |||||
| chr8:38998467
|
C | G | 1 | a0001c0001t0001g0329 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.97+1307C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998467 | ||||||
| chr8:38998511
|
T | G | 1 | a0001c0001t0001g0209 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.97+1351T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998511 | ||||||
| chr8:38998778
|
T | TGAAAGAA others(350): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.97+1633_97+1634ins others(357): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 38998778 | |||||
| chr8:38998817
|
A | G | 138 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.97+1657A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998817 | ||||||
| chr8:38998928
|
C | A | 1 | a0002c0002t0002g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+1768C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998928 | ||||||
| chr8:38998991
|
TAAG | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0133 | 3 | HG02055.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.97+1834_97+1836del others(3): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 38998991 | |||||
| chr8:38999054
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.97+1894C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999054 | ||||||
| chr8:38999112
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18953.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.97+1952C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999112 | ||||||
| chr8:38999146
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.97+1986G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999146 | ||||||
| chr8:38999249
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.97+2089T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999249 | ||||||
| chr8:38999328
|
CT | C | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.97+2183delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 38999328 | |||||
| chr8:38999340
|
T | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | NA18969.hp2 NA19001.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+2180T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999340 | ||||||
| chr8:38999608
|
C | T | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.97+2448C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999608 | ||||||
| chr8:39000088
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.97+2928G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000088 | ||||||
| chr8:39000118
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97+2958G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000118 | ||||||
| chr8:39000235
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.97+3075G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000235 | ||||||
| chr8:39000289
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.97+3129A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000289 | ||||||
| chr8:39000313
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+3153G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000313 | ||||||
| chr8:39000354
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+3194G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000354 | ||||||
| chr8:39000390
|
A | T | 84 | a0001c0001t0001g0207a0001c0001t0001g0213a0001c0001t0001g0214others(81): Show | 84 | HG00099.hp1 HG00438.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.97+3230A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000390 | ||||||
| chr8:39000482
|
G | T | 1 | a0001c0001t0001g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.97+3322G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000482 | ||||||
| chr8:39000638
|
T | C | 29 | a0001c0001t0001g0032a0001c0001t0001g0124a0001c0001t0001g0186others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.97+3478T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000638 | ||||||
| chr8:39000691
|
TCCTGGGC others(13): Show |
T | 1 | a0001c0001t0001g0325 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.97+3533_97+3552del others(20): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39000691 | |||||
| chr8:39000758
|
C | T | 137 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.97+3598C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000758 | ||||||
| chr8:39000759
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.97+3599A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000759 | ||||||
| chr8:39000912
|
A | T | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 137 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.97+3752A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000912 | ||||||
| chr8:39000965
|
G | A | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 140 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.97+3805G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000965 | ||||||
| chr8:39001417
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97+4257G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001417 | ||||||
| chr8:39001424
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+4264C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001424 | ||||||
| chr8:39001542
|
TAAAC | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 13 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+4389_97+4392del others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39001542 | |||||
| chr8:39001585
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4425G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001585 | ||||||
| chr8:39001849
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97+4689T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001849 | ||||||
| chr8:39001851
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.97+4691G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001851 | ||||||
| chr8:39001994
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.97+4834G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001994 | ||||||
| chr8:39002008
|
T | G | 12 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(9): Show | 12 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4848T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002008 | ||||||
| chr8:39002018
|
G | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+4858G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002018 | ||||||
| chr8:39002033
|
T | TA | 33 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG00280.hp2 HG01192.hp2 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+4893dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002033 | |||||
| chr8:39002033
|
T | TAA | 12 | a0001c0001t0001g0217a0002c0002t0002g0130a0002c0002t0002g0187others(9): Show | 12 | HG02257.hp1 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+4892_97+4893dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002033 | |||||
| chr8:39002033
|
TA | T | 17 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(14): Show | 17 | HG00323.hp2 HG01255.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.97+4893delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002033 | |||||
| chr8:39002034
|
A | T | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.97+4874A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002034 | ||||||
| chr8:39002291
|
G | C | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+5131G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002291 | ||||||
| chr8:39002312
|
C | CT | 148 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.97+5176dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002312 | |||||
| chr8:39002312
|
C | CTT | 21 | a0001c0001t0001g0024a0001c0001t0001g0124a0001c0001t0001g0128others(18): Show | 21 | HG00673.hp2 HG01952.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.97+5175_97+5176dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002312 | |||||
| chr8:39002312
|
CT | C | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(7): Show | 10 | HG02055.hp2 HG03130.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+5176delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002312 | |||||
| chr8:39002371
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+5211T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002371 | ||||||
| chr8:39002475
|
C | T | 108 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(105): Show | 108 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.97+5315C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002475 | ||||||
| chr8:39002511
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0184 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.97+5351C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002511 | ||||||
| chr8:39002548
|
C | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.98-5338C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002548 | ||||||
| chr8:39002658
|
C | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 13 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-5228C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002658 | ||||||
| chr8:39002728
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.98-5158C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002728 | ||||||
| chr8:39002768
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.98-5118C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002768 | ||||||
| chr8:39002805
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.98-5081A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002805 | ||||||
| chr8:39002869
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 13 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-5017C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002869 | ||||||
| chr8:39003025
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-4861C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003025 | ||||||
| chr8:39003065
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.98-4821A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003065 | ||||||
| chr8:39003082
|
G | T | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98-4804G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003082 | ||||||
| chr8:39003225
|
TG | T | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-4659delG | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39003225 | |||||
| chr8:39003358
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-4528C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003358 | ||||||
| chr8:39003480
|
G | A | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.98-4406G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003480 | ||||||
| chr8:39003485
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.98-4401T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003485 | ||||||
| chr8:39003485
|
T | TA | 268 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.98-4387dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39003485 | |||||
| chr8:39003485
|
T | TAA | 7 | a0001c0001t0001g0041a0001c0001t0001g0088a0001c0001t0001g0219others(4): Show | 7 | HG00438.hp2 HG01928.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-4388_98-4387dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39003485 | |||||
| chr8:39003568
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.98-4318G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003568 | ||||||
| chr8:39003739
|
T | A | 3 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314 | 3 | HG00673.hp2 HG02135.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.98-4147T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003739 | ||||||
| chr8:39003828
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0255 | 2 | NA18962.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.98-4058C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003828 | ||||||
| chr8:39003888
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.98-3998C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003888 | ||||||
| chr8:39003896
|
C | G | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-3990C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003896 | ||||||
| chr8:39003936
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.98-3950C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003936 | ||||||
| chr8:39004030
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-3856A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004030 | ||||||
| chr8:39004071
|
A | G | 1 | a0001c0001t0001g0320 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.98-3815A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004071 | ||||||
| chr8:39004285
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.98-3601C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004285 | ||||||
| chr8:39004303
|
T | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3583T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004303 | ||||||
| chr8:39004305
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3581C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004305 | ||||||
| chr8:39004307
|
A | T | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3579A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004307 | ||||||
| chr8:39004308
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3578G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004308 | ||||||
| chr8:39004310
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3576C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004310 | ||||||
| chr8:39004313
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3573A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004313 | ||||||
| chr8:39004314
|
G | C | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3572G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004314 | ||||||
| chr8:39004319
|
T | G | 108 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(105): Show | 108 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.98-3567T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004319 | ||||||
| chr8:39004324
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3562C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004324 | ||||||
| chr8:39004544
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.98-3342A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004544 | ||||||
| chr8:39004790
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-3096G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004790 | ||||||
| chr8:39005210
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.98-2676G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39005210 | ||||||
| chr8:39005530
|
C | A | 1 | a0001c0001t0001g0162 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.98-2356C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39005530 | ||||||
| chr8:39005576
|
G | A | 137 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.98-2310G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39005576 | ||||||
| chr8:39006083
|
C | T | 3 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314 | 3 | HG00673.hp2 HG02135.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.98-1803C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006083 | ||||||
| chr8:39006160
|
T | G | 1 | a0001c0003t0001g0258 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.98-1726T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006160 | ||||||
| chr8:39006401
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.98-1485A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006401 | ||||||
| chr8:39006512
|
G | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-1374G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006512 | ||||||
| chr8:39006520
|
T | C | 62 | a0001c0001t0001g0207a0001c0001t0001g0214a0001c0001t0001g0215others(59): Show | 62 | HG00099.hp1 HG00438.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.98-1366T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006520 | ||||||
| chr8:39006541
|
T | TAAAAAGG others(307): Show |
1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-1328_98-1327ins others(314): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | |||||
| chr8:39006541
|
T | TAAAAAGG others(305): Show |
3 | a0001c0001t0001g0248a0001c0001t0001g0300a0001c0001t0001g0327 | 3 | HG01069.hp2 HG01169.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.98-1328_98-1327ins others(312): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | |||||
| chr8:39006541
|
T | TAAAAAGG others(306): Show |
124 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.98-1328_98-1327ins others(313): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | |||||
| chr8:39006541
|
T | TAAAAAGG others(307): Show |
4 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0220others(1): Show | 4 | HG02630.hp2 HG03516.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1328_98-1327ins others(314): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | |||||
| chr8:39006541
|
T | TAAAAAGG others(308): Show |
1 | a0001c0001t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.98-1328_98-1327ins others(315): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | |||||
| chr8:39006541
|
T | TAAAAAGG others(306): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0255 | 2 | NA18962.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.98-1329_98-1328ins others(313): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | |||||
| chr8:39006543
|
A | AAAAGGTA others(306): Show |
2 | a0003c0004t0001g0301a0003c0004t0001g0302 | 2 | NA18963.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.98-1328_98-1327ins others(313): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006543 | |||||
| chr8:39006582
|
G | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0184 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.98-1304G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006582 | ||||||
| chr8:39006618
|
G | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.98-1268G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006618 | ||||||
| chr8:39006643
|
A | G | 1 | a0003c0004t0001g0302 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.98-1243A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006643 | ||||||
| chr8:39006863
|
G | A | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 137 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.98-1023G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006863 | ||||||
| chr8:39006997
|
G | A | 137 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.98-889G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006997 | ||||||
| chr8:39007165
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.98-721G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007165 | ||||||
| chr8:39007174
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.98-712C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007174 | ||||||
| chr8:39007175
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.98-711A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007175 | ||||||
| chr8:39007312
|
A | G | 22 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0072others(19): Show | 22 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.98-574A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007312 | ||||||
| chr8:39007341
|
C | T | 109 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(106): Show | 109 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.98-545C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007341 | ||||||
| chr8:39007695
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-191T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007695 | ||||||
| chr8:39007733
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-153A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007733 | ||||||
| chr8:39007762
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-124A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007762 | ||||||
| chr8:39008008
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.195+25A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008008 | ||||||
| chr8:39008173
|
C | CT | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 135 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.195+203dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39008173 | |||||
| chr8:39008296
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.195+313G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008296 | ||||||
| chr8:39008366
|
G | A | 137 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.195+383G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008366 | ||||||
| chr8:39008449
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.195+466C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008449 | ||||||
| chr8:39008645
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.195+662A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008645 | ||||||
| chr8:39008699
|
C | T | 108 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(105): Show | 108 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.195+716C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008699 | ||||||
| chr8:39008714
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.195+731A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008714 | ||||||
| chr8:39008829
|
T | C | 2 | a0003c0004t0001g0301a0003c0004t0001g0302 | 2 | NA18963.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.195+846T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008829 | ||||||
| chr8:39008868
|
A | G | 20 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 20 | HG01496.hp1 HG02148.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.195+885A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008868 | ||||||
| chr8:39009063
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.195+1080A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009063 | ||||||
| chr8:39009121
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.195+1138A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009121 | ||||||
| chr8:39009162
|
A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.195+1179A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009162 | ||||||
| chr8:39009349
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.195+1366C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009349 | ||||||
| chr8:39009360
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.195+1377C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009360 | ||||||
| chr8:39009755
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0200 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.195+1772G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009755 | ||||||
| chr8:39009792
|
G | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.195+1809G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009792 | ||||||
| chr8:39009895
|
TG | T | 135 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.196-1751delG | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009895 | |||||
| chr8:39009895
|
TGG | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | HG00280.hp1 HG02055.hp2 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.196-1752_196-1751d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009895 | |||||
| chr8:39009895
|
TGGG | T | 37 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(34): Show | 37 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.196-1753_196-1751d others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009895 | |||||
| chr8:39009898
|
G | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.196-1760G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009898 | ||||||
| chr8:39009905
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.196-1753G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009905 | ||||||
| chr8:39009905
|
G | GCA | 37 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(34): Show | 37 | HG00639.hp2 HG00673.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.196-1753_196-1752i others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009905 | ||||||
| chr8:39009907
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0071a0001c0001t0001g0088others(1): Show | 4 | NA18972.hp1 NA18974.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1751G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009907 | ||||||
| chr8:39009908
|
C | G | 50 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(47): Show | 50 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.196-1750C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009908 | ||||||
| chr8:39009911
|
G | A | 50 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(47): Show | 50 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.196-1747G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009911 | ||||||
| chr8:39009911
|
G | GGA | 3 | a0001c0001t0001g0017a0001c0001t0001g0327a0001c0003t0001g0290 | 3 | HG01081.hp1 HG02922.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.196-1726_196-1725d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009911 | |||||
| chr8:39009930
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.196-1728G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009930 | ||||||
| chr8:39009932
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.196-1726G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009932 | ||||||
| chr8:39009932
|
G | GAGACAAA others(1): Show |
210 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.196-1725_196-1724i others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009932 | |||||
| chr8:39009943
|
A | AAACAAC | 10 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(7): Show | 10 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-1706_196-1701d others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009943 | |||||
| chr8:39009943
|
A | C | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.196-1715A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009943 | ||||||
| chr8:39009958
|
A | C | 57 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(54): Show | 57 | HG00639.hp2 HG00673.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.196-1700A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009958 | ||||||
| chr8:39009962
|
A | AAAAAC | 3 | a0001c0001t0001g0327a0001c0001t0004g0332a0001c0003t0001g0290 | 3 | HG01081.hp1 HG02647.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.196-1694_196-1693i others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009962 | |||||
| chr8:39009964
|
A | AAACAAAC | 6 | a0001c0001t0001g0068a0001c0001t0001g0103a0002c0002t0002g0194others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-1694_196-1693i others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | ||||||
| chr8:39009964
|
A | AAACAAAC others(1): Show |
33 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(30): Show | 33 | HG00639.hp2 HG01109.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.196-1694_196-1693i others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | ||||||
| chr8:39009964
|
A | AAACAAAC others(2): Show |
14 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0033others(11): Show | 14 | HG00673.hp1 HG01192.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-1694_196-1693i others(11): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | ||||||
| chr8:39009964
|
A | AAACAAAC others(3): Show |
1 | a0001c0001t0001g0041 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.196-1694_196-1693i others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | ||||||
| chr8:39009964
|
A | AC | 20 | a0001c0001t0001g0024a0001c0001t0001g0075a0001c0001t0001g0111others(17): Show | 20 | HG00280.hp2 HG00621.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-1683dupC | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009964 | |||||
| chr8:39009964
|
A | ACC | 18 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 18 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-1684_196-1683d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009964 | |||||
| chr8:39009964
|
A | ACCC | 32 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(29): Show | 32 | HG00733.hp2 HG01069.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-1685_196-1683d others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009964 | |||||
| chr8:39009964
|
A | C | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.196-1694A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | ||||||
| chr8:39009965
|
C | A | 3 | a0001c0001t0001g0327a0001c0001t0004g0332a0001c0003t0001g0290 | 3 | HG01081.hp1 HG02647.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.196-1693C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009965 | ||||||
| chr8:39010016
|
A | G | 1 | a0001c0001t0001g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.196-1642A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010016 | ||||||
| chr8:39010431
|
C | T | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.196-1227C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010431 | ||||||
| chr8:39010936
|
T | C | 135 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.196-722T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010936 | ||||||
| chr8:39010942
|
A | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.196-716A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010942 | ||||||
| chr8:39010976
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.196-682C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010976 | ||||||
| chr8:39010984
|
T | C | 87 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(84): Show | 87 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.196-674T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010984 | ||||||
| chr8:39011007
|
T | G | 2 | a0001c0001t0001g0136a0001c0001t0003g0133 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196-651T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011007 | ||||||
| chr8:39011092
|
C | CA | 18 | a0001c0001t0001g0131a0001c0001t0001g0137a0001c0001t0001g0138others(15): Show | 18 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-549dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39011092 | |||||
| chr8:39011349
|
A | C | 2 | a0002c0002t0002g0192a0002c0002t0002g0193 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-309A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011349 | ||||||
| chr8:39011391
|
C | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-267C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011391 | ||||||
| chr8:39011444
|
T | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0024 | 3 | HG02257.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.196-214T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011444 | ||||||
| chr8:39011524
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.196-134C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011524 | ||||||
| chr8:39011588
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.196-70A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011588 | ||||||
| chr8:39012213
|
G | C | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.254+497G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012213 | ||||||
| chr8:39012231
|
G | A | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.254+515G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012231 | ||||||
| chr8:39012314
|
C | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.254+598C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012314 | ||||||
| chr8:39012352
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.254+636T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012352 | ||||||
| chr8:39012737
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.254+1021A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012737 | ||||||
| chr8:39012794
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.254+1078C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012794 | ||||||
| chr8:39012875
|
A | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.255-1090A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012875 | ||||||
| chr8:39012927
|
C | T | 38 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(35): Show | 38 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.255-1038C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012927 | ||||||
| chr8:39012940
|
G | GATA | 3 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314 | 3 | HG00673.hp2 HG02135.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.255-1014_255-1012d others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 39012940 | |||||
| chr8:39013000
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.255-965G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013000 | ||||||
| chr8:39013020
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.255-945A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013020 | ||||||
| chr8:39013081
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.255-884C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013081 | ||||||
| chr8:39013090
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.255-875C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013090 | ||||||
| chr8:39013178
|
A | G | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.255-787A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013178 | ||||||
| chr8:39013383
|
A | AT | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.255-576dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 39013383 | |||||
| chr8:39013391
|
G | C | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.255-574G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013391 | ||||||
| chr8:39013505
|
CT | C | 15 | a0001c0001t0001g0048a0001c0001t0001g0112a0001c0001t0001g0126others(12): Show | 15 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.255-447delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 39013505 | |||||
| chr8:39013806
|
T | G | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.255-159T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013806 | ||||||
| chr8:39014470
|
G | T | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.333+427G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014470 | ||||||
| chr8:39014528
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.333+485C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014528 | ||||||
| chr8:39014563
|
T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.333+520T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014563 | ||||||
| chr8:39014667
|
C | A | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.333+624C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014667 | ||||||
| chr8:39014824
|
C | CTTTAG | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.333+782_333+786dup others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 39014824 | |||||
| chr8:39014868
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.333+825A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014868 | ||||||
| chr8:39015173
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.334-945A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015173 | ||||||
| chr8:39015199
|
C | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | HG00099.hp1 HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.334-919C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015199 | ||||||
| chr8:39015489
|
T | A | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.334-629T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015489 | ||||||
| chr8:39015554
|
A | C | 1 | a0001c0001t0001g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.334-564A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015554 | ||||||
| chr8:39015690
|
A | G | 57 | a0001c0001t0001g0207a0001c0001t0001g0214a0001c0001t0001g0215others(54): Show | 57 | HG00099.hp1 HG00438.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.334-428A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015690 | ||||||
| chr8:39016282
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.410+88G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016282 | ||||||
| chr8:39016286
|
C | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.410+92C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016286 | ||||||
| chr8:39016426
|
A | C | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.410+232A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016426 | ||||||
| chr8:39016708
|
T | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411-511T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016708 | ||||||
| chr8:39016875
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.411-344C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016875 | ||||||
| chr8:39016876
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.411-343G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016876 | ||||||
| chr8:39016925
|
C | T | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.411-294C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016925 | ||||||
| chr8:39017105
|
A | G | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.411-114A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39017105 | ||||||
| chr8:39017179
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411-40C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39017179 | ||||||
| chr8:39017589
|
C | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.606+175C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39017589 | ||||||
| chr8:39017618
|
C | T | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.606+204C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39017618 | ||||||
| chr8:39017931
|
A | G | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.606+517A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39017931 | ||||||
| chr8:39018130
|
G | A | 87 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(84): Show | 87 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.606+716G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39018130 | ||||||
| chr8:39018421
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.607-432A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39018421 | ||||||
| chr8:39018453
|
C | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.607-400C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39018453 | ||||||
| chr8:39018947
|
T | C | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.672+29T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39018947 | ||||||
| chr8:39018949
|
C | T | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.672+31C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39018949 | ||||||
| chr8:39018957
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.672+39G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39018957 | ||||||
| chr8:39019104
|
A | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.672+186A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019104 | ||||||
| chr8:39019317
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.672+399T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019317 | ||||||
| chr8:39019383
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.672+465C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019383 | ||||||
| chr8:39019475
|
T | C | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+557T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019475 | ||||||
| chr8:39019513
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.672+595T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019513 | ||||||
| chr8:39019569
|
G | A | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.672+651G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019569 | ||||||
| chr8:39019597
|
A | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.672+679A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019597 | ||||||
| chr8:39019615
|
A | T | 1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.672+697A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019615 | ||||||
| chr8:39019859
|
A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.672+941A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019859 | ||||||
| chr8:39019896
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.672+978C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019896 | ||||||
| chr8:39019935
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.672+1017G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019935 | ||||||
| chr8:39020067
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.672+1149C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020067 | ||||||
| chr8:39020154
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.672+1236G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020154 | ||||||
| chr8:39020184
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.672+1266G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020184 | ||||||
| chr8:39020217
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01891.hp2 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.672+1299A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020217 | ||||||
| chr8:39020273
|
A | G | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.672+1355A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020273 | ||||||
| chr8:39020387
|
T | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673-1256T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020387 | ||||||
| chr8:39020399
|
C | CT | 9 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG01257.hp1 HG01928.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.673-1242dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 39020399 | |||||
| chr8:39020645
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0078 | 2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.673-998C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020645 | ||||||
| chr8:39020892
|
TA | T | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.673-738delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 39020892 | |||||
| chr8:39021162
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.673-481C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39021162 | ||||||
| chr8:39021225
|
T | G | 1 | a0001c0001t0001g0260 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.673-418T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39021225 | ||||||
| chr8:39021441
|
G | A | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.673-202G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39021441 | ||||||
| chr8:39021503
|
C | T | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.673-140C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39021503 | ||||||
| chr8:39022064
|
T | TTG | 23 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0055others(20): Show | 23 | HG01069.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.744+383_744+384dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022064 | |||||
| chr8:39022064
|
TTG | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(8): Show | 11 | HG02055.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.744+383_744+384del others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022064 | |||||
| chr8:39022064
|
TTGTG | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 37 | HG00621.hp1 HG00735.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.744+381_744+384del others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022064 | |||||
| chr8:39022089
|
TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.744+377_744+388del others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022089 | |||||
| chr8:39022095
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.744+381T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022095 | ||||||
| chr8:39022097
|
T | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0153others(6): Show | 9 | HG02109.hp1 HG03927.hp1 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+383T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022097 | ||||||
| chr8:39022097
|
T | TGTGTGAG others(1): Show |
12 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(9): Show | 12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.744+384_744+385ins others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022097 | |||||
| chr8:39022099
|
A | T | 2 | a0001c0001t0001g0209a0002c0002t0002g0191 | 2 | HG02559.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.744+385A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022099 | ||||||
| chr8:39022101
|
A | T | 1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.744+387A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022101 | ||||||
| chr8:39022239
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.744+525C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022239 | ||||||
| chr8:39022355
|
A | G | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.744+641A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022355 | ||||||
| chr8:39022356
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.744+642C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022356 | ||||||
| chr8:39022882
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.745-274T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022882 | ||||||
| chr8:39023399
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.914+74A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023399 | ||||||
| chr8:39023740
|
G | GT | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.914+438dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | |||||
| chr8:39023740
|
G | GTT | 25 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(22): Show | 25 | HG00621.hp1 HG01106.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.914+437_914+438dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | |||||
| chr8:39023740
|
G | GTTT | 6 | a0001c0001t0001g0042a0001c0001t0001g0077a0001c0001t0001g0109others(3): Show | 6 | HG00735.hp1 HG02083.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.914+436_914+438dup others(3): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | |||||
| chr8:39023740
|
GTTTTTTT others(4): Show |
G | 2 | a0001c0001t0001g0020a0001c0001t0001g0024 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.914+428_914+438del others(11): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | |||||
| chr8:39023740
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0224 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.914+425_914+438del others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | |||||
| chr8:39023764
|
G | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.914+439G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023764 | ||||||
| chr8:39023786
|
G | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | NA18969.hp2 NA19001.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.914+461G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023786 | ||||||
| chr8:39023791
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.914+466G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023791 | ||||||
| chr8:39023871
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.914+546C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023871 | ||||||
| chr8:39023946
|
A | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.914+621A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023946 | ||||||
| chr8:39024028
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.914+703G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024028 | ||||||
| chr8:39024051
|
C | T | 2 | a0003c0004t0001g0301a0003c0004t0001g0302 | 2 | NA18963.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.914+726C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024051 | ||||||
| chr8:39024052
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.914+727G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024052 | ||||||
| chr8:39024111
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0121a0004c0008t0001g0120 | 3 | HG01884.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.914+786C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024111 | ||||||
| chr8:39024343
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+1018G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024343 | ||||||
| chr8:39024548
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.914+1223A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024548 | ||||||
| chr8:39024646
|
A | T | 7 | a0001c0003t0001g0206a0001c0003t0001g0258a0001c0003t0001g0290others(4): Show | 7 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.915-1157A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024646 | ||||||
| chr8:39024756
|
A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.915-1047A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024756 | ||||||
| chr8:39024798
|
C | T | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.915-1005C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024798 | ||||||
| chr8:39024907
|
G | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0160 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.915-896G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024907 | ||||||
| chr8:39025052
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.915-751G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025052 | ||||||
| chr8:39025092
|
C | CT | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.915-701dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39025092 | |||||
| chr8:39025108
|
G | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.915-695G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025108 | ||||||
| chr8:39025149
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.915-654G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025149 | ||||||
| chr8:39025388
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.915-415C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025388 | ||||||
| chr8:39025444
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.915-359G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025444 | ||||||
| chr8:39025592
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.915-211C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025592 | ||||||
| chr8:39025655
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.915-148A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025655 | ||||||
| chr8:39025708
|
G | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.915-95G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025708 | ||||||
| chr8:39025963
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.996+79C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39025963 | ||||||
| chr8:39026023
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.996+139T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39026023 | ||||||
| chr8:39026134
|
T | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.996+250T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39026134 | ||||||
| chr8:39026158
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.996+274A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39026158 | ||||||
| chr8:39026657
|
T | C | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.997-20T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39026657 | ||||||
| chr8:39026823
|
G | GTTCT | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+15_1130+18dup others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39026823 | |||||
| chr8:39026946
|
A | G | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1130+136A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39026946 | ||||||
| chr8:39026959
|
C | CT | 17 | a0001c0001t0001g0124a0001c0001t0001g0186a0001c0001t0001g0204others(14): Show | 17 | HG01070.hp2 HG01106.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.1130+164dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39026959 | |||||
| chr8:39026974
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1130+164T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39026974 | ||||||
| chr8:39027138
|
A | G | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1130+328A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027138 | ||||||
| chr8:39027218
|
C | T | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+408C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027218 | ||||||
| chr8:39027462
|
A | T | 9 | a0001c0001t0001g0215a0001c0001t0001g0257a0001c0001t0001g0279others(6): Show | 9 | HG01928.hp1 HG01952.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1130+652A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027462 | ||||||
| chr8:39027470
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0003g0133 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1130+660A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027470 | ||||||
| chr8:39027782
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+972A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027782 | ||||||
| chr8:39027798
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1130+988C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027798 | ||||||
| chr8:39027909
|
A | T | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1130+1099A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027909 | ||||||
| chr8:39028013
|
A | G | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1130+1203A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028013 | ||||||
| chr8:39028115
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1130+1305T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028115 | ||||||
| chr8:39028186
|
G | A | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1130+1376G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028186 | ||||||
| chr8:39028190
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1130+1380T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028190 | ||||||
| chr8:39028256
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+1446C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028256 | ||||||
| chr8:39028365
|
TA | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1130+1565delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39028365 | |||||
| chr8:39028382
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1130+1572A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028382 | ||||||
| chr8:39028475
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1130+1665C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028475 | ||||||
| chr8:39028554
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1130+1744G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028554 | ||||||
| chr8:39029071
|
A | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1130+2261A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029071 | ||||||
| chr8:39029131
|
G | GT | 268 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1130+2336dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39029131 | |||||
| chr8:39029133
|
T | TG | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0004g0332 | 3 | HG01168.hp2 HG01169.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1130+2323_1130+232 others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029133 | ||||||
| chr8:39029237
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1130+2427G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029237 | ||||||
| chr8:39029242
|
A | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0235 | 2 | HG02056.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1130+2432A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029242 | ||||||
| chr8:39029277
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140 | 3 | HG02615.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1130+2467G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029277 | ||||||
| chr8:39029322
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1130+2512C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029322 | ||||||
| chr8:39029341
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1130+2531G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029341 | ||||||
| chr8:39029380
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+2570T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029380 | ||||||
| chr8:39029673
|
G | A | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1130+2863G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029673 | ||||||
| chr8:39029747
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0172a0001c0001t0001g0182 | 3 | NA18966.hp2 NA18973.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1130+2937G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029747 | ||||||
| chr8:39030239
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+3429G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39030239 | ||||||
| chr8:39030604
|
G | A | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+3794G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39030604 | ||||||
| chr8:39030679
|
CT | C | 17 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1130+3871delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39030679 | |||||
| chr8:39030766
|
G | A | 5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130+3956G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39030766 | ||||||
| chr8:39031381
|
C | T | 6 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(3): Show | 6 | HG02155.hp2 NA18943.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130+4571C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031381 | ||||||
| chr8:39031416
|
A | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1130+4606A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031416 | ||||||
| chr8:39031425
|
C | G | 1 | a0002c0002t0002g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1130+4615C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031425 | ||||||
| chr8:39031432
|
T | C | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+4622T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031432 | ||||||
| chr8:39031460
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1130+4650G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031460 | ||||||
| chr8:39031534
|
A | C | 1 | a0002c0002t0002g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1130+4724A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031534 | ||||||
| chr8:39031580
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0184 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1130+4770C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031580 | ||||||
| chr8:39031686
|
C | G | 2 | a0001c0001t0001g0136a0001c0001t0003g0133 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1130+4876C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031686 | ||||||
| chr8:39032008
|
C | T | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1130+5198C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032008 | ||||||
| chr8:39032079
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+5269C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032079 | ||||||
| chr8:39032216
|
G | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+5406G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032216 | ||||||
| chr8:39032323
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+5513C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032323 | ||||||
| chr8:39032352
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+5542G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032352 | ||||||
| chr8:39032363
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1130+5553C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032363 | ||||||
| chr8:39032403
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1130+5593T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032403 | ||||||
| chr8:39032448
|
A | G | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1130+5638A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032448 | ||||||
| chr8:39032643
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1130+5833C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032643 | ||||||
| chr8:39032670
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+5860A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032670 | ||||||
| chr8:39032790
|
C | T | 136 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1130+5980C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032790 | ||||||
| chr8:39032791
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1130+5981G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032791 | ||||||
| chr8:39032859
|
A | T | 7 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0079others(4): Show | 7 | HG00621.hp1 HG02132.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.1130+6049A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032859 | ||||||
| chr8:39033136
|
A | G | 5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130+6326A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39033136 | ||||||
| chr8:39033198
|
T | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0184 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1130+6388T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39033198 | ||||||
| chr8:39033510
|
A | T | 1 | a0001c0001t0001g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1130+6700A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39033510 | ||||||
| chr8:39033802
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1130+6992T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39033802 | ||||||
| chr8:39034073
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1130+7263T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39034073 | ||||||
| chr8:39034415
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131-7531A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39034415 | ||||||
| chr8:39034554
|
T | C | 2 | a0001c0001t0001g0082a0004c0008t0001g0120 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1131-7392T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39034554 | ||||||
| chr8:39034649
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1131-7297A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39034649 | ||||||
| chr8:39035054
|
A | C | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1131-6892A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035054 | ||||||
| chr8:39035084
|
T | G | 1 | a0001c0001t0001g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1131-6862T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035084 | ||||||
| chr8:39035275
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1131-6671C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035275 | ||||||
| chr8:39035376
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1131-6570T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035376 | ||||||
| chr8:39035394
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1131-6552T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035394 | ||||||
| chr8:39035402
|
C | T | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1131-6544C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035402 | ||||||
| chr8:39035674
|
G | C | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-6272G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035674 | ||||||
| chr8:39035772
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1131-6174G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035772 | ||||||
| chr8:39035803
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(29): Show | 32 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.1131-6143C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035803 | ||||||
| chr8:39035804
|
G | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131-6142G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035804 | ||||||
| chr8:39035815
|
TCAAAACA others(3): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131-6110_1131-610 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39035815 | |||||
| chr8:39035922
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131-6024C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035922 | ||||||
| chr8:39035958
|
T | C | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 140 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.1131-5988T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035958 | ||||||
| chr8:39036296
|
A | G | 2 | a0001c0001t0003g0133a0001c0001t0004g0332 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1131-5650A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036296 | ||||||
| chr8:39036373
|
TC | T | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1131-5571delC | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39036373 | |||||
| chr8:39036473
|
A | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131-5473A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036473 | ||||||
| chr8:39036548
|
C | T | 131 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1131-5398C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036548 | ||||||
| chr8:39036729
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1131-5217A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036729 | ||||||
| chr8:39036765
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1131-5181A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036765 | ||||||
| chr8:39036815
|
G | A | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1131-5131G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036815 | ||||||
| chr8:39036930
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1131-5016T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036930 | ||||||
| chr8:39037033
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1131-4913A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037033 | ||||||
| chr8:39037050
|
C | CT | 26 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0091others(23): Show | 26 | HG01261.hp1 HG01361.hp1 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.1131-4872dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037050 | |||||
| chr8:39037050
|
CT | C | 77 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0025others(74): Show | 77 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1131-4872delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037050 | |||||
| chr8:39037050
|
CTT | C | 124 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1131-4873_1131-487 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037050 | |||||
| chr8:39037080
|
G | T | 5 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(2): Show | 5 | HG01106.hp1 HG01952.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131-4866G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037080 | ||||||
| chr8:39037082
|
AG | A | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1131-4863delG | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037082 | ||||||
| chr8:39037112
|
A | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1131-4834A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037112 | ||||||
| chr8:39037150
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1131-4796G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037150 | ||||||
| chr8:39037206
|
C | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1131-4740C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037206 | ||||||
| chr8:39037441
|
A | AGT | 8 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0024others(5): Show | 8 | HG00280.hp2 HG01256.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131-4488_1131-448 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037441 | |||||
| chr8:39037441
|
AGT | A | 15 | a0001c0001t0001g0298a0002c0002t0002g0130a0002c0002t0002g0187others(12): Show | 15 | HG01109.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1131-4488_1131-448 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037441 | |||||
| chr8:39037458
|
G | GT | 95 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(92): Show | 95 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1131-4472dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037458 | |||||
| chr8:39037458
|
G | GTGT | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(17): Show | 20 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1131-4487_1131-448 others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037458 | |||||
| chr8:39037458
|
G | GTGTGT | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0013others(9): Show | 12 | HG00621.hp1 HG00735.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-4487_1131-448 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037458 | |||||
| chr8:39037458
|
G | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0323a0001c0001t0003g0133 | 3 | HG02055.hp2 NA19012.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1131-4488G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037458 | ||||||
| chr8:39037459
|
T | TG | 11 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0055others(8): Show | 11 | HG00738.hp2 HG01069.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1131-4487_1131-448 others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037459 | ||||||
| chr8:39037509
|
A | G | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1131-4437A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037509 | ||||||
| chr8:39037553
|
G | A | 3 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314 | 3 | HG00673.hp2 HG02135.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1131-4393G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037553 | ||||||
| chr8:39037787
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1131-4159A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037787 | ||||||
| chr8:39037861
|
T | G | 1 | a0001c0001t0001g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1131-4085T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037861 | ||||||
| chr8:39038614
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1131-3332G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39038614 | ||||||
| chr8:39038865
|
T | C | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1131-3081T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39038865 | ||||||
| chr8:39038960
|
G | GT | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1131-2978dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39038960 | |||||
| chr8:39039031
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1131-2915A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039031 | ||||||
| chr8:39039048
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1131-2898A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039048 | ||||||
| chr8:39039184
|
A | G | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-2762A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039184 | ||||||
| chr8:39039202
|
G | A | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1131-2744G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039202 | ||||||
| chr8:39039518
|
A | G | 1 | a0001c0001t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1131-2428A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039518 | ||||||
| chr8:39039530
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1131-2416G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039530 | ||||||
| chr8:39039674
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1131-2272C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039674 | ||||||
| chr8:39039884
|
G | A | 1 | a0002c0002t0002g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1131-2062G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039884 | ||||||
| chr8:39039951
|
A | C | 40 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(37): Show | 40 | HG00673.hp1 HG01109.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.1131-1995A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039951 | ||||||
| chr8:39039976
|
A | G | 2 | a0001c0001t0003g0133a0001c0001t0004g0332 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1131-1970A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039976 | ||||||
| chr8:39040004
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1131-1942A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040004 | ||||||
| chr8:39040041
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1131-1905C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040041 | ||||||
| chr8:39040076
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1131-1870G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040076 | ||||||
| chr8:39040159
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1131-1787C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040159 | ||||||
| chr8:39040237
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1131-1709C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040237 | ||||||
| chr8:39040303
|
C | T | 2 | a0001c0001t0003g0133a0001c0001t0004g0332 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1131-1643C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040303 | ||||||
| chr8:39040525
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG03710.hp2 NA18747.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1131-1421C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040525 | ||||||
| chr8:39040685
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1131-1261T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040685 | ||||||
| chr8:39040766
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1131-1180C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040766 | ||||||
| chr8:39040769
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-1177A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040769 | ||||||
| chr8:39040856
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131-1090T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040856 | ||||||
| chr8:39041132
|
A | T | 126 | a0001c0001t0001g0032a0001c0001t0001g0124a0001c0001t0001g0126others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1131-814A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041132 | ||||||
| chr8:39041229
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1131-717C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041229 | ||||||
| chr8:39041287
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1131-659G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041287 | ||||||
| chr8:39041288
|
C | G | 135 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1131-658C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041288 | ||||||
| chr8:39041338
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1131-608C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041338 | ||||||
| chr8:39041369
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1131-577T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041369 | ||||||
| chr8:39041495
|
TC | T | 135 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1131-449delC | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39041495 | |||||
| chr8:39041798
|
T | C | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-148T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041798 | ||||||
| chr8:39041897
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1131-49A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041897 | ||||||
| chr8:39042133
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1302+16G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042133 | ||||||
| chr8:39042229
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+112A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042229 | ||||||
| chr8:39042253
|
G | A | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1302+136G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042253 | ||||||
| chr8:39042367
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1302+250A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042367 | ||||||
| chr8:39042575
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1302+458A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042575 | ||||||
| chr8:39043134
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1302+1017G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043134 | ||||||
| chr8:39043158
|
T | C | 3 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0100 | 3 | NA18961.hp2 NA18985.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1302+1041T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043158 | ||||||
| chr8:39043221
|
T | C | 1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1302+1104T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043221 | ||||||
| chr8:39043227
|
T | C | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1302+1110T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043227 | ||||||
| chr8:39043748
|
A | T | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+1631A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043748 | ||||||
| chr8:39043818
|
A | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140 | 3 | HG02615.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1302+1701A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043818 | ||||||
| chr8:39043931
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0003g0133 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1302+1814A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043931 | ||||||
| chr8:39044032
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+1915A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044032 | ||||||
| chr8:39044219
|
T | G | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+2102T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044219 | ||||||
| chr8:39044358
|
T | C | 135 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1302+2241T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044358 | ||||||
| chr8:39044484
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+2367G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044484 | ||||||
| chr8:39044547
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1302+2430C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044547 | ||||||
| chr8:39044582
|
TCAGCCCT others(20): Show |
T | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+2494_1302+252 others(31): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044582 | |||||
| chr8:39044663
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0172a0001c0001t0001g0182 | 3 | NA18966.hp2 NA18973.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1302+2546C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044663 | ||||||
| chr8:39044688
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1302+2571G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044688 | ||||||
| chr8:39044689
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+2572C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044689 | ||||||
| chr8:39044774
|
C | T | 2 | a0001c0003t0001g0290a0001c0003t0001g0294 | 2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1302+2657C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044774 | ||||||
| chr8:39044842
|
T | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 48 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.1302+2725T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044842 | ||||||
| chr8:39044886
|
A | ATG | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1302+2770_1302+277 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044886 | |||||
| chr8:39044910
|
A | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0074a0001c0001t0001g0077others(15): Show | 18 | HG00621.hp1 HG00639.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+2793A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044910 | ||||||
| chr8:39044913
|
T | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0054others(1): Show | 4 | HG01261.hp1 HG02135.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+2796T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044913 | ||||||
| chr8:39044920
|
A | ATATATAT others(59): Show |
2 | a0001c0001t0001g0157a0001c0001t0001g0160 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1302+2808_1302+280 others(70): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044920 | |||||
| chr8:39044920
|
A | G | 53 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(50): Show | 53 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1302+2803A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044920 | ||||||
| chr8:39044942
|
C | A | 201 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1302+2825C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044942 | ||||||
| chr8:39044945
|
T | G | 85 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(82): Show | 85 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1302+2828T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044945 | ||||||
| chr8:39044952
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1302+2835G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044952 | ||||||
| chr8:39044952
|
GTA | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG00280.hp2 HG01256.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+2839_1302+284 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044952 | |||||
| chr8:39044956
|
A | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0085a0002c0002t0002g0130others(13): Show | 16 | HG00621.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302+2839A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044956 | ||||||
| chr8:39044956
|
ATG | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0257a0001c0001t0001g0311 | 3 | HG01928.hp1 HG01952.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1302+2846_1302+284 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044956 | |||||
| chr8:39044967
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0085 | 2 | HG00621.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1302+2850C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044967 | ||||||
| chr8:39044974
|
C | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+2857C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044974 | ||||||
| chr8:39044977
|
T | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0089 | 3 | HG01070.hp1 HG01071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1302+2860T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044977 | ||||||
| chr8:39044979
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1302+2862T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044979 | ||||||
| chr8:39044985
|
TATATGTG others(77): Show |
T | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1302+2880_1302+296 others(88): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044985 | |||||
| chr8:39044988
|
A | G | 24 | a0001c0001t0001g0012a0001c0001t0001g0085a0001c0001t0001g0157others(21): Show | 24 | HG00621.hp1 HG00621.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1302+2871A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044988 | ||||||
| chr8:39044999
|
C | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0209a0001c0001t0001g0222others(1): Show | 4 | HG00621.hp1 HG02647.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+2882C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044999 | ||||||
| chr8:39045006
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0222 | 2 | NA18963.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1302+2889C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045006 | ||||||
| chr8:39045006
|
C | CTATGTAT others(25): Show |
1 | a0001c0001t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1302+2927_1302+295 others(36): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045006 | |||||
| chr8:39045010
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1302+2893G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045010 | ||||||
| chr8:39045018
|
A | ATG | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1302+2910_1302+291 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045018 | |||||
| chr8:39045020
|
G | A | 77 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0034others(74): Show | 77 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1302+2903G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045020 | ||||||
| chr8:39045020
|
GTGTGTGT others(89): Show |
G | 2 | a0001c0001t0001g0209a0001c0001t0001g0222 | 2 | NA18963.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1302+2912_1302+300 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045020 | |||||
| chr8:39045022
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1302+2905G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045022 | ||||||
| chr8:39045028
|
GCA | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0308 | 3 | HG01891.hp1 HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1302+2912_1302+291 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045028 | ||||||
| chr8:39045031
|
T | C | 112 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(109): Show |
intron_variant | MODIFIER | c.1302+2914T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045031 | ||||||
| chr8:39045032
|
A | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0308 | 3 | HG01891.hp1 HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1302+2915A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045032 | ||||||
| chr8:39045038
|
A | C | 111 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(108): Show |
intron_variant | MODIFIER | c.1302+2921A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045038 | ||||||
| chr8:39045041
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1302+2924T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045041 | ||||||
| chr8:39045042
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1302+2925G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045042 | ||||||
| chr8:39045043
|
T | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(29): Show | 32 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.1302+2926T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045043 | ||||||
| chr8:39045048
|
GTATGTGT others(15): Show |
G | 2 | a0001c0001t0001g0179a0001c0001t0001g0181 | 2 | HG01243.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1302+3001_1302+302 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045048 | |||||
| chr8:39045048
|
GTATGTGT others(59): Show |
G | 4 | a0001c0001t0001g0261a0001c0001t0001g0306a0001c0001t0001g0316others(1): Show | 4 | NA18953.hp2 NA18972.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+2957_1302+302 others(70): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045048 | |||||
| chr8:39045050
|
A | ATG | 60 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(57): Show | 60 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.1302+2942_1302+294 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045050 | |||||
| chr8:39045052
|
G | A | 13 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0085others(10): Show | 13 | HG00438.hp2 HG00621.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+2935G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045052 | ||||||
| chr8:39045052
|
GTGTGTGT others(57): Show |
G | 54 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1302+2944_1302+300 others(68): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045052 | |||||
| chr8:39045054
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1302+2937G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045054 | ||||||
| chr8:39045058
|
GTGCATAC others(85): Show |
G | 12 | a0001c0001t0001g0032a0001c0001t0001g0216a0001c0001t0001g0260others(9): Show | 12 | HG00099.hp2 HG00673.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1302+2944_1302+303 others(96): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045058 | |||||
| chr8:39045058
|
GTGCATAC others(113): Show |
G | 2 | a0001c0001t0001g0186a0001c0001t0001g0287 | 2 | HG03492.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1302+2944_1302+306 others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045058 | |||||
| chr8:39045058
|
GTGCATAC others(141): Show |
G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+2944_1302+309 others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045058 | |||||
| chr8:39045061
|
CATACATA others(87): Show |
C | 1 | a0001c0001t0001g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1302+2957_1302+305 others(98): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045061 | |||||
| chr8:39045063
|
T | C | 73 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(70): Show | 73 | HG00438.hp2 HG00673.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.1302+2946T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045063 | ||||||
| chr8:39045069
|
C | CCTATGTA others(3): Show |
33 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(30): Show | 33 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+2952_1302+295 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045069 | ||||||
| chr8:39045069
|
C | CCTATGTA others(35): Show |
3 | a0002c0002t0002g0191a0002c0002t0002g0192a0002c0002t0002g0193 | 3 | HG02559.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1302+2952_1302+295 others(46): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045069 | ||||||
| chr8:39045070
|
A | ATATGTAT others(3): Show |
1 | a0001c0001t0001g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1302+2958_1302+295 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045070 | |||||
| chr8:39045070
|
A | C | 36 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(33): Show | 36 | HG00673.hp1 HG01109.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+2953A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045070 | ||||||
| chr8:39045070
|
A | G | 36 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(33): Show | 36 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+2953A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045070 | ||||||
| chr8:39045072
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1302+2955A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045072 | ||||||
| chr8:39045074
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 88 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.1302+2957G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045074 | ||||||
| chr8:39045076
|
G | A | 74 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(71): Show | 74 | HG00639.hp2 HG00673.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1302+2959G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045076 | ||||||
| chr8:39045078
|
G | GTATATA | 17 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0074others(14): Show | 17 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1302+2962_1302+296 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045078 | |||||
| chr8:39045078
|
G | GTATATAT others(27): Show |
18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(15): Show | 18 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+2962_1302+296 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045078 | |||||
| chr8:39045078
|
G | GTATATAT others(55): Show |
4 | a0001c0001t0001g0007a0001c0001t0001g0077a0001c0001t0001g0079others(1): Show | 4 | HG02647.hp1 NA18964.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+2962_1302+296 others(66): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045078 | |||||
| chr8:39045079
|
TGTGCATA others(5): Show |
T | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(16): Show | 19 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302+2963_1302+297 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045079 | ||||||
| chr8:39045079
|
TGTGCATA others(27): Show |
T | 30 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(27): Show | 30 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1302+2963_1302+299 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045079 | ||||||
| chr8:39045080
|
GTGCATAC others(5): Show |
G | 36 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(33): Show | 36 | HG00673.hp1 HG01109.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+2965_1302+297 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045080 | |||||
| chr8:39045080
|
GTGCATAC others(27): Show |
G | 1 | a0001c0001t0001g0273 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1302+2965_1302+299 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045080 | |||||
| chr8:39045081
|
TGCATACA others(3): Show |
T | 16 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0048others(13): Show | 16 | HG00639.hp2 HG00733.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+2965_1302+297 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045081 | ||||||
| chr8:39045081
|
TGCATACA others(25): Show |
T | 21 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0050others(18): Show | 21 | HG00738.hp2 HG01069.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+2965_1302+299 others(36): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045081 | ||||||
| chr8:39045083
|
C | T | 39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(36): Show | 39 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1302+2966C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045083 | ||||||
| chr8:39045085
|
T | C | 12 | a0001c0001t0001g0036a0002c0002t0002g0130a0002c0002t0002g0187others(9): Show | 12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1302+2968T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045085 | ||||||
| chr8:39045091
|
C | CCTATGTA others(3): Show |
11 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(8): Show | 11 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+2974_1302+297 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045091 | ||||||
| chr8:39045092
|
A | C | 1 | a0001c0001t0001g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1302+2975A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045092 | ||||||
| chr8:39045092
|
A | G | 11 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(8): Show | 11 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+2975A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045092 | ||||||
| chr8:39045094
|
A | G | 16 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0048others(13): Show | 16 | HG00639.hp2 HG00733.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+2977A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045094 | ||||||
| chr8:39045096
|
G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(53): Show | 56 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1302+2979G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045096 | ||||||
| chr8:39045098
|
G | A | 23 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(20): Show | 23 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1302+2981G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045098 | ||||||
| chr8:39045098
|
G | GTATA | 5 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0077others(2): Show | 5 | HG00621.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+2982_1302+298 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045098 | |||||
| chr8:39045100
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0077others(2): Show | 5 | HG00621.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+2983G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045100 | ||||||
| chr8:39045100
|
G | GTATATA | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 37 | HG00323.hp1 HG00735.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1302+2984_1302+298 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045100 | |||||
| chr8:39045101
|
TGTGCATA others(5): Show |
T | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1302+2985_1302+299 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045101 | ||||||
| chr8:39045102
|
G | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(15): Show | 18 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+2985G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045102 | ||||||
| chr8:39045103
|
TGCATACA others(3): Show |
T | 23 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(20): Show | 23 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1302+2987_1302+299 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045103 | ||||||
| chr8:39045104
|
G | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(15): Show | 18 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+2987G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045104 | ||||||
| chr8:39045105
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(39): Show | 42 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1302+2988C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045105 | ||||||
| chr8:39045105
|
CATACATA others(99): Show |
C | 7 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0098others(4): Show | 7 | HG00733.hp2 HG01993.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3001_1302+310 others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045105 | |||||
| chr8:39045107
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0239a0002c0002t0002g0189others(1): Show | 4 | HG01192.hp1 HG03017.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+2990T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045107 | ||||||
| chr8:39045113
|
C | CCTATGTA others(3): Show |
3 | a0001c0001t0001g0239a0002c0002t0002g0189a0002c0010t0002g0198 | 3 | HG01192.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1302+2996_1302+299 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045113 | ||||||
| chr8:39045113
|
C | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(15): Show | 18 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+2996C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045113 | ||||||
| chr8:39045114
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1302+2997A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045114 | ||||||
| chr8:39045114
|
A | G | 3 | a0001c0001t0001g0239a0002c0002t0002g0189a0002c0010t0002g0198 | 3 | HG01192.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1302+2997A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045114 | ||||||
| chr8:39045116
|
A | G | 62 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(59): Show | 62 | HG00438.hp2 HG00735.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.1302+2999A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045116 | ||||||
| chr8:39045118
|
G | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 84 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1302+3001G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045118 | ||||||
| chr8:39045118
|
G | GTA | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(15): Show | 18 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+3002_1302+300 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045118 | |||||
| chr8:39045118
|
G | GTGTGTGC others(13): Show |
6 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01106.hp2 HG01123.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+3007_1302+300 others(24): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045118 | |||||
| chr8:39045118
|
GTGTGTGT others(41): Show |
G | 1 | a0001c0001t0001g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1302+3003_1302+305 others(52): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045118 | |||||
| chr8:39045120
|
G | A | 52 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(49): Show | 52 | HG00673.hp1 HG00735.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1302+3003G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045120 | ||||||
| chr8:39045120
|
G | GTATA | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302+3004_1302+300 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045120 | |||||
| chr8:39045120
|
G | GTATATAT others(7): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0085 | 3 | HG00621.hp1 NA18964.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1302+3004_1302+300 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045120 | |||||
| chr8:39045120
|
G | GTGTATAT others(27): Show |
4 | a0001c0001t0001g0162a0001c0001t0001g0174a0001c0001t0001g0178others(1): Show | 4 | HG00621.hp2 NA18945.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3006_1302+300 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045120 | |||||
| chr8:39045122
|
G | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 40 | HG00621.hp1 HG00735.hp2 HG02083.hp2 others(37): Show |
intron_variant | MODIFIER | c.1302+3005G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045122 | ||||||
| chr8:39045122
|
G | GTATATA | 43 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(40): Show | 43 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1302+3006_1302+300 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045122 | |||||
| chr8:39045122
|
G | GTATATAT others(27): Show |
2 | a0001c0001t0001g0157a0001c0001t0001g0182 | 2 | NA18522.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1302+3006_1302+300 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045122 | |||||
| chr8:39045122
|
G | GTATATAT others(55): Show |
3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG02723.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1302+3006_1302+300 others(66): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045122 | |||||
| chr8:39045122
|
G | GTGTGTAT others(21): Show |
1 | a0001c0001t0001g0183 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1302+3009_1302+301 others(32): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045122 | |||||
| chr8:39045123
|
TGTGC | T | 30 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(27): Show | 30 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1302+3007_1302+301 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045123 | ||||||
| chr8:39045124
|
GTGCATAC others(35): Show |
G | 7 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0065others(4): Show | 7 | NA18961.hp2 NA18965.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3009_1302+305 others(46): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045124 | |||||
| chr8:39045124
|
GTGCATAC others(63): Show |
G | 27 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3009_1302+307 others(74): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045124 | |||||
| chr8:39045127
|
C | CATACATA others(21): Show |
6 | a0001c0001t0001g0111a0001c0001t0001g0135a0001c0001t0001g0145others(3): Show | 6 | HG01106.hp2 HG02083.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+3135_1302+316 others(32): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045127 | |||||
| chr8:39045127
|
C | CATACATA others(49): Show |
3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0164 | 3 | HG02165.hp2 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1302+3107_1302+316 others(60): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045127 | |||||
| chr8:39045127
|
C | CATACATA others(77): Show |
1 | a0001c0001t0001g0144 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1302+3079_1302+316 others(88): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045127 | |||||
| chr8:39045127
|
C | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(86): Show | 89 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1302+3010C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045127 | ||||||
| chr8:39045127
|
CATACATA others(21): Show |
C | 2 | a0001c0001t0001g0002a0001c0001t0001g0201 | 2 | HG01346.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1302+3135_1302+316 others(32): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045127 | |||||
| chr8:39045129
|
T | C | 3 | a0001c0001t0001g0239a0001c0001t0004g0332a0002c0010t0002g0198 | 3 | HG01192.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1302+3012T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045129 | ||||||
| chr8:39045135
|
C | CATATGTG others(1): Show |
19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302+3022_1302+302 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045135 | |||||
| chr8:39045135
|
CAT | C | 11 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0074others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+3023_1302+302 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045135 | |||||
| chr8:39045138
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0004g0332 | 2 | HG01192.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1302+3021A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045138 | ||||||
| chr8:39045140
|
A | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0004g0332 | 3 | HG02647.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+3023A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045140 | ||||||
| chr8:39045144
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1302+3027G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045144 | ||||||
| chr8:39045148
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1302+3031A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045148 | ||||||
| chr8:39045149
|
TATGTGTA others(3): Show |
T | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3035_1302+304 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045149 | |||||
| chr8:39045150
|
A | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0001t0001g0239others(3): Show | 6 | HG00639.hp2 HG01192.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3033A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045150 | ||||||
| chr8:39045151
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1302+3034T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045151 | ||||||
| chr8:39045155
|
T | C | 15 | a0001c0001t0001g0032a0001c0001t0001g0170a0001c0001t0001g0185others(12): Show | 15 | HG00099.hp2 HG00323.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1302+3038T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045155 | ||||||
| chr8:39045157
|
T | C | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0004g0332 | 3 | HG00639.hp2 HG01192.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1302+3040T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045157 | ||||||
| chr8:39045159
|
C | CATACATA others(17): Show |
1 | a0001c0001t0001g0172 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1302+3050_1302+307 others(28): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045159 | |||||
| chr8:39045160
|
A | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3043A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045160 | ||||||
| chr8:39045163
|
C | CATATGTG others(1): Show |
10 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0074others(7): Show | 10 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3050_1302+305 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045163 | |||||
| chr8:39045163
|
C | CATATGTG others(27): Show |
1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1302+3050_1302+305 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045163 | |||||
| chr8:39045163
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3046C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045163 | ||||||
| chr8:39045163
|
CAT | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0089others(1): Show | 4 | HG01361.hp1 HG02135.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3051_1302+305 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045163 | |||||
| chr8:39045165
|
T | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3048T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045165 | ||||||
| chr8:39045166
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1302+3049A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045166 | ||||||
| chr8:39045168
|
A | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0240others(1): Show | 4 | HG00639.hp2 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3051A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045168 | ||||||
| chr8:39045170
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1302+3053G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045170 | ||||||
| chr8:39045172
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0089others(1): Show | 4 | HG01361.hp1 HG02135.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3055G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045172 | ||||||
| chr8:39045172
|
GTA | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0065others(4): Show | 7 | NA18961.hp2 NA18965.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3061_1302+306 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045172 | |||||
| chr8:39045175
|
T | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3058T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045175 | ||||||
| chr8:39045176
|
A | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0045others(10): Show | 13 | HG01192.hp1 HG01361.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3059A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045176 | ||||||
| chr8:39045178
|
A | ACATATAG others(3): Show |
1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3061_1302+306 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045178 | ||||||
| chr8:39045178
|
A | G | 16 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0045others(13): Show | 16 | HG01192.hp1 HG01361.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+3061A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045178 | ||||||
| chr8:39045183
|
T | C | 9 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0065others(6): Show | 9 | HG03492.hp1 NA18961.hp2 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3066T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045183 | ||||||
| chr8:39045184
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0103 | 2 | HG02109.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3067A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045184 | ||||||
| chr8:39045185
|
T | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0089others(3): Show | 6 | HG00639.hp2 HG01361.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3068T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045185 | ||||||
| chr8:39045187
|
C | CCT | 4 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0089others(1): Show | 4 | HG01361.hp1 HG02135.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3070_1302+307 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045187 | ||||||
| chr8:39045187
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3070C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045187 | ||||||
| chr8:39045188
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1302+3071A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045188 | ||||||
| chr8:39045189
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0004g0332 | 3 | HG02109.hp1 HG02647.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3072T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045189 | ||||||
| chr8:39045190
|
A | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0103 | 2 | HG02109.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3073A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045190 | ||||||
| chr8:39045191
|
C | CATATATG others(3): Show |
1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3088_1302+309 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045191 | |||||
| chr8:39045191
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0001g0240 | 3 | HG00639.hp2 HG02109.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3074C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045191 | ||||||
| chr8:39045191
|
CAT | C | 31 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(28): Show | 31 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1302+3079_1302+308 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045191 | |||||
| chr8:39045192
|
A | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3075A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045192 | ||||||
| chr8:39045193
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1302+3076T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045193 | ||||||
| chr8:39045194
|
A | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0089others(2): Show | 5 | HG00639.hp2 HG01361.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+3077A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045194 | ||||||
| chr8:39045194
|
ATATG | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3079_1302+308 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045194 | |||||
| chr8:39045195
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0103 | 2 | HG02109.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3078T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045195 | ||||||
| chr8:39045196
|
A | G | 7 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0089others(4): Show | 7 | HG00639.hp2 HG01361.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3079A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045196 | ||||||
| chr8:39045200
|
G | A | 31 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(28): Show | 31 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1302+3083G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045200 | ||||||
| chr8:39045200
|
G | GTACACC | 3 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01361.hp1 HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3085_1302+308 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045200 | |||||
| chr8:39045200
|
GTA | G | 27 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3089_1302+309 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045200 | |||||
| chr8:39045204
|
A | G | 60 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(57): Show | 60 | HG00438.hp2 HG00673.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.1302+3087A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045204 | ||||||
| chr8:39045205
|
T | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0001t0001g0090others(1): Show | 4 | HG01361.hp1 HG02135.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3088T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045205 | ||||||
| chr8:39045206
|
A | G | 70 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(67): Show | 70 | HG00438.hp2 HG00673.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1302+3089A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045206 | ||||||
| chr8:39045211
|
T | C | 34 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(31): Show | 34 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+3094T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045211 | ||||||
| chr8:39045212
|
A | G | 12 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(9): Show | 12 | HG00639.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1302+3095A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045212 | ||||||
| chr8:39045213
|
T | C | 36 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(33): Show | 36 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+3096T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045213 | ||||||
| chr8:39045215
|
C | CCT | 33 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(30): Show | 33 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+3098_1302+309 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045215 | ||||||
| chr8:39045217
|
T | C | 10 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(7): Show | 10 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3100T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045217 | ||||||
| chr8:39045218
|
A | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3101A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045218 | ||||||
| chr8:39045219
|
C | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3102C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045219 | ||||||
| chr8:39045220
|
A | C | 2 | a0001c0001t0001g0043a0001c0001t0004g0332 | 2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+3103A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045220 | ||||||
| chr8:39045222
|
A | G | 33 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(30): Show | 33 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+3105A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045222 | ||||||
| chr8:39045223
|
T | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3106T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045223 | ||||||
| chr8:39045224
|
A | AGGTG | 3 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01361.hp1 HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3107_1302+310 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045224 | ||||||
| chr8:39045224
|
A | G | 35 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(32): Show | 35 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1302+3107A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045224 | ||||||
| chr8:39045225
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1302+3108T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045225 | ||||||
| chr8:39045228
|
G | GTACACC | 27 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(24): Show | 27 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045228 | |||||
| chr8:39045228
|
G | GTACCCC | 3 | a0001c0001t0001g0092a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | NA18953.hp1 NA18981.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045228 | |||||
| chr8:39045228
|
GTATA | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0240a0001c0001t0004g0332 | 3 | HG00639.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+3115_1302+311 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045228 | |||||
| chr8:39045228
|
GTATATA | G | 8 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045228 | |||||
| chr8:39045230
|
A | ACACACAC others(1): Show |
3 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01361.hp1 HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045230 | ||||||
| chr8:39045230
|
A | ACACC | 3 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0068 | 3 | HG01074.hp1 HG03927.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045230 | ||||||
| chr8:39045233
|
T | C | 33 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(30): Show | 33 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1302+3116T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045233 | ||||||
| chr8:39045234
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0240a0001c0001t0004g0332 | 3 | HG00639.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+3117A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045234 | ||||||
| chr8:39045240
|
A | G | 32 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(29): Show | 32 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+3123A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045240 | ||||||
| chr8:39045241
|
T | C | 15 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3124T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045241 | ||||||
| chr8:39045243
|
C | CCT | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(6): Show | 9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3126_1302+312 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045243 | ||||||
| chr8:39045244
|
A | C | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1302+3127A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045244 | ||||||
| chr8:39045245
|
T | C | 8 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0053others(5): Show | 8 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+3128T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045245 | ||||||
| chr8:39045247
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1302+3130C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045247 | ||||||
| chr8:39045248
|
A | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0053others(3): Show | 6 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3131A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045248 | ||||||
| chr8:39045249
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG02135.hp1 HG03831.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1302+3132T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045249 | ||||||
| chr8:39045250
|
A | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3133A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045250 | ||||||
| chr8:39045250
|
A | G | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(6): Show | 9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3133A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045250 | ||||||
| chr8:39045252
|
A | AGGTG | 8 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0094others(5): Show | 8 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3135_1302+313 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045252 | ||||||
| chr8:39045252
|
A | G | 13 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(10): Show | 13 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3135A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045252 | ||||||
| chr8:39045253
|
T | C | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1302+3136T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045253 | ||||||
| chr8:39045253
|
T | G | 22 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(19): Show | 22 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1302+3136T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045253 | ||||||
| chr8:39045254
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3137G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045254 | ||||||
| chr8:39045254
|
G | GTGTATAT others(17): Show |
1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3155_1302+315 others(28): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045254 | |||||
| chr8:39045256
|
G | A | 2 | a0001c0001t0001g0249a0003c0004t0001g0302 | 2 | HG03688.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1302+3139G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045256 | ||||||
| chr8:39045256
|
G | GTACACC | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(6): Show | 9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3141_1302+314 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045256 | |||||
| chr8:39045256
|
GTATA | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0240 | 3 | HG00639.hp2 HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1302+3143_1302+314 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045256 | |||||
| chr8:39045256
|
GTATATA | G | 21 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(18): Show | 21 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+3141_1302+314 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045256 | |||||
| chr8:39045258
|
A | ACACACAC others(1): Show |
8 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0094others(5): Show | 8 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3141_1302+314 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045258 | ||||||
| chr8:39045258
|
A | G | 4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG02080.hp1 HG02135.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3141A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045258 | ||||||
| chr8:39045259
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0068a0001c0001t0001g0089others(1): Show | 4 | HG02135.hp1 HG03831.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3142T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045259 | ||||||
| chr8:39045260
|
A | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | HG02080.hp1 HG02135.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3143A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045260 | ||||||
| chr8:39045261
|
T | C | 12 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(9): Show | 12 | HG00639.hp2 HG01074.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1302+3144T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045261 | ||||||
| chr8:39045262
|
A | ACACACAC others(35): Show |
1 | a0001c0001t0001g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1302+3145_1302+314 others(46): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045262 | ||||||
| chr8:39045262
|
A | ACACACAC others(113): Show |
1 | a0001c0001t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1302+3145_1302+314 others(124): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045262 | ||||||
| chr8:39045262
|
A | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0043others(10): Show | 13 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3145A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045262 | ||||||
| chr8:39045263
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0004g0332 | 2 | HG02647.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1302+3146T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045263 | ||||||
| chr8:39045263
|
T | TGTGC | 8 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0094others(5): Show | 8 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3149_1302+315 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045263 | |||||
| chr8:39045268
|
A | G | 21 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0026others(18): Show | 21 | HG00438.hp2 HG01256.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+3151A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045268 | ||||||
| chr8:39045269
|
T | C | 29 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(26): Show | 29 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1302+3152T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045269 | ||||||
| chr8:39045272
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1302+3155A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045272 | ||||||
| chr8:39045273
|
T | C | 39 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(36): Show | 39 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1302+3156T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045273 | ||||||
| chr8:39045276
|
A | C | 28 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(25): Show | 28 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1302+3159A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045276 | ||||||
| chr8:39045276
|
ATATG | A | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(6): Show | 9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3163_1302+316 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045276 | |||||
| chr8:39045277
|
T | C | 10 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0092others(7): Show | 10 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3160T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045277 | ||||||
| chr8:39045278
|
A | ATATG | 13 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0170others(10): Show | 13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3162_1302+316 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045278 | |||||
| chr8:39045278
|
A | C | 10 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0092others(7): Show | 10 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3161A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045278 | ||||||
| chr8:39045278
|
ATG | A | 20 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(17): Show | 20 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1302+3163_1302+316 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045278 | |||||
| chr8:39045280
|
G | A | 18 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0053others(15): Show | 18 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+3163G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045280 | ||||||
| chr8:39045280
|
GTA | G | 10 | a0001c0001t0001g0082a0001c0001t0001g0113a0001c0001t0001g0114others(7): Show | 10 | HG01884.hp2 HG02622.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3167_1302+316 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045280 | |||||
| chr8:39045282
|
A | G | 8 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0053others(5): Show | 8 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+3165A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045282 | ||||||
| chr8:39045283
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1302+3166T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045283 | ||||||
| chr8:39045283
|
T | TATGTGTG others(13): Show |
1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1302+3183_1302+318 others(24): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045283 | |||||
| chr8:39045283
|
T | TATGTGTG others(13): Show |
1 | a0005c0009t0001g0163 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1302+3215_1302+323 others(24): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045283 | |||||
| chr8:39045284
|
A | G | 38 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(35): Show | 38 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1302+3167A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045284 | ||||||
| chr8:39045285
|
T | C | 8 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0053others(5): Show | 8 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+3168T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045285 | ||||||
| chr8:39045285
|
T | G | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(6): Show | 9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3168T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045285 | ||||||
| chr8:39045286
|
G | A | 13 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0170others(10): Show | 13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3169G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045286 | ||||||
| chr8:39045287
|
T | C | 30 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(27): Show | 30 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1302+3170T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045287 | ||||||
| chr8:39045292
|
G | A | 14 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0134others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+3175G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045292 | ||||||
| chr8:39045293
|
T | TACAC | 44 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0039others(41): Show | 44 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+3177_1302+318 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045293 | |||||
| chr8:39045295
|
C | CAT | 13 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0170others(10): Show | 13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3179_1302+318 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045295 | |||||
| chr8:39045297
|
CCTATACA others(9): Show |
C | 2 | a0001c0001t0001g0099a0001c0001t0001g0117 | 2 | HG03239.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1302+3181_1302+319 others(20): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045297 | ||||||
| chr8:39045298
|
C | A | 14 | a0001c0001t0001g0036a0001c0001t0001g0075a0001c0001t0001g0076others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+3181C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045298 | ||||||
| chr8:39045299
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1302+3182T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045299 | ||||||
| chr8:39045300
|
A | ATG | 13 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0170others(10): Show | 13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3184_1302+318 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045300 | |||||
| chr8:39045301
|
T | C | 125 | a0001c0001t0001g0032a0001c0001t0001g0124a0001c0001t0001g0126others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1302+3184T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045301 | ||||||
| chr8:39045303
|
C | T | 58 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(55): Show | 58 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1302+3186C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045303 | ||||||
| chr8:39045304
|
A | G | 44 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0039others(41): Show | 44 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+3187A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045304 | ||||||
| chr8:39045305
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1302+3188T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045305 | ||||||
| chr8:39045307
|
T | C | 44 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0039others(41): Show | 44 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+3190T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045307 | ||||||
| chr8:39045313
|
T | TACAC | 14 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(11): Show | 14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1302+3197_1302+320 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045313 | |||||
| chr8:39045313
|
T | TGTACAC | 31 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(28): Show | 31 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1302+3196_1302+319 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045313 | ||||||
| chr8:39045321
|
T | C | 130 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1302+3204T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045321 | ||||||
| chr8:39045323
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3206C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045323 | ||||||
| chr8:39045323
|
C | T | 47 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(44): Show | 47 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1302+3206C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045323 | ||||||
| chr8:39045324
|
A | G | 48 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(45): Show | 48 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.1302+3207A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045324 | ||||||
| chr8:39045325
|
T | TGC | 16 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(13): Show | 16 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+3209_1302+321 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045325 | |||||
| chr8:39045327
|
T | C | 32 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(29): Show | 32 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+3210T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045327 | ||||||
| chr8:39045331
|
T | TACATACA others(15): Show |
1 | a0002c0002t0002g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1302+3214_1302+321 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045331 | ||||||
| chr8:39045332
|
G | A | 14 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0058others(11): Show | 14 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.1302+3215G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045332 | ||||||
| chr8:39045333
|
T | C | 13 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0058others(10): Show | 13 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3216T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045333 | ||||||
| chr8:39045333
|
T | TACAC | 10 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0039others(7): Show | 10 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3217_1302+322 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045333 | |||||
| chr8:39045333
|
T | TGTACAC | 21 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0045others(18): Show | 21 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+3216_1302+321 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045333 | ||||||
| chr8:39045335
|
C | T | 13 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0058others(10): Show | 13 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3218C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045335 | ||||||
| chr8:39045337
|
CCTAT | C | 15 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3221_1302+322 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045337 | ||||||
| chr8:39045338
|
C | A | 13 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0058others(10): Show | 13 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3221C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045338 | ||||||
| chr8:39045341
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(3): Show | 6 | HG02056.hp1 HG02165.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+3224T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045341 | ||||||
| chr8:39045342
|
A | AGGTGCGT others(427): Show |
1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3225_1302+322 others(438): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045342 | ||||||
| chr8:39045342
|
A | ATGTG | 32 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(29): Show | 32 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+3225_1302+322 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045342 | ||||||
| chr8:39045343
|
C | G | 13 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0058others(10): Show | 13 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3226C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045343 | ||||||
| chr8:39045343
|
CATGTGTG others(1): Show |
C | 15 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3228_1302+323 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045343 | |||||
| chr8:39045344
|
A | G | 47 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(44): Show | 47 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.1302+3227A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045344 | ||||||
| chr8:39045352
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1302+3235A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045352 | ||||||
| chr8:39045353
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1302+3236C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045353 | ||||||
| chr8:39045354
|
A | C | 15 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3237A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045354 | ||||||
| chr8:39045355
|
T | C | 42 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(39): Show | 42 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1302+3238T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045355 | ||||||
| chr8:39045357
|
C | T | 15 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3240C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045357 | ||||||
| chr8:39045358
|
A | ACC | 46 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(43): Show | 46 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1302+3241_1302+324 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045358 | ||||||
| chr8:39045358
|
A | C | 2 | a0001c0001t0001g0170a0001c0001t0004g0332 | 2 | HG02647.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1302+3241A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045358 | ||||||
| chr8:39045360
|
A | G | 15 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3243A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045360 | ||||||
| chr8:39045362
|
A | ATGTG | 32 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(29): Show | 32 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+3245_1302+324 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045362 | ||||||
| chr8:39045362
|
A | G | 16 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(13): Show | 16 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+3245A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045362 | ||||||
| chr8:39045363
|
G | C | 51 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(48): Show | 51 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1302+3246G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045363 | ||||||
| chr8:39045363
|
G | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0098others(4): Show | 7 | HG00733.hp2 HG01993.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3246G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045363 | ||||||
| chr8:39045364
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1302+3247G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045364 | ||||||
| chr8:39045365
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1302+3248T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045365 | ||||||
| chr8:39045365
|
T | TGC | 6 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0098others(3): Show | 6 | HG00733.hp2 HG01993.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3249_1302+325 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045365 | |||||
| chr8:39045367
|
T | C | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3250T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045367 | ||||||
| chr8:39045370
|
G | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0266a0001c0001t0001g0300others(1): Show | 4 | HG01169.hp1 HG04204.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3253G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045370 | ||||||
| chr8:39045372
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3255A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045372 | ||||||
| chr8:39045375
|
T | C | 104 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(101): Show | 104 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.1302+3258T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045375 | ||||||
| chr8:39045375
|
T | TACACGCA others(65): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1302+3262_1302+326 others(76): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045375 | |||||
| chr8:39045375
|
T | TACACGCA others(89): Show |
1 | a0001c0001t0001g0081 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1302+3262_1302+326 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045375 | |||||
| chr8:39045376
|
A | ACACG | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(27): Show | 30 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1302+3262_1302+326 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045376 | |||||
| chr8:39045380
|
C | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(27): Show | 30 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1302+3263C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045380 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(89): Show |
1 | a0002c0002t0002g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(115): Show |
1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(126): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(163): Show |
1 | a0002c0002t0002g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(174): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(63): Show |
3 | a0002c0002t0002g0188a0002c0002t0002g0194a0002c0002t0002g0195 | 3 | HG02258.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1302+3267_1302+326 others(74): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(89): Show |
1 | a0002c0002t0002g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(115): Show |
1 | a0002c0002t0002g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(126): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(141): Show |
1 | a0002c0002t0002g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(152): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(93): Show |
1 | a0002c0002t0002g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(104): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ACGTGTGT others(141): Show |
1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(152): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ATGTACGT others(73): Show |
1 | a0001c0001t0001g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(84): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ATGTACGT others(149): Show |
2 | a0001c0001t0001g0266a0001c0003t0001g0293 | 2 | HG06807.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1302+3267_1302+326 others(160): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ATGTG | 58 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(55): Show | 58 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1302+3267_1302+326 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ATGTGCGT others(881): Show |
1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(892): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ATGTGCGT others(21): Show |
1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(32): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ATGTGCGT others(23): Show |
3 | a0001c0001t0001g0131a0002c0002t0002g0192a0002c0002t0002g0193 | 3 | HG02965.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1302+3267_1302+326 others(34): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045384
|
A | ATGTGCGT others(153): Show |
1 | a0001c0001t0001g0300 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(164): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | ||||||
| chr8:39045385
|
G | C | 78 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0036others(75): Show | 78 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1302+3268G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045385 | ||||||
| chr8:39045385
|
G | GGTGTGTC others(171): Show |
1 | a0001c0001t0001g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(182): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(119): Show |
1 | a0001c0001t0001g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(95): Show |
1 | a0001c0006t0001g0256 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(106): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(121): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0213a0001c0003t0001g0294 | 3 | HG00738.hp1 HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(132): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(147): Show |
1 | a0001c0003t0001g0290 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(158): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(67): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0208a0001c0001t0001g0219others(1): Show | 4 | HG02055.hp1 HG02738.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(78): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(93): Show |
16 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0209others(13): Show | 16 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(104): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(171): Show |
1 | a0001c0001t0001g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(182): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(119): Show |
18 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(15): Show | 18 | HG00099.hp1 HG01255.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(145): Show |
15 | a0001c0001t0001g0186a0001c0001t0001g0246a0001c0001t0001g0247others(12): Show | 15 | HG00639.hp1 HG01123.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(171): Show |
16 | a0001c0001t0001g0126a0001c0001t0001g0207a0001c0001t0001g0253others(13): Show | 16 | HG00323.hp1 HG01168.hp1 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(182): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(197): Show |
8 | a0001c0001t0001g0127a0001c0001t0001g0205a0001c0001t0001g0255others(5): Show | 8 | HG00735.hp2 HG02523.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(208): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(223): Show |
2 | a0001c0001t0001g0268a0001c0001t0001g0308 | 2 | HG01891.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(234): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(249): Show |
1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(260): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(275): Show |
1 | a0001c0001t0001g0216 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(286): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(145): Show |
1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(143): Show |
1 | a0001c0001t0001g0273 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(154): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(171): Show |
1 | a0001c0001t0001g0286 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(182): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(173): Show |
1 | a0001c0001t0001g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(184): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(69): Show |
1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(80): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(95): Show |
1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(106): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(121): Show |
2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | NA18954.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(132): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(145): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0282 | 2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(223): Show |
1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(234): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(71): Show |
1 | a0001c0001t0001g0270 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(82): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(97): Show |
3 | a0001c0001t0001g0230a0001c0001t0001g0271a0001c0001t0001g0291 | 3 | HG02083.hp2 NA18952.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(108): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(123): Show |
4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0272others(1): Show | 4 | NA18992.hp1 NA19009.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(134): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(149): Show |
1 | a0001c0001t0001g0328 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(160): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(175): Show |
1 | a0001c0001t0001g0287 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(186): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(121): Show |
7 | a0001c0001t0001g0236a0001c0001t0001g0257a0001c0001t0001g0311others(4): Show | 7 | HG01928.hp1 HG01952.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(132): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(147): Show |
4 | a0001c0001t0001g0229a0001c0001t0001g0250a0001c0001t0001g0251others(1): Show | 4 | HG01106.hp1 HG02622.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(158): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(173): Show |
2 | a0001c0001t0001g0227a0001c0001t0001g0279 | 2 | HG01952.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(184): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(199): Show |
1 | a0001c0001t0001g0288 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(210): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(251): Show |
1 | a0001c0001t0001g0278 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(262): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTC others(277): Show |
1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(288): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTG others(45): Show |
1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1302+3292_1302+329 others(56): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | GGTGTGTG others(19): Show |
1 | a0002c0002t0002g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1302+3270_1302+329 others(30): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | |||||
| chr8:39045385
|
G | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(31): Show | 34 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+3268G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045385 | ||||||
| chr8:39045387
|
T | TGC | 34 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(31): Show | 34 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+3271_1302+327 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045387 | |||||
| chr8:39045387
|
T | TGTGTGTA others(19): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0149a0001c0001t0001g0184 | 3 | HG01361.hp2 HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1302+3322_1302+334 others(30): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045387 | |||||
| chr8:39045387
|
T | TGTGTGTA others(45): Show |
1 | a0001c0001t0001g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1302+3296_1302+334 others(56): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045387 | |||||
| chr8:39045387
|
TGTGTGTA others(19): Show |
T | 2 | a0001c0001t0001g0147a0001c0001t0001g0175 | 2 | HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1302+3322_1302+334 others(30): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045387 | |||||
| chr8:39045389
|
T | TGTCTACA others(119): Show |
1 | a0001c0001t0001g0313 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045389 | |||||
| chr8:39045389
|
T | TGTCTACA others(119): Show |
1 | a0001c0001t0001g0312 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045389 | |||||
| chr8:39045389
|
T | TGTCTACA others(145): Show |
1 | a0001c0001t0001g0314 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045389 | |||||
| chr8:39045389
|
T | TGTCTACA others(199): Show |
1 | a0001c0001t0001g0275 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(210): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045389 | |||||
| chr8:39045394
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3277A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045394 | ||||||
| chr8:39045395
|
C | CACACACC others(39): Show |
23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 23 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1302+3295_1302+329 others(50): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045395 | |||||
| chr8:39045395
|
C | CACACACC others(63): Show |
5 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0080others(2): Show | 5 | HG00621.hp1 HG02132.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+3295_1302+329 others(74): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045395 | |||||
| chr8:39045395
|
C | CACACACC others(87): Show |
1 | a0001c0001t0001g0079 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1302+3295_1302+329 others(98): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045395 | |||||
| chr8:39045398
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3281A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045398 | ||||||
| chr8:39045407
|
T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3290T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045407 | ||||||
| chr8:39045407
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3290T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045407 | ||||||
| chr8:39045409
|
TGC | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0100others(1): Show | 4 | HG02572.hp1 NA18961.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3296_1302+329 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045409 | |||||
| chr8:39045411
|
C | CGTGTGTA others(15): Show |
1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1302+3295_1302+329 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045411 | |||||
| chr8:39045412
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+3295G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045412 | ||||||
| chr8:39045413
|
C | T | 271 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1302+3296C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045413 | ||||||
| chr8:39045415
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1302+3298T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045415 | ||||||
| chr8:39045419
|
TAC | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3309_1302+331 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045419 | |||||
| chr8:39045420
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3303A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045420 | ||||||
| chr8:39045424
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3307A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045424 | ||||||
| chr8:39045433
|
T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3316T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045433 | ||||||
| chr8:39045433
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3316T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045433 | ||||||
| chr8:39045439
|
C | T | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+3322C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045439 | ||||||
| chr8:39045439
|
CGTGTGTA others(19): Show |
C | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1302+3353_1302+337 others(30): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045439 | |||||
| chr8:39045445
|
TAC | T | 18 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+3335_1302+333 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045445 | |||||
| chr8:39045446
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3329A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045446 | ||||||
| chr8:39045450
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3333A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045450 | ||||||
| chr8:39045454
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0084 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1302+3337C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045454 | ||||||
| chr8:39045459
|
T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3342T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045459 | ||||||
| chr8:39045459
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3342T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045459 | ||||||
| chr8:39045464
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1302+3347G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045464 | ||||||
| chr8:39045471
|
TAC | T | 31 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(28): Show | 31 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1302+3361_1302+336 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045471 | |||||
| chr8:39045472
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3355A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045472 | ||||||
| chr8:39045473
|
C | CACACACC others(17): Show |
3 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0225 | 3 | HG02155.hp1 HG02602.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(28): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(169): Show |
2 | a0001c0001t0001g0038a0001c0001t0001g0112 | 2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(180): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(271): Show |
1 | a0001c0001t0001g0058 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(282): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(197): Show |
1 | a0001c0001t0001g0034 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(208): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(195): Show |
3 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0125 | 3 | NA18961.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(206): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(219): Show |
2 | a0001c0001t0001g0102a0001c0001t0001g0119 | 2 | HG01496.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(230): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(145): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0070 | 2 | HG02698.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(169): Show |
4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0066others(1): Show | 4 | HG01109.hp1 HG04115.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(180): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(193): Show |
1 | a0001c0001t0001g0101 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(204): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(119): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0106 | 2 | NA18982.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(143): Show |
7 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG02523.hp1 HG03017.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(154): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(167): Show |
1 | a0001c0001t0001g0027 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(178): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(93): Show |
3 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0092 | 3 | HG03927.hp1 NA18960.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(104): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(117): Show |
4 | a0001c0001t0001g0035a0001c0001t0001g0061a0001c0001t0001g0107others(1): Show | 4 | HG02572.hp1 HG04199.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(128): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(141): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0104a0001c0001t0001g0223 | 3 | HG00673.hp1 NA18977.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(152): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(213): Show |
1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(224): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(67): Show |
1 | a0001c0001t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(78): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(91): Show |
1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(102): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(115): Show |
2 | a0001c0001t0001g0033a0001c0001t0001g0071 | 2 | NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(126): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(139): Show |
1 | a0001c0001t0001g0088 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(150): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(41): Show |
1 | a0001c0001t0001g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(52): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(65): Show |
3 | a0001c0001t0001g0103a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG01256.hp1 HG01258.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(76): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(89): Show |
1 | a0001c0001t0001g0108 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACACC others(69): Show |
1 | a0001c0001t0001g0139 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(80): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045473
|
C | CACACCTA others(15): Show |
5 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0097others(2): Show | 5 | HG00733.hp2 HG01928.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+3360_1302+336 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | |||||
| chr8:39045476
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3359A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045476 | ||||||
| chr8:39045485
|
T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3368T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045485 | ||||||
| chr8:39045485
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3368T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045485 | ||||||
| chr8:39045496
|
A | G | 6 | a0001c0001t0001g0056a0001c0001t0001g0200a0001c0001t0001g0215others(3): Show | 6 | HG02055.hp2 HG02148.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3379A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045496 | ||||||
| chr8:39045510
|
G | A | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1302+3393G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045510 | ||||||
| chr8:39045540
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1302+3423A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045540 | ||||||
| chr8:39045540
|
ATATATGT others(7): Show |
A | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1302+3439_1302+345 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045540 | |||||
| chr8:39045556
|
ATATGTGT others(7): Show |
A | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3443_1302+345 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045556 | |||||
| chr8:39045568
|
G | GTATA | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 27 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3452_1302+345 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | |||||
| chr8:39045568
|
G | GTATATA | 4 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0075others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3452_1302+345 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | |||||
| chr8:39045568
|
G | GTATATAT others(3): Show |
10 | a0002c0002t0002g0187a0002c0002t0002g0188a0002c0002t0002g0189others(7): Show | 10 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1302+3452_1302+345 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | |||||
| chr8:39045568
|
G | GTATATAT others(5): Show |
2 | a0002c0002t0002g0130a0002c0002t0002g0190 | 2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1302+3452_1302+345 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | |||||
| chr8:39045568
|
G | GTATATAT others(7): Show |
1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3452_1302+345 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | |||||
| chr8:39045568
|
GTGTA | G | 133 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1302+3453_1302+345 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | |||||
| chr8:39045570
|
G | A | 51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 51 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.1302+3453G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045570 | ||||||
| chr8:39045570
|
G | GTA | 3 | a0001c0001t0001g0110a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG02723.hp1 HG02895.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1302+3470_1302+347 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045570 | |||||
| chr8:39045570
|
GTA | G | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1302+3470_1302+347 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045570 | |||||
| chr8:39045587
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1302+3470T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045587 | ||||||
| chr8:39045609
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1302+3492C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045609 | ||||||
| chr8:39045663
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3546C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045663 | ||||||
| chr8:39045707
|
T | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+3590T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045707 | ||||||
| chr8:39045796
|
T | A | 4 | a0002c0002t0002g0187a0002c0002t0002g0189a0002c0002t0002g0197others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3679T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045796 | ||||||
| chr8:39045815
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3698A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045815 | ||||||
| chr8:39045872
|
G | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(326): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1302+3755G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045872 | ||||||
| chr8:39045927
|
T | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+3810T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045927 | ||||||
| chr8:39045954
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1302+3837A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045954 | ||||||
| chr8:39045979
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1302+3862G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045979 | ||||||
| chr8:39046435
|
C | T | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+4318C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046435 | ||||||
| chr8:39046497
|
T | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0178 | 3 | HG00621.hp2 NA18945.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1302+4380T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046497 | ||||||
| chr8:39046510
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+4393C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046510 | ||||||
| chr8:39046685
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1302+4568C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046685 | ||||||
| chr8:39046775
|
AT | A | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+4671delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39046775 | |||||
| chr8:39046797
|
G | T | 2 | a0002c0002t0002g0192a0002c0002t0002g0193 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1302+4680G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046797 | ||||||
| chr8:39047024
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1302+4907C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047024 | ||||||
| chr8:39047044
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1302+4927C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047044 | ||||||
| chr8:39047395
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+5278T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047395 | ||||||
| chr8:39047410
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1302+5293C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047410 | ||||||
| chr8:39047456
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1302+5339A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047456 | ||||||
| chr8:39047614
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1302+5497T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047614 | ||||||
| chr8:39047696
|
A | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+5579A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047696 | ||||||
| chr8:39047825
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+5708G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047825 | ||||||
| chr8:39048065
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1302+5948C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048065 | ||||||
| chr8:39048298
|
G | A | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1302+6181G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048298 | ||||||
| chr8:39048567
|
C | G | 1 | a0001c0007t0001g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1303-5914C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048567 | ||||||
| chr8:39048574
|
T | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0156 | 2 | HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1303-5907T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048574 | ||||||
| chr8:39048623
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0226a0001c0001t0001g0327 | 3 | NA18987.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1303-5858C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048623 | ||||||
| chr8:39048984
|
G | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1303-5497G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048984 | ||||||
| chr8:39048998
|
G | GT | 6 | a0001c0001t0001g0045a0001c0001t0001g0125a0001c0001t0001g0134others(3): Show | 6 | HG01361.hp1 HG02074.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-5464dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39048998 | |||||
| chr8:39048998
|
GT | G | 166 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1303-5464delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39048998 | |||||
| chr8:39048998
|
GTT | G | 15 | a0001c0001t0001g0136a0002c0002t0002g0130a0002c0002t0002g0187others(12): Show | 15 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1303-5465_1303-546 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39048998 | |||||
| chr8:39049651
|
C | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0112 | 2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1303-4830C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39049651 | ||||||
| chr8:39049696
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1303-4785C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39049696 | ||||||
| chr8:39049757
|
T | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0212 | 2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1303-4724T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39049757 | ||||||
| chr8:39050008
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0112 | 2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1303-4473A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050008 | ||||||
| chr8:39050144
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1303-4337G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050144 | ||||||
| chr8:39050350
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1303-4131T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050350 | ||||||
| chr8:39050393
|
T | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1303-4088T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050393 | ||||||
| chr8:39050452
|
C | CT | 173 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1303-4016dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050452 | |||||
| chr8:39050452
|
CT | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG00639.hp2 HG03704.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303-4016delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050452 | |||||
| chr8:39050500
|
G | A | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1303-3981G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050500 | ||||||
| chr8:39050565
|
T | G | 1 | a0001c0001t0001g0280 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1303-3916T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050565 | ||||||
| chr8:39050571
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1303-3910G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050571 | ||||||
| chr8:39050703
|
A | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1303-3778A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050703 | ||||||
| chr8:39050751
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1303-3730T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050751 | ||||||
| chr8:39050830
|
G | GT | 11 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0066others(8): Show | 11 | HG00621.hp2 HG02683.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1303-3626dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050830 | |||||
| chr8:39050830
|
GT | G | 216 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1303-3626delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050830 | |||||
| chr8:39050830
|
GTT | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0080others(5): Show | 8 | HG01168.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1303-3627_1303-362 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050830 | |||||
| chr8:39050863
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1303-3618A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050863 | ||||||
| chr8:39051140
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0075others(2): Show | 5 | HG02970.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-3341C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051140 | ||||||
| chr8:39051340
|
T | G | 1 | a0001c0006t0001g0256 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1303-3141T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051340 | ||||||
| chr8:39051390
|
G | C | 1 | a0001c0001t0001g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1303-3091G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051390 | ||||||
| chr8:39051612
|
C | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-2869C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051612 | ||||||
| chr8:39051637
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1303-2844G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051637 | ||||||
| chr8:39051742
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1303-2739T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051742 | ||||||
| chr8:39052042
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1303-2439G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052042 | ||||||
| chr8:39052130
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1303-2351C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052130 | ||||||
| chr8:39052342
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1303-2139A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052342 | ||||||
| chr8:39052530
|
CTA | C | 7 | a0001c0001t0001g0254a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 7 | HG02074.hp2 NA18944.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-1944_1303-194 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39052530 | |||||
| chr8:39052542
|
C | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1303-1939C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052542 | ||||||
| chr8:39052728
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1303-1753A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052728 | ||||||
| chr8:39052897
|
A | G | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1303-1584A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052897 | ||||||
| chr8:39053097
|
G | A | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1303-1384G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053097 | ||||||
| chr8:39053114
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1303-1367T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053114 | ||||||
| chr8:39053225
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1303-1256A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053225 | ||||||
| chr8:39053327
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1303-1154A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053327 | ||||||
| chr8:39053472
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1303-1009C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053472 | ||||||
| chr8:39053872
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1303-609T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053872 | ||||||
| chr8:39054121
|
A | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG01256.hp1 HG01258.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1303-360A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054121 | ||||||
| chr8:39054137
|
C | G | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1303-344C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054137 | ||||||
| chr8:39054291
|
T | C | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1303-190T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054291 | ||||||
| chr8:39054419
|
T | G | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1303-62T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054419 | ||||||
| chr8:39054434
|
C | A | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1303-47C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054434 | ||||||
| chr8:39054602
|
G | GA | 143 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1395+49dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 39054602 | |||||
| chr8:39054602
|
GA | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(33): Show | 36 | HG00621.hp1 HG01255.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1395+49delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 39054602 | |||||
| chr8:39054602
|
GAA | G | 16 | a0001c0001t0001g0072a0001c0001t0001g0109a0002c0002t0002g0130others(13): Show | 16 | HG01257.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1395+48_1395+49del others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 39054602 | |||||
| chr8:39054714
|
G | A | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395+141G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054714 | ||||||
| chr8:39054736
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1395+163C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054736 | ||||||
| chr8:39054875
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1395+302T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054875 | ||||||
| chr8:39054947
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+374G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054947 | ||||||
| chr8:39054989
|
A | C | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1395+416A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054989 | ||||||
| chr8:39055148
|
C | T | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1396-429C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39055148 | ||||||
| chr8:39055287
|
G | T | 287 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1396-290G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39055287 | ||||||
| chr8:39055323
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1396-254G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39055323 | ||||||
| chr8:39055805
|
G | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1591+33G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39055805 | ||||||
| chr8:39056037
|
A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1591+265A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056037 | ||||||
| chr8:39056380
|
GT | G | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1591+613delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39056380 | |||||
| chr8:39056544
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1591+772C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056544 | ||||||
| chr8:39056555
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0003g0133 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1591+783G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056555 | ||||||
| chr8:39056657
|
T | G | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1591+885T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056657 | ||||||
| chr8:39056719
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1591+947A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056719 | ||||||
| chr8:39056898
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1591+1126A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056898 | ||||||
| chr8:39057019
|
CTATGTTT others(3): Show |
C | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1591+1260_1591+126 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39057019 | |||||
| chr8:39057061
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1591+1289C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057061 | ||||||
| chr8:39057084
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1591+1312A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057084 | ||||||
| chr8:39057344
|
T | TAATATAT others(20): Show |
1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1591+1583_1591+160 others(31): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39057344 | |||||
| chr8:39057493
|
TTG | T | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1591+1726_1591+172 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39057493 | |||||
| chr8:39057749
|
A | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1591+1977A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057749 | ||||||
| chr8:39057874
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1591+2102C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057874 | ||||||
| chr8:39057891
|
C | CTTTTTAG others(6): Show |
1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1591+2120_1591+212 others(17): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39057891 | |||||
| chr8:39057924
|
C | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1591+2152C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057924 | ||||||
| chr8:39058085
|
G | T | 132 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1591+2313G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39058085 | ||||||
| chr8:39058818
|
C | T | 57 | a0001c0001t0001g0032a0001c0001t0001g0207a0001c0001t0001g0214others(54): Show | 57 | HG00099.hp2 HG00438.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1591+3046C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39058818 | ||||||
| chr8:39059082
|
A | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0052others(2): Show | 5 | HG01074.hp1 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1591+3310A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059082 | ||||||
| chr8:39059182
|
G | C | 1 | a0001c0001t0001g0273 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1591+3410G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059182 | ||||||
| chr8:39059217
|
G | A | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1591+3445G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059217 | ||||||
| chr8:39059426
|
T | TA | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1591+3654_1591+365 others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059426 | ||||||
| chr8:39059484
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1591+3712C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059484 | ||||||
| chr8:39059485
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1591+3713C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059485 | ||||||
| chr8:39059660
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1591+3888C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059660 | ||||||
| chr8:39059930
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1591+4158T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059930 | ||||||
| chr8:39060141
|
G | C | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1591+4369G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060141 | ||||||
| chr8:39060200
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1591+4428A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060200 | ||||||
| chr8:39060330
|
G | A | 48 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(45): Show | 48 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1591+4558G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060330 | ||||||
| chr8:39060354
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1591+4582G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060354 | ||||||
| chr8:39060837
|
G | T | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1591+5065G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060837 | ||||||
| chr8:39061154
|
T | C | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1591+5382T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061154 | ||||||
| chr8:39061182
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1591+5410G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061182 | ||||||
| chr8:39061190
|
T | G | 1 | a0001c0001t0001g0288 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1591+5418T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061190 | ||||||
| chr8:39061249
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1591+5477A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061249 | ||||||
| chr8:39061472
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1591+5700A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061472 | ||||||
| chr8:39061516
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1591+5744T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061516 | ||||||
| chr8:39061546
|
C | A | 8 | a0001c0001t0001g0254a0001c0001t0001g0262a0001c0001t0001g0263others(5): Show | 8 | HG02074.hp2 NA18944.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1591+5774C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061546 | ||||||
| chr8:39061888
|
T | C | 53 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(50): Show | 53 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.1591+6116T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061888 | ||||||
| chr8:39062003
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1591+6231G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39062003 | ||||||
| chr8:39062613
|
A | G | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1591+6841A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39062613 | ||||||
| chr8:39062870
|
G | A | 132 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1591+7098G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39062870 | ||||||
| chr8:39062994
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1591+7222C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39062994 | ||||||
| chr8:39063217
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1591+7445G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063217 | ||||||
| chr8:39063461
|
G | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1591+7689G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063461 | ||||||
| chr8:39063579
|
A | G | 1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1592-7719A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063579 | ||||||
| chr8:39063686
|
C | T | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1592-7612C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063686 | ||||||
| chr8:39063777
|
A | G | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1592-7521A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063777 | ||||||
| chr8:39063794
|
C | G | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1592-7504C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063794 | ||||||
| chr8:39063947
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1592-7351C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063947 | ||||||
| chr8:39064026
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1592-7272C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064026 | ||||||
| chr8:39064081
|
T | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0029 | 2 | NA19074.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1592-7217T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064081 | ||||||
| chr8:39064082
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1592-7216C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064082 | ||||||
| chr8:39064216
|
G | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1592-7082G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064216 | ||||||
| chr8:39064339
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1592-6959T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064339 | ||||||
| chr8:39064463
|
G | A | 20 | a0001c0001t0001g0216a0001c0001t0001g0254a0001c0001t0001g0261others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.1592-6835G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064463 | ||||||
| chr8:39064505
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-6793T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064505 | ||||||
| chr8:39064514
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-6784T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064514 | ||||||
| chr8:39064595
|
T | A | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1592-6703T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064595 | ||||||
| chr8:39064630
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0066a0001c0001t0001g0105others(1): Show | 4 | HG02698.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1592-6668C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064630 | ||||||
| chr8:39064702
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0078 | 2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1592-6596C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064702 | ||||||
| chr8:39064790
|
G | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1592-6508G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064790 | ||||||
| chr8:39064972
|
T | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1592-6326T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064972 | ||||||
| chr8:39065012
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0173 | 2 | HG01106.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1592-6286C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065012 | ||||||
| chr8:39065202
|
G | GT | 9 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0242others(6): Show | 9 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1592-6087dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065202 | |||||
| chr8:39065212
|
G | GT | 51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 51 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(48): Show |
intron_variant | MODIFIER | c.1592-6074dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065212 | |||||
| chr8:39065217
|
T | C | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1592-6081T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065217 | ||||||
| chr8:39065439
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1592-5859G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065439 | ||||||
| chr8:39065501
|
A | T | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1592-5797A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065501 | ||||||
| chr8:39065584
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1592-5714C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065584 | ||||||
| chr8:39065620
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0121a0004c0008t0001g0120 | 3 | HG01884.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1592-5678A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065620 | ||||||
| chr8:39065647
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1592-5651G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065647 | ||||||
| chr8:39065659
|
C | CA | 7 | a0001c0001t0001g0111a0001c0001t0001g0142a0001c0001t0001g0143others(4): Show | 7 | HG01192.hp2 HG02055.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1592-5616dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065659 | |||||
| chr8:39065659
|
CA | C | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(117): Show | 120 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1592-5616delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065659 | |||||
| chr8:39065659
|
CAA | C | 130 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1592-5617_1592-561 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065659 | |||||
| chr8:39065710
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0175 | 2 | HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1592-5588C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065710 | ||||||
| chr8:39065800
|
G | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1592-5498G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065800 | ||||||
| chr8:39065908
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0107 | 2 | NA18944.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1592-5390C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065908 | ||||||
| chr8:39065934
|
A | G | 39 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(36): Show | 39 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1592-5364A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065934 | ||||||
| chr8:39066040
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1592-5258C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066040 | ||||||
| chr8:39066042
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1592-5256G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066042 | ||||||
| chr8:39066067
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1592-5231C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066067 | ||||||
| chr8:39066115
|
T | C | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1592-5183T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066115 | ||||||
| chr8:39066130
|
T | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0224 | 2 | HG01070.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1592-5168T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066130 | ||||||
| chr8:39066163
|
T | G | 1 | a0001c0001t0001g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1592-5135T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066163 | ||||||
| chr8:39066204
|
A | G | 1 | a0004c0008t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1592-5094A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066204 | ||||||
| chr8:39066486
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0078 | 2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1592-4812G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066486 | ||||||
| chr8:39066560
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1592-4738A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066560 | ||||||
| chr8:39066703
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1592-4595C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066703 | ||||||
| chr8:39066742
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1592-4556G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066742 | ||||||
| chr8:39066773
|
A | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1592-4525A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066773 | ||||||
| chr8:39066779
|
G | T | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1592-4519G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066779 | ||||||
| chr8:39066800
|
G | C | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1592-4498G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066800 | ||||||
| chr8:39066877
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0226a0001c0001t0001g0327 | 3 | NA18987.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1592-4421G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066877 | ||||||
| chr8:39066878
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1592-4420A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066878 | ||||||
| chr8:39066993
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1592-4305A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066993 | ||||||
| chr8:39067084
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1592-4214G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067084 | ||||||
| chr8:39067311
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0235 | 2 | HG02056.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1592-3987G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067311 | ||||||
| chr8:39067379
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1592-3919C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067379 | ||||||
| chr8:39067494
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1592-3804A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067494 | ||||||
| chr8:39067622
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1592-3676T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067622 | ||||||
| chr8:39067954
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1592-3344A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067954 | ||||||
| chr8:39067974
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1592-3324A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067974 | ||||||
| chr8:39068027
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1592-3271G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068027 | ||||||
| chr8:39068057
|
G | C | 1 | a0001c0001t0001g0325 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1592-3241G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068057 | ||||||
| chr8:39068153
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02155.hp2 NA18954.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1592-3145G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068153 | ||||||
| chr8:39068440
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1592-2858C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068440 | ||||||
| chr8:39068449
|
T | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1592-2849T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068449 | ||||||
| chr8:39068508
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1592-2790C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068508 | ||||||
| chr8:39068633
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1592-2665C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068633 | ||||||
| chr8:39068675
|
C | CA | 11 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0172others(8): Show | 11 | HG01109.hp2 HG02040.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1592-2584dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CA | C | 59 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1592-2584delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAA | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(47): Show | 50 | HG00738.hp1 HG01074.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.1592-2585_1592-258 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAA | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0024others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1592-2586_1592-258 others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAA | C | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0124others(5): Show | 8 | HG02132.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1592-2587_1592-258 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAA | C | 7 | a0002c0002t0002g0130a0002c0002t0002g0191a0002c0002t0002g0192others(4): Show | 7 | HG02559.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1592-2588_1592-258 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0170a0001c0001t0001g0178a0001c0001t0001g0249 | 3 | HG00621.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1592-2593_1592-258 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0162 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1592-2594_1592-258 others(15): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0136a0001c0001t0001g0141 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1592-2595_1592-258 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(6): Show |
C | 13 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0061others(10): Show | 13 | HG01192.hp1 HG01361.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1592-2596_1592-258 others(17): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(7): Show |
C | 75 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(72): Show | 75 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.1592-2597_1592-258 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0265others(1): Show | 4 | NA18944.hp1 NA18974.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1592-2598_1592-258 others(19): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0016a0001c0001t0001g0205 | 2 | HG02523.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1592-2599_1592-258 others(20): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(15): Show |
C | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1592-2605_1592-258 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068675
|
CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1592-2608_1592-258 others(29): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | |||||
| chr8:39068749
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1592-2549A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068749 | ||||||
| chr8:39069020
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-2278C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069020 | ||||||
| chr8:39069081
|
G | C | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1592-2217G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069081 | ||||||
| chr8:39069260
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-2038C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069260 | ||||||
| chr8:39069489
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1592-1809A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069489 | ||||||
| chr8:39069507
|
G | T | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1592-1791G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069507 | ||||||
| chr8:39069766
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1592-1532A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069766 | ||||||
| chr8:39069783
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-1515T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069783 | ||||||
| chr8:39069815
|
A | G | 1 | a0002c0002t0002g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1592-1483A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069815 | ||||||
| chr8:39069853
|
A | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0226a0001c0001t0001g0327 | 3 | NA18987.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1592-1445A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069853 | ||||||
| chr8:39069904
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1592-1394A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069904 | ||||||
| chr8:39069950
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1592-1348C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069950 | ||||||
| chr8:39069979
|
TA | T | 173 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1592-1295delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39069979 | |||||
| chr8:39069979
|
TAA | T | 95 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(92): Show | 95 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1592-1296_1592-129 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39069979 | |||||
| chr8:39070152
|
CA | C | 253 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1592-1125delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39070152 | |||||
| chr8:39070191
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1592-1107C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070191 | ||||||
| chr8:39070241
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-1057T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070241 | ||||||
| chr8:39070612
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1592-686G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070612 | ||||||
| chr8:39070713
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1592-585G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070713 | ||||||
| chr8:39070806
|
A | T | 2 | a0001c0001t0003g0133a0001c0001t0004g0332 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1592-492A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070806 | ||||||
| chr8:39071067
|
A | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1592-231A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39071067 | ||||||
| chr8:39071132
|
G | T | 21 | a0001c0001t0001g0213a0001c0001t0001g0291a0001c0001t0001g0296others(18): Show | 21 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1592-166G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39071132 | ||||||
| chr8:39071164
|
A | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1592-134A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39071164 | ||||||
| chr8:39071216
|
G | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1592-82G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39071216 | ||||||
| chr8:39071450
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1697+47C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071450 | ||||||
| chr8:39071465
|
C | CT | 19 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0115others(16): Show | 19 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1697+82dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39071465 | |||||
| chr8:39071465
|
C | CTT | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 37 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1697+81_1697+82dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39071465 | |||||
| chr8:39071465
|
CT | C | 132 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1697+82delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39071465 | |||||
| chr8:39071540
|
C | G | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1697+137C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071540 | ||||||
| chr8:39071569
|
T | C | 274 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1697+166T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071569 | ||||||
| chr8:39071619
|
A | G | 2 | a0001c0001t0003g0133a0001c0001t0004g0332 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1697+216A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071619 | ||||||
| chr8:39071624
|
G | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1697+221G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071624 | ||||||
| chr8:39071754
|
T | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1697+351T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071754 | ||||||
| chr8:39071764
|
C | T | 2 | a0002c0002t0002g0187a0002c0010t0002g0198 | 2 | HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1697+361C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071764 | ||||||
| chr8:39072128
|
T | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1697+725T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39072128 | ||||||
| chr8:39072619
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1697+1216G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39072619 | ||||||
| chr8:39072702
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1697+1299A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39072702 | ||||||
| chr8:39073221
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1697+1818G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073221 | ||||||
| chr8:39073672
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1697+2269C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073672 | ||||||
| chr8:39073738
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1697+2335T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073738 | ||||||
| chr8:39073808
|
A | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1697+2405A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073808 | ||||||
| chr8:39073848
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0278 | 2 | NA18984.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1697+2445T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073848 | ||||||
| chr8:39074011
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1697+2608C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074011 | ||||||
| chr8:39074073
|
A | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0079a0001c0001t0001g0080others(2): Show | 5 | HG00621.hp1 HG02132.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1697+2670A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074073 | ||||||
| chr8:39074229
|
T | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1697+2826T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074229 | ||||||
| chr8:39074247
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1697+2844G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074247 | ||||||
| chr8:39074375
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1698-2853T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074375 | ||||||
| chr8:39074555
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0269 | 2 | NA18960.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1698-2673A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074555 | ||||||
| chr8:39074674
|
C | A | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1698-2554C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074674 | ||||||
| chr8:39074903
|
C | CT | 13 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0103others(10): Show | 13 | HG01255.hp2 HG01891.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1698-2303dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39074903 | |||||
| chr8:39074903
|
CT | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0143a0001c0001t0001g0240others(3): Show | 6 | HG00639.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1698-2303delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39074903 | |||||
| chr8:39075078
|
T | C | 90 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(87): Show | 90 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1698-2150T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075078 | ||||||
| chr8:39075107
|
A | G | 1 | a0002c0002t0002g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1698-2121A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075107 | ||||||
| chr8:39075176
|
G | A | 1 | a0001c0007t0001g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1698-2052G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075176 | ||||||
| chr8:39075187
|
G | T | 39 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(36): Show | 39 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1698-2041G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075187 | ||||||
| chr8:39075338
|
C | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1698-1890C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075338 | ||||||
| chr8:39075450
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0103 | 2 | NA18943.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1698-1778T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075450 | ||||||
| chr8:39075622
|
T | C | 4 | a0001c0001t0001g0134a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02886.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1698-1606T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075622 | ||||||
| chr8:39075646
|
G | C | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1698-1582G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075646 | ||||||
| chr8:39075686
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1698-1542G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075686 | ||||||
| chr8:39075748
|
C | T | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1698-1480C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075748 | ||||||
| chr8:39075825
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1698-1403G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075825 | ||||||
| chr8:39076452
|
A | T | 2 | a0001c0001t0003g0133a0001c0001t0004g0332 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1698-776A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076452 | ||||||
| chr8:39076538
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1698-690A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076538 | ||||||
| chr8:39076739
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1698-489T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076739 | ||||||
| chr8:39076814
|
A | G | 132 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1698-414A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076814 | ||||||
| chr8:39076983
|
G | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1698-245G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076983 | ||||||
| chr8:39077064
|
C | T | 129 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1698-164C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39077064 | ||||||
| chr8:39077065
|
G | A | 5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698-163G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39077065 | ||||||
| chr8:39077218
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0255 | 2 | NA18962.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1698-10C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39077218 | ||||||
| chr8:39077590
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1881+179C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077590 | ||||||
| chr8:39077627
|
A | C | 8 | a0001c0001t0001g0146a0001c0001t0001g0156a0001c0001t0001g0162others(5): Show | 8 | HG00621.hp2 HG02074.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1881+216A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077627 | ||||||
| chr8:39077702
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0175 | 2 | HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1881+291T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077702 | ||||||
| chr8:39077705
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1881+294C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077705 | ||||||
| chr8:39077768
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1881+357A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077768 | ||||||
| chr8:39077778
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1881+367C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077778 | ||||||
| chr8:39078175
|
C | A | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1881+764C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078175 | ||||||
| chr8:39078308
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1881+897A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078308 | ||||||
| chr8:39078362
|
C | CA | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1881+968dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39078362 | |||||
| chr8:39078362
|
C | CAAA | 117 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1881+966_1881+968d others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39078362 | |||||
| chr8:39078362
|
CA | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0046others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1881+968delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39078362 | |||||
| chr8:39078379
|
A | AAAT | 8 | a0001c0001t0001g0216a0001c0001t0001g0261a0001c0001t0001g0306others(5): Show | 8 | HG00673.hp2 HG02135.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.1881+968_1881+969i others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078379 | ||||||
| chr8:39078425
|
TATCTA | T | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1881+1019_1881+102 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39078425 | |||||
| chr8:39078507
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1881+1096C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078507 | ||||||
| chr8:39078654
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1881+1243G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078654 | ||||||
| chr8:39078768
|
G | A | 133 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1881+1357G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078768 | ||||||
| chr8:39079257
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1881+1846G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079257 | ||||||
| chr8:39079340
|
C | CT | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1881+1929_1881+193 others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079340 | ||||||
| chr8:39079379
|
T | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1881+1968T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079379 | ||||||
| chr8:39079415
|
T | TTCCATGT others(10): Show |
1 | a0001c0001t0001g0058 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1881+2012_1881+202 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39079415 | |||||
| chr8:39079468
|
T | C | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1881+2057T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079468 | ||||||
| chr8:39079588
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1881+2177T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079588 | ||||||
| chr8:39079594
|
A | AT | 81 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(78): Show | 81 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1881+2201dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39079594 | |||||
| chr8:39079595
|
T | A | 132 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1881+2184T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079595 | ||||||
| chr8:39079725
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1881+2314C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079725 | ||||||
| chr8:39079771
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1881+2360G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079771 | ||||||
| chr8:39079781
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1881+2370C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079781 | ||||||
| chr8:39079973
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1881+2562A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079973 | ||||||
| chr8:39080097
|
ATTAT | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0186 | 3 | HG03492.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1882-2537_1882-253 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39080097 | |||||
| chr8:39080185
|
C | CA | 274 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1882-2449dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39080185 | |||||
| chr8:39080190
|
AAAT | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | NA18969.hp2 NA19001.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882-2450_1882-244 others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080190 | ||||||
| chr8:39080247
|
G | T | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1882-2394G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080247 | ||||||
| chr8:39080412
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1882-2229T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080412 | ||||||
| chr8:39080424
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1882-2217A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080424 | ||||||
| chr8:39080548
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0184 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1882-2093G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080548 | ||||||
| chr8:39080561
|
A | G | 90 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(87): Show | 90 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1882-2080A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080561 | ||||||
| chr8:39080587
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0056 | 3 | HG01993.hp2 HG03491.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1882-2054C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080587 | ||||||
| chr8:39080681
|
T | C | 2 | a0001c0001t0003g0133a0001c0001t0004g0332 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1882-1960T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080681 | ||||||
| chr8:39080724
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0053 | 2 | HG01074.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1882-1917C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080724 | ||||||
| chr8:39080725
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1882-1916G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080725 | ||||||
| chr8:39080846
|
G | C | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1882-1795G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080846 | ||||||
| chr8:39080853
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1788C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080853 | ||||||
| chr8:39080855
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1786A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080855 | ||||||
| chr8:39080857
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1784T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080857 | ||||||
| chr8:39080859
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1782G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080859 | ||||||
| chr8:39080860
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1781C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080860 | ||||||
| chr8:39080861
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1780T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080861 | ||||||
| chr8:39080863
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1778C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080863 | ||||||
| chr8:39080864
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1777G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080864 | ||||||
| chr8:39080869
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1772G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080869 | ||||||
| chr8:39080870
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1771G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080870 | ||||||
| chr8:39080873
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1768G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080873 | ||||||
| chr8:39080875
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1766T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080875 | ||||||
| chr8:39080876
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1765G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080876 | ||||||
| chr8:39080877
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1764G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080877 | ||||||
| chr8:39080879
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1762G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080879 | ||||||
| chr8:39080880
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1761G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080880 | ||||||
| chr8:39080882
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1759G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080882 | ||||||
| chr8:39080883
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1758G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080883 | ||||||
| chr8:39080884
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1757C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080884 | ||||||
| chr8:39080885
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1756C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080885 | ||||||
| chr8:39080889
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1752G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080889 | ||||||
| chr8:39080891
|
T | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1750T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080891 | ||||||
| chr8:39080892
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1749G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080892 | ||||||
| chr8:39080903
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1738T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080903 | ||||||
| chr8:39080905
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1736G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080905 | ||||||
| chr8:39080907
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1734A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080907 | ||||||
| chr8:39080908
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1733G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080908 | ||||||
| chr8:39080910
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1731A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080910 | ||||||
| chr8:39080911
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1730G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080911 | ||||||
| chr8:39080914
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1727T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080914 | ||||||
| chr8:39080915
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1726G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080915 | ||||||
| chr8:39080916
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1725T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080916 | ||||||
| chr8:39080917
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1724G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080917 | ||||||
| chr8:39080919
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1722G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080919 | ||||||
| chr8:39080921
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1720G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080921 | ||||||
| chr8:39080922
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1719G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080922 | ||||||
| chr8:39080926
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1715G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080926 | ||||||
| chr8:39080932
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1709C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080932 | ||||||
| chr8:39080933
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1708C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080933 | ||||||
| chr8:39080936
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1705C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080936 | ||||||
| chr8:39080937
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1704C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080937 | ||||||
| chr8:39080938
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1703C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080938 | ||||||
| chr8:39080944
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1697G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080944 | ||||||
| chr8:39080946
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1695G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080946 | ||||||
| chr8:39080948
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1693G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080948 | ||||||
| chr8:39080948
|
G | GT | 158 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1882-1673dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39080948 | |||||
| chr8:39080948
|
G | GTT | 9 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0083others(6): Show | 9 | HG00733.hp1 HG01168.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1882-1674_1882-167 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39080948 | |||||
| chr8:39080950
|
T | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1691T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080950 | ||||||
| chr8:39080953
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1688T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080953 | ||||||
| chr8:39080954
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1687T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080954 | ||||||
| chr8:39080956
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1685T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080956 | ||||||
| chr8:39080957
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1684T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080957 | ||||||
| chr8:39080960
|
T | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1681T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080960 | ||||||
| chr8:39080961
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1680T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080961 | ||||||
| chr8:39080966
|
T | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1675T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080966 | ||||||
| chr8:39080967
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1674T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080967 | ||||||
| chr8:39080972
|
GCAGGGTC others(4): Show |
G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1668_1882-165 others(15): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080972 | ||||||
| chr8:39081009
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1882-1632A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081009 | ||||||
| chr8:39081088
|
C | G | 133 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1882-1553C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081088 | ||||||
| chr8:39081109
|
G | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1882-1532G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081109 | ||||||
| chr8:39081228
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1882-1413C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081228 | ||||||
| chr8:39081287
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1882-1354G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081287 | ||||||
| chr8:39081409
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1882-1232A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081409 | ||||||
| chr8:39081414
|
A | G | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1882-1227A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081414 | ||||||
| chr8:39081813
|
A | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1882-828A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081813 | ||||||
| chr8:39081991
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1882-650G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081991 | ||||||
| chr8:39082020
|
G | A | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1882-621G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39082020 | ||||||
| chr8:39082134
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1882-507A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39082134 | ||||||
| chr8:39082214
|
C | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1882-427C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39082214 | ||||||
| chr8:39082570
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1882-71T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39082570 | ||||||
| chr8:39082773
|
GAAATCTC others(9): Show |
G | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1962+53_1962+68del others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 17/21 | chr8 | 39082773 | ||||||
| chr8:39082811
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1962+90G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 17/21 | chr8 | 39082811 | ||||||
| chr8:39082873
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0067 | 2 | HG00673.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1963-95A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 17/21 | chr8 | 39082873 | ||||||
| chr8:39082948
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1963-20G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 17/21 | chr8 | 39082948 | ||||||
| chr8:39083096
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2068+23A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083096 | ||||||
| chr8:39083147
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2068+74C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083147 | ||||||
| chr8:39083168
|
A | T | 1 | a0001c0001t0001g0170 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2068+95A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083168 | ||||||
| chr8:39083293
|
A | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+220A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083293 | ||||||
| chr8:39083302
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2068+229C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083302 | ||||||
| chr8:39083403
|
G | A | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2068+330G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083403 | ||||||
| chr8:39083415
|
A | G | 22 | a0001c0001t0001g0213a0001c0001t0001g0291a0001c0001t0001g0296others(19): Show | 22 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2068+342A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083415 | ||||||
| chr8:39083630
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0278 | 2 | NA18984.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2068+557A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083630 | ||||||
| chr8:39083787
|
CAG | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0078others(1): Show | 4 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+715_2068+716d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083787 | ||||||
| chr8:39084128
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2068+1055C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084128 | ||||||
| chr8:39084220
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0214a0001c0001t0001g0282 | 3 | HG00099.hp2 HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2068+1147A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084220 | ||||||
| chr8:39084285
|
G | T | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2068+1212G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084285 | ||||||
| chr8:39084430
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2068+1357A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084430 | ||||||
| chr8:39084502
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2068+1429C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084502 | ||||||
| chr8:39084537
|
T | G | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2068+1464T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084537 | ||||||
| chr8:39084583
|
C | CT | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2068+1522dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39084583 | |||||
| chr8:39084728
|
C | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0054others(3): Show | 6 | HG00738.hp2 HG01069.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068+1655C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084728 | ||||||
| chr8:39084803
|
G | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0052others(2): Show | 5 | HG01074.hp1 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2068+1730G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084803 | ||||||
| chr8:39084999
|
A | G | 7 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0079others(4): Show | 7 | HG00621.hp1 HG02132.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.2068+1926A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084999 | ||||||
| chr8:39085220
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2068+2147C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085220 | ||||||
| chr8:39085433
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2068+2360T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085433 | ||||||
| chr8:39085597
|
CA | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+2526delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39085597 | |||||
| chr8:39085600
|
G | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+2527G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085600 | ||||||
| chr8:39085741
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0282 | 2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2068+2668T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085741 | ||||||
| chr8:39085772
|
T | C | 223 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2068+2699T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085772 | ||||||
| chr8:39085929
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2068+2856A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085929 | ||||||
| chr8:39086048
|
T | C | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2068+2975T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086048 | ||||||
| chr8:39086163
|
TG | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+3091delG | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086163 | ||||||
| chr8:39086214
|
G | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2068+3141G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086214 | ||||||
| chr8:39086431
|
G | A | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2068+3358G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086431 | ||||||
| chr8:39086493
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2068+3420A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086493 | ||||||
| chr8:39086852
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | NA19074.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.2069-3195A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086852 | ||||||
| chr8:39087209
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0024 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2069-2838G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087209 | ||||||
| chr8:39087278
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2069-2769T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087278 | ||||||
| chr8:39087304
|
C | G | 1 | a0001c0001t0001g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2069-2743C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087304 | ||||||
| chr8:39087465
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2069-2582G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087465 | ||||||
| chr8:39087831
|
C | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-2216C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087831 | ||||||
| chr8:39087878
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2069-2169T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087878 | ||||||
| chr8:39087961
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2069-2086A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087961 | ||||||
| chr8:39087966
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2069-2081A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087966 | ||||||
| chr8:39088144
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2069-1903G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088144 | ||||||
| chr8:39088150
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2069-1897A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088150 | ||||||
| chr8:39088181
|
C | T | 12 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(9): Show | 12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2069-1866C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088181 | ||||||
| chr8:39088239
|
GATAA | G | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2069-1804_2069-180 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39088239 | |||||
| chr8:39088270
|
C | CT | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2069-1764dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39088270 | |||||
| chr8:39088310
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2069-1737C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088310 | ||||||
| chr8:39088508
|
C | T | 12 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(9): Show | 12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2069-1539C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088508 | ||||||
| chr8:39088521
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2069-1526C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088521 | ||||||
| chr8:39088527
|
G | GAT | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2069-1519_2069-151 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39088527 | |||||
| chr8:39088548
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2069-1499C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088548 | ||||||
| chr8:39088558
|
G | A | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2069-1489G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088558 | ||||||
| chr8:39088688
|
A | C | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2069-1359A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088688 | ||||||
| chr8:39088728
|
G | A | 286 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.2069-1319G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088728 | ||||||
| chr8:39088777
|
C | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2069-1270C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088777 | ||||||
| chr8:39089021
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-1026G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089021 | ||||||
| chr8:39089086
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0024 | 3 | HG02257.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2069-961A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089086 | ||||||
| chr8:39089117
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2069-930C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089117 | ||||||
| chr8:39089172
|
C | A | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2069-875C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089172 | ||||||
| chr8:39089286
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2069-761A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089286 | ||||||
| chr8:39089309
|
A | G | 92 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(89): Show | 92 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.2069-738A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089309 | ||||||
| chr8:39089399
|
G | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2069-648G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089399 | ||||||
| chr8:39089417
|
G | A | 14 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(11): Show | 14 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2069-630G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089417 | ||||||
| chr8:39089720
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2069-327A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089720 | ||||||
| chr8:39089755
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(1): Show | 4 | HG01346.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-292A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089755 | ||||||
| chr8:39089804
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0160 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2069-243C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089804 | ||||||
| chr8:39089963
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2069-84A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089963 | ||||||
| chr8:39090308
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2210+120G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090308 | ||||||
| chr8:39090355
|
A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2210+167A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090355 | ||||||
| chr8:39090503
|
G | T | 1 | a0001c0001t0001g0103 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2210+315G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090503 | ||||||
| chr8:39090638
|
G | T | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2210+450G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090638 | ||||||
| chr8:39090639
|
T | A | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2210+451T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090639 | ||||||
| chr8:39090640
|
T | A | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2210+452T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090640 | ||||||
| chr8:39090725
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2211-534C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090725 | ||||||
| chr8:39091514
|
GC | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(37): Show | 40 | HG00673.hp1 HG01109.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.2298+170delC | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39091514 | |||||
| chr8:39091530
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0307a0001c0001t0001g0317 | 3 | HG02698.hp2 NA19086.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2298+184C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39091530 | ||||||
| chr8:39091531
|
G | A | 6 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(3): Show | 6 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2298+185G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39091531 | ||||||
| chr8:39091866
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2298+520C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39091866 | ||||||
| chr8:39092013
|
C | T | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2298+667C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092013 | ||||||
| chr8:39092014
|
T | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2298+668T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092014 | ||||||
| chr8:39092128
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2298+782G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092128 | ||||||
| chr8:39092166
|
T | C | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2298+820T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092166 | ||||||
| chr8:39092195
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+849A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092195 | ||||||
| chr8:39092300
|
AT | A | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2298+956delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092300 | |||||
| chr8:39092324
|
A | G | 1 | a0001c0001t0001g0323 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2298+978A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092324 | ||||||
| chr8:39092331
|
T | TAC | 14 | a0001c0001t0001g0017a0001c0001t0001g0117a0001c0001t0001g0131others(11): Show | 14 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2298+1009_2298+101 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092331 | |||||
| chr8:39092331
|
T | TACAC | 87 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(84): Show | 87 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.2298+1007_2298+101 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092331 | |||||
| chr8:39092331
|
T | TACACAC | 16 | a0001c0001t0001g0067a0001c0001t0001g0098a0001c0001t0001g0099others(13): Show | 16 | HG00673.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2298+1005_2298+101 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092331 | |||||
| chr8:39092331
|
TAC | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2298+1009_2298+101 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092331 | |||||
| chr8:39092473
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2298+1127C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092473 | ||||||
| chr8:39092599
|
T | C | 1 | a0001c0003t0001g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2298+1253T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092599 | ||||||
| chr8:39092725
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2298+1379G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092725 | ||||||
| chr8:39092859
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2298+1513A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092859 | ||||||
| chr8:39092937
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2298+1591G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092937 | ||||||
| chr8:39093395
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2298+2049C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39093395 | ||||||
| chr8:39093830
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2298+2484C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39093830 | ||||||
| chr8:39093923
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2298+2577C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39093923 | ||||||
| chr8:39093981
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0003g0133 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2298+2635A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39093981 | ||||||
| chr8:39094047
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2298+2701C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094047 | ||||||
| chr8:39094186
|
A | G | 14 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2298+2840A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094186 | ||||||
| chr8:39094256
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2298+2910G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094256 | ||||||
| chr8:39094260
|
C | A | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2298+2914C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094260 | ||||||
| chr8:39094670
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0160 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2298+3324G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094670 | ||||||
| chr8:39094849
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0184 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2298+3503A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094849 | ||||||
| chr8:39094892
|
C | T | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2298+3546C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094892 | ||||||
| chr8:39094924
|
A | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.2298+3578A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094924 | ||||||
| chr8:39095045
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2298+3699G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095045 | ||||||
| chr8:39095283
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2298+3937A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095283 | ||||||
| chr8:39095321
|
C | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2298+3975C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095321 | ||||||
| chr8:39095406
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2298+4060T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095406 | ||||||
| chr8:39095476
|
C | T | 21 | a0001c0001t0001g0213a0001c0001t0001g0291a0001c0001t0001g0296others(18): Show | 21 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2298+4130C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095476 | ||||||
| chr8:39095850
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2298+4504C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095850 | ||||||
| chr8:39095855
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2298+4509C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095855 | ||||||
| chr8:39096046
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2298+4700C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096046 | ||||||
| chr8:39096077
|
T | TA | 134 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2298+4738dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39096077 | |||||
| chr8:39096096
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2298+4750T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096096 | ||||||
| chr8:39096100
|
TAATAGTT others(252): Show |
T | 28 | a0001c0001t0001g0124a0001c0001t0001g0186a0001c0001t0001g0205others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2298+4758_2298+501 others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39096100 | |||||
| chr8:39096136
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2298+4790T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096136 | ||||||
| chr8:39096236
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(42): Show | 45 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2298+4890T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096236 | ||||||
| chr8:39096362
|
T | A | 28 | a0001c0001t0001g0124a0001c0001t0001g0186a0001c0001t0001g0205others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2298+5016T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096362 | ||||||
| chr8:39096533
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2298+5187A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096533 | ||||||
| chr8:39097228
|
C | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.2299-4635C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097228 | ||||||
| chr8:39097282
|
G | C | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-4581G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097282 | ||||||
| chr8:39097292
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2299-4571T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097292 | ||||||
| chr8:39097392
|
CGCCTCCC others(5): Show |
C | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2299-4470_2299-445 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097392 | ||||||
| chr8:39097548
|
C | T | 87 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(84): Show | 87 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.2299-4315C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097548 | ||||||
| chr8:39097552
|
C | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2299-4311C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097552 | ||||||
| chr8:39097560
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2299-4303C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097560 | ||||||
| chr8:39097633
|
T | A | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-4230T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097633 | ||||||
| chr8:39097634
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2299-4229A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097634 | ||||||
| chr8:39097738
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2299-4125C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097738 | ||||||
| chr8:39097970
|
G | C | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-3893G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097970 | ||||||
| chr8:39098015
|
C | CTTCAACT others(14): Show |
1 | a0001c0001t0001g0167 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2299-3847_2299-382 others(25): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39098015 | |||||
| chr8:39098049
|
G | A | 130 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.2299-3814G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098049 | ||||||
| chr8:39098300
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2299-3563G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098300 | ||||||
| chr8:39098450
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2299-3413A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098450 | ||||||
| chr8:39098567
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2299-3296A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098567 | ||||||
| chr8:39098706
|
G | C | 1 | a0001c0001t0001g0321 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2299-3157G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098706 | ||||||
| chr8:39098940
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2299-2923A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098940 | ||||||
| chr8:39099087
|
A | C | 133 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2299-2776A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099087 | ||||||
| chr8:39099191
|
C | G | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2299-2672C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099191 | ||||||
| chr8:39099234
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0226a0001c0001t0001g0327 | 3 | NA18987.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2299-2629A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099234 | ||||||
| chr8:39099260
|
A | G | 130 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.2299-2603A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099260 | ||||||
| chr8:39099325
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0004g0332 | 3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-2538G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099325 | ||||||
| chr8:39099460
|
T | G | 2 | a0001c0001t0001g0136a0001c0001t0003g0133 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-2403T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099460 | ||||||
| chr8:39099499
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2299-2364T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099499 | ||||||
| chr8:39099660
|
A | C | 12 | a0002c0002t0002g0130a0002c0002t0002g0187a0002c0002t0002g0188others(9): Show | 12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2299-2203A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099660 | ||||||
| chr8:39099668
|
T | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(40): Show | 43 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.2299-2195T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099668 | ||||||
| chr8:39099875
|
GTT | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0030others(11): Show | 14 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2299-1967_2299-196 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39099875 | |||||
| chr8:39099875
|
GTTT | G | 239 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2299-1968_2299-196 others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39099875 | |||||
| chr8:39099875
|
GTTTT | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2299-1969_2299-196 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39099875 | |||||
| chr8:39099881
|
T | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0079a0001c0001t0001g0080others(2): Show | 5 | HG00621.hp1 HG02132.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.2299-1982T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099881 | ||||||
| chr8:39099882
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2299-1981T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099882 | ||||||
| chr8:39099951
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2299-1912C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099951 | ||||||
| chr8:39100025
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0097 | 3 | HG01257.hp1 HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2299-1838G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100025 | ||||||
| chr8:39100081
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0066a0001c0001t0001g0105others(1): Show | 4 | HG02698.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2299-1782C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100081 | ||||||
| chr8:39100216
|
G | A | 129 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.2299-1647G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100216 | ||||||
| chr8:39100257
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2299-1606A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100257 | ||||||
| chr8:39100334
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2299-1529G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100334 | ||||||
| chr8:39100536
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2299-1327A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100536 | ||||||
| chr8:39100715
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2299-1148G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100715 | ||||||
| chr8:39100767
|
A | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2299-1096A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100767 | ||||||
| chr8:39100790
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2299-1073A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100790 | ||||||
| chr8:39100864
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2299-999A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100864 | ||||||
| chr8:39101046
|
A | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(91): Show | 94 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.2299-817A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101046 | ||||||
| chr8:39101198
|
G | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2299-665G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101198 | ||||||
| chr8:39101366
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2299-497T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101366 | ||||||
| chr8:39101678
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0172a0001c0001t0001g0182 | 3 | NA18966.hp2 NA18973.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2299-185C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101678 | ||||||
| chr8:39101847
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2299-16T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101847 | ||||||
| chr8:39101979
|
G | A | 93 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(90): Show | 93 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.2366+49G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39101979 | ||||||
| chr8:39102032
|
T | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2366+102T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102032 | ||||||
| chr8:39102069
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2366+139G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102069 | ||||||
| chr8:39102082
|
C | T | 8 | a0001c0001t0001g0299a0001c0003t0001g0206a0001c0003t0001g0258others(5): Show | 8 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.2366+152C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102082 | ||||||
| chr8:39102551
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2366+621G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102551 | ||||||
| chr8:39102675
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2366+745G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102675 | ||||||
| chr8:39102698
|
A | G | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 5 | HG00280.hp2 HG01256.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.2366+768A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102698 | ||||||
| chr8:39102787
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2367-820A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102787 | ||||||
| chr8:39102983
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2367-624A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102983 | ||||||
| chr8:39102986
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2367-621C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102986 | ||||||
| chr8:39103225
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2367-382G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39103225 | ||||||
| chr8:39103406
|
ATT | A | 3 | a0002c0002t0002g0194a0002c0002t0002g0195a0002c0002t0002g0196 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2367-199_2367-198d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 39103406 |