| geneid | 8749 |
|---|---|
| ensemblid | ENSG00000168619.16 |
| hgncid | 196 |
| symbol | ADAM18 |
| name | ADAM metallopeptidase domain 18 |
| refseq_nuc | NM_014237.3 |
| refseq_prot | NP_055052.1 |
| ensembl_nuc | ENST00000265707.10 |
| ensembl_prot | ENSP00000265707.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 39584568 |
| end | 39730065 |
| strand | + |
| ver | v1.2 |
| region | chr8:39584568-39730065 |
| region5000 | chr8:39579568-39735065 |
| regionname0 | ADAM18_chr8_39584568_39730065 |
| regionname5000 | ADAM18_chr8_39579568_39735065 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 739 | 303 | 57 | 71 | 130 | 8 | 36 | 93 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0002 | 0/0 | 739 | 12 | 10 | 1 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0003 | 0/0 | 739 | 10 | 9 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0004 | 0/0 | 739 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0005 | 0/0 | 739 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0006 | 0/0 | 739 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0007 | 0/0 | 739 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0008 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0009 | 0/0 | 739 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0010 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0011 | 0/0 | 739 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0012 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0013 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0014 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2220 | 148 | 18 | 32 | 84 | 4 | 10 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0002 | 0/1 | 2220 | 145 | 32 | 38 | 44 | 4 | 26 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0003 | 0/0 | 2220 | 12 | 10 | 1 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0004 | 0/0 | 2220 | 10 | 9 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0005 | 0/0 | 2220 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0006 | 0/0 | 2220 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0007 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0008 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0009 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0010 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0011 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0012 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0013 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0014 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0015 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0016 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0017 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0018 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0019 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0020 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0021 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0022 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0023 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| c0024 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| 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 | 181 | 342 | 87 | 74 | 134 | 8 | 38 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| t0002 | 0/0 | 181 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| t0003 | 0/0 | 181 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2220 | 148 | 18 | 32 | 84 | 4 | 10 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0002 | 0/1 | 2220 | 145 | 32 | 38 | 44 | 4 | 26 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0007 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0008 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0010 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0012 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0014 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0015 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0002c0003 | 0/0 | 2220 | 12 | 10 | 1 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0003c0004 | 0/0 | 2220 | 10 | 9 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0004c0005 | 0/0 | 2220 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0004c0019 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0004c0022 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0005c0011 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0005c0016 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0006c0006 | 0/0 | 2220 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0007c0009 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0008c0024 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0009c0023 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0010c0013 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0011c0021 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0012c0020 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0013c0017 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0014c0018 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2400 | 148 | 18 | 32 | 84 | 4 | 10 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0002t0001 | 0/1 | 2400 | 145 | 32 | 38 | 44 | 4 | 26 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0007t0001 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0008t0003 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0010t0001 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0012t0001 | 0/0 | 2400 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0014t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0001c0015t0001 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0002c0003t0001 | 0/0 | 2400 | 12 | 10 | 1 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0003c0004t0001 | 0/0 | 2400 | 7 | 6 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0003c0004t0002 | 0/0 | 2400 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0004c0005t0001 | 0/0 | 2400 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0004c0019t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0004c0022t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0005c0011t0001 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0005c0016t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0006c0006t0001 | 0/0 | 2400 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0007c0009t0001 | 0/0 | 2400 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0008c0024t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0009c0023t0001 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0010c0013t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0011c0021t0001 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0012c0020t0001 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0013c0017t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| a0014c0018t0001 | 0/0 | 2400 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | copy fasta | chr8 | 39579568 | 39735065 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0007t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0007t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0008t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0008t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0010t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0010t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0012t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0014t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0015t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0019t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0022t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0005c0011t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0005c0011t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0005c0016t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0006c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0006c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0006c0006t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0007c0009t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0007c0009t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0008c0024t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0009c0023t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0010c0013t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0011c0021t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0012c0020t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0013c0017t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0014c0018t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0143 | EUR | GBR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | GBR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0152 | EUR | FIN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | FIN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0045 | EUR | FIN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0021 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00738 | hp2 | a0001 | c0015 | t0001 | g0029 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01167 | hp2 | a0009 | c0023 | t0001 | g0014 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01192 | hp2 | a0011 | c0021 | t0001 | g0224 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01884 | hp1 | a0010 | c0013 | t0001 | g0161 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02055 | hp1 | a0004 | c0022 | t0001 | g0192 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02055 | hp2 | a0001 | c0008 | t0003 | g0013 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CDX | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02257 | hp2 | a0003 | c0004 | t0002 | g0008 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02280 | hp2 | a0004 | c0005 | t0001 | g0290 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02572 | hp2 | a0004 | c0005 | t0001 | g0309 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0116 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0210 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02630 | hp1 | a0005 | c0011 | t0001 | g0188 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02717 | hp2 | a0006 | c0006 | t0001 | g0266 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0213 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0285 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02895 | hp2 | a0004 | c0019 | t0001 | g0106 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0022 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0179 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0023 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0132 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0144 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03041 | hp1 | a0001 | c0014 | t0001 | g0217 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03098 | hp1 | a0001 | c0008 | t0003 | g0012 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03098 | hp2 | a0004 | c0005 | t0001 | g0294 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03130 | hp1 | a0003 | c0004 | t0002 | g0007 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03139 | hp1 | a0003 | c0004 | t0002 | g0006 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03139 | hp2 | a0001 | c0007 | t0001 | g0195 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0227 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03209 | hp1 | a0001 | c0010 | t0001 | g0033 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03209 | hp2 | a0005 | c0016 | t0001 | g0156 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03239 | hp2 | a0003 | c0004 | t0001 | g0243 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03516 | hp1 | a0008 | c0024 | t0001 | g0211 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03516 | hp2 | a0001 | c0010 | t0001 | g0042 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03579 | hp1 | a0006 | c0006 | t0001 | g0265 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04199 | hp1 | a0014 | c0018 | t0001 | g0038 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18522 | hp1 | a0003 | c0004 | t0001 | g0214 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | CHB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18906 | hp1 | a0005 | c0011 | t0001 | g0245 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18961 | hp1 | a0012 | c0020 | t0001 | g0077 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18980 | hp1 | a0001 | c0012 | t0001 | g0005 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18986 | hp2 | a0001 | c0012 | t0001 | g0005 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19043 | hp1 | a0006 | c0006 | t0001 | g0264 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19043 | hp2 | a0013 | c0017 | t0001 | g0253 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19074 | hp1 | a0007 | c0009 | t0001 | g0151 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19077 | hp2 | a0007 | c0009 | t0001 | g0114 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0215 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20129 | hp1 | a0004 | c0005 | t0001 | g0316 | AFR | ASW | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ASW | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0260 | EUR | TSI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0342 | EUR | TSI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | GIH | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | GIH | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | USA | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | USA | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | USA | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20300 | hp2 | a0004 | c0005 | t0001 | g0320 | AFR | USA | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA21309 | hp1 | a0003 | c0004 | t0001 | g0212 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0148 | REF | REF | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39610551
|
A | C | 1 | a0006 | 3 | HG02717.hp2 HG03579.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.367A>C | p.Ile123Leu | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/20 | 422/2400 | 367/2220 | 123/739 | chr8 | 39610551 | ||
| chr8:39610609
|
A | T | 2 | a0003a0008 | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
missense_variant | MODERATE | c.425A>T | p.Gln142Leu | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/20 | 480/2400 | 425/2220 | 142/739 | chr8 | 39610609 | ||
| chr8:39637309
|
G | T | 2 | a0002a0009 | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
missense_variant | MODERATE | c.634G>T | p.Val212Phe | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 8/20 | 689/2400 | 634/2220 | 212/739 | chr8 | 39637309 | ||
| chr8:39648379
|
G | A | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1082G>A | p.Ser361Asn | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/20 | 1137/2400 | 1082/2220 | 361/739 | chr8 | 39648379 | ||
| chr8:39648410
|
A | T | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1113A>T | p.Lys371Asn | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/20 | 1168/2400 | 1113/2220 | 371/739 | chr8 | 39648410 | ||
| chr8:39668113
|
G | A | 1 | a0011 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.1442G>A | p.Arg481His | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/20 | 1497/2400 | 1442/2220 | 481/739 | chr8 | 39668113 | ||
| chr8:39668137
|
A | G | 1 | a0012 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.1466A>G | p.Tyr489Cys | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/20 | 1521/2400 | 1466/2220 | 489/739 | chr8 | 39668137 | ||
| chr8:39680074
|
C | T | 1 | a0014 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1669C>T | p.His557Tyr | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/20 | 1724/2400 | 1669/2220 | 557/739 | chr8 | 39680074 | ||
| chr8:39692661
|
C | T | 1 | a0007 | 2 | NA19074.hp1 NA19077.hp2 |
missense_variant | MODERATE | c.1883C>T | p.Thr628Ile | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/20 | 1938/2400 | 1883/2220 | 628/739 | chr8 | 39692661 | ||
| chr8:39706848
|
A | G | 3 | a0002a0009a0013 | 14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
missense_variant | MODERATE | c.1961A>G | p.Lys654Arg | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/20 | 2016/2400 | 1961/2220 | 654/739 | chr8 | 39706848 | ||
| chr8:39723859
|
G | T | 1 | a0005 | 3 | HG02630.hp1 HG03209.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.2129G>T | p.Arg710Ile | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2184/2400 | 2129/2220 | 710/739 | chr8 | 39723859 | ||
| chr8:39723876
|
T | A | 3 | a0004a0008a0009 | 9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.2146T>A | p.Ser716Thr | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2201/2400 | 2146/2220 | 716/739 | chr8 | 39723876 | ||
| chr8:39723898
|
A | G | 3 | a0004a0008a0009 | 9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.2168A>G | p.Glu723Gly | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2223/2400 | 2168/2220 | 723/739 | chr8 | 39723898 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39584664
|
G | A | 1 | a0001c0007 | 2 | HG03139.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.42G>A | p.Leu14Leu | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/20 | 97/2400 | 42/2220 | 14/739 | chr8 | 39584664 | ||
| chr8:39637555
|
T | C | 3 | a0001c0008a0002c0003a0009c0023 | 15 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(12): Show |
synonymous_variant | LOW | c.679T>C | p.Leu227Leu | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/20 | 734/2400 | 679/2220 | 227/739 | chr8 | 39637555 | ||
| chr8:39638510
|
T | C | 18 | a0001c0002a0001c0008a0001c0010others(15): Show | 191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
synonymous_variant | LOW | c.873T>C | p.Thr291Thr | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/20 | 928/2400 | 873/2220 | 291/739 | chr8 | 39638510 | ||
| chr8:39663842
|
G | A | 1 | a0001c0014 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1278G>A | p.Lys426Lys | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/20 | 1333/2400 | 1278/2220 | 426/739 | chr8 | 39663842 | ||
| chr8:39668147
|
C | T | 1 | a0004c0019 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1476C>T | p.Asn492Asn | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/20 | 1531/2400 | 1476/2220 | 492/739 | chr8 | 39668147 | ||
| chr8:39668162
|
T | C | 1 | a0001c0015 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1491T>C | p.Thr497Thr | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/20 | 1546/2400 | 1491/2220 | 497/739 | chr8 | 39668162 | ||
| chr8:39680097
|
C | T | 5 | a0001c0010a0002c0003a0003c0004others(2): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
synonymous_variant | LOW | c.1692C>T | p.Asp564Asp | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/20 | 1747/2400 | 1692/2220 | 564/739 | chr8 | 39680097 | ||
| chr8:39723770
|
C | T | 1 | a0001c0012 | 2 | NA18980.hp1 NA18986.hp2 |
synonymous_variant | LOW | c.2040C>T | p.Gly680Gly | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2095/2400 | 2040/2220 | 680/739 | chr8 | 39723770 | ||
| chr8:39723854
|
T | C | 1 | a0009c0023 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.2124T>C | p.Phe708Phe | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2179/2400 | 2124/2220 | 708/739 | chr8 | 39723854 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39584586
|
C | G | 1 | a0003c0004t0002 | 3 | HG02257.hp2 HG03130.hp1 HG03139.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/20 | chr8 | 39584586 | ||||||
| chr8:39584607
|
G | C | 1 | a0001c0008t0003 | 2 | HG02055.hp2 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-16G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/20 | 16 | chr8 | 39584607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39584773
|
T | G | 290 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(287): Show | 295 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.55+96T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/19 | chr8 | 39584773 | ||||||
| chr8:39584985
|
ACTC | A | 3 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008 | 3 | HG02257.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.56-287_56-285delCT others(1): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr8 | 39584985 | |||||
| chr8:39585065
|
A | AT | 6 | a0001c0001t0001g0286a0001c0002t0001g0285a0001c0002t0001g0287others(3): Show | 6 | HG00621.hp1 HG02280.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-202dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr8 | 39585065 | |||||
| chr8:39585130
|
T | C | 2 | a0001c0002t0001g0009a0001c0002t0001g0010 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.56-146T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/19 | chr8 | 39585130 | ||||||
| chr8:39586117
|
T | C | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.132+765T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586117 | ||||||
| chr8:39586131
|
G | T | 17 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.132+779G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586131 | ||||||
| chr8:39586260
|
C | T | 4 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+908C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586260 | ||||||
| chr8:39586261
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.132+909A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586261 | ||||||
| chr8:39586513
|
C | T | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+1161C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586513 | ||||||
| chr8:39586535
|
T | C | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.132+1183T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586535 | ||||||
| chr8:39586604
|
G | A | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+1252G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586604 | ||||||
| chr8:39586605
|
T | C | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+1253T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586605 | ||||||
| chr8:39586615
|
T | G | 151 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(148): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.132+1263T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586615 | ||||||
| chr8:39586641
|
C | T | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.132+1289C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586641 | ||||||
| chr8:39586699
|
C | G | 1 | a0001c0001t0001g0342 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+1347C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586699 | ||||||
| chr8:39586755
|
A | ACTAT | 30 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0247others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.132+1448_132+1451d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586755
|
A | ACTATCTA others(1): Show |
4 | a0001c0001t0001g0252a0001c0002t0001g0157a0003c0004t0002g0008others(1): Show | 4 | HG00738.hp1 HG02257.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1444_132+1451d others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586755
|
A | ACTATCTA others(5): Show |
2 | a0001c0001t0001g0254a0001c0001t0001g0341 | 2 | HG00597.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.132+1440_132+1451d others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586755
|
ACTAT | A | 102 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(99): Show | 104 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.132+1448_132+1451d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586755
|
ACTATCTA others(1): Show |
A | 34 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(31): Show | 34 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.132+1444_132+1451d others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586755
|
ACTATCTA others(5): Show |
A | 22 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(19): Show | 23 | HG01081.hp1 HG01167.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.132+1440_132+1451d others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586755
|
ACTATCTA others(9): Show |
A | 6 | a0001c0001t0001g0160a0001c0002t0001g0255a0001c0002t0001g0256others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+1436_132+1451d others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586755
|
ACTATCTA others(13): Show |
A | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.132+1432_132+1451d others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586755
|
ACTATCTA others(17): Show |
A | 5 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(2): Show | 5 | HG00642.hp2 HG00738.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+1428_132+1451d others(26): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | |||||
| chr8:39586789
|
T | TATC | 3 | a0001c0002t0001g0039a0001c0002t0001g0040a0014c0018t0001g0038 | 3 | HG02698.hp2 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.132+1438_132+1440d others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586789 | |||||
| chr8:39586792
|
CTATCTAT others(3): Show |
C | 1 | a0001c0001t0001g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.132+1452_132+1461d others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586792 | |||||
| chr8:39586794
|
ATC | A | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG01257.hp2 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.132+1444_132+1445d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586794 | |||||
| chr8:39586794
|
ATCTATCT others(5): Show |
A | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+1444_132+1455d others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586794 | |||||
| chr8:39586796
|
C | G | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1444C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586796 | ||||||
| chr8:39586798
|
ATCTATAT others(1): Show |
A | 13 | a0001c0001t0001g0046a0001c0002t0001g0001a0001c0002t0001g0045others(10): Show | 14 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.132+1448_132+1455d others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586798 | |||||
| chr8:39586800
|
C | A | 3 | a0001c0002t0001g0263a0006c0006t0001g0264a0006c0006t0001g0265 | 3 | HG02300.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.132+1448C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586800 | ||||||
| chr8:39586800
|
CTA | C | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG01257.hp2 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.132+1452_132+1453d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586800 | |||||
| chr8:39586802
|
A | ATC | 4 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0155others(1): Show | 4 | HG01074.hp2 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+1451_132+1452i others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586802 | |||||
| chr8:39586802
|
A | C | 3 | a0001c0002t0001g0263a0006c0006t0001g0264a0006c0006t0001g0265 | 3 | HG02300.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.132+1450A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586802 | ||||||
| chr8:39586802
|
ATATC | A | 21 | a0001c0001t0001g0090a0001c0002t0001g0086a0001c0002t0001g0087others(18): Show | 21 | HG00544.hp2 HG00609.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.132+1463_132+1466d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586802 | |||||
| chr8:39586804
|
A | C | 29 | a0001c0001t0001g0135a0001c0002t0001g0009a0001c0002t0001g0010others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.132+1452A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586804 | ||||||
| chr8:39586806
|
C | A | 29 | a0001c0001t0001g0135a0001c0002t0001g0009a0001c0002t0001g0010others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.132+1454C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586806 | ||||||
| chr8:39586806
|
C | CTA | 5 | a0001c0002t0001g0085a0001c0002t0001g0153a0001c0002t0001g0154others(2): Show | 5 | HG01074.hp2 HG01099.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1456_132+1457d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586806 | |||||
| chr8:39587387
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.132+2035C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587387 | ||||||
| chr8:39587594
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.132+2242G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587594 | ||||||
| chr8:39587620
|
T | C | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.132+2268T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587620 | ||||||
| chr8:39587721
|
C | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+2369C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587721 | ||||||
| chr8:39587826
|
A | G | 1 | a0001c0002t0001g0055 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.132+2474A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587826 | ||||||
| chr8:39587923
|
T | G | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+2571T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587923 | ||||||
| chr8:39588079
|
A | G | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2727A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588079 | ||||||
| chr8:39588173
|
C | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+2821C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588173 | ||||||
| chr8:39588231
|
T | TTG | 109 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(106): Show | 110 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.132+2880_132+2881i others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39588231 | |||||
| chr8:39588233
|
T | G | 167 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(164): Show | 171 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.132+2881T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588233 | ||||||
| chr8:39588324
|
T | G | 1 | a0001c0002t0001g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.132+2972T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588324 | ||||||
| chr8:39588352
|
C | T | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+3000C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588352 | ||||||
| chr8:39588618
|
C | G | 1 | a0001c0012t0001g0005 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.132+3266C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588618 | ||||||
| chr8:39588634
|
CT | C | 107 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(104): Show | 108 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.132+3283delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588634 | ||||||
| chr8:39588747
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0286 | 2 | HG00621.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.132+3395G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588747 | ||||||
| chr8:39588837
|
G | A | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.132+3485G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588837 | ||||||
| chr8:39589047
|
C | A | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+3695C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589047 | ||||||
| chr8:39589071
|
G | A | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+3719G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589071 | ||||||
| chr8:39589233
|
C | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.132+3881C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589233 | ||||||
| chr8:39589444
|
G | C | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+4092G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589444 | ||||||
| chr8:39589485
|
T | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0153 | 2 | HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.132+4133T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589485 | ||||||
| chr8:39589553
|
C | T | 151 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(148): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.132+4201C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589553 | ||||||
| chr8:39589653
|
T | C | 1 | a0001c0002t0001g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.132+4301T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589653 | ||||||
| chr8:39589698
|
A | G | 8 | a0001c0002t0001g0054a0001c0002t0001g0101a0001c0002t0001g0102others(5): Show | 8 | HG01993.hp2 HG02273.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.132+4346A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589698 | ||||||
| chr8:39589809
|
A | G | 107 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(104): Show | 108 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.132+4457A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589809 | ||||||
| chr8:39589913
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.132+4561G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589913 | ||||||
| chr8:39589967
|
G | A | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.132+4615G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589967 | ||||||
| chr8:39590203
|
A | G | 1 | a0001c0002t0001g0035 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.132+4851A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590203 | ||||||
| chr8:39590351
|
C | T | 4 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+4999C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590351 | ||||||
| chr8:39590459
|
T | C | 69 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(66): Show | 70 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.132+5107T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590459 | ||||||
| chr8:39590607
|
A | T | 1 | a0001c0002t0001g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.132+5255A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590607 | ||||||
| chr8:39590741
|
T | C | 290 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(287): Show | 295 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.132+5389T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590741 | ||||||
| chr8:39591064
|
T | A | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+5712T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591064 | ||||||
| chr8:39591166
|
C | T | 2 | a0001c0001t0001g0317a0001c0001t0001g0331 | 2 | NA18952.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.132+5814C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591166 | ||||||
| chr8:39591302
|
A | G | 52 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(49): Show | 55 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.132+5950A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591302 | ||||||
| chr8:39591375
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132+6023A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591375 | ||||||
| chr8:39591447
|
C | T | 70 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(67): Show | 71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+6095C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591447 | ||||||
| chr8:39591502
|
C | T | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.132+6150C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591502 | ||||||
| chr8:39591559
|
G | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+6207G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591559 | ||||||
| chr8:39591581
|
C | T | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+6229C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591581 | ||||||
| chr8:39591668
|
C | T | 70 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(67): Show | 71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+6316C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591668 | ||||||
| chr8:39591747
|
A | C | 2 | a0001c0002t0001g0116a0001c0002t0001g0152 | 2 | HG00280.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.132+6395A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591747 | ||||||
| chr8:39591783
|
A | G | 1 | a0001c0010t0001g0033 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.132+6431A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591783 | ||||||
| chr8:39592054
|
A | T | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+6702A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592054 | ||||||
| chr8:39592117
|
G | A | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.132+6765G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592117 | ||||||
| chr8:39592230
|
G | A | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+6878G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592230 | ||||||
| chr8:39592280
|
T | G | 107 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(104): Show | 108 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.132+6928T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592280 | ||||||
| chr8:39592381
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.132+7029C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592381 | ||||||
| chr8:39592561
|
C | T | 2 | a0001c0002t0001g0059a0001c0002t0001g0108 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.132+7209C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592561 | ||||||
| chr8:39592671
|
A | G | 1 | a0003c0004t0001g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.132+7319A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592671 | ||||||
| chr8:39592765
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132+7413C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592765 | ||||||
| chr8:39592862
|
C | T | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+7510C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592862 | ||||||
| chr8:39592996
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.132+7644C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592996 | ||||||
| chr8:39593049
|
A | G | 2 | a0001c0002t0001g0009a0001c0002t0001g0010 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.132+7697A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593049 | ||||||
| chr8:39593219
|
C | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0181others(3): Show | 6 | HG01256.hp1 HG01258.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+7867C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593219 | ||||||
| chr8:39593421
|
T | C | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+8069T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593421 | ||||||
| chr8:39593514
|
A | G | 1 | a0002c0003t0001g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.132+8162A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593514 | ||||||
| chr8:39593664
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.132+8312T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593664 | ||||||
| chr8:39593666
|
T | C | 3 | a0001c0002t0001g0060a0001c0002t0001g0061a0001c0002t0001g0062 | 3 | NA18957.hp2 NA18966.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.132+8314T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593666 | ||||||
| chr8:39593876
|
T | G | 1 | a0001c0002t0001g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.132+8524T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593876 | ||||||
| chr8:39594013
|
T | C | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+8661T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594013 | ||||||
| chr8:39594035
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.132+8683G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594035 | ||||||
| chr8:39594069
|
T | G | 70 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(67): Show | 71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+8717T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594069 | ||||||
| chr8:39594094
|
T | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG01168.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.132+8742T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594094 | ||||||
| chr8:39594481
|
G | T | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+9129G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594481 | ||||||
| chr8:39594618
|
T | C | 1 | a0001c0002t0001g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.132+9266T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594618 | ||||||
| chr8:39594706
|
G | A | 4 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+9354G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594706 | ||||||
| chr8:39594793
|
G | GT | 15 | a0001c0008t0003g0013a0002c0003t0001g0015a0002c0003t0001g0016others(12): Show | 15 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.132+9464dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39594793 | |||||
| chr8:39594793
|
GT | G | 238 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(235): Show | 243 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.132+9464delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39594793 | |||||
| chr8:39594793
|
GTT | G | 7 | a0001c0001t0001g0186a0001c0001t0001g0242a0001c0001t0001g0244others(4): Show | 7 | HG00639.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+9463_132+9464d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39594793 | |||||
| chr8:39594795
|
T | G | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+9443T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594795 | ||||||
| chr8:39594928
|
C | T | 105 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(102): Show | 106 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.132+9576C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594928 | ||||||
| chr8:39594986
|
A | G | 8 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+9634A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594986 | ||||||
| chr8:39595058
|
G | A | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+9706G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39595058 | ||||||
| chr8:39595331
|
G | A | 1 | a0001c0002t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.132+9979G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39595331 | ||||||
| chr8:39595899
|
T | A | 1 | a0001c0001t0001g0291 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.133-10408T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39595899 | ||||||
| chr8:39596003
|
T | C | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-10304T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596003 | ||||||
| chr8:39596134
|
C | T | 48 | a0001c0001t0001g0135a0001c0002t0001g0001a0001c0002t0001g0009others(45): Show | 49 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.133-10173C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596134 | ||||||
| chr8:39596199
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.133-10108C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596199 | ||||||
| chr8:39596325
|
T | C | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.133-9982T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596325 | ||||||
| chr8:39596575
|
C | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.133-9732C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596575 | ||||||
| chr8:39596906
|
T | A | 111 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(108): Show | 112 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.133-9401T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596906 | ||||||
| chr8:39596997
|
C | T | 25 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(22): Show | 25 | HG00733.hp1 HG01167.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.133-9310C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596997 | ||||||
| chr8:39597051
|
A | T | 3 | a0003c0004t0001g0179a0003c0004t0001g0213a0003c0004t0001g0214 | 3 | HG02723.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.133-9256A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597051 | ||||||
| chr8:39597058
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.133-9249T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597058 | ||||||
| chr8:39597158
|
G | T | 106 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.133-9149G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597158 | ||||||
| chr8:39597322
|
T | C | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-8985T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597322 | ||||||
| chr8:39597403
|
G | T | 1 | a0001c0001t0001g0238 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.133-8904G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597403 | ||||||
| chr8:39597407
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-8900A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597407 | ||||||
| chr8:39597607
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.133-8700G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597607 | ||||||
| chr8:39597697
|
G | T | 5 | a0001c0001t0001g0269a0001c0001t0001g0275a0001c0001t0001g0276others(2): Show | 5 | NA18950.hp1 NA18962.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-8610G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597697 | ||||||
| chr8:39597703
|
A | C | 1 | a0001c0002t0001g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.133-8604A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597703 | ||||||
| chr8:39597969
|
T | C | 1 | a0005c0011t0001g0188 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.133-8338T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597969 | ||||||
| chr8:39598147
|
T | C | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.133-8160T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598147 | ||||||
| chr8:39598283
|
T | A | 1 | a0001c0002t0001g0064 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.133-8024T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598283 | ||||||
| chr8:39598370
|
G | A | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133-7937G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598370 | ||||||
| chr8:39598762
|
C | T | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-7545C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598762 | ||||||
| chr8:39598767
|
C | CA | 47 | a0001c0001t0001g0172a0001c0001t0001g0180a0001c0001t0001g0183others(44): Show | 49 | HG00733.hp1 HG00738.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.133-7525dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39598767 | |||||
| chr8:39598767
|
CA | C | 26 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0207others(23): Show | 26 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.133-7525delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39598767 | |||||
| chr8:39598874
|
C | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.133-7433C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598874 | ||||||
| chr8:39599062
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.133-7245C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599062 | ||||||
| chr8:39599102
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.133-7205C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599102 | ||||||
| chr8:39599516
|
G | A | 149 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(146): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.133-6791G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599516 | ||||||
| chr8:39599708
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | NA18944.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.133-6599C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599708 | ||||||
| chr8:39599872
|
A | T | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-6435A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599872 | ||||||
| chr8:39599895
|
C | A | 8 | a0003c0004t0001g0210a0003c0004t0001g0212a0003c0004t0001g0215others(5): Show | 8 | HG02257.hp2 HG02622.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-6412C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599895 | ||||||
| chr8:39599949
|
T | A | 1 | a0002c0003t0001g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.133-6358T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599949 | ||||||
| chr8:39600113
|
T | C | 2 | a0003c0004t0001g0210a0003c0004t0001g0215 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133-6194T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600113 | ||||||
| chr8:39600149
|
T | G | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.133-6158T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600149 | ||||||
| chr8:39600167
|
G | A | 3 | a0001c0001t0001g0298a0001c0001t0001g0318a0001c0001t0001g0334 | 3 | HG00609.hp1 NA18948.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.133-6140G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600167 | ||||||
| chr8:39600232
|
A | G | 287 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(284): Show | 292 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.133-6075A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600232 | ||||||
| chr8:39600405
|
T | C | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-5902T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600405 | ||||||
| chr8:39600436
|
A | G | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.133-5871A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600436 | ||||||
| chr8:39600811
|
G | C | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.133-5496G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600811 | ||||||
| chr8:39600880
|
C | T | 152 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(149): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.133-5427C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600880 | ||||||
| chr8:39600968
|
C | A | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.133-5339C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600968 | ||||||
| chr8:39600987
|
G | T | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133-5320G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600987 | ||||||
| chr8:39601004
|
G | A | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-5303G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601004 | ||||||
| chr8:39601088
|
G | A | 5 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0088others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-5219G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601088 | ||||||
| chr8:39601126
|
C | T | 1 | a0001c0002t0001g0084 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.133-5181C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601126 | ||||||
| chr8:39601202
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-5105C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601202 | ||||||
| chr8:39601461
|
T | G | 1 | a0001c0002t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.133-4846T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601461 | ||||||
| chr8:39601531
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.133-4776A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601531 | ||||||
| chr8:39601626
|
T | C | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.133-4681T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601626 | ||||||
| chr8:39601653
|
C | G | 2 | a0001c0002t0001g0115a0001c0002t0001g0157 | 2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.133-4654C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601653 | ||||||
| chr8:39601700
|
C | A | 1 | a0011c0021t0001g0224 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.133-4607C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601700 | ||||||
| chr8:39601786
|
T | C | 106 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.133-4521T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601786 | ||||||
| chr8:39602079
|
G | T | 1 | a0001c0002t0001g0083 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.133-4228G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602079 | ||||||
| chr8:39602329
|
G | A | 1 | a0001c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.133-3978G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602329 | ||||||
| chr8:39602543
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.133-3764C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602543 | ||||||
| chr8:39602560
|
C | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.133-3747C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602560 | ||||||
| chr8:39602592
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.133-3715G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602592 | ||||||
| chr8:39602716
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.133-3591T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602716 | ||||||
| chr8:39602749
|
GCTTTTTT others(18): Show |
G | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.133-3553_133-3529d others(27): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39602749 | |||||
| chr8:39603113
|
G | A | 1 | a0013c0017t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.133-3194G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603113 | ||||||
| chr8:39603140
|
A | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-3167A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603140 | ||||||
| chr8:39603261
|
A | G | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.133-3046A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603261 | ||||||
| chr8:39603312
|
G | C | 1 | a0001c0002t0001g0067 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.133-2995G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603312 | ||||||
| chr8:39603602
|
A | T | 106 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.133-2705A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603602 | ||||||
| chr8:39603852
|
CTGTT | C | 10 | a0001c0002t0001g0047a0001c0002t0001g0093a0001c0002t0001g0094others(7): Show | 10 | HG00544.hp2 HG01496.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-2453_133-2450d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39603852 | |||||
| chr8:39604047
|
A | G | 1 | a0001c0002t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.133-2260A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604047 | ||||||
| chr8:39604088
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.133-2219C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604088 | ||||||
| chr8:39604250
|
T | C | 1 | a0001c0002t0001g0086 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.133-2057T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604250 | ||||||
| chr8:39604255
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.133-2052C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604255 | ||||||
| chr8:39604256
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.133-2051G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604256 | ||||||
| chr8:39604384
|
A | T | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.133-1923A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604384 | ||||||
| chr8:39604403
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.133-1904T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604403 | ||||||
| chr8:39604478
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.133-1829G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604478 | ||||||
| chr8:39604560
|
G | A | 1 | a0001c0002t0001g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.133-1747G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604560 | ||||||
| chr8:39604648
|
C | T | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.133-1659C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604648 | ||||||
| chr8:39604708
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-1599G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604708 | ||||||
| chr8:39604735
|
C | T | 1 | a0004c0005t0001g0316 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.133-1572C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604735 | ||||||
| chr8:39605252
|
T | G | 15 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(12): Show | 15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-1055T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605252 | ||||||
| chr8:39605466
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.133-841A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605466 | ||||||
| chr8:39605524
|
T | C | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.133-783T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605524 | ||||||
| chr8:39605544
|
T | C | 318 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(315): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.133-763T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605544 | ||||||
| chr8:39605545
|
G | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.133-762G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605545 | ||||||
| chr8:39605615
|
G | T | 5 | a0001c0002t0001g0116a0001c0002t0001g0147a0001c0002t0001g0148others(2): Show | 5 | HG00280.hp1 HG01256.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-692G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605615 | ||||||
| chr8:39605619
|
T | C | 3 | a0001c0002t0001g0048a0001c0002t0001g0095a0001c0002t0001g0107 | 3 | NA18965.hp2 NA18985.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.133-688T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605619 | ||||||
| chr8:39605677
|
T | A | 11 | a0001c0001t0001g0193a0001c0001t0001g0225a0001c0001t0001g0246others(8): Show | 11 | HG00323.hp2 HG00733.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.133-630T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605677 | ||||||
| chr8:39605683
|
A | T | 1 | a0003c0004t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.133-624A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605683 | ||||||
| chr8:39605747
|
T | G | 15 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(12): Show | 15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-560T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605747 | ||||||
| chr8:39605809
|
C | T | 6 | a0001c0001t0001g0135a0001c0002t0001g0001a0001c0002t0001g0051others(3): Show | 7 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-498C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605809 | ||||||
| chr8:39606095
|
C | T | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-212C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39606095 | ||||||
| chr8:39606201
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.133-106G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39606201 | ||||||
| chr8:39606304
|
T | C | 71 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(68): Show | 72 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.133-3T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39606304 | ||||||
| chr8:39606619
|
C | T | 52 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(49): Show | 55 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.188+257C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39606619 | ||||||
| chr8:39606754
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.188+392G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39606754 | ||||||
| chr8:39607244
|
T | G | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+882T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607244 | ||||||
| chr8:39607463
|
C | T | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.188+1101C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607463 | ||||||
| chr8:39607519
|
G | A | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+1157G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607519 | ||||||
| chr8:39607530
|
G | A | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.188+1168G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607530 | ||||||
| chr8:39607587
|
T | G | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.188+1225T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607587 | ||||||
| chr8:39607742
|
A | AT | 105 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(102): Show | 106 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.189-1287dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr8 | 39607742 | |||||
| chr8:39607742
|
AT | A | 12 | a0001c0001t0001g0336a0001c0002t0001g0109a0002c0003t0001g0011others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-1287delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr8 | 39607742 | |||||
| chr8:39607774
|
G | A | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-1268G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607774 | ||||||
| chr8:39607813
|
GT | G | 92 | a0001c0001t0001g0187a0001c0002t0001g0002a0001c0002t0001g0003others(89): Show | 95 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.189-1218delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr8 | 39607813 | |||||
| chr8:39607824
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.189-1218T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607824 | ||||||
| chr8:39607939
|
A | G | 1 | a0002c0003t0001g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-1103A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607939 | ||||||
| chr8:39608095
|
C | T | 1 | a0001c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.189-947C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608095 | ||||||
| chr8:39608108
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.189-934G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608108 | ||||||
| chr8:39608177
|
A | ATATATC | 30 | a0001c0001t0001g0160a0001c0001t0001g0187a0001c0001t0001g0201others(27): Show | 30 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.189-850_189-845dup others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr8 | 39608177 | |||||
| chr8:39608187
|
A | G | 1 | a0001c0002t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.189-855A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608187 | ||||||
| chr8:39608264
|
A | G | 1 | a0001c0015t0001g0029 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.189-778A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608264 | ||||||
| chr8:39608417
|
A | G | 2 | a0001c0001t0001g0172a0004c0022t0001g0192 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.189-625A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608417 | ||||||
| chr8:39608511
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.189-531C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608511 | ||||||
| chr8:39608701
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.189-341A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608701 | ||||||
| chr8:39608832
|
T | A | 1 | a0001c0002t0001g0259 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189-210T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608832 | ||||||
| chr8:39608884
|
T | C | 1 | a0001c0002t0001g0030 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.189-158T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608884 | ||||||
| chr8:39609275
|
G | T | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.267+155G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 4/19 | chr8 | 39609275 | ||||||
| chr8:39609432
|
C | A | 1 | a0001c0001t0001g0322 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.268-53C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 4/19 | chr8 | 39609432 | ||||||
| chr8:39609456
|
T | C | 1 | a0001c0002t0001g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.268-29T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 4/19 | chr8 | 39609456 | ||||||
| chr8:39609475
|
T | C | 2 | a0001c0002t0001g0054a0001c0002t0001g0101 | 2 | NA18960.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.268-10T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 4/19 | chr8 | 39609475 | ||||||
| chr8:39609576
|
T | C | 8 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0261others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+15T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609576 | ||||||
| chr8:39609606
|
A | T | 1 | a0001c0001t0001g0315 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.344+45A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609606 | ||||||
| chr8:39609805
|
A | G | 106 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.344+244A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609805 | ||||||
| chr8:39609846
|
C | G | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+285C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609846 | ||||||
| chr8:39609921
|
C | G | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.344+360C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609921 | ||||||
| chr8:39610140
|
G | A | 1 | a0001c0002t0001g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.345-389G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39610140 | ||||||
| chr8:39610173
|
A | G | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-356A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39610173 | ||||||
| chr8:39610187
|
T | G | 3 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0025 | 3 | HG02965.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.345-342T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39610187 | ||||||
| chr8:39610377
|
GC | G | 7 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-145delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr8 | 39610377 | |||||
| chr8:39610452
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.345-77C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39610452 | ||||||
| chr8:39611054
|
A | T | 2 | a0001c0002t0001g0289a0004c0005t0001g0290 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.522+348A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611054 | ||||||
| chr8:39611076
|
G | A | 3 | a0003c0004t0001g0179a0003c0004t0001g0213a0003c0004t0001g0214 | 3 | HG02723.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.522+370G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611076 | ||||||
| chr8:39611315
|
A | G | 1 | a0001c0002t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.522+609A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611315 | ||||||
| chr8:39611330
|
G | T | 151 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(148): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.522+624G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611330 | ||||||
| chr8:39611380
|
T | A | 151 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(148): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.522+674T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611380 | ||||||
| chr8:39611423
|
G | GA | 282 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(279): Show | 287 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.522+727dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39611423 | |||||
| chr8:39611443
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+737G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611443 | ||||||
| chr8:39611736
|
A | G | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.522+1030A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611736 | ||||||
| chr8:39611745
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.522+1039C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611745 | ||||||
| chr8:39611909
|
A | G | 1 | a0001c0001t0001g0335 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.522+1203A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611909 | ||||||
| chr8:39611948
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.522+1242T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611948 | ||||||
| chr8:39612098
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.522+1392A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612098 | ||||||
| chr8:39612132
|
G | GA | 16 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(13): Show | 16 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.522+1437dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39612132 | |||||
| chr8:39612508
|
C | T | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+1802C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612508 | ||||||
| chr8:39612617
|
T | G | 145 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(142): Show | 149 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.522+1911T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612617 | ||||||
| chr8:39612698
|
T | G | 1 | a0001c0002t0001g0125 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.522+1992T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612698 | ||||||
| chr8:39612908
|
C | T | 2 | a0001c0001t0001g0172a0004c0022t0001g0192 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.522+2202C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612908 | ||||||
| chr8:39613099
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.522+2393C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613099 | ||||||
| chr8:39613148
|
T | G | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.522+2442T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613148 | ||||||
| chr8:39613289
|
A | T | 4 | a0001c0001t0001g0269a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | NA18950.hp1 NA18962.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+2583A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613289 | ||||||
| chr8:39613316
|
A | G | 1 | a0002c0003t0001g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.522+2610A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613316 | ||||||
| chr8:39613349
|
A | G | 2 | a0001c0001t0001g0298a0001c0001t0001g0318 | 2 | HG00609.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.522+2643A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613349 | ||||||
| chr8:39613489
|
G | C | 40 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(37): Show | 40 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.522+2783G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613489 | ||||||
| chr8:39613748
|
A | G | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.522+3042A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613748 | ||||||
| chr8:39613912
|
A | G | 1 | a0001c0002t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.522+3206A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613912 | ||||||
| chr8:39614137
|
A | G | 2 | a0005c0011t0001g0188a0005c0011t0001g0245 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.522+3431A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614137 | ||||||
| chr8:39614146
|
C | T | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+3440C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614146 | ||||||
| chr8:39614290
|
G | A | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.522+3584G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614290 | ||||||
| chr8:39614714
|
C | T | 151 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(148): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.522+4008C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614714 | ||||||
| chr8:39614896
|
AG | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0194a0001c0001t0001g0226 | 3 | HG00438.hp1 HG00621.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.522+4191delG | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614896 | ||||||
| chr8:39614941
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.522+4235G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614941 | ||||||
| chr8:39615101
|
A | G | 1 | a0006c0006t0001g0266 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.522+4395A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615101 | ||||||
| chr8:39615112
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+4406A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615112 | ||||||
| chr8:39615226
|
TA | T | 46 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0026others(43): Show | 48 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.522+4533delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39615226 | |||||
| chr8:39615236
|
A | G | 1 | a0001c0002t0001g0292 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.522+4530A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615236 | ||||||
| chr8:39615247
|
A | G | 5 | a0001c0002t0001g0259a0001c0002t0001g0292a0004c0005t0001g0294others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.522+4541A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615247 | ||||||
| chr8:39615426
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.522+4720A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615426 | ||||||
| chr8:39615531
|
A | G | 70 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(67): Show | 71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.522+4825A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615531 | ||||||
| chr8:39615604
|
T | C | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.522+4898T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615604 | ||||||
| chr8:39615635
|
C | G | 15 | a0001c0001t0001g0167a0001c0001t0001g0185a0001c0001t0001g0204others(12): Show | 15 | HG00323.hp2 HG02132.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.522+4929C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615635 | ||||||
| chr8:39615636
|
T | C | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.522+4930T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615636 | ||||||
| chr8:39615697
|
A | G | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.522+4991A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615697 | ||||||
| chr8:39615744
|
A | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.522+5038A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615744 | ||||||
| chr8:39615778
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+5072A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615778 | ||||||
| chr8:39615902
|
G | A | 4 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0002t0001g0258others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+5196G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615902 | ||||||
| chr8:39616084
|
C | G | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.522+5378C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616084 | ||||||
| chr8:39616181
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.522+5475A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616181 | ||||||
| chr8:39616286
|
T | C | 7 | a0001c0001t0001g0196a0001c0001t0001g0216a0001c0001t0001g0219others(4): Show | 7 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+5580T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616286 | ||||||
| chr8:39616502
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.522+5796C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616502 | ||||||
| chr8:39616503
|
G | A | 10 | a0001c0002t0001g0002a0001c0002t0001g0063a0001c0002t0001g0065others(7): Show | 11 | HG02257.hp1 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.522+5797G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616503 | ||||||
| chr8:39616512
|
C | A | 1 | a0001c0002t0001g0139 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.522+5806C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616512 | ||||||
| chr8:39616657
|
G | A | 1 | a0001c0002t0001g0142 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.522+5951G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616657 | ||||||
| chr8:39616797
|
G | A | 2 | a0001c0002t0001g0125a0001c0002t0001g0126 | 2 | HG01943.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.522+6091G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616797 | ||||||
| chr8:39616860
|
A | G | 1 | a0001c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.522+6154A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616860 | ||||||
| chr8:39617166
|
A | G | 1 | a0001c0002t0001g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.522+6460A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617166 | ||||||
| chr8:39617229
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.522+6523A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617229 | ||||||
| chr8:39617460
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.522+6754C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617460 | ||||||
| chr8:39617536
|
A | T | 1 | a0001c0002t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.522+6830A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617536 | ||||||
| chr8:39617573
|
A | G | 4 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0002t0001g0258others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+6867A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617573 | ||||||
| chr8:39617586
|
C | T | 1 | a0001c0002t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.522+6880C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617586 | ||||||
| chr8:39617784
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.522+7078C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617784 | ||||||
| chr8:39618041
|
G | C | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.522+7335G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618041 | ||||||
| chr8:39618202
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.522+7496C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618202 | ||||||
| chr8:39618234
|
C | A | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.522+7528C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618234 | ||||||
| chr8:39618379
|
A | T | 1 | a0005c0016t0001g0156 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.522+7673A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618379 | ||||||
| chr8:39618466
|
T | C | 1 | a0001c0002t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.522+7760T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618466 | ||||||
| chr8:39618504
|
AAC | A | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.522+7802_522+7803d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39618504 | |||||
| chr8:39618572
|
G | A | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.522+7866G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618572 | ||||||
| chr8:39618690
|
G | A | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+7984G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618690 | ||||||
| chr8:39618691
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.522+7985C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618691 | ||||||
| chr8:39618734
|
G | A | 2 | a0001c0002t0001g0009a0001c0002t0001g0010 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.522+8028G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618734 | ||||||
| chr8:39618750
|
T | G | 1 | a0001c0002t0001g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.522+8044T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618750 | ||||||
| chr8:39618753
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.522+8047C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618753 | ||||||
| chr8:39618754
|
G | A | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.522+8048G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618754 | ||||||
| chr8:39618840
|
C | T | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.522+8134C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618840 | ||||||
| chr8:39618881
|
G | A | 1 | a0001c0002t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.522+8175G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618881 | ||||||
| chr8:39618948
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.522+8242T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618948 | ||||||
| chr8:39619280
|
G | A | 8 | a0001c0002t0001g0045a0001c0002t0001g0085a0001c0002t0001g0086others(5): Show | 8 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.522+8574G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619280 | ||||||
| chr8:39619355
|
T | G | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.522+8649T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619355 | ||||||
| chr8:39619411
|
T | A | 6 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+8705T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619411 | ||||||
| chr8:39619459
|
T | C | 151 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(148): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.522+8753T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619459 | ||||||
| chr8:39619573
|
AC | A | 71 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(68): Show | 72 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.522+8868delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619573 | ||||||
| chr8:39619673
|
G | A | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.522+8967G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619673 | ||||||
| chr8:39620000
|
A | C | 1 | a0001c0001t0001g0281 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.522+9294A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620000 | ||||||
| chr8:39620013
|
C | T | 3 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0044 | 3 | HG01069.hp1 HG02738.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.522+9307C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620013 | ||||||
| chr8:39620019
|
C | T | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+9313C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620019 | ||||||
| chr8:39620097
|
A | G | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.523-9277A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620097 | ||||||
| chr8:39620102
|
G | A | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-9272G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620102 | ||||||
| chr8:39620302
|
T | C | 1 | a0004c0005t0001g0294 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.523-9072T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620302 | ||||||
| chr8:39620329
|
A | C | 151 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(148): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.523-9045A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620329 | ||||||
| chr8:39620341
|
G | A | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.523-9033G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620341 | ||||||
| chr8:39620357
|
C | CA | 8 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(5): Show | 8 | HG00438.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.523-9000dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39620357 | |||||
| chr8:39620357
|
CAA | C | 10 | a0001c0008t0003g0013a0003c0004t0001g0179a0003c0004t0001g0212others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.523-9001_523-9000d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39620357 | |||||
| chr8:39620358
|
A | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-9016A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620358 | ||||||
| chr8:39620366
|
A | G | 106 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.523-9008A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620366 | ||||||
| chr8:39620372
|
A | C | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-9002A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620372 | ||||||
| chr8:39620373
|
A | C | 186 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(183): Show | 190 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.523-9001A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620373 | ||||||
| chr8:39620373
|
AAC | A | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-8999_523-8998d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39620373 | |||||
| chr8:39620374
|
A | C | 149 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(146): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.523-9000A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620374 | ||||||
| chr8:39620374
|
AC | A | 118 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(115): Show | 119 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.523-8999delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620374 | ||||||
| chr8:39620375
|
C | A | 145 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(142): Show | 149 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.523-8999C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620375 | ||||||
| chr8:39620375
|
C | CA | 6 | a0001c0002t0001g0043a0001c0002t0001g0057a0001c0002t0001g0075others(3): Show | 6 | HG03491.hp1 HG03516.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-8990dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39620375 | |||||
| chr8:39620380
|
A | C | 3 | a0001c0002t0001g0093a0001c0002t0001g0123a0001c0002t0001g0124 | 3 | HG00544.hp2 NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.523-8994A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620380 | ||||||
| chr8:39620414
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.523-8960A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620414 | ||||||
| chr8:39620420
|
A | C | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-8954A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620420 | ||||||
| chr8:39620422
|
C | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.523-8952C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620422 | ||||||
| chr8:39620537
|
C | A | 6 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.523-8837C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620537 | ||||||
| chr8:39620609
|
A | C | 1 | a0011c0021t0001g0224 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.523-8765A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620609 | ||||||
| chr8:39620702
|
A | G | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.523-8672A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620702 | ||||||
| chr8:39620847
|
A | G | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-8527A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620847 | ||||||
| chr8:39621098
|
T | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0304 | 2 | NA18969.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.523-8276T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621098 | ||||||
| chr8:39621265
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.523-8109C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621265 | ||||||
| chr8:39621309
|
T | TCA | 74 | a0001c0001t0001g0135a0001c0001t0001g0160a0001c0001t0001g0167others(71): Show | 74 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.523-8017_523-8016d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
T | TCACA | 21 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0177others(18): Show | 22 | HG01069.hp2 HG01071.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.523-8019_523-8016d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
T | TCACACA | 5 | a0001c0001t0001g0300a0001c0001t0001g0335a0001c0002t0001g0048others(2): Show | 5 | HG02572.hp2 NA18957.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-8021_523-8016d others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
T | TCACACAC others(3): Show |
1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.523-8025_523-8016d others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
TCA | T | 42 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0170others(39): Show | 42 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.523-8017_523-8016d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
TCACA | T | 9 | a0001c0001t0001g0184a0001c0001t0001g0208a0001c0001t0001g0231others(6): Show | 9 | HG00597.hp2 HG01257.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.523-8019_523-8016d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
TCACACA | T | 19 | a0001c0002t0001g0076a0001c0002t0001g0109a0001c0002t0001g0110others(16): Show | 19 | HG00733.hp1 HG01167.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.523-8021_523-8016d others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
TCACACAC others(1): Show |
T | 41 | a0001c0001t0001g0173a0001c0002t0001g0003a0001c0002t0001g0004others(38): Show | 43 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.523-8023_523-8016d others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
TCACACAC others(3): Show |
T | 18 | a0001c0001t0001g0281a0001c0002t0001g0002a0001c0002t0001g0026others(15): Show | 19 | HG02055.hp2 HG02257.hp1 HG02602.hp1 others(16): Show |
intron_variant | MODIFIER | c.523-8025_523-8016d others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
TCACACAC others(5): Show |
T | 40 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(37): Show | 40 | HG00544.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.523-8027_523-8016d others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
TCACACAC others(7): Show |
T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0278 | 3 | HG00597.hp1 NA18955.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.523-8029_523-8016d others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621309
|
TCACACAC others(9): Show |
T | 1 | a0001c0001t0001g0203 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.523-8031_523-8016d others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | |||||
| chr8:39621495
|
A | G | 1 | a0001c0002t0001g0095 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.523-7879A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621495 | ||||||
| chr8:39621530
|
G | T | 1 | a0002c0003t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.523-7844G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621530 | ||||||
| chr8:39621656
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.523-7718G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621656 | ||||||
| chr8:39621668
|
A | G | 2 | a0001c0002t0001g0123a0001c0002t0001g0124 | 2 | NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.523-7706A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621668 | ||||||
| chr8:39622226
|
T | C | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.523-7148T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622226 | ||||||
| chr8:39622295
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-7079A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622295 | ||||||
| chr8:39622370
|
T | G | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-7004T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622370 | ||||||
| chr8:39622781
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.523-6593T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622781 | ||||||
| chr8:39622847
|
T | C | 107 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(104): Show | 108 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.523-6527T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622847 | ||||||
| chr8:39622876
|
A | G | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.523-6498A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622876 | ||||||
| chr8:39623027
|
C | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.523-6347C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623027 | ||||||
| chr8:39623190
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523-6184T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623190 | ||||||
| chr8:39623298
|
G | A | 3 | a0001c0002t0001g0097a0001c0002t0001g0129a0001c0002t0001g0154 | 3 | HG01074.hp2 HG01109.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.523-6076G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623298 | ||||||
| chr8:39623306
|
A | G | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.523-6068A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623306 | ||||||
| chr8:39623347
|
T | G | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.523-6027T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623347 | ||||||
| chr8:39623507
|
AT | A | 287 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(284): Show | 292 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.523-5853delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39623507 | |||||
| chr8:39623617
|
G | A | 1 | a0002c0003t0001g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.523-5757G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623617 | ||||||
| chr8:39623635
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.523-5739C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623635 | ||||||
| chr8:39623813
|
G | C | 106 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.523-5561G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623813 | ||||||
| chr8:39623916
|
A | C | 2 | a0001c0002t0001g0003a0001c0002t0001g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.523-5458A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623916 | ||||||
| chr8:39624025
|
T | C | 59 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163others(56): Show | 60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.523-5349T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39624025 | ||||||
| chr8:39624491
|
A | G | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-4883A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39624491 | ||||||
| chr8:39625044
|
T | C | 15 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(12): Show | 15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-4330T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625044 | ||||||
| chr8:39625083
|
G | C | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.523-4291G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625083 | ||||||
| chr8:39625257
|
G | A | 1 | a0001c0002t0001g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.523-4117G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625257 | ||||||
| chr8:39625400
|
T | C | 1 | a0001c0001t0001g0311 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.523-3974T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625400 | ||||||
| chr8:39625560
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.523-3814C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625560 | ||||||
| chr8:39625591
|
A | G | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.523-3783A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625591 | ||||||
| chr8:39625727
|
T | G | 2 | a0001c0002t0001g0064a0001c0002t0001g0078 | 2 | NA18747.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.523-3647T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625727 | ||||||
| chr8:39625745
|
A | G | 7 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(4): Show | 7 | HG00733.hp1 HG01167.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.523-3629A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625745 | ||||||
| chr8:39625782
|
A | G | 2 | a0003c0004t0001g0210a0003c0004t0001g0215 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.523-3592A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625782 | ||||||
| chr8:39626160
|
G | C | 151 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(148): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.523-3214G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626160 | ||||||
| chr8:39626252
|
G | A | 106 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.523-3122G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626252 | ||||||
| chr8:39626529
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.523-2845G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626529 | ||||||
| chr8:39626562
|
C | T | 1 | a0001c0002t0001g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.523-2812C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626562 | ||||||
| chr8:39626607
|
A | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-2767A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626607 | ||||||
| chr8:39626818
|
C | G | 1 | a0001c0002t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.523-2556C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626818 | ||||||
| chr8:39626974
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG02080.hp2 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-2400C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626974 | ||||||
| chr8:39627203
|
G | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0178 | 2 | HG02129.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.523-2171G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627203 | ||||||
| chr8:39627356
|
A | G | 2 | a0001c0002t0001g0009a0001c0002t0001g0010 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.523-2018A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627356 | ||||||
| chr8:39627377
|
C | G | 3 | a0001c0002t0001g0064a0001c0002t0001g0078a0001c0002t0001g0083 | 3 | NA18747.hp2 NA18945.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.523-1997C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627377 | ||||||
| chr8:39627445
|
G | T | 1 | a0001c0001t0001g0284 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.523-1929G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627445 | ||||||
| chr8:39627708
|
T | C | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-1666T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627708 | ||||||
| chr8:39627759
|
T | C | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-1615T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627759 | ||||||
| chr8:39627966
|
T | C | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.523-1408T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627966 | ||||||
| chr8:39628250
|
A | G | 3 | a0001c0001t0001g0310a0001c0001t0001g0321a0001c0001t0001g0342 | 3 | HG00280.hp2 HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.523-1124A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628250 | ||||||
| chr8:39628297
|
T | C | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.523-1077T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628297 | ||||||
| chr8:39628309
|
T | C | 2 | a0003c0004t0002g0007a0003c0004t0002g0008 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.523-1065T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628309 | ||||||
| chr8:39628416
|
A | AATAG | 95 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0164others(92): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.523-918_523-915dup others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | |||||
| chr8:39628416
|
A | AATAGATA others(1): Show |
14 | a0001c0001t0001g0187a0001c0001t0001g0251a0001c0002t0001g0002others(11): Show | 15 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-922_523-915dup others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | |||||
| chr8:39628416
|
A | AATAGATA others(5): Show |
1 | a0001c0002t0001g0066 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.523-926_523-915dup others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | |||||
| chr8:39628416
|
AATAG | A | 96 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.523-918_523-915del others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | |||||
| chr8:39628416
|
AATAGATA others(1): Show |
A | 20 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(17): Show | 20 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.523-922_523-915del others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | |||||
| chr8:39628416
|
AATAGATA others(5): Show |
A | 2 | a0001c0001t0001g0249a0014c0018t0001g0038 | 2 | HG04199.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.523-926_523-915del others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | |||||
| chr8:39628416
|
AATAGATA others(9): Show |
A | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-930_523-915del others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | |||||
| chr8:39628554
|
G | T | 1 | a0003c0004t0002g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.523-820G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628554 | ||||||
| chr8:39628624
|
T | A | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-750T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628624 | ||||||
| chr8:39628686
|
T | C | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-688T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628686 | ||||||
| chr8:39628964
|
G | T | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.523-410G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628964 | ||||||
| chr8:39629183
|
C | A | 1 | a0001c0001t0001g0319 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.523-191C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39629183 | ||||||
| chr8:39629332
|
A | G | 1 | a0003c0004t0001g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.523-42A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39629332 | ||||||
| chr8:39629503
|
C | T | 254 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(251): Show | 259 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.588+64C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39629503 | ||||||
| chr8:39629869
|
G | C | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.588+430G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39629869 | ||||||
| chr8:39629891
|
G | T | 1 | a0001c0002t0001g0103 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.588+452G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39629891 | ||||||
| chr8:39630011
|
A | G | 18 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(15): Show | 18 | HG00733.hp1 HG01167.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.588+572A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630011 | ||||||
| chr8:39630341
|
G | A | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+902G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630341 | ||||||
| chr8:39630350
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.588+911C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630350 | ||||||
| chr8:39630439
|
A | T | 1 | a0007c0009t0001g0151 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.588+1000A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630439 | ||||||
| chr8:39630472
|
T | C | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+1033T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630472 | ||||||
| chr8:39630624
|
C | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.588+1185C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630624 | ||||||
| chr8:39630740
|
A | G | 1 | a0002c0003t0001g0018 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.588+1301A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630740 | ||||||
| chr8:39630791
|
G | A | 1 | a0001c0002t0001g0048 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.588+1352G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630791 | ||||||
| chr8:39630811
|
G | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.588+1372G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630811 | ||||||
| chr8:39630833
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.588+1394G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630833 | ||||||
| chr8:39631155
|
C | A | 1 | a0001c0002t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.588+1716C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631155 | ||||||
| chr8:39631373
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.588+1934C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631373 | ||||||
| chr8:39631433
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.588+1994C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631433 | ||||||
| chr8:39631513
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.588+2074T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631513 | ||||||
| chr8:39631560
|
A | G | 1 | a0001c0002t0001g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588+2121A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631560 | ||||||
| chr8:39631733
|
A | G | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.588+2294A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631733 | ||||||
| chr8:39631734
|
T | C | 2 | a0001c0002t0001g0261a0001c0002t0001g0262 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.588+2295T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631734 | ||||||
| chr8:39631773
|
A | G | 1 | a0001c0002t0001g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.588+2334A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631773 | ||||||
| chr8:39631817
|
C | T | 3 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | HG01257.hp2 HG01258.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.588+2378C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631817 | ||||||
| chr8:39631862
|
T | C | 1 | a0001c0002t0001g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.588+2423T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631862 | ||||||
| chr8:39631936
|
T | C | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+2497T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631936 | ||||||
| chr8:39631992
|
C | G | 1 | a0002c0003t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.588+2553C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631992 | ||||||
| chr8:39632134
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.588+2695T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632134 | ||||||
| chr8:39632252
|
C | T | 6 | a0001c0002t0001g0259a0001c0002t0001g0292a0004c0005t0001g0294others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+2813C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632252 | ||||||
| chr8:39632706
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.588+3267C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632706 | ||||||
| chr8:39632719
|
AT | A | 11 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.588+3282delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39632719 | |||||
| chr8:39632867
|
C | G | 1 | a0001c0002t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.588+3428C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632867 | ||||||
| chr8:39632929
|
T | A | 6 | a0001c0001t0001g0196a0001c0001t0001g0216a0001c0001t0001g0219others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+3490T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632929 | ||||||
| chr8:39633149
|
T | A | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.588+3710T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633149 | ||||||
| chr8:39633193
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0238 | 2 | HG02027.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.588+3754A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633193 | ||||||
| chr8:39633282
|
T | C | 1 | a0001c0002t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.588+3843T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633282 | ||||||
| chr8:39633434
|
A | G | 54 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(51): Show | 57 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(54): Show |
intron_variant | MODIFIER | c.589-3830A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633434 | ||||||
| chr8:39633441
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.589-3823A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633441 | ||||||
| chr8:39633509
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-3755G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633509 | ||||||
| chr8:39633582
|
G | A | 190 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(187): Show | 194 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.589-3682G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633582 | ||||||
| chr8:39633661
|
A | G | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.589-3603A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633661 | ||||||
| chr8:39633830
|
TA | T | 7 | a0001c0002t0001g0010a0001c0002t0001g0259a0001c0002t0001g0292others(4): Show | 7 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-3421delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39633830 | |||||
| chr8:39634152
|
G | T | 1 | a0004c0005t0001g0316 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.589-3112G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634152 | ||||||
| chr8:39634364
|
G | T | 2 | a0001c0001t0001g0172a0004c0022t0001g0192 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.589-2900G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634364 | ||||||
| chr8:39634463
|
G | A | 38 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(35): Show | 38 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.589-2801G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634463 | ||||||
| chr8:39634548
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.589-2716G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634548 | ||||||
| chr8:39634567
|
G | A | 4 | a0001c0001t0001g0270a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00597.hp1 NA18954.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-2697G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634567 | ||||||
| chr8:39634568
|
C | T | 6 | a0001c0001t0001g0196a0001c0001t0001g0216a0001c0001t0001g0219others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2696C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634568 | ||||||
| chr8:39634722
|
A | G | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-2542A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634722 | ||||||
| chr8:39634748
|
A | C | 6 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2516A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634748 | ||||||
| chr8:39635024
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.589-2240G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39635024 | ||||||
| chr8:39635443
|
T | G | 1 | a0001c0002t0001g0145 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.589-1821T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39635443 | ||||||
| chr8:39635870
|
G | C | 1 | a0013c0017t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-1394G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39635870 | ||||||
| chr8:39636001
|
G | GT | 15 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(12): Show | 15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.589-1256dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39636001 | |||||
| chr8:39636009
|
G | GT | 22 | a0001c0001t0001g0046a0001c0001t0001g0193a0001c0001t0001g0221others(19): Show | 22 | HG00621.hp2 HG00733.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.589-1242dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39636009 | |||||
| chr8:39636009
|
G | T | 16 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(13): Show | 16 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-1255G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636009 | ||||||
| chr8:39636040
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0277 | 2 | NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.589-1224A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636040 | ||||||
| chr8:39636042
|
G | A | 186 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(183): Show | 190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.589-1222G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636042 | ||||||
| chr8:39636081
|
A | C | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.589-1183A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636081 | ||||||
| chr8:39636115
|
C | T | 1 | a0013c0017t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-1149C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636115 | ||||||
| chr8:39636193
|
A | T | 2 | a0006c0006t0001g0264a0006c0006t0001g0265 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.589-1071A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636193 | ||||||
| chr8:39636396
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-868T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636396 | ||||||
| chr8:39636523
|
A | T | 1 | a0004c0005t0001g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.589-741A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636523 | ||||||
| chr8:39636628
|
A | T | 161 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(158): Show | 165 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.589-636A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636628 | ||||||
| chr8:39636770
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.589-494C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636770 | ||||||
| chr8:39636793
|
T | G | 15 | a0001c0008t0003g0012a0001c0008t0003g0013a0002c0003t0001g0011others(12): Show | 15 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-471T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636793 | ||||||
| chr8:39636899
|
T | G | 1 | a0001c0001t0001g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.589-365T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636899 | ||||||
| chr8:39636983
|
A | T | 161 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(158): Show | 165 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.589-281A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636983 | ||||||
| chr8:39637016
|
ATT | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(69): Show | 73 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.589-245_589-244del others(2): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637016 | |||||
| chr8:39637017
|
TTTTA | T | 60 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(57): Show | 63 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(60): Show |
intron_variant | MODIFIER | c.589-245_589-242del others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | |||||
| chr8:39637017
|
TTTTATA | T | 26 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(23): Show | 26 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.589-245_589-240del others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | |||||
| chr8:39637017
|
TTTTATAT others(7): Show |
T | 1 | a0001c0002t0001g0292 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.589-245_589-232del others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | |||||
| chr8:39637017
|
TTTTATAT others(9): Show |
T | 4 | a0001c0002t0001g0259a0004c0005t0001g0294a0004c0005t0001g0309others(1): Show | 4 | HG02572.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-245_589-230del others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | |||||
| chr8:39637017
|
TTTTATAT others(11): Show |
T | 1 | a0004c0005t0001g0320 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.589-245_589-228del others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | |||||
| chr8:39637018
|
TTTA | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0206a0001c0001t0001g0275 | 3 | NA18977.hp1 NA18977.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.589-244_589-242del others(3): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637018 | |||||
| chr8:39637019
|
T | A | 2 | a0001c0002t0001g0124a0007c0009t0001g0151 | 2 | NA18975.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.589-245T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637019 | ||||||
| chr8:39637019
|
TTA | T | 24 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0169others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.589-199_589-198del others(2): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATA | T | 38 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0172others(35): Show | 38 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.589-201_589-198del others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATATA | T | 29 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0159others(26): Show | 30 | HG01074.hp1 HG01175.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.589-203_589-198del others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATATAT others(1): Show |
T | 28 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0191others(25): Show | 28 | HG00280.hp2 HG00544.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.589-205_589-198del others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATATAT others(3): Show |
T | 7 | a0001c0001t0001g0193a0001c0001t0001g0200a0001c0001t0001g0226others(4): Show | 7 | HG00621.hp2 HG00733.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-207_589-198del others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATATAT others(5): Show |
T | 9 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0207others(6): Show | 9 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-209_589-198del others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATATAT others(7): Show |
T | 7 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0241others(4): Show | 7 | HG01884.hp2 HG02148.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-211_589-198del others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATATAT others(9): Show |
T | 1 | a0001c0001t0001g0135 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.589-213_589-198del others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATATAT others(13): Show |
T | 1 | a0002c0003t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.589-217_589-198del others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637019
|
TTATATAT others(15): Show |
T | 3 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0025 | 3 | HG02965.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.589-219_589-198del others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | |||||
| chr8:39637029
|
A | G | 1 | a0007c0009t0001g0151 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-235A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637029 | ||||||
| chr8:39637031
|
A | G | 1 | a0007c0009t0001g0151 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-233A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637031 | ||||||
| chr8:39637033
|
A | T | 1 | a0001c0002t0001g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.589-231A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637033 | ||||||
| chr8:39637034
|
T | C | 20 | a0001c0002t0001g0001a0001c0002t0001g0050a0001c0002t0001g0055others(17): Show | 21 | HG00609.hp2 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.589-230T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637034 | ||||||
| chr8:39637035
|
A | T | 4 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0002t0001g0258others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-229A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637035 | ||||||
| chr8:39637036
|
T | C | 124 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(121): Show | 128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.589-228T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637036 | ||||||
| chr8:39637038
|
T | C | 60 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(57): Show | 63 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(60): Show |
intron_variant | MODIFIER | c.589-226T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637038 | ||||||
| chr8:39637040
|
T | C | 26 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(23): Show | 26 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.589-224T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637040 | ||||||
| chr8:39637042
|
T | C | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.589-222T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637042 | ||||||
| chr8:39637043
|
A | G | 1 | a0007c0009t0001g0151 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-221A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637043 | ||||||
| chr8:39637050
|
T | C | 1 | a0007c0009t0001g0151 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-214T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637050 | ||||||
| chr8:39637053
|
A | G | 148 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(145): Show | 152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.589-211A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637053 | ||||||
| chr8:39637055
|
A | G | 160 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(157): Show | 164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.589-209A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637055 | ||||||
| chr8:39637067
|
G | A | 1 | a0007c0009t0001g0151 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-197G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637067 | ||||||
| chr8:39637196
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.589-68C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637196 | ||||||
| chr8:39637233
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.589-31A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637233 | ||||||
| chr8:39637740
|
A | G | 1 | a0001c0002t0001g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.827+37A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39637740 | ||||||
| chr8:39637806
|
G | A | 187 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(184): Show | 191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.827+103G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39637806 | ||||||
| chr8:39637959
|
T | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.827+256T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39637959 | ||||||
| chr8:39638009
|
G | T | 1 | a0001c0002t0001g0119 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.827+306G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39638009 | ||||||
| chr8:39638130
|
G | A | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.828-335G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39638130 | ||||||
| chr8:39638229
|
T | A | 1 | a0001c0002t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.828-236T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39638229 | ||||||
| chr8:39638267
|
TA | T | 61 | a0001c0002t0001g0001a0001c0002t0001g0039a0001c0002t0001g0040others(58): Show | 62 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.828-195delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr8 | 39638267 | |||||
| chr8:39638291
|
GATTTAGT | G | 17 | a0001c0002t0001g0002a0001c0002t0001g0063a0001c0002t0001g0065others(14): Show | 18 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.828-155_828-149del others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr8 | 39638291 | |||||
| chr8:39638375
|
T | TAAAATTT others(236): Show |
6 | a0001c0002t0001g0259a0001c0002t0001g0292a0004c0005t0001g0294others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.828-77_828-76insGC others(241): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr8 | 39638375 | |||||
| chr8:39638423
|
T | A | 1 | a0002c0003t0001g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.828-42T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39638423 | ||||||
| chr8:39638683
|
G | A | 161 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(158): Show | 165 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.909+137G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638683 | ||||||
| chr8:39638695
|
A | G | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.909+149A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638695 | ||||||
| chr8:39638772
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.909+226C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638772 | ||||||
| chr8:39638786
|
A | G | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.909+240A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638786 | ||||||
| chr8:39638796
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.909+250C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638796 | ||||||
| chr8:39639135
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+589T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639135 | ||||||
| chr8:39639161
|
G | T | 1 | a0002c0003t0001g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+615G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639161 | ||||||
| chr8:39639451
|
C | T | 187 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(184): Show | 191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.909+905C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639451 | ||||||
| chr8:39639492
|
C | T | 149 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(146): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.909+946C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639492 | ||||||
| chr8:39639557
|
T | C | 2 | a0001c0002t0001g0003a0001c0002t0001g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.909+1011T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639557 | ||||||
| chr8:39639567
|
ATT | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.909+1023_909+1024d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr8 | 39639567 | |||||
| chr8:39639572
|
G | C | 2 | a0001c0002t0001g0003a0001c0002t0001g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.909+1026G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639572 | ||||||
| chr8:39639573
|
AC | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.909+1028delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639573 | ||||||
| chr8:39639603
|
A | C | 187 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(184): Show | 191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.909+1057A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639603 | ||||||
| chr8:39639618
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.909+1072G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639618 | ||||||
| chr8:39639790
|
G | A | 1 | a0004c0005t0001g0294 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.909+1244G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639790 | ||||||
| chr8:39639844
|
T | G | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.909+1298T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639844 | ||||||
| chr8:39639974
|
G | T | 1 | a0001c0002t0001g0126 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.909+1428G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639974 | ||||||
| chr8:39640119
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.909+1573C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640119 | ||||||
| chr8:39640303
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.909+1757A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640303 | ||||||
| chr8:39640441
|
G | A | 187 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(184): Show | 191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.909+1895G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640441 | ||||||
| chr8:39640815
|
A | AT | 149 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(146): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.909+2279dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr8 | 39640815 | |||||
| chr8:39640834
|
T | A | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+2288T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640834 | ||||||
| chr8:39640851
|
T | C | 5 | a0001c0002t0001g0054a0001c0002t0001g0101a0001c0002t0001g0102others(2): Show | 5 | NA18948.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+2305T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640851 | ||||||
| chr8:39640867
|
GT | G | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+2331delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr8 | 39640867 | |||||
| chr8:39641340
|
C | G | 149 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(146): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.909+2794C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641340 | ||||||
| chr8:39641354
|
G | A | 1 | a0002c0003t0001g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.909+2808G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641354 | ||||||
| chr8:39641470
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.909+2924C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641470 | ||||||
| chr8:39641475
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.909+2929C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641475 | ||||||
| chr8:39641557
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0233 | 2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.909+3011C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641557 | ||||||
| chr8:39641678
|
C | A | 1 | a0013c0017t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.909+3132C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641678 | ||||||
| chr8:39641678
|
C | T | 1 | a0005c0011t0001g0245 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.909+3132C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641678 | ||||||
| chr8:39641679
|
G | T | 161 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(158): Show | 165 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.909+3133G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641679 | ||||||
| chr8:39641773
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.909+3227C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641773 | ||||||
| chr8:39641857
|
A | G | 6 | a0001c0002t0001g0259a0001c0002t0001g0292a0004c0005t0001g0294others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+3311A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641857 | ||||||
| chr8:39641873
|
A | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.909+3327A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641873 | ||||||
| chr8:39642052
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0202 | 2 | NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.910-3286A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642052 | ||||||
| chr8:39642212
|
T | C | 7 | a0001c0001t0001g0297a0001c0001t0001g0313a0001c0001t0001g0322others(4): Show | 7 | HG01106.hp1 HG01257.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-3126T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642212 | ||||||
| chr8:39642336
|
G | T | 3 | a0001c0002t0001g0097a0001c0002t0001g0129a0001c0002t0001g0154 | 3 | HG01074.hp2 HG01109.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.910-3002G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642336 | ||||||
| chr8:39642390
|
G | T | 15 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(12): Show | 15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.910-2948G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642390 | ||||||
| chr8:39642706
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.910-2632T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642706 | ||||||
| chr8:39642717
|
T | C | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.910-2621T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642717 | ||||||
| chr8:39642762
|
G | A | 1 | a0003c0004t0002g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.910-2576G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642762 | ||||||
| chr8:39642830
|
G | A | 149 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(146): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.910-2508G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642830 | ||||||
| chr8:39642987
|
A | G | 73 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(70): Show | 76 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.910-2351A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642987 | ||||||
| chr8:39643077
|
C | G | 1 | a0001c0002t0001g0126 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.910-2261C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643077 | ||||||
| chr8:39643142
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.910-2196G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643142 | ||||||
| chr8:39643329
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.910-2009A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643329 | ||||||
| chr8:39643397
|
A | G | 3 | a0001c0002t0001g0097a0001c0002t0001g0129a0001c0002t0001g0154 | 3 | HG01074.hp2 HG01109.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.910-1941A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643397 | ||||||
| chr8:39643493
|
G | T | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.910-1845G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643493 | ||||||
| chr8:39643523
|
A | C | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-1815A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643523 | ||||||
| chr8:39643593
|
A | T | 1 | a0002c0003t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.910-1745A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643593 | ||||||
| chr8:39643673
|
C | G | 3 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008 | 3 | HG02257.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.910-1665C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643673 | ||||||
| chr8:39643787
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.910-1551C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643787 | ||||||
| chr8:39644133
|
G | C | 187 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(184): Show | 191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.910-1205G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644133 | ||||||
| chr8:39644163
|
G | C | 6 | a0001c0002t0001g0259a0001c0002t0001g0292a0004c0005t0001g0294others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-1175G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644163 | ||||||
| chr8:39644213
|
GATAA | G | 6 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-1120_910-1117d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr8 | 39644213 | |||||
| chr8:39644319
|
A | G | 186 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(183): Show | 190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.910-1019A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644319 | ||||||
| chr8:39644476
|
C | T | 1 | a0003c0004t0002g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.910-862C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644476 | ||||||
| chr8:39644698
|
C | T | 162 | a0001c0001t0001g0222a0001c0002t0001g0001a0001c0002t0001g0002others(159): Show | 166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.910-640C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644698 | ||||||
| chr8:39644710
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.910-628G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644710 | ||||||
| chr8:39645113
|
G | A | 1 | a0001c0002t0001g0060 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.910-225G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39645113 | ||||||
| chr8:39645288
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.910-50A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39645288 | ||||||
| chr8:39645294
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-44A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39645294 | ||||||
| chr8:39645518
|
T | C | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1046+44T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645518 | ||||||
| chr8:39645558
|
C | T | 4 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+84C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645558 | ||||||
| chr8:39645560
|
G | A | 181 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1046+86G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645560 | ||||||
| chr8:39645592
|
G | C | 15 | a0001c0008t0003g0012a0001c0008t0003g0013a0002c0003t0001g0011others(12): Show | 15 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046+118G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645592 | ||||||
| chr8:39645642
|
T | C | 6 | a0001c0002t0001g0259a0001c0002t0001g0292a0004c0005t0001g0294others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1046+168T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645642 | ||||||
| chr8:39645688
|
A | T | 1 | a0001c0001t0001g0207 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1046+214A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645688 | ||||||
| chr8:39645759
|
A | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+285A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645759 | ||||||
| chr8:39645932
|
C | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+458C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645932 | ||||||
| chr8:39645984
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1046+510G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645984 | ||||||
| chr8:39646095
|
A | G | 1 | a0001c0001t0001g0312 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1046+621A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646095 | ||||||
| chr8:39646192
|
A | T | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1046+718A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646192 | ||||||
| chr8:39646222
|
T | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+748T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646222 | ||||||
| chr8:39646223
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+749A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646223 | ||||||
| chr8:39646267
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+793A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646267 | ||||||
| chr8:39646563
|
G | A | 10 | a0001c0002t0001g0002a0001c0002t0001g0063a0001c0002t0001g0065others(7): Show | 11 | HG02257.hp1 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046+1089G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646563 | ||||||
| chr8:39646721
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1046+1247C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646721 | ||||||
| chr8:39646904
|
A | AG | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+1435dupG | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr8 | 39646904 | |||||
| chr8:39646993
|
G | T | 3 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | HG01257.hp2 HG01258.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1047-1351G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646993 | ||||||
| chr8:39647136
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-1208G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647136 | ||||||
| chr8:39647215
|
A | T | 1 | a0001c0002t0001g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1047-1129A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647215 | ||||||
| chr8:39647222
|
G | A | 1 | a0001c0002t0001g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1047-1122G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647222 | ||||||
| chr8:39647223
|
G | T | 165 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(162): Show | 169 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1047-1121G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647223 | ||||||
| chr8:39647234
|
C | CA | 101 | a0001c0001t0001g0090a0001c0001t0001g0184a0001c0001t0001g0199others(98): Show | 104 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.1047-1093dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr8 | 39647234 | |||||
| chr8:39647234
|
C | CAA | 81 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(78): Show | 82 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1047-1094_1047-109 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr8 | 39647234 | |||||
| chr8:39647320
|
C | T | 1 | a0001c0002t0001g0058 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047-1024C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647320 | ||||||
| chr8:39647436
|
T | C | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047-908T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647436 | ||||||
| chr8:39647488
|
A | G | 1 | a0004c0005t0001g0316 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1047-856A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647488 | ||||||
| chr8:39647584
|
C | T | 2 | a0006c0006t0001g0264a0006c0006t0001g0265 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1047-760C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647584 | ||||||
| chr8:39647656
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1047-688G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647656 | ||||||
| chr8:39647672
|
G | A | 82 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(79): Show | 83 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1047-672G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647672 | ||||||
| chr8:39647775
|
A | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(2): Show | 5 | HG00609.hp1 HG02523.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-569A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647775 | ||||||
| chr8:39647794
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1047-550C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647794 | ||||||
| chr8:39647827
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0237 | 2 | NA18612.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1047-517A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647827 | ||||||
| chr8:39647863
|
A | G | 193 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(190): Show | 197 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1047-481A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647863 | ||||||
| chr8:39647909
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0202 | 2 | NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1047-435A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647909 | ||||||
| chr8:39647961
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1047-383G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647961 | ||||||
| chr8:39647998
|
G | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-346G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647998 | ||||||
| chr8:39648026
|
G | A | 1 | a0004c0005t0001g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1047-318G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39648026 | ||||||
| chr8:39648183
|
G | C | 42 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0034others(39): Show | 44 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1047-161G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39648183 | ||||||
| chr8:39648307
|
C | A | 171 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(168): Show | 175 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1047-37C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39648307 | ||||||
| chr8:39648562
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1230+35T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39648562 | ||||||
| chr8:39648671
|
T | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+144T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39648671 | ||||||
| chr8:39648694
|
T | G | 16 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013others(13): Show | 16 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1230+167T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39648694 | ||||||
| chr8:39649247
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+720T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649247 | ||||||
| chr8:39649282
|
T | A | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1230+755T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649282 | ||||||
| chr8:39649299
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1230+772G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649299 | ||||||
| chr8:39649346
|
A | T | 12 | a0003c0004t0001g0179a0003c0004t0001g0210a0003c0004t0001g0212others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1230+819A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649346 | ||||||
| chr8:39649348
|
G | A | 1 | a0001c0002t0001g0138 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+821G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649348 | ||||||
| chr8:39649350
|
T | A | 193 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(190): Show | 197 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1230+823T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649350 | ||||||
| chr8:39649380
|
G | GTA | 40 | a0001c0002t0001g0004a0001c0002t0001g0034a0001c0002t0001g0035others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.1230+867_1230+868d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39649380 | |||||
| chr8:39649380
|
G | GTATA | 4 | a0001c0002t0001g0003a0001c0002t0001g0080a0001c0002t0001g0081others(1): Show | 5 | HG01168.hp1 HG01169.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+865_1230+868d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39649380 | |||||
| chr8:39649380
|
GTA | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+867_1230+868d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39649380 | |||||
| chr8:39649403
|
A | T | 1 | a0001c0002t0001g0133 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1230+876A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649403 | ||||||
| chr8:39649526
|
A | G | 1 | a0001c0002t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1230+999A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649526 | ||||||
| chr8:39649822
|
C | CT | 166 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(163): Show | 170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1230+1297dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39649822 | |||||
| chr8:39650006
|
A | T | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1230+1479A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650006 | ||||||
| chr8:39650170
|
C | T | 1 | a0001c0002t0001g0096 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1230+1643C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650170 | ||||||
| chr8:39650246
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1230+1719T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650246 | ||||||
| chr8:39650350
|
T | G | 171 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(168): Show | 175 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1230+1823T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650350 | ||||||
| chr8:39650506
|
A | G | 4 | a0001c0001t0001g0185a0001c0001t0001g0204a0001c0001t0001g0230others(1): Show | 4 | HG02132.hp2 NA18612.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+1979A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650506 | ||||||
| chr8:39650732
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1230+2205T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650732 | ||||||
| chr8:39650812
|
C | G | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+2285C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650812 | ||||||
| chr8:39650840
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+2313G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650840 | ||||||
| chr8:39650873
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+2346C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650873 | ||||||
| chr8:39650966
|
A | G | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+2439A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650966 | ||||||
| chr8:39651243
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+2716C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39651243 | ||||||
| chr8:39651393
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+2866A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39651393 | ||||||
| chr8:39651468
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1230+2941C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39651468 | ||||||
| chr8:39651570
|
A | G | 166 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(163): Show | 170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1230+3043A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39651570 | ||||||
| chr8:39651574
|
CTTAATCC others(13): Show |
C | 16 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013others(13): Show | 16 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1230+3050_1230+306 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651574 | |||||
| chr8:39651607
|
GT | G | 193 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(190): Show | 197 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1230+3084delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651607 | |||||
| chr8:39651637
|
GT | G | 166 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(163): Show | 170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1230+3112delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651637 | |||||
| chr8:39651923
|
GC | G | 43 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0034others(40): Show | 45 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.1230+3399delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651923 | |||||
| chr8:39651972
|
AG | A | 166 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(163): Show | 170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1230+3447delG | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651972 | |||||
| chr8:39652206
|
A | G | 1 | a0001c0002t0001g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1230+3679A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652206 | ||||||
| chr8:39652399
|
G | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+3872G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652399 | ||||||
| chr8:39652571
|
G | C | 14 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(11): Show | 14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1230+4044G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652571 | ||||||
| chr8:39652638
|
C | T | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+4111C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652638 | ||||||
| chr8:39652643
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4116A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652643 | ||||||
| chr8:39652695
|
C | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4168C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652695 | ||||||
| chr8:39652702
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4175C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652702 | ||||||
| chr8:39652840
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4313T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652840 | ||||||
| chr8:39652863
|
A | G | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1230+4336A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652863 | ||||||
| chr8:39652984
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4457A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652984 | ||||||
| chr8:39653160
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4633T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653160 | ||||||
| chr8:39653160
|
T | TA | 5 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(2): Show | 5 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4634dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39653160 | |||||
| chr8:39653192
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4665C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653192 | ||||||
| chr8:39653221
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4694C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653221 | ||||||
| chr8:39653289
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1230+4762G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653289 | ||||||
| chr8:39653296
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1230+4769T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653296 | ||||||
| chr8:39653312
|
A | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4785A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653312 | ||||||
| chr8:39653397
|
T | C | 193 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(190): Show | 197 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1230+4870T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653397 | ||||||
| chr8:39653404
|
T | C | 1 | a0001c0002t0001g0047 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1230+4877T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653404 | ||||||
| chr8:39653457
|
A | C | 1 | a0001c0001t0001g0203 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1230+4930A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653457 | ||||||
| chr8:39653471
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4944A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653471 | ||||||
| chr8:39653494
|
A | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4967A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653494 | ||||||
| chr8:39653554
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5027T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653554 | ||||||
| chr8:39653636
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5109A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653636 | ||||||
| chr8:39653723
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5196C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653723 | ||||||
| chr8:39653730
|
G | A | 2 | a0001c0002t0001g0095a0001c0002t0001g0107 | 2 | NA18985.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1230+5203G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653730 | ||||||
| chr8:39653824
|
G | T | 70 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(67): Show | 71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1230+5297G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653824 | ||||||
| chr8:39653935
|
T | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5408T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653935 | ||||||
| chr8:39654021
|
A | G | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5494A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654021 | ||||||
| chr8:39654040
|
CTTCCACA others(53): Show |
C | 2 | a0001c0007t0001g0195a0001c0007t0001g0227 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1230+5514_1230+557 others(64): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654040 | ||||||
| chr8:39654064
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5537T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654064 | ||||||
| chr8:39654092
|
T | C | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1230+5565T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654092 | ||||||
| chr8:39654115
|
A | G | 81 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(78): Show | 82 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1230+5588A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654115 | ||||||
| chr8:39654134
|
CCACTGAC others(371): Show |
C | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+5610_1230+598 others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39654134 | |||||
| chr8:39654152
|
TC | T | 5 | a0001c0002t0001g0068a0001c0002t0001g0074a0001c0002t0001g0095others(2): Show | 5 | HG01975.hp2 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+5627delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39654152 | |||||
| chr8:39654153
|
C | CT | 7 | a0001c0002t0001g0009a0001c0002t0001g0035a0001c0002t0001g0089others(4): Show | 7 | HG00642.hp1 HG01109.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+5626_1230+562 others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654153 | ||||||
| chr8:39654153
|
C | CTTTTTTT | 4 | a0001c0002t0001g0255a0001c0002t0001g0257a0001c0002t0001g0258others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+5626_1230+562 others(11): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654153 | ||||||
| chr8:39654154
|
C | CT | 11 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0181others(8): Show | 11 | HG01071.hp2 HG01192.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+5647dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39654154 | |||||
| chr8:39654154
|
C | T | 178 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(175): Show | 182 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1230+5627C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654154 | ||||||
| chr8:39654200
|
A | C | 32 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(29): Show | 32 | HG00733.hp1 HG01167.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1230+5673A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654200 | ||||||
| chr8:39654200
|
A | T | 154 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(151): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1230+5673A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654200 | ||||||
| chr8:39654244
|
G | T | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5717G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654244 | ||||||
| chr8:39654261
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5734G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654261 | ||||||
| chr8:39654298
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1230+5771C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654298 | ||||||
| chr8:39654359
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1230+5832C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654359 | ||||||
| chr8:39654525
|
G | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5998G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654525 | ||||||
| chr8:39654664
|
A | AG | 186 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(183): Show | 190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1230+6137_1230+613 others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654664 | ||||||
| chr8:39654803
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+6276T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654803 | ||||||
| chr8:39654938
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1230+6411C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654938 | ||||||
| chr8:39655027
|
G | C | 13 | a0001c0010t0001g0033a0001c0010t0001g0042a0003c0004t0001g0179others(10): Show | 13 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1230+6500G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655027 | ||||||
| chr8:39655238
|
A | T | 195 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(192): Show | 199 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1230+6711A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655238 | ||||||
| chr8:39655260
|
CCCAGTG | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+6737_1230+674 others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39655260 | |||||
| chr8:39655573
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+7046A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655573 | ||||||
| chr8:39655729
|
A | C | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+7202A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655729 | ||||||
| chr8:39655828
|
C | CATAAAAA others(11): Show |
1 | a0008c0024t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1230+7301_1230+730 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655828 | ||||||
| chr8:39656066
|
G | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+7539G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656066 | ||||||
| chr8:39656163
|
A | G | 1 | a0001c0002t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1231-7632A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656163 | ||||||
| chr8:39656306
|
A | G | 82 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(79): Show | 83 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1231-7489A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656306 | ||||||
| chr8:39656380
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1231-7415G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656380 | ||||||
| chr8:39656410
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1231-7385C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656410 | ||||||
| chr8:39656411
|
G | A | 1 | a0008c0024t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1231-7384G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656411 | ||||||
| chr8:39656432
|
T | G | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-7363T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656432 | ||||||
| chr8:39656482
|
T | C | 4 | a0001c0002t0001g0002a0001c0002t0001g0065a0001c0002t0001g0069others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-7313T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656482 | ||||||
| chr8:39656656
|
A | T | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1231-7139A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656656 | ||||||
| chr8:39656657
|
G | C | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-7138G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656657 | ||||||
| chr8:39656790
|
T | A | 160 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(157): Show | 164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1231-7005T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656790 | ||||||
| chr8:39656837
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1231-6958T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656837 | ||||||
| chr8:39656844
|
C | G | 70 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(67): Show | 71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1231-6951C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656844 | ||||||
| chr8:39657113
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1231-6682A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657113 | ||||||
| chr8:39657200
|
A | G | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-6595A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657200 | ||||||
| chr8:39657318
|
G | GT | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-6472dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39657318 | |||||
| chr8:39657364
|
T | G | 1 | a0002c0003t0001g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1231-6431T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657364 | ||||||
| chr8:39657562
|
C | T | 1 | a0001c0002t0001g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1231-6233C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657562 | ||||||
| chr8:39657808
|
A | G | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-5987A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657808 | ||||||
| chr8:39657820
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1231-5975A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657820 | ||||||
| chr8:39657822
|
A | C | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-5973A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657822 | ||||||
| chr8:39657916
|
CAT | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0208a0001c0001t0001g0236others(1): Show | 4 | HG02074.hp2 NA18949.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-5878_1231-587 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657916 | ||||||
| chr8:39658054
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1231-5741G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658054 | ||||||
| chr8:39658085
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1231-5710C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658085 | ||||||
| chr8:39658194
|
A | G | 1 | a0001c0002t0001g0045 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1231-5601A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658194 | ||||||
| chr8:39658408
|
A | T | 1 | a0002c0003t0001g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1231-5387A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658408 | ||||||
| chr8:39658650
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1231-5145A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658650 | ||||||
| chr8:39658808
|
T | G | 4 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(1): Show | 4 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-4987T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658808 | ||||||
| chr8:39658963
|
T | A | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1231-4832T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658963 | ||||||
| chr8:39659206
|
T | A | 1 | a0001c0001t0001g0298 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1231-4589T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659206 | ||||||
| chr8:39659406
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1231-4389T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659406 | ||||||
| chr8:39659410
|
T | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1231-4385T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659410 | ||||||
| chr8:39659557
|
A | T | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-4238A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659557 | ||||||
| chr8:39659729
|
A | T | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1231-4066A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659729 | ||||||
| chr8:39659875
|
C | G | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1231-3920C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659875 | ||||||
| chr8:39660053
|
A | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0276 | 2 | NA18950.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1231-3742A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39660053 | ||||||
| chr8:39660084
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-3711C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39660084 | ||||||
| chr8:39660322
|
T | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-3473T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39660322 | ||||||
| chr8:39661117
|
T | TA | 13 | a0001c0001t0001g0313a0002c0003t0001g0011a0002c0003t0001g0015others(10): Show | 13 | HG00733.hp1 HG01106.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1231-2668dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661117 | |||||
| chr8:39661122
|
A | T | 1 | a0001c0001t0001g0302 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1231-2673A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661122 | ||||||
| chr8:39661129
|
C | A | 160 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(157): Show | 164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1231-2666C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661129 | ||||||
| chr8:39661144
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1231-2651T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661144 | ||||||
| chr8:39661154
|
C | CT | 90 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1231-2623dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661154 | |||||
| chr8:39661154
|
C | CTT | 6 | a0001c0001t0001g0223a0001c0001t0001g0231a0001c0001t0001g0267others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-2624_1231-262 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661154 | |||||
| chr8:39661154
|
CT | C | 74 | a0001c0001t0001g0172a0001c0001t0001g0270a0001c0002t0001g0002others(71): Show | 77 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.1231-2623delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661154 | |||||
| chr8:39661157
|
T | C | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1231-2638T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661157 | ||||||
| chr8:39661158
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-2637T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661158 | ||||||
| chr8:39661207
|
C | T | 1 | a0001c0002t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1231-2588C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661207 | ||||||
| chr8:39661222
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-2573G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661222 | ||||||
| chr8:39661298
|
G | A | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-2497G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661298 | ||||||
| chr8:39661319
|
A | AT | 74 | a0001c0001t0001g0090a0001c0001t0001g0135a0001c0001t0001g0160others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1231-2448dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | |||||
| chr8:39661319
|
A | ATT | 74 | a0001c0001t0001g0046a0001c0001t0001g0159a0001c0001t0001g0162others(71): Show | 75 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1231-2449_1231-244 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | |||||
| chr8:39661319
|
A | ATTT | 20 | a0001c0001t0001g0167a0001c0001t0001g0173a0001c0001t0001g0183others(17): Show | 20 | HG00438.hp1 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-2450_1231-244 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | |||||
| chr8:39661319
|
ATTTTTTT others(4): Show |
A | 5 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0088others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-2458_1231-244 others(15): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | |||||
| chr8:39661319
|
ATTTTTTT others(5): Show |
A | 144 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(141): Show | 148 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1231-2459_1231-244 others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | |||||
| chr8:39661319
|
ATTTTTTT others(6): Show |
A | 6 | a0001c0002t0001g0044a0001c0002t0001g0116a0001c0002t0001g0131others(3): Show | 6 | HG01069.hp1 HG01070.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-2460_1231-244 others(17): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | |||||
| chr8:39661349
|
T | G | 155 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(152): Show | 159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1231-2446T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661349 | ||||||
| chr8:39661406
|
C | T | 8 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-2389C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661406 | ||||||
| chr8:39661409
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1231-2386C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661409 | ||||||
| chr8:39661410
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1231-2385G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661410 | ||||||
| chr8:39661418
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1231-2377C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661418 | ||||||
| chr8:39661449
|
C | T | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1231-2346C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661449 | ||||||
| chr8:39661536
|
A | G | 13 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1231-2259A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661536 | ||||||
| chr8:39661928
|
T | TTA | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1231-1855_1231-185 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661928 | |||||
| chr8:39662110
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1231-1685T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662110 | ||||||
| chr8:39662337
|
T | A | 228 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(225): Show | 232 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1231-1458T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662337 | ||||||
| chr8:39662400
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1231-1395G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662400 | ||||||
| chr8:39662563
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1231-1232G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662563 | ||||||
| chr8:39662608
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-1187T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662608 | ||||||
| chr8:39662757
|
T | G | 1 | a0001c0001t0001g0279 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1231-1038T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662757 | ||||||
| chr8:39662781
|
C | T | 19 | a0001c0002t0001g0045a0001c0002t0001g0054a0001c0002t0001g0085others(16): Show | 19 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1231-1014C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662781 | ||||||
| chr8:39662800
|
T | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-995T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662800 | ||||||
| chr8:39662903
|
G | A | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-892G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662903 | ||||||
| chr8:39662905
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-890G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662905 | ||||||
| chr8:39662990
|
G | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-805G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662990 | ||||||
| chr8:39663001
|
T | C | 1 | a0001c0002t0001g0292 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1231-794T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663001 | ||||||
| chr8:39663225
|
T | C | 59 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(56): Show | 59 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1231-570T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663225 | ||||||
| chr8:39663235
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1231-560C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663235 | ||||||
| chr8:39663369
|
A | G | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-426A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663369 | ||||||
| chr8:39663377
|
T | G | 1 | a0001c0002t0001g0037 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1231-418T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663377 | ||||||
| chr8:39663425
|
C | CA | 143 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(140): Show | 147 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1231-354dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663425 | |||||
| chr8:39663471
|
C | T | 1 | a0011c0021t0001g0224 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1231-324C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663471 | ||||||
| chr8:39663577
|
T | C | 228 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(225): Show | 232 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1231-218T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663577 | ||||||
| chr8:39663598
|
C | CA | 66 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0173others(63): Show | 66 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1231-168dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | |||||
| chr8:39663598
|
C | CAA | 20 | a0001c0001t0001g0167a0001c0001t0001g0197a0001c0001t0001g0205others(17): Show | 20 | HG02027.hp1 HG02074.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-169_1231-168d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | |||||
| chr8:39663598
|
CA | C | 56 | a0001c0001t0001g0203a0001c0001t0001g0237a0001c0001t0001g0277others(53): Show | 59 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.1231-168delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | |||||
| chr8:39663598
|
CAA | C | 15 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(12): Show | 15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1231-169_1231-168d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | |||||
| chr8:39663598
|
CAAAA | C | 6 | a0001c0001t0001g0196a0001c0002t0001g0255a0001c0002t0001g0256others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-171_1231-168d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | |||||
| chr8:39663625
|
A | G | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1231-170A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663625 | ||||||
| chr8:39663748
|
T | C | 1 | a0004c0005t0001g0320 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1231-47T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663748 | ||||||
| chr8:39663755
|
T | C | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-40T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663755 | ||||||
| chr8:39663900
|
T | C | 228 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(225): Show | 232 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1326+10T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39663900 | ||||||
| chr8:39664028
|
A | T | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1326+138A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664028 | ||||||
| chr8:39664324
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1326+434T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664324 | ||||||
| chr8:39664635
|
G | A | 59 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(56): Show | 59 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1326+745G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664635 | ||||||
| chr8:39664665
|
T | C | 1 | a0001c0002t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1326+775T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664665 | ||||||
| chr8:39664853
|
A | G | 6 | a0001c0001t0001g0180a0001c0001t0001g0190a0001c0001t0001g0220others(3): Show | 6 | HG00738.hp1 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326+963A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664853 | ||||||
| chr8:39664932
|
G | T | 82 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(79): Show | 85 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.1326+1042G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664932 | ||||||
| chr8:39664933
|
T | G | 82 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(79): Show | 85 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.1326+1043T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664933 | ||||||
| chr8:39664934
|
TGAA | T | 82 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(79): Show | 85 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.1326+1045_1326+104 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664934 | ||||||
| chr8:39665094
|
G | A | 228 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(225): Show | 232 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1326+1204G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665094 | ||||||
| chr8:39665115
|
C | A | 1 | a0001c0001t0001g0335 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1326+1225C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665115 | ||||||
| chr8:39665456
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326+1566A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665456 | ||||||
| chr8:39665549
|
G | A | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326+1659G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665549 | ||||||
| chr8:39665773
|
C | A | 1 | a0003c0004t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1326+1883C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665773 | ||||||
| chr8:39665803
|
C | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326+1913C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665803 | ||||||
| chr8:39665833
|
T | A | 1 | a0001c0002t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1326+1943T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665833 | ||||||
| chr8:39665877
|
TAAA | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326+1989_1326+199 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr8 | 39665877 | |||||
| chr8:39665882
|
G | T | 1 | a0001c0002t0001g0035 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1326+1992G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665882 | ||||||
| chr8:39665892
|
A | T | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1326+2002A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665892 | ||||||
| chr8:39665900
|
G | T | 59 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(56): Show | 59 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1326+2010G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665900 | ||||||
| chr8:39665961
|
T | C | 1 | a0001c0010t0001g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1327-2037T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665961 | ||||||
| chr8:39666016
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1327-1982C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666016 | ||||||
| chr8:39666365
|
G | A | 1 | a0013c0017t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1327-1633G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666365 | ||||||
| chr8:39666482
|
A | G | 1 | a0001c0002t0001g0028 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1327-1516A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666482 | ||||||
| chr8:39666512
|
G | A | 1 | a0001c0002t0001g0086 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1327-1486G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666512 | ||||||
| chr8:39666652
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0278 | 2 | NA18955.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1327-1346G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666652 | ||||||
| chr8:39666781
|
G | A | 6 | a0001c0002t0001g0050a0001c0002t0001g0092a0001c0002t0001g0098others(3): Show | 6 | HG00609.hp2 NA18950.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1327-1217G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666781 | ||||||
| chr8:39666917
|
T | G | 228 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(225): Show | 232 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1327-1081T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666917 | ||||||
| chr8:39667128
|
G | A | 59 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(56): Show | 59 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1327-870G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667128 | ||||||
| chr8:39667129
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0237 | 2 | NA18612.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1327-869C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667129 | ||||||
| chr8:39667295
|
G | A | 5 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0088others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-703G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667295 | ||||||
| chr8:39667401
|
C | CA | 29 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0164others(26): Show | 30 | HG00621.hp1 HG00733.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1327-578dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr8 | 39667401 | |||||
| chr8:39667401
|
CA | C | 12 | a0001c0001t0001g0191a0001c0001t0001g0225a0001c0001t0001g0233others(9): Show | 12 | HG00323.hp2 HG01074.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1327-578delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr8 | 39667401 | |||||
| chr8:39667427
|
G | A | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1327-571G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667427 | ||||||
| chr8:39667478
|
T | C | 1 | a0001c0010t0001g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1327-520T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667478 | ||||||
| chr8:39667478
|
T | G | 1 | a0001c0002t0001g0259 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1327-520T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667478 | ||||||
| chr8:39667543
|
A | T | 1 | a0003c0004t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1327-455A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667543 | ||||||
| chr8:39667591
|
A | G | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1327-407A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667591 | ||||||
| chr8:39667655
|
C | T | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1327-343C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667655 | ||||||
| chr8:39667875
|
T | C | 1 | a0004c0005t0001g0309 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1327-123T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667875 | ||||||
| chr8:39668213
|
C | T | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525+17C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668213 | ||||||
| chr8:39668225
|
A | G | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1525+29A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668225 | ||||||
| chr8:39668231
|
C | A | 195 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(192): Show | 199 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1525+35C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668231 | ||||||
| chr8:39668310
|
A | C | 95 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(92): Show | 96 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.1525+114A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668310 | ||||||
| chr8:39668820
|
T | C | 1 | a0001c0002t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1525+624T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668820 | ||||||
| chr8:39669182
|
G | A | 5 | a0001c0002t0001g0054a0001c0002t0001g0101a0001c0002t0001g0102others(2): Show | 5 | NA18948.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+986G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669182 | ||||||
| chr8:39669314
|
A | T | 186 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(183): Show | 190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1525+1118A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669314 | ||||||
| chr8:39669368
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0219 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1525+1172G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669368 | ||||||
| chr8:39669464
|
C | G | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1525+1268C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669464 | ||||||
| chr8:39669474
|
C | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0154 | 2 | HG01074.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1525+1278C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669474 | ||||||
| chr8:39669538
|
T | C | 195 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(192): Show | 199 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1525+1342T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669538 | ||||||
| chr8:39669549
|
G | C | 1 | a0001c0001t0001g0270 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1525+1353G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669549 | ||||||
| chr8:39669588
|
G | T | 1 | a0001c0002t0001g0292 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1525+1392G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669588 | ||||||
| chr8:39669762
|
C | A | 6 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525+1566C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669762 | ||||||
| chr8:39669846
|
T | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+1650T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669846 | ||||||
| chr8:39669885
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1525+1689A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669885 | ||||||
| chr8:39670069
|
T | C | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525+1873T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670069 | ||||||
| chr8:39670132
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1525+1936C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670132 | ||||||
| chr8:39670205
|
C | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | NA18944.hp2 NA19002.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525+2009C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670205 | ||||||
| chr8:39670241
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1525+2045C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670241 | ||||||
| chr8:39670462
|
A | G | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525+2266A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670462 | ||||||
| chr8:39670495
|
A | G | 1 | a0001c0012t0001g0005 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1525+2299A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670495 | ||||||
| chr8:39670693
|
C | T | 13 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525+2497C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670693 | ||||||
| chr8:39671283
|
A | G | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525+3087A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671283 | ||||||
| chr8:39671750
|
C | T | 1 | a0001c0002t0001g0058 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1525+3554C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671750 | ||||||
| chr8:39671781
|
A | C | 5 | a0001c0002t0001g0054a0001c0002t0001g0101a0001c0002t0001g0102others(2): Show | 5 | NA18948.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+3585A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671781 | ||||||
| chr8:39671834
|
A | T | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525+3638A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671834 | ||||||
| chr8:39671886
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1525+3690G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671886 | ||||||
| chr8:39671931
|
A | T | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525+3735A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671931 | ||||||
| chr8:39671977
|
A | G | 96 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(93): Show | 99 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.1525+3781A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671977 | ||||||
| chr8:39672081
|
T | C | 154 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(151): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1525+3885T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672081 | ||||||
| chr8:39672101
|
T | G | 154 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(151): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1525+3905T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672101 | ||||||
| chr8:39672432
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1525+4236G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672432 | ||||||
| chr8:39672485
|
G | T | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525+4289G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672485 | ||||||
| chr8:39672583
|
T | C | 7 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(4): Show | 7 | HG00733.hp1 HG01167.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1525+4387T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672583 | ||||||
| chr8:39672694
|
T | C | 1 | a0001c0002t0001g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1525+4498T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672694 | ||||||
| chr8:39672726
|
C | T | 1 | a0001c0002t0001g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1525+4530C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672726 | ||||||
| chr8:39672765
|
A | C | 2 | a0001c0010t0001g0033a0001c0010t0001g0042 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1525+4569A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672765 | ||||||
| chr8:39672891
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1526-4540G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672891 | ||||||
| chr8:39673501
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0250 | 2 | NA18995.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1526-3930C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39673501 | ||||||
| chr8:39673775
|
C | T | 16 | a0001c0001t0001g0206a0001c0001t0001g0268a0001c0001t0001g0269others(13): Show | 16 | HG00544.hp1 HG00597.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1526-3656C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39673775 | ||||||
| chr8:39673928
|
C | A | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG01243.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-3503C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39673928 | ||||||
| chr8:39673929
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1526-3502G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39673929 | ||||||
| chr8:39674032
|
T | C | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1526-3399T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674032 | ||||||
| chr8:39674232
|
T | C | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1526-3199T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674232 | ||||||
| chr8:39674256
|
C | T | 1 | a0002c0003t0001g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1526-3175C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674256 | ||||||
| chr8:39674711
|
T | A | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1526-2720T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674711 | ||||||
| chr8:39674712
|
C | T | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1526-2719C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674712 | ||||||
| chr8:39674790
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1526-2641C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674790 | ||||||
| chr8:39674947
|
T | G | 195 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(192): Show | 199 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1526-2484T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674947 | ||||||
| chr8:39674952
|
C | A | 154 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(151): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1526-2479C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674952 | ||||||
| chr8:39674969
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1526-2462G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674969 | ||||||
| chr8:39675009
|
C | T | 1 | a0001c0008t0003g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1526-2422C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675009 | ||||||
| chr8:39675295
|
A | G | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1526-2136A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675295 | ||||||
| chr8:39675420
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1526-2011T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675420 | ||||||
| chr8:39675437
|
C | G | 6 | a0001c0002t0001g0116a0001c0002t0001g0145a0001c0002t0001g0147others(3): Show | 6 | HG00280.hp1 HG01256.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1526-1994C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675437 | ||||||
| chr8:39675754
|
T | C | 1 | a0004c0005t0001g0320 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1526-1677T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675754 | ||||||
| chr8:39675782
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-1649A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675782 | ||||||
| chr8:39675852
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1526-1579G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675852 | ||||||
| chr8:39676110
|
C | T | 154 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(151): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1526-1321C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676110 | ||||||
| chr8:39676207
|
G | A | 83 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(80): Show | 84 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1526-1224G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676207 | ||||||
| chr8:39676343
|
C | T | 1 | a0004c0005t0001g0316 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1526-1088C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676343 | ||||||
| chr8:39676379
|
G | A | 1 | a0004c0005t0001g0316 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1526-1052G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676379 | ||||||
| chr8:39676399
|
C | T | 1 | a0012c0020t0001g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1526-1032C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676399 | ||||||
| chr8:39676498
|
G | T | 6 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0052others(3): Show | 7 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1526-933G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676498 | ||||||
| chr8:39676583
|
C | T | 1 | a0006c0006t0001g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1526-848C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676583 | ||||||
| chr8:39676604
|
CA | C | 342 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(339): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1526-826delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676604 | ||||||
| chr8:39676610
|
C | T | 1 | a0001c0002t0001g0096 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1526-821C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676610 | ||||||
| chr8:39676613
|
C | T | 342 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(339): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1526-818C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676613 | ||||||
| chr8:39676615
|
C | T | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1526-816C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676615 | ||||||
| chr8:39676622
|
C | T | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1526-809C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676622 | ||||||
| chr8:39676692
|
C | T | 13 | a0001c0010t0001g0033a0001c0010t0001g0042a0003c0004t0001g0179others(10): Show | 13 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1526-739C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676692 | ||||||
| chr8:39676767
|
G | A | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1526-664G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676767 | ||||||
| chr8:39676771
|
A | G | 53 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(50): Show | 56 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.1526-660A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676771 | ||||||
| chr8:39676918
|
G | A | 8 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(5): Show | 8 | HG00738.hp1 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1526-513G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676918 | ||||||
| chr8:39677141
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1526-290A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677141 | ||||||
| chr8:39677192
|
A | G | 2 | a0001c0002t0001g0054a0001c0002t0001g0101 | 2 | NA18960.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1526-239A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677192 | ||||||
| chr8:39677200
|
A | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-231A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677200 | ||||||
| chr8:39677239
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1526-192T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677239 | ||||||
| chr8:39677375
|
C | G | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1526-56C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677375 | ||||||
| chr8:39677543
|
A | G | 1 | a0001c0002t0001g0048 | 1 | NA18965.hp2 | splice_region_variant&intron_variant | LOW | c.1631+7A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677543 | ||||||
| chr8:39677569
|
T | G | 1 | a0002c0003t0001g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1631+33T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677569 | ||||||
| chr8:39677661
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1631+125A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677661 | ||||||
| chr8:39677709
|
C | A | 1 | a0013c0017t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1631+173C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677709 | ||||||
| chr8:39677762
|
G | A | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1631+226G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677762 | ||||||
| chr8:39677797
|
T | C | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1631+261T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677797 | ||||||
| chr8:39677835
|
G | A | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1631+299G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677835 | ||||||
| chr8:39677931
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1631+395T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677931 | ||||||
| chr8:39678310
|
T | C | 53 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(50): Show | 56 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.1631+774T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678310 | ||||||
| chr8:39678467
|
A | T | 33 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1631+931A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678467 | ||||||
| chr8:39678490
|
A | C | 3 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0289 | 3 | HG03041.hp2 HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1631+954A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678490 | ||||||
| chr8:39678501
|
A | C | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1631+965A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678501 | ||||||
| chr8:39678531
|
C | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1631+995C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678531 | ||||||
| chr8:39678725
|
C | T | 1 | a0001c0002t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1631+1189C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678725 | ||||||
| chr8:39678893
|
G | C | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1632-1144G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678893 | ||||||
| chr8:39679023
|
G | C | 1 | a0001c0002t0001g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1632-1014G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679023 | ||||||
| chr8:39679060
|
G | T | 1 | a0006c0006t0001g0266 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1632-977G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679060 | ||||||
| chr8:39679209
|
T | C | 1 | a0009c0023t0001g0014 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1632-828T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679209 | ||||||
| chr8:39679259
|
T | C | 1 | a0001c0002t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1632-778T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679259 | ||||||
| chr8:39679765
|
C | T | 155 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(152): Show | 159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1632-272C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679765 | ||||||
| chr8:39679771
|
A | C | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1632-266A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679771 | ||||||
| chr8:39679853
|
T | A | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1632-184T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679853 | ||||||
| chr8:39679912
|
C | T | 192 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(189): Show | 196 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1632-125C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679912 | ||||||
| chr8:39680377
|
C | G | 1 | a0011c0021t0001g0224 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1821+151C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39680377 | ||||||
| chr8:39680635
|
A | T | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1821+409A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39680635 | ||||||
| chr8:39680716
|
C | T | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+490C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39680716 | ||||||
| chr8:39680851
|
C | CACTT | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+627_1821+630d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39680851 | |||||
| chr8:39680882
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1821+656C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39680882 | ||||||
| chr8:39681220
|
C | A | 13 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+994C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681220 | ||||||
| chr8:39681248
|
G | T | 1 | a0001c0002t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1821+1022G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681248 | ||||||
| chr8:39681281
|
C | A | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1821+1055C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681281 | ||||||
| chr8:39681441
|
G | C | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1821+1215G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681441 | ||||||
| chr8:39681552
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1821+1326G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681552 | ||||||
| chr8:39681595
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1821+1369C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681595 | ||||||
| chr8:39681812
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1821+1586C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681812 | ||||||
| chr8:39681821
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1821+1595T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681821 | ||||||
| chr8:39681950
|
A | G | 1 | a0004c0005t0001g0316 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1821+1724A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681950 | ||||||
| chr8:39682029
|
G | C | 1 | a0001c0002t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1821+1803G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682029 | ||||||
| chr8:39682191
|
C | T | 1 | a0001c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1821+1965C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682191 | ||||||
| chr8:39682268
|
C | A | 1 | a0001c0001t0001g0329 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1821+2042C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682268 | ||||||
| chr8:39682269
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1821+2043G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682269 | ||||||
| chr8:39682370
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG01168.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1821+2144G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682370 | ||||||
| chr8:39682397
|
G | A | 70 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(67): Show | 73 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.1821+2171G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682397 | ||||||
| chr8:39682430
|
T | C | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+2204T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682430 | ||||||
| chr8:39682604
|
G | A | 1 | a0001c0002t0001g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1821+2378G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682604 | ||||||
| chr8:39682643
|
C | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(88): Show | 94 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1821+2417C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682643 | ||||||
| chr8:39682644
|
C | G | 2 | a0001c0001t0001g0301a0001c0001t0001g0303 | 2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1821+2418C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682644 | ||||||
| chr8:39683029
|
G | A | 1 | a0001c0002t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1821+2803G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39683029 | ||||||
| chr8:39683309
|
G | A | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+3083G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39683309 | ||||||
| chr8:39683396
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1821+3170C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39683396 | ||||||
| chr8:39683932
|
T | C | 1 | a0001c0002t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1821+3706T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39683932 | ||||||
| chr8:39684017
|
C | T | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+3791C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684017 | ||||||
| chr8:39684058
|
T | G | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1821+3832T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684058 | ||||||
| chr8:39684219
|
T | C | 1 | a0001c0002t0001g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1821+3993T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684219 | ||||||
| chr8:39684249
|
T | C | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+4023T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684249 | ||||||
| chr8:39684321
|
G | A | 6 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+4095G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684321 | ||||||
| chr8:39684459
|
C | T | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1821+4233C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684459 | ||||||
| chr8:39684497
|
A | C | 1 | a0001c0002t0001g0043 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1821+4271A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684497 | ||||||
| chr8:39684572
|
A | C | 1 | a0001c0002t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1821+4346A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684572 | ||||||
| chr8:39684883
|
G | C | 2 | a0001c0002t0001g0053a0001c0002t0001g0100 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1821+4657G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684883 | ||||||
| chr8:39684978
|
G | A | 1 | a0007c0009t0001g0151 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1821+4752G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684978 | ||||||
| chr8:39685056
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1821+4830T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685056 | ||||||
| chr8:39685155
|
T | C | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+4929T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685155 | ||||||
| chr8:39685318
|
T | C | 318 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(315): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1821+5092T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685318 | ||||||
| chr8:39685474
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1821+5248G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685474 | ||||||
| chr8:39685506
|
C | T | 1 | a0001c0002t0001g0155 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1821+5280C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685506 | ||||||
| chr8:39685545
|
T | C | 5 | a0002c0003t0001g0020a0002c0003t0001g0022a0002c0003t0001g0023others(2): Show | 5 | HG02074.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821+5319T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685545 | ||||||
| chr8:39685626
|
G | A | 13 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(10): Show | 13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+5400G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685626 | ||||||
| chr8:39685939
|
C | T | 69 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(66): Show | 72 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1821+5713C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685939 | ||||||
| chr8:39686006
|
A | G | 1 | a0003c0004t0001g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1821+5780A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686006 | ||||||
| chr8:39686087
|
C | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1821+5861C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686087 | ||||||
| chr8:39686116
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1821+5890G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686116 | ||||||
| chr8:39686164
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0194 | 2 | HG00438.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1821+5938C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686164 | ||||||
| chr8:39686242
|
T | A | 13 | a0001c0010t0001g0033a0001c0010t0001g0042a0003c0004t0001g0179others(10): Show | 13 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1821+6016T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686242 | ||||||
| chr8:39686307
|
G | A | 1 | a0002c0003t0001g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1821+6081G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686307 | ||||||
| chr8:39686316
|
T | A | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1821+6090T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686316 | ||||||
| chr8:39686382
|
G | C | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1821+6156G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686382 | ||||||
| chr8:39686446
|
G | A | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1822-6154G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686446 | ||||||
| chr8:39686468
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0178others(1): Show | 4 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1822-6132A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686468 | ||||||
| chr8:39686580
|
G | A | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1822-6020G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686580 | ||||||
| chr8:39686644
|
C | A | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1822-5956C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686644 | ||||||
| chr8:39686662
|
G | A | 1 | a0004c0019t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1822-5938G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686662 | ||||||
| chr8:39686705
|
G | A | 26 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0011others(23): Show | 26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1822-5895G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686705 | ||||||
| chr8:39686780
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1822-5820C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686780 | ||||||
| chr8:39686781
|
G | A | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1822-5819G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686781 | ||||||
| chr8:39686841
|
T | A | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1822-5759T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686841 | ||||||
| chr8:39687215
|
A | G | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822-5385A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687215 | ||||||
| chr8:39687569
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1822-5031G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687569 | ||||||
| chr8:39687597
|
C | A | 1 | a0001c0001t0001g0291 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1822-5003C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687597 | ||||||
| chr8:39687599
|
T | A | 1 | a0001c0002t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1822-5001T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687599 | ||||||
| chr8:39687646
|
G | A | 154 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(151): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1822-4954G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687646 | ||||||
| chr8:39687714
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1822-4886A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687714 | ||||||
| chr8:39687716
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0238 | 2 | HG02027.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1822-4884G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687716 | ||||||
| chr8:39687841
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1822-4759G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687841 | ||||||
| chr8:39687908
|
T | C | 29 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013others(26): Show | 29 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1822-4692T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687908 | ||||||
| chr8:39688141
|
A | G | 188 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(185): Show | 192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1822-4459A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688141 | ||||||
| chr8:39688186
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(11): Show | 14 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1822-4414A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688186 | ||||||
| chr8:39688317
|
T | G | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1822-4283T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688317 | ||||||
| chr8:39688791
|
T | C | 1 | a0001c0002t0001g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1822-3809T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688791 | ||||||
| chr8:39688961
|
C | T | 30 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013others(27): Show | 30 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1822-3639C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688961 | ||||||
| chr8:39688993
|
G | T | 1 | a0001c0002t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1822-3607G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688993 | ||||||
| chr8:39689283
|
C | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0218a0001c0001t0001g0240others(3): Show | 6 | HG01074.hp1 HG02148.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822-3317C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689283 | ||||||
| chr8:39689284
|
G | A | 54 | a0001c0001t0001g0200a0001c0002t0001g0002a0001c0002t0001g0003others(51): Show | 57 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(54): Show |
intron_variant | MODIFIER | c.1822-3316G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689284 | ||||||
| chr8:39689469
|
G | A | 1 | a0001c0002t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1822-3131G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689469 | ||||||
| chr8:39689692
|
T | C | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1822-2908T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689692 | ||||||
| chr8:39689741
|
G | A | 13 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1822-2859G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689741 | ||||||
| chr8:39689890
|
C | T | 167 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(164): Show | 171 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1822-2710C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689890 | ||||||
| chr8:39689955
|
C | T | 14 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(11): Show | 14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1822-2645C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689955 | ||||||
| chr8:39689973
|
G | A | 101 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(98): Show | 102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1822-2627G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689973 | ||||||
| chr8:39690100
|
G | T | 1 | a0001c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1822-2500G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690100 | ||||||
| chr8:39690108
|
G | A | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-2492G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690108 | ||||||
| chr8:39690123
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1822-2477C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690123 | ||||||
| chr8:39690258
|
G | A | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-2342G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690258 | ||||||
| chr8:39690262
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1822-2338C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690262 | ||||||
| chr8:39690274
|
G | T | 13 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1822-2326G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690274 | ||||||
| chr8:39690277
|
C | A | 1 | a0001c0002t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1822-2323C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690277 | ||||||
| chr8:39690328
|
G | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1822-2272G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690328 | ||||||
| chr8:39690414
|
G | A | 1 | a0001c0002t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1822-2186G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690414 | ||||||
| chr8:39690460
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1822-2140G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690460 | ||||||
| chr8:39690528
|
G | C | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1822-2072G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690528 | ||||||
| chr8:39690652
|
C | T | 5 | a0001c0010t0001g0033a0001c0010t0001g0042a0003c0004t0001g0179others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1822-1948C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690652 | ||||||
| chr8:39690839
|
C | T | 145 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(142): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1822-1761C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690839 | ||||||
| chr8:39690859
|
C | T | 182 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(179): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.1822-1741C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690859 | ||||||
| chr8:39690867
|
G | T | 2 | a0002c0003t0001g0011a0013c0017t0001g0253 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1822-1733G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690867 | ||||||
| chr8:39690907
|
A | G | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1822-1693A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690907 | ||||||
| chr8:39691128
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1822-1472G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39691128 | ||||||
| chr8:39691340
|
G | T | 175 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(172): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1822-1260G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39691340 | ||||||
| chr8:39691567
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1822-1033A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39691567 | ||||||
| chr8:39691734
|
A | C | 2 | a0005c0011t0001g0188a0005c0011t0001g0245 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1822-866A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39691734 | ||||||
| chr8:39691740
|
TATC | T | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-857_1822-855d others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691740 | |||||
| chr8:39691751
|
CTTACTCA others(23): Show |
C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1822-847_1822-818d others(32): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691751 | |||||
| chr8:39691884
|
TA | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0218a0001c0001t0001g0251 | 3 | HG02451.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1822-713delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691884 | |||||
| chr8:39691909
|
GAAGTAAT others(4): Show |
G | 3 | a0001c0001t0001g0191a0001c0001t0001g0218a0001c0001t0001g0251 | 3 | HG02451.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1822-687_1822-677d others(13): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691909 | |||||
| chr8:39691996
|
TAAAA | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1822-601_1822-598d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691996 | |||||
| chr8:39692000
|
A | C | 1 | a0001c0002t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1822-600A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692000 | ||||||
| chr8:39692260
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0084 | 2 | NA18970.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1822-340A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692260 | ||||||
| chr8:39692295
|
C | T | 2 | a0001c0002t0001g0054a0001c0002t0001g0101 | 2 | NA18960.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1822-305C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692295 | ||||||
| chr8:39692301
|
G | A | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-299G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692301 | ||||||
| chr8:39692348
|
A | G | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 291 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1822-252A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692348 | ||||||
| chr8:39692379
|
T | A | 1 | a0001c0002t0001g0098 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1822-221T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692379 | ||||||
| chr8:39692705
|
G | T | 1 | a0001c0002t0001g0048 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1902+25G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39692705 | ||||||
| chr8:39692737
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1902+57A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39692737 | ||||||
| chr8:39693178
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0202 | 2 | NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1902+498T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693178 | ||||||
| chr8:39693210
|
T | A | 1 | a0001c0001t0001g0312 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1902+530T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693210 | ||||||
| chr8:39693442
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1902+762T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693442 | ||||||
| chr8:39693446
|
C | G | 2 | a0001c0002t0001g0089a0001c0002t0001g0138 | 2 | HG01109.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1902+766C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693446 | ||||||
| chr8:39693524
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1902+844T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693524 | ||||||
| chr8:39693529
|
C | T | 3 | a0001c0002t0001g0093a0001c0002t0001g0123a0001c0002t0001g0124 | 3 | HG00544.hp2 NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1902+849C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693529 | ||||||
| chr8:39693575
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+895A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693575 | ||||||
| chr8:39693632
|
T | A | 144 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(141): Show | 145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1902+952T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693632 | ||||||
| chr8:39693682
|
A | C | 13 | a0001c0010t0001g0033a0001c0010t0001g0042a0003c0004t0001g0179others(10): Show | 13 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1902+1002A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693682 | ||||||
| chr8:39693700
|
C | G | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1902+1020C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693700 | ||||||
| chr8:39693763
|
A | C | 1 | a0001c0001t0001g0312 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1902+1083A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693763 | ||||||
| chr8:39694113
|
T | A | 1 | a0001c0001t0001g0234 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1902+1433T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39694113 | ||||||
| chr8:39694487
|
A | G | 162 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(159): Show | 163 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1902+1807A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39694487 | ||||||
| chr8:39694854
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1902+2174C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39694854 | ||||||
| chr8:39694855
|
G | A | 7 | a0001c0001t0001g0297a0001c0001t0001g0313a0001c0001t0001g0322others(4): Show | 7 | HG01106.hp1 HG01257.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1902+2175G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39694855 | ||||||
| chr8:39695013
|
G | A | 1 | a0001c0002t0001g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1902+2333G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695013 | ||||||
| chr8:39695086
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1902+2406T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695086 | ||||||
| chr8:39695333
|
T | C | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1902+2653T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695333 | ||||||
| chr8:39695742
|
T | C | 101 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(98): Show | 102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1902+3062T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695742 | ||||||
| chr8:39695833
|
C | T | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1902+3153C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695833 | ||||||
| chr8:39696109
|
T | C | 158 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(155): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1902+3429T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696109 | ||||||
| chr8:39696166
|
C | A | 6 | a0001c0002t0001g0002a0001c0002t0001g0063a0001c0002t0001g0065others(3): Show | 7 | HG02257.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1902+3486C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696166 | ||||||
| chr8:39696169
|
T | G | 29 | a0001c0001t0001g0169a0001c0001t0001g0274a0001c0001t0001g0291others(26): Show | 29 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1902+3489T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696169 | ||||||
| chr8:39696248
|
A | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+3568A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696248 | ||||||
| chr8:39696264
|
A | G | 50 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(47): Show | 51 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1902+3584A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696264 | ||||||
| chr8:39696269
|
T | A | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3589T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696269 | ||||||
| chr8:39696270
|
ATATT | A | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3592_1902+359 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39696270 | |||||
| chr8:39696277
|
G | C | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3597G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696277 | ||||||
| chr8:39696278
|
G | T | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3598G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696278 | ||||||
| chr8:39696280
|
T | A | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3600T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696280 | ||||||
| chr8:39696284
|
AATTCCTT others(29): Show |
A | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3605_1902+364 others(40): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696284 | ||||||
| chr8:39696556
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+3876T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696556 | ||||||
| chr8:39696839
|
G | T | 1 | a0013c0017t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1902+4159G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696839 | ||||||
| chr8:39696865
|
T | C | 1 | a0001c0002t0001g0131 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1902+4185T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696865 | ||||||
| chr8:39696871
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1902+4191C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696871 | ||||||
| chr8:39696922
|
T | A | 2 | a0001c0010t0001g0033a0001c0010t0001g0042 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1902+4242T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696922 | ||||||
| chr8:39697007
|
G | A | 101 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(98): Show | 102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1902+4327G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697007 | ||||||
| chr8:39697149
|
A | G | 1 | a0003c0004t0001g0179 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1902+4469A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697149 | ||||||
| chr8:39697166
|
C | T | 2 | a0001c0001t0001g0229a0010c0013t0001g0161 | 2 | HG01884.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1902+4486C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697166 | ||||||
| chr8:39697167
|
G | A | 1 | a0004c0005t0001g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1902+4487G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697167 | ||||||
| chr8:39697217
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1902+4537A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697217 | ||||||
| chr8:39697293
|
G | C | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1902+4613G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697293 | ||||||
| chr8:39697532
|
C | G | 3 | a0001c0002t0001g0076a0001c0002t0001g0110a0001c0002t0001g0111 | 3 | NA18971.hp2 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1902+4852C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697532 | ||||||
| chr8:39697617
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1902+4937C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697617 | ||||||
| chr8:39697904
|
A | G | 1 | a0001c0002t0001g0055 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1902+5224A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697904 | ||||||
| chr8:39698004
|
C | A | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1902+5324C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698004 | ||||||
| chr8:39698139
|
G | A | 101 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(98): Show | 102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1902+5459G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698139 | ||||||
| chr8:39698189
|
C | T | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 291 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1902+5509C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698189 | ||||||
| chr8:39698230
|
T | A | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1902+5550T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698230 | ||||||
| chr8:39698277
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0178 | 2 | HG02129.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1902+5597T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698277 | ||||||
| chr8:39698290
|
T | A | 101 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(98): Show | 102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1902+5610T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698290 | ||||||
| chr8:39698347
|
C | G | 1 | a0001c0002t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1902+5667C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698347 | ||||||
| chr8:39698365
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1902+5685G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698365 | ||||||
| chr8:39698472
|
A | T | 1 | a0001c0001t0001g0207 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1902+5792A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698472 | ||||||
| chr8:39698563
|
G | A | 2 | a0001c0002t0001g0123a0001c0002t0001g0124 | 2 | NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1902+5883G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698563 | ||||||
| chr8:39698737
|
G | T | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1902+6057G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698737 | ||||||
| chr8:39698845
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1902+6165T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698845 | ||||||
| chr8:39698867
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1902+6187C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698867 | ||||||
| chr8:39699047
|
A | G | 1 | a0012c0020t0001g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1902+6367A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699047 | ||||||
| chr8:39699144
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1902+6464G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699144 | ||||||
| chr8:39699196
|
A | G | 1 | a0003c0004t0001g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1902+6516A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699196 | ||||||
| chr8:39699346
|
G | T | 4 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(1): Show | 4 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1902+6666G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699346 | ||||||
| chr8:39699454
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1902+6774G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699454 | ||||||
| chr8:39699532
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0237a0001c0001t0001g0280 | 3 | NA18612.hp2 NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1902+6852A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699532 | ||||||
| chr8:39700126
|
C | T | 101 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(98): Show | 102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1903-6664C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700126 | ||||||
| chr8:39700202
|
G | C | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6588G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700202 | ||||||
| chr8:39700272
|
T | C | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6518T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700272 | ||||||
| chr8:39700350
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1903-6440T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700350 | ||||||
| chr8:39700446
|
C | T | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6344C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700446 | ||||||
| chr8:39700449
|
A | C | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6341A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700449 | ||||||
| chr8:39700459
|
G | GA | 12 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(9): Show | 12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1903-6325dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39700459 | |||||
| chr8:39700470
|
C | T | 1 | a0008c0024t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1903-6320C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700470 | ||||||
| chr8:39700504
|
G | A | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6286G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700504 | ||||||
| chr8:39700581
|
C | A | 1 | a0001c0002t0001g0075 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1903-6209C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700581 | ||||||
| chr8:39700886
|
G | A | 1 | a0002c0003t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1903-5904G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700886 | ||||||
| chr8:39700887
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-5903G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700887 | ||||||
| chr8:39701034
|
C | T | 40 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(37): Show | 40 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1903-5756C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701034 | ||||||
| chr8:39701117
|
C | CA | 71 | a0001c0001t0001g0090a0001c0001t0001g0135a0001c0001t0001g0160others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1903-5641dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAA | 31 | a0001c0001t0001g0046a0001c0001t0001g0198a0001c0001t0001g0199others(28): Show | 31 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1903-5642_1903-564 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAA | 29 | a0001c0001t0001g0169a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 30 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1903-5643_1903-564 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAA | 40 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0171others(37): Show | 41 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1903-5644_1903-564 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAA | 33 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0168others(30): Show | 33 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1903-5645_1903-564 others(9): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAA | 8 | a0001c0001t0001g0159a0001c0001t0001g0167a0001c0002t0001g0050others(5): Show | 8 | HG01943.hp2 HG02148.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.1903-5646_1903-564 others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(3): Show |
2 | a0001c0002t0001g0104a0001c0002t0001g0261 | 2 | HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1903-5650_1903-564 others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0001g0044 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1903-5653_1903-564 others(17): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(7): Show |
2 | a0001c0002t0001g0030a0001c0002t0001g0058 | 2 | HG02004.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1903-5654_1903-564 others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(8): Show |
10 | a0001c0002t0001g0026a0001c0002t0001g0031a0001c0002t0001g0032others(7): Show | 10 | HG01081.hp1 HG01952.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1903-5655_1903-564 others(19): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(9): Show |
3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0036 | 3 | HG00642.hp2 HG01099.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1903-5656_1903-564 others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(11): Show |
3 | a0001c0002t0001g0009a0001c0002t0001g0085a0005c0011t0001g0188 | 3 | HG01099.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1903-5658_1903-564 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(12): Show |
7 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0101others(4): Show | 7 | HG00323.hp1 HG01993.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903-5659_1903-564 others(23): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(13): Show |
3 | a0001c0002t0001g0054a0001c0002t0001g0102a0001c0002t0001g0263 | 3 | HG02300.hp1 NA18954.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1903-5660_1903-564 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(14): Show |
5 | a0001c0002t0001g0087a0001c0002t0001g0089a0001c0002t0001g0103others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-5661_1903-564 others(25): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1903-5666_1903-564 others(30): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
C | CAAAAAAA others(32): Show |
1 | a0005c0011t0001g0245 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1903-5641_1903-564 others(43): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0002t0001g0108a0001c0002t0001g0255a0001c0002t0001g0256others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903-5648_1903-564 others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0086 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1903-5650_1903-564 others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0002t0001g0158a0010c0013t0001g0161 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1903-5651_1903-564 others(15): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701117
|
CAAAAAAA others(6): Show |
C | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-5653_1903-564 others(17): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | |||||
| chr8:39701143
|
A | AG | 7 | a0002c0003t0001g0011a0002c0003t0001g0016a0002c0003t0001g0017others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-5647_1903-564 others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701143 | ||||||
| chr8:39701143
|
A | G | 7 | a0002c0003t0001g0015a0002c0003t0001g0020a0002c0003t0001g0021others(4): Show | 7 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903-5647A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701143 | ||||||
| chr8:39701263
|
C | G | 6 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1903-5527C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701263 | ||||||
| chr8:39701356
|
C | T | 14 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163others(11): Show | 15 | HG00621.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1903-5434C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701356 | ||||||
| chr8:39701374
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1903-5416G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701374 | ||||||
| chr8:39701505
|
G | T | 1 | a0001c0002t0001g0263 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1903-5285G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701505 | ||||||
| chr8:39701620
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1903-5170C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701620 | ||||||
| chr8:39701871
|
G | A | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1903-4919G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701871 | ||||||
| chr8:39701910
|
C | T | 4 | a0001c0001t0001g0208a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG02074.hp2 NA18949.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903-4880C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701910 | ||||||
| chr8:39702130
|
C | G | 2 | a0007c0009t0001g0114a0007c0009t0001g0151 | 2 | NA19074.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1903-4660C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702130 | ||||||
| chr8:39702173
|
C | T | 14 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163others(11): Show | 15 | HG00621.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1903-4617C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702173 | ||||||
| chr8:39702216
|
G | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1903-4574G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702216 | ||||||
| chr8:39702337
|
G | T | 1 | a0001c0001t0001g0325 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1903-4453G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702337 | ||||||
| chr8:39702345
|
T | A | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG01243.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903-4445T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702345 | ||||||
| chr8:39702448
|
C | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-4342C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702448 | ||||||
| chr8:39702557
|
C | T | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-4233C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702557 | ||||||
| chr8:39702605
|
T | C | 5 | a0001c0002t0001g0054a0001c0002t0001g0101a0001c0002t0001g0102others(2): Show | 5 | NA18948.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-4185T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702605 | ||||||
| chr8:39702664
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-4126G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702664 | ||||||
| chr8:39702746
|
C | T | 114 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(111): Show | 115 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.1903-4044C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702746 | ||||||
| chr8:39702780
|
G | C | 2 | a0001c0001t0001g0305a0001c0001t0001g0335 | 2 | NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1903-4010G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702780 | ||||||
| chr8:39703110
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1903-3680C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703110 | ||||||
| chr8:39703273
|
T | C | 1 | a0003c0004t0001g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1903-3517T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703273 | ||||||
| chr8:39703430
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1903-3360C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703430 | ||||||
| chr8:39703552
|
T | A | 3 | a0001c0002t0001g0259a0001c0008t0003g0012a0001c0008t0003g0013 | 3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1903-3238T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703552 | ||||||
| chr8:39703556
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1903-3234G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703556 | ||||||
| chr8:39703593
|
G | A | 1 | a0011c0021t0001g0224 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1903-3197G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703593 | ||||||
| chr8:39703914
|
A | T | 1 | a0001c0001t0001g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1903-2876A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703914 | ||||||
| chr8:39704077
|
A | G | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1903-2713A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704077 | ||||||
| chr8:39704119
|
T | C | 1 | a0001c0002t0001g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1903-2671T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704119 | ||||||
| chr8:39704326
|
G | A | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-2464G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704326 | ||||||
| chr8:39704360
|
A | G | 6 | a0001c0002t0001g0050a0001c0002t0001g0092a0001c0002t0001g0098others(3): Show | 6 | HG00609.hp2 NA18950.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903-2430A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704360 | ||||||
| chr8:39704387
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-2403T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704387 | ||||||
| chr8:39704528
|
C | T | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1903-2262C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704528 | ||||||
| chr8:39704537
|
T | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135 | 3 | HG00639.hp2 HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1903-2253T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704537 | ||||||
| chr8:39704975
|
T | A | 175 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(172): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1903-1815T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704975 | ||||||
| chr8:39705071
|
T | C | 102 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 103 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1903-1719T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705071 | ||||||
| chr8:39705185
|
A | C | 4 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(1): Show | 4 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903-1605A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705185 | ||||||
| chr8:39705247
|
T | A | 1 | a0001c0001t0001g0302 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1903-1543T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705247 | ||||||
| chr8:39705271
|
C | T | 1 | a0001c0002t0001g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1903-1519C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705271 | ||||||
| chr8:39705506
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1903-1284C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705506 | ||||||
| chr8:39705653
|
C | T | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1903-1137C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705653 | ||||||
| chr8:39705778
|
G | A | 158 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(155): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1903-1012G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705778 | ||||||
| chr8:39706319
|
A | G | 1 | a0001c0001t0001g0328 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1903-471A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39706319 | ||||||
| chr8:39706632
|
C | T | 289 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(286): Show | 291 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1903-158C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39706632 | ||||||
| chr8:39706714
|
ATATCAGA others(13): Show |
A | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1903-59_1903-40del others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39706714 | |||||
| chr8:39706905
|
G | T | 1 | a0001c0001t0001g0314 | 1 | HG02080.hp1 | splice_donor_variant&intron_variant | HIGH | c.2017+1G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39706905 | ||||||
| chr8:39706996
|
A | G | 1 | a0001c0002t0001g0089 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2017+92A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39706996 | ||||||
| chr8:39707036
|
A | G | 2 | a0001c0010t0001g0033a0001c0010t0001g0042 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2017+132A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707036 | ||||||
| chr8:39707072
|
T | C | 1 | a0001c0002t0001g0124 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2017+168T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707072 | ||||||
| chr8:39707222
|
T | C | 84 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(81): Show | 85 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2017+318T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707222 | ||||||
| chr8:39707568
|
C | G | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2017+664C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707568 | ||||||
| chr8:39707769
|
A | G | 1 | a0001c0002t0001g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2017+865A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707769 | ||||||
| chr8:39707929
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2017+1025A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707929 | ||||||
| chr8:39707964
|
G | C | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2017+1060G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707964 | ||||||
| chr8:39708008
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2017+1104C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708008 | ||||||
| chr8:39708029
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2017+1125C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708029 | ||||||
| chr8:39708069
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2017+1165G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708069 | ||||||
| chr8:39708217
|
G | A | 1 | a0001c0002t0001g0133 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2017+1313G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708217 | ||||||
| chr8:39708312
|
A | G | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+1408A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708312 | ||||||
| chr8:39708354
|
T | G | 3 | a0003c0004t0001g0179a0003c0004t0001g0213a0003c0004t0001g0214 | 3 | HG02723.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2017+1450T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708354 | ||||||
| chr8:39708377
|
T | G | 2 | a0001c0010t0001g0033a0001c0010t0001g0042 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2017+1473T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708377 | ||||||
| chr8:39708661
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2017+1757G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708661 | ||||||
| chr8:39708671
|
C | A | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+1767C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708671 | ||||||
| chr8:39708701
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2017+1797G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708701 | ||||||
| chr8:39708749
|
G | T | 1 | a0001c0002t0001g0130 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2017+1845G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708749 | ||||||
| chr8:39708901
|
C | G | 299 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(296): Show | 302 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.2017+1997C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708901 | ||||||
| chr8:39708916
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2017+2012G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708916 | ||||||
| chr8:39709068
|
T | C | 183 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(180): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2017+2164T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709068 | ||||||
| chr8:39709106
|
TG | T | 6 | a0001c0001t0001g0315a0001c0001t0001g0325a0001c0001t0001g0337others(3): Show | 6 | HG00438.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017+2204delG | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39709106 | |||||
| chr8:39709120
|
A | G | 1 | a0001c0002t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2017+2216A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709120 | ||||||
| chr8:39709135
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2017+2231G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709135 | ||||||
| chr8:39709205
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2017+2301C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709205 | ||||||
| chr8:39709524
|
G | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0194a0001c0001t0001g0226 | 3 | HG00438.hp1 HG00621.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.2017+2620G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709524 | ||||||
| chr8:39709641
|
G | A | 288 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(285): Show | 290 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.2017+2737G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709641 | ||||||
| chr8:39709748
|
T | C | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+2844T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709748 | ||||||
| chr8:39709814
|
T | C | 87 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(84): Show | 88 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2017+2910T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709814 | ||||||
| chr8:39709838
|
A | G | 3 | a0006c0006t0001g0264a0006c0006t0001g0265a0006c0006t0001g0266 | 3 | HG02717.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2017+2934A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709838 | ||||||
| chr8:39710113
|
G | A | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2017+3209G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710113 | ||||||
| chr8:39710189
|
G | C | 1 | a0003c0004t0001g0243 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2017+3285G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710189 | ||||||
| chr8:39710214
|
G | A | 1 | a0001c0012t0001g0005 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2017+3310G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710214 | ||||||
| chr8:39710262
|
G | T | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+3358G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710262 | ||||||
| chr8:39710270
|
C | T | 1 | a0001c0002t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2017+3366C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710270 | ||||||
| chr8:39710299
|
A | C | 14 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(11): Show | 14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017+3395A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710299 | ||||||
| chr8:39710503
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+3599T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710503 | ||||||
| chr8:39710808
|
T | C | 2 | a0001c0002t0001g0053a0001c0002t0001g0100 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2017+3904T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710808 | ||||||
| chr8:39710863
|
A | G | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.2017+3959A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710863 | ||||||
| chr8:39711677
|
T | A | 4 | a0001c0002t0001g0059a0001c0002t0001g0108a0001c0002t0001g0287others(1): Show | 4 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017+4773T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39711677 | ||||||
| chr8:39711925
|
C | T | 1 | a0001c0002t0001g0107 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2017+5021C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39711925 | ||||||
| chr8:39711958
|
C | T | 14 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(11): Show | 14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017+5054C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39711958 | ||||||
| chr8:39711959
|
G | A | 1 | a0003c0004t0001g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2017+5055G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39711959 | ||||||
| chr8:39712003
|
T | G | 1 | a0002c0003t0001g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2017+5099T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712003 | ||||||
| chr8:39712008
|
A | C | 1 | a0001c0002t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2017+5104A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712008 | ||||||
| chr8:39712032
|
G | GC | 159 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(156): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.2017+5137dupC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39712032 | |||||
| chr8:39712147
|
C | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2017+5243C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712147 | ||||||
| chr8:39712158
|
A | C | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2017+5254A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712158 | ||||||
| chr8:39712252
|
C | G | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2017+5348C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712252 | ||||||
| chr8:39712382
|
CAAGAT | C | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+5482_2017+548 others(9): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39712382 | |||||
| chr8:39712431
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2017+5527A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712431 | ||||||
| chr8:39712715
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2017+5811A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712715 | ||||||
| chr8:39712737
|
G | A | 1 | a0003c0004t0001g0243 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2017+5833G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712737 | ||||||
| chr8:39712750
|
G | T | 290 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(287): Show | 292 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.2017+5846G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712750 | ||||||
| chr8:39712823
|
A | G | 175 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(172): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2017+5919A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712823 | ||||||
| chr8:39712912
|
G | C | 102 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 103 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.2017+6008G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712912 | ||||||
| chr8:39713012
|
A | G | 1 | a0002c0003t0001g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2017+6108A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713012 | ||||||
| chr8:39713360
|
C | T | 175 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(172): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2017+6456C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713360 | ||||||
| chr8:39713567
|
C | A | 1 | a0011c0021t0001g0224 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2017+6663C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713567 | ||||||
| chr8:39713682
|
A | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(2): Show | 5 | HG00609.hp1 HG02523.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2017+6778A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713682 | ||||||
| chr8:39713766
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2017+6862G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713766 | ||||||
| chr8:39713767
|
C | CA | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+6865dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39713767 | |||||
| chr8:39713767
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2017+6863C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713767 | ||||||
| chr8:39713774
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2017+6870T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713774 | ||||||
| chr8:39713819
|
A | C | 1 | a0003c0004t0001g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2017+6915A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713819 | ||||||
| chr8:39713841
|
G | A | 14 | a0002c0003t0001g0011a0002c0003t0001g0015a0002c0003t0001g0016others(11): Show | 14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017+6937G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713841 | ||||||
| chr8:39713860
|
A | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017+6956A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713860 | ||||||
| chr8:39714076
|
G | A | 78 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(75): Show | 79 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.2017+7172G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714076 | ||||||
| chr8:39714090
|
C | T | 175 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(172): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2017+7186C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714090 | ||||||
| chr8:39714219
|
C | T | 3 | a0001c0002t0001g0108a0001c0002t0001g0287a0001c0002t0001g0288 | 3 | HG02145.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2017+7315C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714219 | ||||||
| chr8:39714370
|
A | G | 183 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(180): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2017+7466A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714370 | ||||||
| chr8:39714475
|
A | G | 3 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0289 | 3 | HG03041.hp2 HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2017+7571A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714475 | ||||||
| chr8:39714710
|
A | T | 1 | a0004c0005t0001g0309 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2017+7806A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714710 | ||||||
| chr8:39714930
|
G | A | 145 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(142): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.2017+8026G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714930 | ||||||
| chr8:39715230
|
T | C | 291 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(288): Show | 293 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2017+8326T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715230 | ||||||
| chr8:39715357
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2018-8391C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715357 | ||||||
| chr8:39715358
|
G | A | 8 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2018-8390G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715358 | ||||||
| chr8:39715389
|
T | C | 1 | a0001c0001t0001g0302 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2018-8359T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715389 | ||||||
| chr8:39715474
|
G | GA | 174 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(171): Show | 175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2018-8264dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39715474 | |||||
| chr8:39715549
|
C | A | 173 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(170): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.2018-8199C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715549 | ||||||
| chr8:39715579
|
A | G | 1 | a0001c0002t0001g0098 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2018-8169A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715579 | ||||||
| chr8:39715716
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2018-8032C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715716 | ||||||
| chr8:39715887
|
C | T | 7 | a0001c0001t0001g0298a0001c0001t0001g0300a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp1 HG02523.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.2018-7861C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715887 | ||||||
| chr8:39715904
|
G | A | 5 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-7844G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715904 | ||||||
| chr8:39715955
|
C | T | 2 | a0004c0005t0001g0320a0004c0019t0001g0106 | 2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2018-7793C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715955 | ||||||
| chr8:39715956
|
G | A | 145 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(142): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.2018-7792G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715956 | ||||||
| chr8:39716006
|
C | G | 161 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.2018-7742C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716006 | ||||||
| chr8:39716086
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2018-7662C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716086 | ||||||
| chr8:39716105
|
G | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0237a0001c0001t0001g0280 | 3 | NA18612.hp2 NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2018-7643G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716105 | ||||||
| chr8:39716161
|
TTTTG | T | 175 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(172): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2018-7575_2018-757 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39716161 | |||||
| chr8:39716270
|
T | C | 2 | a0001c0002t0001g0053a0001c0002t0001g0100 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2018-7478T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716270 | ||||||
| chr8:39716302
|
C | A | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2018-7446C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716302 | ||||||
| chr8:39716377
|
C | T | 8 | a0003c0004t0001g0210a0003c0004t0001g0212a0003c0004t0001g0215others(5): Show | 8 | HG01192.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2018-7371C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716377 | ||||||
| chr8:39716535
|
A | T | 291 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(288): Show | 293 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2018-7213A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716535 | ||||||
| chr8:39716541
|
C | G | 173 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(170): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.2018-7207C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716541 | ||||||
| chr8:39716662
|
C | A | 1 | a0011c0021t0001g0224 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2018-7086C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716662 | ||||||
| chr8:39716848
|
T | A | 1 | a0001c0001t0001g0300 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2018-6900T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716848 | ||||||
| chr8:39716989
|
G | A | 3 | a0003c0004t0001g0179a0003c0004t0001g0213a0003c0004t0001g0214 | 3 | HG02723.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2018-6759G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716989 | ||||||
| chr8:39716997
|
A | G | 3 | a0001c0002t0001g0108a0001c0002t0001g0287a0001c0002t0001g0288 | 3 | HG02145.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2018-6751A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716997 | ||||||
| chr8:39717125
|
G | A | 1 | a0001c0001t0001g0328 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2018-6623G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717125 | ||||||
| chr8:39717203
|
A | G | 1 | a0011c0021t0001g0224 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2018-6545A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717203 | ||||||
| chr8:39717299
|
T | TTTAG | 287 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(284): Show | 289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.2018-6446_2018-644 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39717299 | |||||
| chr8:39717401
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2018-6347T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717401 | ||||||
| chr8:39717419
|
C | G | 1 | a0001c0002t0001g0067 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2018-6329C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717419 | ||||||
| chr8:39717514
|
C | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0244 | 3 | HG01243.hp2 HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2018-6234C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717514 | ||||||
| chr8:39717609
|
A | C | 7 | a0001c0002t0001g0292a0004c0005t0001g0290a0004c0005t0001g0294others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2018-6139A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717609 | ||||||
| chr8:39717674
|
A | G | 1 | a0002c0003t0001g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2018-6074A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717674 | ||||||
| chr8:39717720
|
A | G | 6 | a0001c0002t0001g0104a0001c0002t0001g0261a0001c0002t0001g0262others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.2018-6028A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717720 | ||||||
| chr8:39717805
|
G | A | 274 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(271): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.2018-5943G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717805 | ||||||
| chr8:39717825
|
A | C | 15 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0018others(12): Show | 15 | HG01192.hp2 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2018-5923A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717825 | ||||||
| chr8:39718042
|
A | T | 1 | a0001c0002t0001g0258 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2018-5706A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718042 | ||||||
| chr8:39718079
|
A | C | 1 | a0005c0011t0001g0188 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2018-5669A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718079 | ||||||
| chr8:39718137
|
C | G | 3 | a0001c0002t0001g0108a0001c0002t0001g0287a0001c0002t0001g0288 | 3 | HG02145.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2018-5611C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718137 | ||||||
| chr8:39718196
|
C | G | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2018-5552C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718196 | ||||||
| chr8:39718334
|
G | A | 292 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(289): Show | 294 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2018-5414G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718334 | ||||||
| chr8:39718529
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2018-5219A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718529 | ||||||
| chr8:39718761
|
A | AAAATACT others(13): Show |
90 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(87): Show | 91 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2018-4985_2018-496 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39718761 | |||||
| chr8:39718761
|
A | AATTT | 3 | a0001c0001t0001g0201a0001c0001t0001g0304a0002c0003t0001g0016 | 3 | HG02886.hp1 NA18969.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2018-4986_2018-498 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39718761 | |||||
| chr8:39719070
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2018-4678C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719070 | ||||||
| chr8:39719324
|
T | C | 9 | a0004c0005t0001g0290a0004c0005t0001g0294a0004c0005t0001g0309others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2018-4424T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719324 | ||||||
| chr8:39719351
|
G | T | 174 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0168others(171): Show | 176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2018-4397G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719351 | ||||||
| chr8:39719408
|
C | T | 4 | a0001c0002t0001g0034a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | NA18955.hp1 NA18957.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-4340C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719408 | ||||||
| chr8:39719443
|
C | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2018-4305C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719443 | ||||||
| chr8:39719533
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2018-4215C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719533 | ||||||
| chr8:39719561
|
A | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-4187A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719561 | ||||||
| chr8:39719784
|
A | G | 319 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(316): Show | 323 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.2018-3964A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719784 | ||||||
| chr8:39719920
|
A | G | 2 | a0001c0002t0001g0053a0001c0002t0001g0100 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2018-3828A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719920 | ||||||
| chr8:39720070
|
AGAT | A | 99 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.2018-3673_2018-367 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39720070 | |||||
| chr8:39720296
|
G | A | 1 | a0003c0004t0001g0243 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2018-3452G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720296 | ||||||
| chr8:39720323
|
G | A | 9 | a0004c0005t0001g0290a0004c0005t0001g0294a0004c0005t0001g0309others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2018-3425G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720323 | ||||||
| chr8:39720395
|
G | A | 2 | a0001c0008t0003g0012a0001c0008t0003g0013 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2018-3353G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720395 | ||||||
| chr8:39720444
|
T | G | 174 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0168others(171): Show | 176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2018-3304T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720444 | ||||||
| chr8:39720660
|
G | A | 94 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(91): Show | 95 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2018-3088G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720660 | ||||||
| chr8:39720780
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2018-2968G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720780 | ||||||
| chr8:39720844
|
A | C | 144 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(141): Show | 146 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.2018-2904A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720844 | ||||||
| chr8:39720855
|
T | C | 1 | a0001c0002t0001g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2018-2893T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720855 | ||||||
| chr8:39721000
|
C | A | 1 | a0001c0012t0001g0005 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2018-2748C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721000 | ||||||
| chr8:39721062
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2018-2686G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721062 | ||||||
| chr8:39721241
|
G | GT | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-2506dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39721241 | |||||
| chr8:39721272
|
A | T | 4 | a0001c0002t0001g0034a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | NA18955.hp1 NA18957.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-2476A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721272 | ||||||
| chr8:39721293
|
A | G | 4 | a0001c0010t0001g0033a0001c0010t0001g0042a0002c0003t0001g0019others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-2455A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721293 | ||||||
| chr8:39721312
|
G | A | 219 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(216): Show | 222 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.2018-2436G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721312 | ||||||
| chr8:39721558
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2018-2190C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721558 | ||||||
| chr8:39721657
|
G | T | 2 | a0001c0002t0001g0060a0001c0002t0001g0061 | 2 | NA18957.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2018-2091G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721657 | ||||||
| chr8:39721660
|
A | G | 5 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(2): Show | 5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-2088A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721660 | ||||||
| chr8:39721670
|
T | C | 1 | a0001c0002t0001g0067 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2018-2078T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721670 | ||||||
| chr8:39721723
|
G | A | 153 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(150): Show | 155 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.2018-2025G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721723 | ||||||
| chr8:39722098
|
G | A | 110 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(107): Show | 111 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2018-1650G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722098 | ||||||
| chr8:39722190
|
C | CGT | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0198others(3): Show | 6 | HG01261.hp2 HG02602.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.2018-1531_2018-153 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722190 | |||||
| chr8:39722190
|
C | CGTGT | 5 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0184others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1533_2018-153 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722190 | |||||
| chr8:39722207
|
GTGTGTGT others(5): Show |
G | 3 | a0004c0005t0001g0316a0004c0022t0001g0192a0008c0024t0001g0211 | 3 | HG02055.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2018-1539_2018-152 others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722207 | |||||
| chr8:39722207
|
GTGTGTGT others(9): Show |
G | 1 | a0004c0005t0001g0320 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2018-1539_2018-152 others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722207 | |||||
| chr8:39722209
|
G | A | 1 | a0004c0005t0001g0309 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018-1539G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722209 | ||||||
| chr8:39722211
|
G | A | 1 | a0004c0005t0001g0309 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018-1537G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722211 | ||||||
| chr8:39722212
|
T | C | 1 | a0004c0005t0001g0309 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018-1536T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722212 | ||||||
| chr8:39722213
|
G | A | 3 | a0004c0005t0001g0290a0004c0005t0001g0309a0004c0019t0001g0106 | 3 | HG02280.hp2 HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2018-1535G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722213 | ||||||
| chr8:39722213
|
GTGTGTAT others(11): Show |
G | 2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2018-1533_2018-151 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722213 | |||||
| chr8:39722213
|
GTGTGTAT others(13): Show |
G | 4 | a0001c0002t0001g0053a0001c0002t0001g0100a0001c0002t0001g0258others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-1533_2018-151 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722213 | |||||
| chr8:39722213
|
GTGTGTAT others(15): Show |
G | 6 | a0001c0002t0001g0255a0002c0003t0001g0015a0002c0003t0001g0016others(3): Show | 6 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2018-1533_2018-151 others(26): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722213 | |||||
| chr8:39722215
|
G | A | 5 | a0004c0005t0001g0290a0004c0005t0001g0294a0004c0005t0001g0309others(2): Show | 5 | HG01167.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1533G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722215 | ||||||
| chr8:39722215
|
GTGTATAT others(11): Show |
G | 1 | a0001c0002t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2018-1531_2018-151 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722215 | |||||
| chr8:39722215
|
GTGTATAT others(15): Show |
G | 5 | a0001c0002t0001g0104a0001c0002t0001g0261a0001c0002t0001g0262others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1531_2018-151 others(26): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722215 | |||||
| chr8:39722216
|
T | C | 2 | a0004c0005t0001g0290a0004c0019t0001g0106 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2018-1532T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722216 | ||||||
| chr8:39722217
|
G | A | 6 | a0001c0002t0001g0082a0004c0005t0001g0290a0004c0005t0001g0294others(3): Show | 6 | HG01167.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2018-1531G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722217 | ||||||
| chr8:39722217
|
G | GTA | 2 | a0001c0002t0001g0004a0001c0002t0001g0110 | 3 | HG03490.hp1 HG03492.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2018-1487_2018-148 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTA | G | 18 | a0001c0001t0001g0135a0001c0001t0001g0167a0001c0001t0001g0181others(15): Show | 18 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2018-1487_2018-148 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATA | G | 25 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0172others(22): Show | 25 | HG00609.hp1 HG00673.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.2018-1489_2018-148 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATA | G | 25 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0197others(22): Show | 26 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2018-1491_2018-148 others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(1): Show |
G | 15 | a0001c0001t0001g0159a0001c0001t0001g0185a0001c0001t0001g0233others(12): Show | 15 | HG00280.hp2 HG01168.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.2018-1493_2018-148 others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(3): Show |
G | 15 | a0001c0001t0001g0187a0001c0001t0001g0191a0001c0001t0001g0218others(12): Show | 15 | HG00544.hp1 HG01192.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2018-1495_2018-148 others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(5): Show |
G | 33 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0168others(30): Show | 33 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.2018-1497_2018-148 others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(7): Show |
G | 11 | a0001c0001t0001g0205a0001c0001t0001g0342a0001c0002t0001g0068others(8): Show | 11 | HG02109.hp2 HG02615.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2018-1499_2018-148 others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(9): Show |
G | 21 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0166others(18): Show | 23 | HG00621.hp1 HG01884.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-1501_2018-148 others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(11): Show |
G | 5 | a0001c0001t0001g0206a0001c0001t0001g0247a0001c0008t0003g0012others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2018-1503_2018-148 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(13): Show |
G | 13 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0030others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.2018-1505_2018-148 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(15): Show |
G | 5 | a0001c0001t0001g0321a0001c0002t0001g0026a0001c0002t0001g0055others(2): Show | 5 | HG01106.hp2 HG01109.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1507_2018-148 others(26): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722217
|
GTATATAT others(17): Show |
G | 82 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(79): Show | 83 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.2018-1509_2018-148 others(28): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | |||||
| chr8:39722218
|
T | C | 2 | a0004c0005t0001g0294a0009c0023t0001g0014 | 2 | HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2018-1530T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722218 | ||||||
| chr8:39722219
|
A | G | 26 | a0001c0001t0001g0173a0001c0001t0001g0182a0001c0001t0001g0183others(23): Show | 26 | HG00438.hp1 HG01074.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.2018-1529A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722219 | ||||||
| chr8:39722221
|
A | G | 35 | a0001c0001t0001g0135a0001c0001t0001g0167a0001c0001t0001g0173others(32): Show | 35 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2018-1527A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722221 | ||||||
| chr8:39722223
|
A | G | 40 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0167others(37): Show | 40 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2018-1525A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722223 | ||||||
| chr8:39722224
|
T | C | 3 | a0004c0005t0001g0316a0004c0022t0001g0192a0008c0024t0001g0211 | 3 | HG02055.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2018-1524T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722224 | ||||||
| chr8:39722225
|
A | G | 51 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0165others(48): Show | 52 | HG00609.hp1 HG00673.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.2018-1523A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722225 | ||||||
| chr8:39722227
|
A | G | 44 | a0001c0001t0001g0159a0001c0001t0001g0165a0001c0001t0001g0169others(41): Show | 45 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2018-1521A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722227 | ||||||
| chr8:39722228
|
T | C | 1 | a0004c0005t0001g0320 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2018-1520T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722228 | ||||||
| chr8:39722229
|
A | G | 38 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0001g0172others(35): Show | 39 | HG00280.hp2 HG00544.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.2018-1519A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722229 | ||||||
| chr8:39722231
|
A | G | 50 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0164others(47): Show | 50 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2018-1517A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722231 | ||||||
| chr8:39722233
|
A | G | 45 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0168others(42): Show | 45 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.2018-1515A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722233 | ||||||
| chr8:39722235
|
A | G | 32 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0166others(29): Show | 34 | HG00621.hp1 HG01884.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.2018-1513A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722235 | ||||||
| chr8:39722237
|
A | G | 25 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0166others(22): Show | 27 | HG00621.hp1 HG02040.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.2018-1511A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722237 | ||||||
| chr8:39722239
|
A | G | 36 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0166others(33): Show | 37 | HG00621.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2018-1509A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722239 | ||||||
| chr8:39722241
|
A | G | 34 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0166others(31): Show | 35 | HG00621.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2018-1507A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722241 | ||||||
| chr8:39722243
|
A | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0330a0001c0002t0001g0026others(1): Show | 4 | HG02165.hp2 HG02602.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-1505A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722243 | ||||||
| chr8:39722315
|
T | TTA | 34 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0166others(31): Show | 35 | HG00621.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2018-1423_2018-142 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722315 | |||||
| chr8:39722402
|
C | T | 1 | a0003c0004t0001g0243 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2018-1346C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722402 | ||||||
| chr8:39722566
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2018-1182A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722566 | ||||||
| chr8:39722627
|
C | A | 1 | a0002c0003t0001g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2018-1121C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722627 | ||||||
| chr8:39722666
|
T | C | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2018-1082T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722666 | ||||||
| chr8:39722692
|
A | G | 1 | a0001c0012t0001g0005 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2018-1056A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722692 | ||||||
| chr8:39722752
|
G | A | 1 | a0001c0002t0001g0263 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2018-996G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722752 | ||||||
| chr8:39722841
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2018-907C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722841 | ||||||
| chr8:39723002
|
G | GA | 318 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(315): Show | 322 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.2018-744dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39723002 | |||||
| chr8:39723085
|
A | G | 1 | a0003c0004t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2018-663A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723085 | ||||||
| chr8:39723143
|
A | G | 59 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0168others(56): Show | 60 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2018-605A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723143 | ||||||
| chr8:39723179
|
AC | A | 108 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(105): Show | 109 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2018-568delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723179 | ||||||
| chr8:39723284
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2018-464C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723284 | ||||||
| chr8:39723485
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-263T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723485 | ||||||
| chr8:39723993
|
T | C | 5 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(2): Show | 5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2177+86T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39723993 | ||||||
| chr8:39724210
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2177+303A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724210 | ||||||
| chr8:39724258
|
C | G | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2177+351C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724258 | ||||||
| chr8:39724258
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2177+351C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724258 | ||||||
| chr8:39724335
|
G | A | 5 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(2): Show | 5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2177+428G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724335 | ||||||
| chr8:39724415
|
T | C | 1 | a0001c0002t0001g0044 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2177+508T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724415 | ||||||
| chr8:39724645
|
A | G | 2 | a0001c0001t0001g0336a0004c0005t0001g0309 | 2 | HG01943.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2177+738A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724645 | ||||||
| chr8:39724676
|
T | C | 318 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(315): Show | 322 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.2177+769T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724676 | ||||||
| chr8:39724700
|
G | A | 1 | a0001c0002t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2177+793G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724700 | ||||||
| chr8:39724847
|
A | G | 94 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(91): Show | 95 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2177+940A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724847 | ||||||
| chr8:39724950
|
A | AT | 317 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(314): Show | 321 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.2177+1049dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr8 | 39724950 | |||||
| chr8:39724957
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2177+1050A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724957 | ||||||
| chr8:39725177
|
C | T | 6 | a0001c0002t0001g0057a0001c0002t0001g0108a0001c0002t0001g0287others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2177+1270C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725177 | ||||||
| chr8:39725202
|
C | T | 59 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(56): Show | 60 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2177+1295C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725202 | ||||||
| chr8:39725325
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2177+1418T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725325 | ||||||
| chr8:39725344
|
G | A | 1 | a0003c0004t0002g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2177+1437G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725344 | ||||||
| chr8:39725352
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2177+1445A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725352 | ||||||
| chr8:39725479
|
C | T | 2 | a0001c0002t0001g0057a0001c0002t0001g0058 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2177+1572C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725479 | ||||||
| chr8:39725520
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2177+1613C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725520 | ||||||
| chr8:39725532
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2177+1625C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725532 | ||||||
| chr8:39725563
|
T | A | 1 | a0001c0002t0001g0075 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2177+1656T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725563 | ||||||
| chr8:39725654
|
T | A | 3 | a0001c0002t0001g0001a0001c0002t0001g0118a0001c0002t0001g0136 | 4 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2177+1747T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725654 | ||||||
| chr8:39725691
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2177+1784T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725691 | ||||||
| chr8:39726073
|
C | T | 4 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2177+2166C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726073 | ||||||
| chr8:39726100
|
G | A | 2 | a0001c0002t0001g0082a0001c0002t0001g0146 | 2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2177+2193G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726100 | ||||||
| chr8:39726187
|
G | A | 145 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(142): Show | 147 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.2177+2280G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726187 | ||||||
| chr8:39726257
|
T | TAC | 143 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(140): Show | 145 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.2177+2368_2177+236 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr8 | 39726257 | |||||
| chr8:39726257
|
TAC | T | 11 | a0004c0005t0001g0290a0004c0005t0001g0294a0004c0005t0001g0309others(8): Show | 11 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2177+2368_2177+236 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr8 | 39726257 | |||||
| chr8:39726278
|
TTG | T | 9 | a0001c0002t0001g0002a0001c0002t0001g0065a0001c0002t0001g0068others(6): Show | 10 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2177+2387_2177+238 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr8 | 39726278 | |||||
| chr8:39726296
|
A | G | 11 | a0001c0002t0001g0045a0001c0002t0001g0085a0001c0002t0001g0086others(8): Show | 11 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2177+2389A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726296 | ||||||
| chr8:39726348
|
A | G | 1 | a0001c0002t0001g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2177+2441A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726348 | ||||||
| chr8:39726359
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0286 | 2 | HG00621.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2177+2452G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726359 | ||||||
| chr8:39726374
|
G | A | 1 | a0001c0002t0001g0048 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2177+2467G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726374 | ||||||
| chr8:39726472
|
A | G | 9 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(6): Show | 9 | HG00738.hp1 HG01081.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2177+2565A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726472 | ||||||
| chr8:39726477
|
G | A | 112 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(109): Show | 113 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2177+2570G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726477 | ||||||
| chr8:39726498
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0277 | 2 | NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2177+2591A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726498 | ||||||
| chr8:39726551
|
T | C | 9 | a0004c0005t0001g0290a0004c0005t0001g0294a0004c0005t0001g0309others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2177+2644T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726551 | ||||||
| chr8:39726586
|
G | A | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2177+2679G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726586 | ||||||
| chr8:39726649
|
C | G | 70 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(67): Show | 71 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2177+2742C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726649 | ||||||
| chr8:39727044
|
A | G | 1 | a0001c0002t0001g0119 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2178-2854A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727044 | ||||||
| chr8:39727251
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2178-2647G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727251 | ||||||
| chr8:39727289
|
C | G | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-2609C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727289 | ||||||
| chr8:39727310
|
C | T | 1 | a0001c0002t0001g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2178-2588C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727310 | ||||||
| chr8:39727335
|
C | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2178-2563C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727335 | ||||||
| chr8:39727657
|
ACTTAACT others(13): Show |
A | 1 | a0005c0016t0001g0156 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2178-2240_2178-222 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727657 | ||||||
| chr8:39727765
|
A | G | 5 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(2): Show | 5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2178-2133A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727765 | ||||||
| chr8:39728024
|
T | C | 1 | a0001c0002t0001g0037 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2178-1874T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728024 | ||||||
| chr8:39728050
|
A | G | 219 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0135others(216): Show | 222 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.2178-1848A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728050 | ||||||
| chr8:39728123
|
A | T | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2178-1775A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728123 | ||||||
| chr8:39728227
|
T | C | 9 | a0004c0005t0001g0290a0004c0005t0001g0294a0004c0005t0001g0309others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2178-1671T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728227 | ||||||
| chr8:39728561
|
T | C | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-1337T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728561 | ||||||
| chr8:39728728
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2178-1170G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728728 | ||||||
| chr8:39728825
|
A | G | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-1073A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728825 | ||||||
| chr8:39728839
|
G | A | 8 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(5): Show | 8 | HG00738.hp1 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2178-1059G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728839 | ||||||
| chr8:39728913
|
A | G | 1 | a0010c0013t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2178-985A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728913 | ||||||
| chr8:39728977
|
C | T | 14 | a0001c0001t0001g0247a0001c0002t0001g0026a0001c0002t0001g0027others(11): Show | 14 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.2178-921C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728977 | ||||||
| chr8:39728993
|
G | A | 5 | a0002c0003t0001g0015a0002c0003t0001g0016a0002c0003t0001g0017others(2): Show | 5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2178-905G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728993 | ||||||
| chr8:39729042
|
T | A | 6 | a0001c0002t0001g0068a0001c0002t0001g0255a0001c0002t0001g0256others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2178-856T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729042 | ||||||
| chr8:39729062
|
C | T | 1 | a0001c0002t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2178-836C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729062 | ||||||
| chr8:39729083
|
C | T | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-815C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729083 | ||||||
| chr8:39729213
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2178-685T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729213 | ||||||
| chr8:39729254
|
G | A | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-644G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729254 | ||||||
| chr8:39729520
|
G | A | 2 | a0001c0001t0001g0300a0001c0001t0001g0302 | 2 | NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2178-378G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729520 |